NOAEL Studies Cosmetic Ingredient

O-PHENYLPHENOL NOAEL Studies

CAS: 90-43-7

Raw No Observed Adverse Effect Level endpoint records grouped by source. This page does not render calculated Margin of Safety values.

California Proposition 65 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
California Proposition 65 California Proposition 65 listing ABcancer listing type - - 2000-08-04 California Proposition 65 listing -
EFSA 7 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EFSA NOAEL =39 mg/kg bw/day Rat oral: unspecified 730 days chronic/long term toxicity EFSA - 2009 - OutputID 1173 - histopathology neoplastic - systemic - Peer review of the pesticide risk assessment of the active substance 2-phenylphenol - doi:10.2903/j.efsa.2009.217r
EFSA NOAEL =100 mg/kg bw/day Rabbit - - reproduction toxicity EFSA - 2009 - OutputID 1173 - body weight - systemic - Peer review of the pesticide risk assessment of the active substance 2-phenylphenol - doi:10.2903/j.efsa.2009.217r
EFSA NOAEL =500 mg/kg bw/day Rat - - reproduction toxicity EFSA - 2009 - OutputID 1173 - reproductive - Peer review of the pesticide risk assessment of the active substance 2-phenylphenol - doi:10.2903/j.efsa.2009.217r
EFSA ADI =0.4 mg/kg bw/day Consumers - - ADI EFSA - 2009 - OutputID 1173 - Consumers - Peer review of the pesticide risk assessment of the active substance 2-phenylphenol - doi:10.2903/j.efsa.2009.217r
EFSA NOAEL =39 mg/kg bw/day Rat oral chronic; 2 years chronic LONG_REF=EFSA (2009). Peer review of the pesticide risk assessment of the active substance 2-phenylphenol. doi:10.2903/j.efsa.2009.217r.; TITLE=Peer review of the pesticide risk assessment of the active substance 2-phenylphenol; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2009.217r; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2009; ORIGINAL_YEAR=2009; TOXICOLOGICAL_EFFECT=histopathology: neoplastic; STUDY_GROUP=EFSA:15617597:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_e9a27c53863e80df78c261e5efb07fef
EFSA NOAEL =100 mg/kg bw/day Rabbit oral - reproduction developmental LONG_REF=EFSA (2009). Peer review of the pesticide risk assessment of the active substance 2-phenylphenol. doi:10.2903/j.efsa.2009.217r.; TITLE=Peer review of the pesticide risk assessment of the active substance 2-phenylphenol; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2009.217r; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2009; ORIGINAL_YEAR=2009; TOXICOLOGICAL_EFFECT=body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=EFSA:15617594:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_4e86175022c56810337452a86874ecb6
EFSA NOAEL =500 mg/kg bw/day Rat oral - reproduction developmental LONG_REF=EFSA (2009). Peer review of the pesticide risk assessment of the active substance 2-phenylphenol. doi:10.2903/j.efsa.2009.217r.; TITLE=Peer review of the pesticide risk assessment of the active substance 2-phenylphenol; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2009.217r; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2009; ORIGINAL_YEAR=2009; STUDY_GROUP=EFSA:15617593:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_ae294a2294bffc4709b2a1fb4d0f2ee3
IARC Monographs 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
IARC Monographs IARC carcinogenicity classification 3 IARC group - - 1998 IARC Monographs -
WHO/JECFA 17 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
WHO/JECFA ADI range:0-0.020.02 mg/kg bw/day - - - Health guidance value document_id=jmpr_jmpmono_v85pr14; title=729. Phenylphenol, 2- and its sodium salt (Pesticide residues in food: 1985 evaluations Part II Toxicology); path=mirror/documents/jmpr/jmpmono/v85pr14.htm; row_hash=4dac8100e487cd7b; raw_unit=mg/kg b.w.; context=ESTIMATE OF TEMPORARY ACCEPTABLE DAILY INTAKE FOR MAN 0-0.02 mg/kg b.w.
WHO/JECFA ADI range:0-0.40.4 mg/kg bw/day Rat - 2-year Health guidance value document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=e8fd575f6e716261; raw_unit=mg/kg bw; context=The Meeting established an ADI of 0-0.4 mg/kg bw for 2-phenylphenol, on the basis of the NOAEL of 39 mg/kg per day in the 2-year study of toxicity (based on decreased body-weight gain and hyperplasia of the urinary bladder) and carcinogenicity of the urinary bladder in male rats and a safety factor of 100.
WHO/JECFA NOAEL =39 mg/kg bw/day - - - Toxicology study document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=19219f39bd545aa0; raw_unit=mg/kg bw per day; context=The NOAEL for toxicity was 800 ppm, equal to 39 mg/kg bw per day, on the basis of reduced body-weight gain and hyperplasia in the urinary bladder at all doses.
WHO/JECFA NOAEL =92 mg/kg bw/day Mouse - - Developmental toxicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=027f3eeecd940b7c; raw_unit=mg/kg bw per day; context=The NOAEL for systemic and developmental toxicity was 92 mg/kg bw per day, on the basis of decreased body weight and morphological lesions in the kidneys, urinary bladder, and ureter and a decrease in pup body weight (Eigenberg, 1995). (ii) Developmental toxicity 2-Phenylphenol and sodium 2-phenylphenol Mice Groups of 20-21 pregnan
WHO/JECFA NOAEL =95 mg/kg bw/day - - - Carcinogenicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=a309c1323e0048a8; raw_unit=mg/kg bw per day; context=The NOAEL was 2500 ppm, equal to 95 mg/kg bw per day, on the basis of urinary bladder tumours at all doses (Hiraga, 1983b;
WHO/JECFA NOAEL =100 mg/kg bw/day - - - Developmental toxicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=ed04f24cabe2434b; raw_unit=mg/kg bw per day; context=The NOAEL was 100 mg/kg bw per day for fetotoxicity and 400 mg/kg bw per day, the highest dose tested, for developmental toxicity (Ogata et al., 1978).
WHO/JECFA NOAEL =150 mg/kg bw/day - - - Developmental toxicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=49f26599ffd868dc; raw_unit=mg/kg bw per day; context=The NOAEL was 150 mg/kg bw per day for maternal toxicity, 300 mg/kg bw per day for fetotoxicity, and 600 mg/kg bw per day, the highest dose tested, for developmental toxicity (Kaneda et al., 1978).
WHO/JECFA NOAEL =180 mg/kg bw/day - - - Toxicology study document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=e08e4ec9b84fda5a; raw_unit=mg/kg bw per day; context=The NOAEL was 2500 ppm, equal to 180 mg/kg bw per day, on the basis of reduced body-weight gain at 5000 ppm (Iguchi et al., 1979;
WHO/JECFA NOAEL =250 mg/kg bw/day - - - Carcinogenicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=b4c6208030a21267; raw_unit=mg/kg bw per day; context=The NOAEL for carcinogenicity was 250 mg/kg bw per day on the basis of an increased incidence of hepatocellular adenomas at 500 mg/kg bw per day (Quast & McGuirk, 1995).
WHO/JECFA NOAEL =270 mg/kg bw/day - - - Carcinogenicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=3c0409dcfb8c1249; raw_unit=mg/kg bw per day; context=The NOAEL was 2500 ppm, equivalent to 270 mg/kg bw per day, on the basis of the increased incidence of urinary bladder tumours (Hiraga & Fujii, 1981).
WHO/JECFA NOAEL =300 mg/kg bw/day - - - Toxicology study document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=d8cea569b34d850f; raw_unit=mg/kg bw per day; context=The NOAEL was 300 mg/kg bw per day (Cosse et al., 1990).
WHO/JECFA NOAEL =460 mg/kg bw/day - - - Reproductive toxicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=c900008bf6056cc8; raw_unit=mg/kg bw per day; context=The NOAEL for reproductive toxicity was 460 mg/kg bw per day and that for carcinogenicity was 36 mg/kg bw per day (Eigenberg, 1990).
WHO/JECFA NOAEL =550 mg/kg bw/day - - - Toxicology study document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=7d51123515cc5aba; raw_unit=mg/kg bw per day; context=The NOAEL was 5000 ppm, equivalent to 550 mg/kg bw per day, on the basis of reduced body-weight gain and increased relative liver weight at 10 000 ppm (Shibata et al., 1985).
WHO/JECFA NOAEL =760 mg/kg bw/day - - - Toxicology study document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=23a7d3ef1d6196c7; raw_unit=mg/kg bw per day; context=The NOAEL was 6300 ppm, equal to 760 mg/kg bw per day, on the basis of reduced body weight and body-weight gain at 13 000 ppm (Iguchi et al., 1984).
WHO/JECFA NOAEL =2100 mg/kg bw/day - - - Developmental toxicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=14b62229d1247e7b; raw_unit=mg/kg bw per day; context=The NOAEL for developmental toxicity was 2100 mg/kg bw per day, the highest dose tested.
WHO/JECFA NOAEL =3000 mg/kg bw/day - - - Carcinogenicity document_id=jmpr_jmpmono_v99pr08; title=Toxicological evaluations; path=mirror/documents/jmpr/jmpmono/v99pr08.htm; row_hash=5d2c3b0f19b5d68b; raw_unit=mg/kg bw per day; context=The NOAEL for carcinogenicity was 20 000 ppm, equal to 3000 mg/kg bw per day, the highest dose tested (Ito, 1983a;
WHO/JECFA ADI <=0.4 mg/kg Human oral - Toxicity Value STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/68c95295e4b02565fc7d2c82; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.who.int/teams/environment-climate-change-and-health/water-sanitation-and-health/chemical-hazards-in-drinking-water; YEAR=2003; ORIGINAL_YEAR=2003; STUDY_GROUP=WHO DWG:15954936:-:--; QC_CATEGORY=Manually extracted from unstructured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_206c98a27f71ccf9e92a4534b7add5b2
NTP ICE acute dermal 5 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE acute dermal EPA classification 3 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=673; Record_ID=acute_dermal_527; Data_Type=In Vivo; Formulation_ID=MIX520; Formulation_Name=Veriguard OD; Percent_Active_Ingredient=15.0; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Dermal Toxicity; Endpoint=EPA classification; Response=3.0; Response_Unit=Unitless; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute dermal EPA classification 4 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=668; Record_ID=acute_dermal_96; Data_Type=In Vivo; Formulation_ID=MIX95; Formulation_Name=Chemsico Aerosol LEG; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Dermal Toxicity; Endpoint=EPA classification; Response=4.0; Response_Unit=Unitless; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute dermal GHS classification 5 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=664; Record_ID=acute_dermal_312; Data_Type=In Vivo; Formulation_ID=MIX305; Formulation_Name=Mediclean Carpet Sanitizer; Percent_Active_Ingredient=4.02; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Dermal Toxicity; Endpoint=GHS classification; Response=5.0; Response_Unit=Unitless; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute dermal LD50 >2000 mg/kg Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=667; Record_ID=acute_dermal_527; Data_Type=In Vivo; Formulation_ID=MIX520; Formulation_Name=Veriguard OD; Percent_Active_Ingredient=15.0; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Dermal Toxicity; Endpoint=LD50; Response_Modifier=>; Response=2000.0; Response_Unit=mg/kg; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute dermal LD50 >5000 mg/kg Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=669; Record_ID=acute_dermal_96; Data_Type=In Vivo; Formulation_ID=MIX95; Formulation_Name=Chemsico Aerosol LEG; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Dermal Toxicity; Endpoint=LD50; Response_Modifier=>; Response=5000.0; Response_Unit=mg/kg; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute inhalation 7 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE acute inhalation EPA Classification 3 unitless - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=1360; Record_ID=acute_inhalation_298; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX378; Formulation_Name=Raid Ant & Roach Killer with Germ Kill CIK; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Inhalation Toxicity; Endpoint=EPA Classification; Response=3; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute inhalation EPA Classification 4 unitless - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=1349; Record_ID=acute_inhalation_440; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX520; Formulation_Name=Veriguard OD; Percent_Active_Ingredient=15.0; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Inhalation Toxicity; Endpoint=EPA Classification; Response=4; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute inhalation LC50 >0.036 mg/L - Inhalation Duration=4 hr In Vivo; AcuteInhalNICEATM; Rat Acute Inhalation Toxicity sheet=Data; excel_row=1348; Record_ID=acute_inhalation_1083; Data_Type=In Vivo; Internal_Data_Source=AcuteInhalNICEATM; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=>; Response=0.036; Response_Unit=mg/L; Reference=REACH; URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/2168/7/3/3/?documentUUID=2c055818-6ebe-445b-a148-666d8d7f478a; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute inhalation LC50 >0.949 mg/L - Inhalation Duration=1 hr In Vivo; AcuteInhalNICEATM; Rat Acute Inhalation Toxicity sheet=Data; excel_row=1357; Record_ID=acute_inhalation_1081; Data_Type=In Vivo; Internal_Data_Source=AcuteInhalNICEATM; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=>; Response=0.949; Response_Unit=mg/L; Reference=REACH; URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/2168/7/3/3/?documentUUID=1450d78a-7992-4513-94af-13e0de39c659; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute inhalation LC50 2.09 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=1354; Record_ID=acute_inhalation_300; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX378; Formulation_Name=Raid Ant & Roach Killer with Germ Kill CIK; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=2.09; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute inhalation LC50 >2.1 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=1355; Record_ID=acute_inhalation_440; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX520; Formulation_Name=Veriguard OD; Percent_Active_Ingredient=15.0; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=>; Response=2.1; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute inhalation LC50 2.16 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=1358; Record_ID=acute_inhalation_491; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX95; Formulation_Name=Chemsico Aerosol LEG; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=2.16; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE acute oral 13 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE acute oral EPA classification =3 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12720; row=3857; data_type=In Vivo; mixture=Mixture; formulation_id=MIX305; formulation_name=Mediclean Carpet Sanitizer; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=4.02; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral EPA classification =4 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12345; row=3866; data_type=In Vivo; mixture=Mixture; formulation_id=MIX95; formulation_name=Chemsico Aerosol LEG; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=0.1; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral EPA classification =4 Unitless Rat (Male) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12878; row=3872; data_type=In Vivo; mixture=Mixture; formulation_id=MIX378; formulation_name=Raid Ant & Roach Killer with Germ Kill CIK; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=0.1; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral GHS classification =4 Unitless Rat (Male/Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12820; row=3884; data_type=In Vivo; mixture=Mixture; formulation_id=MIX650; formulation_name=Orthophenylphenol/Sodium Orthophenylphenate; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=99.9; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral GHS classification =4 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12720; row=3892; data_type=In Vivo; mixture=Mixture; formulation_id=MIX305; formulation_name=Mediclean Carpet Sanitizer; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=4.02; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral GHS classification =5 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12345; row=3871; data_type=In Vivo; mixture=Mixture; formulation_id=MIX95; formulation_name=Chemsico Aerosol LEG; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=0.1; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral GHS classification =5 Unitless Rat (Male) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12878; row=3876; data_type=In Vivo; mixture=Mixture; formulation_id=MIX378; formulation_name=Raid Ant & Roach Killer with Germ Kill CIK; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=0.1; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral LD50 =591 mg/kg bw Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12825; row=3861; data_type=In Vivo; mixture=Mixture; formulation_id=MIX650; formulation_name=Orthophenylphenol/Sodium Orthophenylphenate; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=99.9; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral LD50 =846 mg/kg bw Rat (Male) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12824; row=3869; data_type=In Vivo; mixture=Mixture; formulation_id=MIX650; formulation_name=Orthophenylphenol/Sodium Orthophenylphenate; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=99.9; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral LD50 >2000 mg/kg bw Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_13118; row=3867; data_type=In Vivo; mixture=Mixture; formulation_id=MIX520; formulation_name=Veriguard OD; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=15.0; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral LD50 =2733 mg/kg bw Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12822; row=3862; data_type=In Vivo; mixture=Mixture; formulation_id=MIX650; formulation_name=Orthophenylphenol/Sodium Orthophenylphenate; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=99.9; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral LD50 >5000 mg/kg bw Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12882; row=3858; data_type=In Vivo; mixture=Mixture; formulation_id=MIX378; formulation_name=Raid Ant & Roach Killer with Germ Kill CIK; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=0.1; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE acute oral LD50 >5000 mg/kg bw Rat (Male) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12718; row=3868; data_type=In Vivo; mixture=Mixture; formulation_id=MIX305; formulation_name=Mediclean Carpet Sanitizer; chemical_name=2-Phenylphenol; preferred_name=2-Phenylphenol; percent_active_ingredient=4.02; dtxsid=DTXSID2021151; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID2021151; source_file=acute_oral.xlsx
NTP ICE adme parameters 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE adme parameters Clint 2.077 uL/min/10^6 cells Human - - Measured; httk, Human Hepatic Intrinsic Clearance sheet=Data; excel_row=820; Record_ID=adme_parameters_5; Data_Type=Measured; DTXSID=DTXSID2021151; Assay=httk, Human Hepatic Intrinsic Clearance; Endpoint=Clint; Response=2.077; Response_Unit=ul/min/10^6 cells; Species=Human; Reference=httk2.3.1, Wetmore 2012; URL=https://cran.r-project.org/web/packages/httk/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE adme parameters Fu 0.04105 fraction Human - - Measured; httk, Human Plasma Fraction Unbound sheet=Data; excel_row=819; Record_ID=adme_parameters_5; Data_Type=Measured; DTXSID=DTXSID2021151; Assay=httk, Human Plasma Fraction Unbound; Endpoint=Fu; Response=0.04105; Response_Unit=Unitless Fraction; Species=Human; Reference=httk2.3.1, Wetmore 2012; URL=https://cran.r-project.org/web/packages/httk/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE cancer 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE cancer IARC group 3 unitless - - - WOE; IARC Carcinogenicity sheet=Data; excel_row=2579; Record_ID=cancer_4824; Data_Type=WOE; Formulation_Name=2-Phenylphenol; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=IARC Carcinogenicity; Endpoint=IARC group; Response=3; Response_Unit=Unitless; URL=http://publications.iarc.fr/91; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine 12 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE endocrine AC50 41.37403025207 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=2740; RecordID=ERPathway2016_438; DatasetName=ERPathway2016; DTXSID=DTXSID2021151; Assay=ER Pathway Model, Antagonist; Endpoint=AC50; Response=41.37403025207; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine AC50/EC50/IC50 3430 nM - - - In Vitro; AR Transactivation-Antagonist sheet=Data_invitro; excel_row=13506; Record_ID=endocrine_invitro_4165; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=AR Transactivation-Antagonist; Endpoint=AC50/EC50/IC50; Reported_Response=3430; Reported_Response_Unit=nM; Response=3430; Response_Unit=nM; Reference=Kleinstreuer et al. 2016; 27933809; 10.1021/acs.chemrestox.6b00347|Orton et al. 2011; 21310686; 10.1289/ehp.1002895; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine AC50/EC50/IC50 6300 nM - - - In Vitro; AR Transactivation-Antagonist sheet=Data_invitro; excel_row=13239; Record_ID=endocrine_invitro_4099; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=AR Transactivation-Antagonist; Endpoint=AC50/EC50/IC50; Reported_Response=6300; Reported_Response_Unit=nM; Response=6300; Response_Unit=nM; Reference=Kleinstreuer et al. 2016; 27933809; 10.1021/acs.chemrestox.6b00347|Krüger et al. 2008; 18294747; 10.1016/j.tox.2007.12.028; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine AC50/EC50/IC50 12100 nM - - - In Vitro; AR Transactivation-Antagonist sheet=Data_invitro; excel_row=13241; Record_ID=endocrine_invitro_4100; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=AR Transactivation-Antagonist; Endpoint=AC50/EC50/IC50; Reported_Response=12100; Reported_Response_Unit=nM; Response=12100; Response_Unit=nM; Reference=Kleinstreuer et al. 2016; 27933809; 10.1021/acs.chemrestox.6b00347|Indiveri et al. 2014; 24972338; 10.1016/j.reprotox.2014.06.004; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine ACC 38.34237180221 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=2741; RecordID=ERPathway2016_438; DatasetName=ERPathway2016; DTXSID=DTXSID2021151; Assay=ER Pathway Model, Antagonist; Endpoint=ACC; Response=38.34237180221; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine IC20 49000 nM - - - In Vitro; AR Transactivation-Antagonist sheet=Data_invitro; excel_row=13040; Record_ID=endocrine_invitro_4040; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=AR Transactivation-Antagonist; Endpoint=IC20; Reported_Response=49000; Reported_Response_Unit=IC20 (nM); Response=49000; Response_Unit=nM; Reference=Kleinstreuer et al. 2016; 27933809; 10.1021/acs.chemrestox.6b00347; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine LEL 10000 nM - - - In Vitro; AR Transactivation-Antagonist sheet=Data_invitro; excel_row=14971; Record_ID=endocrine_invitro_4099; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=AR Transactivation-Antagonist; Endpoint=LEL; Reported_Response=10000; Reported_Response_Unit=nM; Response=10000; Response_Unit=nM; Reference=Kleinstreuer et al. 2016; 27933809; 10.1021/acs.chemrestox.6b00347|Krüger et al. 2008; 18294747; 10.1016/j.tox.2007.12.028; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=2736; RecordID=ARPathway2016_1703; DatasetName=ARPathway2016; DTXSID=DTXSID2021151; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine Model Score 0.00543 unitless - - - ERPathway2016; ER Pathway Model, Agonist sheet=Integrated_approaches; excel_row=2742; RecordID=ERPathway2016_438; DatasetName=ERPathway2016; DTXSID=DTXSID2021151; Assay=ER Pathway Model, Agonist; Endpoint=Model Score; Response=0.00543; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine NOEL 1000 mg/kg bw/day Rat Oral Treatment_Duration=10 days; Age_at_First_Dose=PND 55; Age_Ovariectomized_or_Castrated=PND 45; Time_Elapsed_Between_Surgery_and_Treatment=10 days; Time_Elapsed_Between_Last_Dose_and_Necropsy=18 to 36 hours; Number_of_Doses_Tested=7 In Vivo; Hershberger-Agonist sheet=Data_invivo; excel_row=1202; Record_ID=endocrine_invivo_521; Data_Type=In Vivo; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=Hershberger-Agonist; Endpoint=NOEL; Response=1000; Response_Unit=mg/kg/day; Species=Rat; Reported_Strain=Sprague-Dawley; Strain=Sprague-Dawley; Sex=Male (castrated); Route=Oral; Reference_Hormone=Testosterone propionate; Reference_Hormone_Dose=0.4; Reference_Hormone_Dose_Units=mg/kg/day; Reference_Hormone_Route=Subcutaneous; Additional_Information=Browne et al. 2018 unique record identifier 448; Reference=US EPA 2013; Not available; https://www.regulations.gov/document/EPA-HQ-OPP-2013-0524-0010|Browne et al. 2018; 30205136; 10.1016/j.reprotox.2018.08.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine Relative potency 7 % - - - In Vitro; AR Transactivation-Antagonist sheet=Data_invitro; excel_row=15208; Record_ID=endocrine_invitro_4100; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=AR Transactivation-Antagonist; Endpoint=Relative potency; Reported_Response=7; Reported_Response_Unit=%; Response=7; Response_Unit=%; Reference=Kleinstreuer et al. 2016; 27933809; 10.1021/acs.chemrestox.6b00347|Indiveri et al. 2014; 24972338; 10.1016/j.reprotox.2014.06.004; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE endocrine Relative potency 59 % - - - In Vitro; AR Transactivation-Antagonist sheet=Data_invitro; excel_row=15209; Record_ID=endocrine_invitro_4040; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID2021151; Assay=AR Transactivation-Antagonist; Endpoint=Relative potency; Reported_Response=59; Reported_Response_Unit=%; Response=59; Response_Unit=%; Reference=Kleinstreuer et al. 2016; 27933809; 10.1021/acs.chemrestox.6b00347; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE eye irritation 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE eye irritation EPA Classification 1 unitless Rabbit Ocular - In Vivo; Draize Eye Irritation/Corrosion Test sheet=Data; excel_row=748; Record_ID=eye_irritation_1208; Data_Type=In Vivo; Formulation_ID=EyeIrritation6pack_PID1034; Formulation_Name=Veriguard OD; Percent_Active_Ingredient=15.0; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Draize Eye Irritation/Corrosion Test; Endpoint=EPA Classification; Response=1; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE eye irritation EPA Classification 3 unitless Rabbit Ocular - In Vivo; Draize Eye Irritation/Corrosion Test sheet=Data; excel_row=744; Record_ID=eye_irritation_401; Data_Type=In Vivo; Formulation_ID=EyeIrritation6pack_PID222; Formulation_Name=Chemsico Aerosol LEG; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Draize Eye Irritation/Corrosion Test; Endpoint=EPA Classification; Response=3; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE skin irritation 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin irritation EPA classification 1 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=526; Record_ID=skin_irritation_invivo_178; Data_Type=In Vivo; Formulation_ID=MIX650; Formulation_Name=Orthophenylphenol/Sodium Orthophenylphenate; Percent_Active_Ingredient=99.9; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=1; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE skin irritation EPA classification 2 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=522; Record_ID=skin_irritation_invivo_677; Data_Type=In Vivo; Formulation_ID=MIX378; Formulation_Name=Raid Ant & Roach Killer with Germ Kill CIK; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=2; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE skin irritation EPA classification 3 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=524; Record_ID=skin_irritation_invivo_1049; Data_Type=In Vivo; Formulation_ID=MIX95; Formulation_Name=Chemsico Aerosol LEG; Percent_Active_Ingredient=0.1; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=3; Response_Unit=Unitless; Species=Rabbit; Reported_Strain=New Zealand White; Strain=New Zealand White; Sex=Male; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
NTP ICE skin irritation EPA classification 4 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=523; Record_ID=skin_irritation_invivo_855; Data_Type=In Vivo; Formulation_ID=MIX520; Formulation_Name=Veriguard OD; Percent_Active_Ingredient=15; Mixture=Mixture; DTXSID=DTXSID2021151; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=4; Response_Unit=Unitless; Species=Rabbit; Reported_Strain=New Zealand White; Strain=New Zealand White; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID2021151
SCCS Opinion 85 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
SCCS Opinion NOAEL =2 % rat - 2-year carcinogenicity p.94
SCCS Opinion NOAEL =2.5 % rat oral - NOAEL study p.80
SCCS Opinion NOAEL =2.5 % rat oral Sub-chronic repeated dose toxicity p.66
SCCS Opinion NOAEL =4 % rat oral - NOAEL study p.80
SCCS Opinion NOAEL =4 % mouse oral 13-week NOAEL study p.67
SCCS Opinion NOAEL =22.4 mg/kg bw/day rat oral 104-week developmental toxicity p.37
SCCS Opinion NOAEL =25 mg/kg/d rat - developmental developmental toxicity p.35
SCCS Opinion NOAEL =25 mg/kg bw/d - - developmental developmental toxicity p.38
SCCS Opinion NOAEL =25 mg/kg bw/day rat - developmental developmental toxicity p.31
SCCS Opinion NOAEL =25 mg/kg/d rabbit oral developmental reproductive toxicity p.31
SCCS Opinion NOAEL =25 mg/kg bw/d rabbit oral developmental developmental toxicity p.41
SCCS Opinion NOAEL =35 mg/kg bw/d rat oral 2-year reproductive toxicity (Ref. 303), p.32
SCCS Opinion NOAEL =35 mg/kg bw/day - - - reproductive toxicity p.70
SCCS Opinion NOAEL =39 mg/kg bw/d rat oral 2-year reproductive toxicity (Ref. 303), p.32
SCCS Opinion NOAEL =39 mg/kg bw/day rat - chronic carcinogenicity p.35
SCCS Opinion NOAEL =49 mg/kg bw/day rat oral 13 weeks carcinogenicity p.37
SCCS Opinion NOAEL =65 - - - - NOAEL study p.65
SCCS Opinion NOAEL =66 - - - - NOAEL study p.66
SCCS Opinion NOAEL =67 - - - - NOAEL study p.67
SCCS Opinion NOAEL =68 - - - - NOAEL study p.68
SCCS Opinion NOAEL =69 - - - - NOAEL study p.69
SCCS Opinion NOAEL =70 - - - - NOAEL study p.70
SCCS Opinion NOAEL =71 - - - - NOAEL study p.71
SCCS Opinion NOAEL =72 - - - - NOAEL study p.72
SCCS Opinion NOAEL =73 - - - - NOAEL study p.73
SCCS Opinion NOAEL =74 - - - - NOAEL study p.74
SCCS Opinion NOAEL =75 - - - - NOAEL study p.75
SCCS Opinion NOAEL =76 - - - - NOAEL study p.76
SCCS Opinion NOAEL =92 mg/kg/day mouse - - NOAEL study p.25
SCCS Opinion NOAEL =92 mg/kg bw/day rat - chronic reproductive toxicity p.71
SCCS Opinion NOAEL =93 - - - - NOAEL study p.93
SCCS Opinion NOAEL =94 - - - - NOAEL study p.94
SCCS Opinion NOAEL =95 mg/kg bw/day rat dermal 2- year carcinogenicity p.35
SCCS Opinion NOAEL =95 - - - - NOAEL study p.95
SCCS Opinion NOAEL =96 - - - - NOAEL study p.96
SCCS Opinion NOAEL =97 - - - - NOAEL study p.97
SCCS Opinion NOAEL >98 % rat oral 24 months NOAEL study p.24
SCCS Opinion NOAEL =100 mg/kg rabbit - chronic reproductive toxicity p.34
SCCS Opinion NOAEL =100 mg/kg/d rat - developmental developmental toxicity p.35
SCCS Opinion NOAEL =100 mg/kg bw/d rat oral - NOAEL study p.36
SCCS Opinion NOAEL =100 mg/kg bw rat - developmental reproductive toxicity p.37
SCCS Opinion NOAEL =100 % rabbit oral developmental developmental toxicity p.47
SCCS Opinion NOAEL =100 mg/kg bw/day rabbit oral 13-day NOAEL study p.65
SCCS Opinion NOAEL =125 mg/kg bw/day - oral 2-year carcinogenicity p.95
SCCS Opinion NOAEL =150 mg/kg mouse - developmental developmental toxicity p.36
SCCS Opinion NOAEL =150 mg/kg bw/day rat oral Prenatal developmental toxicity p.73
SCCS Opinion NOAEL =200 mg/kg bw/day rat oral Sub-acute repeated dose toxicity p.65
SCCS Opinion NOAEL =224 mg/kg bw/day rat - - carcinogenicity p.102
SCCS Opinion NOAEL =240 mg/kg bw/day mouse dermal 4-week NOAEL study p.69
SCCS Opinion NOAEL =248 mg/kg bw/day - - - NOAEL study p.94
SCCS Opinion NOAEL =250 mg/kg bw/d mouse oral 5d NOAEL study p.26
SCCS Opinion NOAEL =250 mg/kg bw/day rat oral chronic carcinogenicity p.35
SCCS Opinion NOAEL =269 mg/kg bw/day rat - 2-year carcinogenicity p.93
SCCS Opinion NOAEL >300 mg/kg/day mouse oral 5d NOAEL study p.26
SCCS Opinion NOAEL =300 mg/kg bw/d rat oral 9 days NOAEL study p.36
SCCS Opinion NOAEL =300 mg/kg bw/day rat oral Prenatal developmental toxicity p.73
SCCS Opinion NOAEL =353 mg/kg bw/day rat oral 13-week NOAEL study p.68
SCCS Opinion NOAEL =395 mg/kg bw/day rat - 2-year carcinogenicity p.96
SCCS Opinion NOAEL =400 mg/ kg bw/ day mouse oral Prenatal developmental toxicity p.76
SCCS Opinion NOAEL =457 mg/kg rat - - reproductive toxicity p.33
SCCS Opinion NOAEL =457 mg/kg bw/day - - - reproductive toxicity p.70
SCCS Opinion NOAEL =490 mg/kg bw/day rat oral - reproductive toxicity p.70
SCCS Opinion NOAEL =500 mg/kg bw/d - - chronic reproductive toxicity p.34
SCCS Opinion NOAEL =500 mg/kg bw/day dog oral Chronic NOAEL study p.67
SCCS Opinion NOAEL =600 mg/kg bw/d mouse oral developmental developmental toxicity p.36
SCCS Opinion NOAEL =600 mg/kg bw/day rat oral Developmental developmental toxicity p.74
SCCS Opinion NOAEL =625 mg/kg bw/day rat oral 13-week NOAEL study p.68
SCCS Opinion NOAEL =700 mg/kg bw/day rat oral Developmental developmental toxicity p.74
SCCS Opinion NOAEL =750 mg/ kg bw/day rabbit oral Prenatal developmental toxicity p.74
SCCS Opinion NOAEL =761 mg/kg bw/day rat oral 3 months NOAEL study p.66
SCCS Opinion NOAEL =770 mg/kg bw/day rat - - NOAEL study p.96
SCCS Opinion NOAEL =1000 mg/kg bw/day rat oral 3 months NOAEL study p.66
SCCS Opinion NOAEL =1200 mg/kg bw/day rat oral Prenatal developmental toxicity p.74
SCCS Opinion NOAEL =1450 mg/kg bw/day mouse - - reproductive toxicity p.73
SCCS Opinion NOAEL =1500 mg/kg bw/day - - 36 weeks carcinogenicity p.96
SCCS Opinion NOAEL =1865 mg/kg bw/day mouse dermal 4-week repeated dose toxicity p.69
SCCS Opinion NOAEL =2000 mg/kg bw/day rat dermal 52-week NOAEL study p.97
SCCS Opinion NOAEL =2100 mg/kg bw/day mouse oral Developmental reproductive toxicity p.72
SCCS Opinion NOAEL =3009 mg/kg bw/day mouse - - NOAEL study p.95
SCCS Opinion NOAEL =3081 mg/kg bw/day - oral 96-week NOAEL study p.94
SCCS Opinion NOAEL =4294 mg/kg bw/day mouse oral Sub-chronic repeated dose toxicity p.67
SCCS Opinion NOAEL =5375 mg/kg bw/day rat oral 13-week NOAEL study p.68
SCCS Opinion NOAEL =10000 mg/kg bw/day rat oral Sub-acute repeated dose toxicity p.65
SCCS Opinion NOAEL =10000 ppm rat - 2-year carcinogenicity p.93
SCCS Opinion NOAEL =20000 ppm - oral 2-year carcinogenicity p.95
EPA ToxRefDB v3 13 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EPA ToxRefDB v3 LEL =100 mg/kg bw/day rabbit (new zealand white; New Zealand White) oral 7 GD to 19 GD DEV study_id=753; toxval_study_source_id=studyid753_Adult_F0_F_systemic; toxval_effect_list=in life observation-clinical signs-discharge on cageboard|in life observation-clinical signs-urine, discoloration|pathology microscopic-stomach-hemorrhage|in life observation-clinical signs-abnormal feces|in life observation-mortality-mortality|pathology microscopic-stomach-ulcer|in life observation-clinical signs-perineal soiling|pathology microscopic-kidney-inflammation|pathology microscopic-kidney-degeneration; dose_level=2; study_year=1991; study_citation=Zablotny, C.; Breslin, W.; Kociba, R. (1991) Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits. Lab Project Number: K-001024-045. Unpublished Study Prepared By Dow Chemical Co., Health and Env. Sciences. 309 P.; dsstox_substance_id=DTXSID2021151; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =140 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 15 weeks (premating) to 2 generation MGR study_id=756; toxval_study_source_id=studyid756_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-urinary bladder-cellular alteration|in life observation-body weight-body weight|pathology microscopic-urinary bladder-hyperplasia; dose_level=2; study_year=1990; study_citation=Eigenberg, D. (1990) Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02. Unpublished study prepared by Mobay Corp. 2696 p.; dsstox_substance_id=DTXSID2021151; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =250 mg/kg bw/day mouse (b6c3f1; B6C3F1) oral 0 day to 24 month CHR study_id=759; toxval_study_source_id=studyid759_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-liver-accentuated lobular pattern|urinalysis-specific gravity/osmolality-specific gravity/osmolality|organ weight-kidney-relative to body weight|organ weight-liver-relative to body weight|organ weight-brain-relative to body weight|organ weight-liver-absolute|in life observation-body weight-body weight gain|organ weight-brain-absolute|organ weight-adrenal gland-relative to body weight; dose_level=1; study_year=1995; study_citation=Quast, J.; Mcguirk, R. (1995) Ortho-Phenylphenol: Two-Year Dietary Chronic Toxicity/Oncogenicity Study In B6C3F1 Mice: Lab Project Number: K-001024-047. Unpublished Study Prepared By The Dow Chemical Co. 1089 P.; dsstox_substance_id=DTXSID2021151; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =300 mg/kg bw/day rat (sprague dawley; Sprague Dawley) oral 6 GD to 15 GD DEV study_id=755; toxval_study_source_id=studyid755_Adult_F0_F_systemic; toxval_effect_list=in life observation-food consumption-food efficiency|in life observation-food consumption-food consumption|in life observation-body weight-body weight gain|organ weight-liver-absolute|organ weight-liver-relative to body weight; dose_level=2; study_year=1978; study_citation=John, J.; Murray, F.; Crawford, A. et al. (1978) Phase 3 Reformat Of MRIDs 00067616 and 00164362: The Effect(s) Of Orally Administered Orthophenylphenol On Rat Embryonal And Fetal Development: Project Het-K-0001024-33(R). *see study comment*; dsstox_substance_id=DTXSID2021151; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =377 mg/kg bw/day rat (fischer; Fischer 344) oral 0 day to 90 day SUB study_id=752; toxval_study_source_id=studyid752_Adult_F0_M_systemic; toxval_effect_list=organ weight-kidney-relative to body weight|organ weight-liver-relative to body weight|organ weight-testes-relative to body weight|in life observation-body weight-body weight gain|in life observation-water consumption-water consumption|organ weight-brain-relative to body weight|in life observation-body weight-body weight|organ weight-urinary bladder-absolute|organ weight-lung-relative to body weight|organ weight-spleen-relative to body weight|organ weight-adrenal gland-relative to body weight|in life observation-food consumption-food consumption; dose_level=1; study_year=1981; study_citation=Nakamura, K.; Iguchi, S.; Hiraga, K. (1982; reformatted 1990) Dow Chemical U S A Phase 3 Reformat Of Mrid 40760207. Subacute Toxicity Of O-Phenylphenol By Food Administration To Male Rats. Prepared By Tokyo Metropolitan Research Lab. 25 P.; dsstox_substance_id=DTXSID2021151; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =490 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 15 weeks (premating) to 2 generation MGR study_id=756; toxval_study_source_id=studyid756_Adult_F1_F_systemic; toxval_effect_list=in life observation-body weight-body weight; dose_level=3; study_year=1990; study_citation=Eigenberg, D. (1990) Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02. Unpublished study prepared by Mobay Corp. 2696 p.; dsstox_substance_id=DTXSID2021151; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL >700 mg/kg bw/day rat (sprague dawley; Sprague Dawley) oral 6 GD to 15 GD DEV study_id=755; toxval_study_source_id=studyid755_Fetal_Fetal_MF_NA; dose_level=3; study_year=1978; study_citation=John, J.; Murray, F.; Crawford, A. et al. (1978) Phase 3 Reformat Of MRIDs 00067616 and 00164362: The Effect(s) Of Orally Administered Orthophenylphenol On Rat Embryonal And Fetal Development: Project Het-K-0001024-33(R). *see study comment*; dsstox_substance_id=DTXSID2021151; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LOAEL =250 mg/kg bw/day rabbit (new zealand white; New Zealand White) oral 7 GD to 19 GD DEV study_id=753; toxval_study_source_id=studyid753_Adult_F0_F_systemic; toxval_effect_list=in life observation-clinical signs-abnormal feces|in life observation-mortality-mortality|in life observation-clinical signs-perineal soiling; dose_level=3; study_year=1991; study_citation=Zablotny, C.; Breslin, W.; Kociba, R. (1991) Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits. Lab Project Number: K-001024-045. Unpublished Study Prepared By Dow Chemical Co., Health and Env. Sciences. 309 P.; dsstox_substance_id=DTXSID2021151; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LOAEL =763 mg/kg bw/day rat (fischer; Fischer 344) oral 0 day to 90 day SUB study_id=752; toxval_study_source_id=studyid752_Adult_F0_M_systemic; toxval_effect_list=in life observation-body weight-body weight gain|in life observation-body weight-body weight; dose_level=2; study_year=1981; study_citation=Nakamura, K.; Iguchi, S.; Hiraga, K. (1982; reformatted 1990) Dow Chemical U S A Phase 3 Reformat Of Mrid 40760207. Subacute Toxicity Of O-Phenylphenol By Food Administration To Male Rats. Prepared By Tokyo Metropolitan Research Lab. 25 P.; dsstox_substance_id=DTXSID2021151; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL >0 mg/kg bw/day rat (fischer; Fischer 344) oral 0 day to 90 day SUB study_id=752; toxval_study_source_id=studyid752_Adult_F0_M_systemic; toxval_effect_list=organ weight-adrenal gland-relative to body weight|organ weight-brain-relative to body weight|organ weight-liver-relative to body weight|organ weight-urinary bladder-absolute|in life observation-body weight-body weight|organ weight-lung-relative to body weight|in life observation-water consumption-water consumption|organ weight-spleen-relative to body weight|organ weight-kidney-relative to body weight|in life observation-food consumption-food consumption|organ weight-testes-relative to body weight|in life observation-body weight-body weight gain; dose_level=0; study_year=1981; study_citation=Nakamura, K.; Iguchi, S.; Hiraga, K. (1982; reformatted 1990) Dow Chemical U S A Phase 3 Reformat Of Mrid 40760207. Subacute Toxicity Of O-Phenylphenol By Food Administration To Male Rats. Prepared By Tokyo Metropolitan Research Lab. 25 P.; dsstox_substance_id=DTXSID2021151; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL =25 mg/kg bw/day rabbit (new zealand white; New Zealand White) oral 7 GD to 19 GD DEV study_id=753; toxval_study_source_id=studyid753_Adult_F0_F_systemic; toxval_effect_list=in life observation-clinical signs-abnormal feces|in life observation-clinical signs-urine, discoloration|pathology microscopic-stomach-hemorrhage|pathology microscopic-kidney-degeneration|in life observation-clinical signs-discharge on cageboard|pathology microscopic-stomach-ulcer|in life observation-clinical signs-perineal soiling|in life observation-mortality-mortality|pathology microscopic-kidney-inflammation; dose_level=1; study_year=1991; study_citation=Zablotny, C.; Breslin, W.; Kociba, R. (1991) Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits. Lab Project Number: K-001024-045. Unpublished Study Prepared By Dow Chemical Co., Health and Env. Sciences. 309 P.; dsstox_substance_id=DTXSID2021151; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL =40 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 15 weeks (premating) to 2 generation MGR study_id=756; toxval_study_source_id=studyid756_Adult_F0_F_systemic; toxval_effect_list=in life observation-body weight-body weight|pathology microscopic-urinary bladder-cellular alteration|pathology microscopic-urinary bladder-hyperplasia; dose_level=1; study_year=1990; study_citation=Eigenberg, D. (1990) Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02. Unpublished study prepared by Mobay Corp. 2696 p.; dsstox_substance_id=DTXSID2021151; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL =100 mg/kg bw/day rat (sprague dawley; Sprague Dawley) oral 6 GD to 15 GD DEV study_id=755; toxval_study_source_id=studyid755_Adult_F0_F_systemic; toxval_effect_list=in life observation-food consumption-food efficiency|organ weight-liver-relative to body weight|organ weight-liver-absolute|in life observation-body weight-body weight gain|in life observation-food consumption-food consumption; dose_level=1; study_year=1978; study_citation=John, J.; Murray, F.; Crawford, A. et al. (1978) Phase 3 Reformat Of MRIDs 00067616 and 00164362: The Effect(s) Of Orally Administered Orthophenylphenol On Rat Embryonal And Fetal Development: Project Het-K-0001024-33(R). *see study comment*; dsstox_substance_id=DTXSID2021151; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxValDB ECOTOX 7 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB ECOTOX LOEL =2 % diet Rat oral chronic; 168 days chronic LONG_REF=Cancer Lett.48(1): 19-28 Shibata,M.A., H. Tanaka, M. Yamada, S. Tamano, and S. Fukushima Proliferative Response of Renal Pelvic Epithelium in Rats to Oral Administration of Ortho-Phenylphenol, Sodium Ortho-Phenylphenate and Diphenyl 1989; TITLE=Proliferative Response of Renal Pelvic Epithelium in Rats to Oral Administration of Ortho-Phenylphenol, Sodium Ortho-Phenylphenate and Diphenyl; AUTHOR=Shibata,M.A., H. Tanaka, M. Yamada, S. Tamano, and S. Fukushima; DOI=10.1016/0304-3835(89)90198-5; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=96226; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1989; ORIGINAL_YEAR=1989; TOXICOLOGICAL_EFFECT=Genetics: DNA synthesis rate|Growth: Weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|other; STUDY_GROUP=ECOTOX:15599614:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=da703b8d02e579ee447e59ad31052880
ToxValDB ECOTOX LOEL =300 mg/kg bw/day Rat oral short-term; 10 days short-term LONG_REF=- | J. Pestic. Sci.3:365-370 Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol 1978; TITLE=Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol; AUTHOR=Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=35292; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1978; ORIGINAL_YEAR=1978; TOXICOLOGICAL_EFFECT=Growth: Weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ECOTOX:15613586:F:-adult; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; Source overall passed QC, and this record was expert reviewed and revised from ECOTOX source; QC_STATUS=pass; SOURCE_HASH=0a05aa302b8ded8b4db4472b879b9233
ToxValDB ECOTOX LOEL =2000 mg/kg bw/day Mouse oral acute; 1 days acute LONG_REF=Mutat. Res.395(2/3): 189-198 Sasaki,Y.F., A. Saga, M. Akasaka, K. Yoshida, E. Nishidate, Y.Q. Su, N. Matsusaka, and S. Tsuda In Vivo Genotoxicity of Ortho-Phenylphenol, Biphenyl, and Thiabendazole Detected in Multiple Mouse Organs by the Alkaline Single Cell Gel Electrophoresis Assay 1997; TITLE=In Vivo Genotoxicity of Ortho-Phenylphenol, Biphenyl, and Thiabendazole Detected in Multiple Mouse Organs by the Alkaline Single Cell Gel Electrophoresis Assay; AUTHOR=Sasaki,Y.F., A. Saga, M. Akasaka, K. Yoshida, E. Nishidate, Y.Q. Su, N. Matsusaka, and S. Tsuda; DOI=10.1016/s1383-5718(97)00168-x; QUALITY=Control type: Carrier or solvent control; EXTERNAL_SOURCE_ID=95361; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=Genetics: Damage; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECOTOX:15595032:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=4ace0dc5f4e412cb24c65d32410a3ec9
ToxValDB ECOTOX NOEL =2 % Rat oral subchronic; 56 days subchronic LONG_REF=Toxicol. Appl. Pharmacol.99(1): 37-49 Shibata,M.A., M. Yamada, H. Tanaka, M. Kagawa, and S. Fukushima Changes in Urine Composition, Bladder Epithelial Morphology, and DNA Synthesis in Male F344 Rats in Response to Ingestion of Bladder Tumor Promoters 1989; TITLE=Changes in Urine Composition, Bladder Epithelial Morphology, and DNA Synthesis in Male F344 Rats in Response to Ingestion of Bladder Tumor Promoters; AUTHOR=Shibata,M.A., M. Yamada, H. Tanaka, M. Kagawa, and S. Fukushima; DOI=10.1016/0041-008x(89)90109-9; QUALITY=Control type: Multiple entries; EXTERNAL_SOURCE_ID=106692; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1989; ORIGINAL_YEAR=1989; TOXICOLOGICAL_EFFECT=Biochemistry: pH|Genetics: DNA synthesis rate; TOXICOLOGICAL_EFFECT_CATEGORY=other|urinalysis; STUDY_GROUP=ECOTOX_dup_EPA ORD_15609983_15609984:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=586be227872d146791bfdd5325b149c7
ToxValDB ECOTOX NOEL =150 mg/kg bw/day Mouse oral short-term; 10 days short-term LONG_REF=- | J. Pestic. Sci.3:365-370 Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol 1978; TITLE=Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol; AUTHOR=Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=35292; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1978; ORIGINAL_YEAR=1978; TOXICOLOGICAL_EFFECT=Material body weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ECOTOX:15613426:F:-adult; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; Source overall passed QC, and this record was expert reviewed and revised from ECOTOX source; QC_STATUS=pass; SOURCE_HASH=9250b3f31bcaf169662e3ecd7029616d
ToxValDB ECOTOX NOEL =300 mg/kg bw/day Rat oral short-term; 10 days reproduction developmental LONG_REF=- | J. Pestic. Sci.3:365-370 Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol 1978; TITLE=Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol; AUTHOR=Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=35292; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1978; ORIGINAL_YEAR=1978; TOXICOLOGICAL_EFFECT=Fetus: Growth: Weight | Fetus: Morphology: External, skeletal, and internal abnormalities; TOXICOLOGICAL_EFFECT_CATEGORY=development; STUDY_GROUP=ECOTOX:15613587:M/F:-fetus; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; Source overall passed QC, and this record was expert reviewed and revised from ECOTOX source; QC_STATUS=pass; SOURCE_HASH=38ba2be1c58182567716a5bf8e5c57ea
ToxValDB ECOTOX NOEL =500 mg/kg bw/day Mouse oral short-term; 5 days developmental LONG_REF=- | J. Pestic. Sci.3:365-370 Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol 1978; TITLE=Teratogenicity and Dominant-Lethal Studies with o-Phenylphenol; AUTHOR=Kaneda,M., S. Teramoto, A. Shingu, and Y. Shirasu; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=35292; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1978; ORIGINAL_YEAR=1978; TOXICOLOGICAL_EFFECT=Genetics: Dominant lethal mutations; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECOTOX:15613427:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; Source overall passed QC, and this record was expert reviewed and revised from ECOTOX source; QC_STATUS=pass; SOURCE_HASH=465474ae15945053ea03a498113965fd
ToxValDB GESTIS DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB GESTIS DNEL DNEL systemic =19.25 mg/m3 Human inhalation - Toxicity Value STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6543dd69e4b045b9ff7cd87e; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.dguv.de/ifa/gestis/gestis-dnel-liste/index-2.jsp; STUDY_GROUP=GESTIS DNEL:15630089:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_bfe5d964f4d74e614ef056286ceabcc0
ToxValDB ToxRefDB 11 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB ToxRefDB LEL =140 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Eigenberg, D. (1990) Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02. Unpublished study prepared by Mobay Corp. 2696 p.; TITLE=Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02; AUTHOR=Eigenberg, D; EXTERNAL_SOURCE_ID=756; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-urinary bladder-cellular alteration|systemic: in life observation-body weight-body weight|systemic: pathology microscopic-urinary bladder-hyperplasia; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15682384_15682385_15682386_15682387:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_28dde25ea774fce8bf28d3a1f496a3d4
ToxValDB ToxRefDB LEL >250 mg/kg bw/day Rabbit oral short-term (developmental); 13 days developmental LONG_REF=Zablotny, C.; Breslin, W.; Kociba, R. (1991) Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits. Lab Project Number: K-001024-045. Unpublished Study Prepared By Dow Chemical Co., Health & Env. Sciences. 309 P.; TITLE=Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits; AUTHOR=Zablotny, C.; Breslin, W.; Kociba, R; EXTERNAL_SOURCE_ID=753; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; STUDY_GROUP=ToxRefDB_dup_-_15682372_15682373_15682374_15682375:M/F:fetusfetal; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_1897b45e6aa8564791fdfff9e4748f3d
ToxValDB ToxRefDB LEL =300 mg/kg bw/day Dog oral chronic; 52 weeks chronic LONG_REF=Cosse, P.; Stebbins, K.; Stott, W.; Et Al. (1990) Ortho-Phenylphen- Ol: Palatability/Probe, Four-Week And One-Year Oral Toxicity Studies In Beagle Dogs: Lab Project Number: K-001024-038: K-001024-038A: K-001024-039. Unpublished Study Prepared By Dow Chemi; TITLE=Ortho-Phenylphen- Ol: Palatability/Probe, Four-Week And One-Year Oral Toxicity Studies In Beagle Dogs: Lab Project Number: K-001024-038: K-001024-038A: K-001024-039; AUTHOR=Cosse, P.; Stebbins, K.; Stott, W.; Et Al; EXTERNAL_SOURCE_ID=757; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: in life observation-food consumption-food consumption|systemic: in life observation-body weight-body weight gain|systemic: in life observation-food consumption-food efficiency|systemic: in life observation-clinical signs-emesis; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|food and/or water consumption; STUDY_GROUP=ToxRefDB_dup_-_15682416_15682417_15682418_15682419:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_f405ea706e2281fef7129695aa40f9a3
ToxValDB ToxRefDB LEL =377 mg/kg bw/day Rat oral subchronic; 90 days subchronic LONG_REF=Nakamura, K.; Iguchi, S.; Hiraga, K. (1982; reformatted 1990) Dow Chemical U S A Phase 3 Reformat Of Mrid 40760207. Subacute Toxicity Of O-Phenylphenol By Food Administration To Male Rats. Prepared By Tokyo Metropolitan Research Lab. 25 P.; TITLE=Dow Chemical U S A Phase 3 Reformat Of Mrid 40760207. Subacute Toxicity Of O-Phenylphenol By Food Administration To Male Rats; AUTHOR=Nakamura, K.; Iguchi, S.; Hiraga, K; EXTERNAL_SOURCE_ID=752; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1981; ORIGINAL_YEAR=1981; TOXICOLOGICAL_EFFECT=systemic: organ weight-kidney-relative to body weight|systemic: organ weight-liver-relative to body weight|systemic: in life observation-water consumption-water consumption|systemic: organ weight-brain-relative to body weight|systemic: organ weight-testes-relative to body weight|systemic: in life observation-body weight-body weight|systemic: in life observation-body weight-body weight gain|systemic: organ weight-urinary bladder-absolute|systemic: organ weight-lung-relative to body weight|systemic: organ weight-adrenal gland-relative to body weight|systemic: organ weight-spleen-relative to body weight|systemic: in life observation-food consumption-food consumption; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|organ weight; STUDY_GROUP=ToxRefDB_dup_-_15682365_15682366_15682367:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_83639ecc1c1e75922c5a3051525a6b46
ToxValDB ToxRefDB LEL =490 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Eigenberg, D. (1990) Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02. Unpublished study prepared by Mobay Corp. 2696 p.; TITLE=Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02; AUTHOR=Eigenberg, D; EXTERNAL_SOURCE_ID=756; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ToxRefDB_dup_-_15682392_15682393_15682394_15682395:F:F1adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_2b63a819b5d955eec22dfae90a291861
ToxValDB ToxRefDB LEL >700 mg/kg bw/day Rat oral short-term (developmental); 10 days developmental LONG_REF=John, J.; Murray, F.; Crawford, A. et al. (1978) Phase 3 Reformat Of MRIDs 00067616 and 00164362: The Effect(s) Of Orally Administered Orthophenylphenol On Rat Embryonal And Fetal Development: Project Het-K-0001024-33(R). *see study comment*; TITLE=Phase 3 Reformat Of MRIDs 00067616 and 00164362: The Effect(s) Of Orally Administered Orthophenylphenol On Rat Embryonal And Fetal Development; AUTHOR=John, J.; Murray, F.; Crawford, A. et al; EXTERNAL_SOURCE_ID=755; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1978; ORIGINAL_YEAR=1978; STUDY_GROUP=ToxRefDB_dup_-_15682380_15682381_15682382_15682383:M/F:fetusfetal; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_e099b8589b524662f096e94fea690388
ToxValDB ToxRefDB LOAEL =250 mg/kg bw/day Rabbit oral short-term (developmental); 13 days reproduction developmental LONG_REF=Zablotny, C.; Breslin, W.; Kociba, R. (1991) Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits. Lab Project Number: K-001024-045. Unpublished Study Prepared By Dow Chemical Co., Health & Env. Sciences. 309 P.; TITLE=Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits; AUTHOR=Zablotny, C.; Breslin, W.; Kociba, R; EXTERNAL_SOURCE_ID=753; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=systemic: in life observation-mortality-mortality|systemic: in life observation-clinical signs-perineal soiling|systemic: in life observation-clinical signs-abnormal feces; TOXICOLOGICAL_EFFECT_CATEGORY=clinical signs|mortality/survival; STUDY_GROUP=ToxRefDB_dup_-_15682368_15682369_15682370_15682371:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_e0e5d4bb29878f8e632ae2ec1587914f
ToxValDB ToxRefDB LOAEL =763 mg/kg bw/day Rat oral subchronic; 90 days subchronic LONG_REF=Nakamura, K.; Iguchi, S.; Hiraga, K. (1982; reformatted 1990) Dow Chemical U S A Phase 3 Reformat Of Mrid 40760207. Subacute Toxicity Of O-Phenylphenol By Food Administration To Male Rats. Prepared By Tokyo Metropolitan Research Lab. 25 P.; TITLE=Dow Chemical U S A Phase 3 Reformat Of Mrid 40760207. Subacute Toxicity Of O-Phenylphenol By Food Administration To Male Rats; AUTHOR=Nakamura, K.; Iguchi, S.; Hiraga, K; EXTERNAL_SOURCE_ID=752; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1981; ORIGINAL_YEAR=1981; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight|systemic: in life observation-body weight-body weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ToxRefDB_dup_-_15682365_15682366_15682367:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_f8c96ff9ad9466808cde749898cc8955
ToxValDB ToxRefDB NEL =25 mg/kg bw/day Rabbit oral short-term (developmental); 13 days reproduction developmental LONG_REF=Zablotny, C.; Breslin, W.; Kociba, R. (1991) Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits. Lab Project Number: K-001024-045. Unpublished Study Prepared By Dow Chemical Co., Health & Env. Sciences. 309 P.; TITLE=Ortho-Phenylphenol (OPP): Gavage Teratology Study In New Zealand White Rabbits; AUTHOR=Zablotny, C.; Breslin, W.; Kociba, R; EXTERNAL_SOURCE_ID=753; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=systemic: in life observation-clinical signs-urine, discoloration|systemic: pathology microscopic-kidney-degeneration|systemic: pathology microscopic-stomach-ulcer|systemic: in life observation-clinical signs-perineal soiling|systemic: in life observation-mortality-mortality|systemic: in life observation-clinical signs-abnormal feces|systemic: pathology microscopic-stomach-hemorrhage|systemic: pathology microscopic-kidney-inflammation|systemic: in life observation-clinical signs-discharge on cageboard; TOXICOLOGICAL_EFFECT_CATEGORY=clinical signs|mortality/survival|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15682368_15682369_15682370_15682371:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_9faf77e6c44882609e18111b5011d160
ToxValDB ToxRefDB NEL =40 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Eigenberg, D. (1990) Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02. Unpublished study prepared by Mobay Corp. 2696 p.; TITLE=Two-Generation Dietary Reproduction Study in Rats Using Orthophenyl Phenol: Lab Project Number: 85-671-02; AUTHOR=Eigenberg, D; EXTERNAL_SOURCE_ID=756; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight|systemic: pathology microscopic-urinary bladder-cellular alteration|systemic: pathology microscopic-urinary bladder-hyperplasia; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15682384_15682385_15682386_15682387:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_fb3c6feb3e37a07c61c349e62b78a207
ToxValDB ToxRefDB NEL =100 mg/kg bw/day Rat oral short-term (developmental); 10 days reproduction developmental LONG_REF=John, J.; Murray, F.; Crawford, A. et al. (1978) Phase 3 Reformat Of MRIDs 00067616 and 00164362: The Effect(s) Of Orally Administered Orthophenylphenol On Rat Embryonal And Fetal Development: Project Het-K-0001024-33(R). *see study comment*; TITLE=Phase 3 Reformat Of MRIDs 00067616 and 00164362: The Effect(s) Of Orally Administered Orthophenylphenol On Rat Embryonal And Fetal Development; AUTHOR=John, J.; Murray, F.; Crawford, A. et al; EXTERNAL_SOURCE_ID=755; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1978; ORIGINAL_YEAR=1978; TOXICOLOGICAL_EFFECT=systemic: in life observation-food consumption-food efficiency|systemic: organ weight-liver-absolute|systemic: organ weight-liver-relative to body weight|systemic: in life observation-body weight-body weight gain|systemic: in life observation-food consumption-food consumption; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|organ weight; STUDY_GROUP=ToxRefDB_dup_-_15682376_15682377_15682378_15682379:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_0d1d3f86d9ead8a2ffe3dfda507da1c6
ToxValDB Uterotrophic Hershberger DB 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB Uterotrophic Hershberger DB NOEL =250 mg/kg bw/day Rat oral short-term; 10 days Hershberger LONG_REF=O-phenylphenol: Data Evaluation Records (DERs) for EDSP Tier 1 Assays Docket Number: EPA-HQ-OPP-2013-0524. Available at: http://www.regulations.gov/contentStreamer?documentId=EPA-HQ-OPP-2013-0524-0010&disposition=attachment&contentType=pdf; TITLE=O-phenylphenol: Data Evaluation Records (DERs) for EDSP Tier 1 Assays Docket Number: EPA-HQ-OPP-2013-0524; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759abc7e4b0a7c65d37b40a; RECORD_SOURCE_LEVEL=Extraction document; TOXICOLOGICAL_EFFECT=inactive|Negative|Negative|anti-androgenic|decrease in ASTs, NS (1.6 d) delay PPS; accompanied by "minor" increase in liver wt and 8% decrease in BW; NOTE AR binding and ARTA (OSRI) positive; STUDY_GROUP=Uterotrophic Hershberger DB:15714277:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_64e8869c42950b46a900bee46f4d1c23
Regulatory source 157 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
Regulatory source - 2 % - oral 96-week - p.94
Regulatory source - 2.5 % rat oral - - p.80
Regulatory source - 2.5 % rat oral 13-week - p.66
Regulatory source - 4 % rat oral - - p.80
Regulatory source - 4 % - - 13 weeks - p.80
Regulatory source - 4 % mouse oral 13-week - p.67
Regulatory source - 4 % rat oral 13-week - p.68
Regulatory source - 65 - - - - - p.65
Regulatory source - 66 - - - - - p.66
Regulatory source - 67 - - - - - p.67
Regulatory source - 68 - - - - - p.68
Regulatory source - 69 - - - - - p.69
Regulatory source - 70 - - - - - p.70
Regulatory source - 71 - - - - - p.71
Regulatory source - 72 - - - - - p.72
Regulatory source - 73 - - - - - p.73
Regulatory source - 74 - - - - - p.74
Regulatory source - 75 - - - - - p.75
Regulatory source - 76 - - - - - p.76
Regulatory source - 92 mg/kg/day mouse - - - p.25
Regulatory source - 93 - - - - - p.93
Regulatory source - 94 - - - - - p.94
Regulatory source - 95 - - - - - p.95
Regulatory source - 96 - - - - - p.96
Regulatory source - 97 - - - - - p.97
Regulatory source - >98 % rat oral 24 months - p.24
Regulatory source - 100 mg/kg bw/d rat oral - - p.36
Regulatory source - 100 % - oral - - p.48
Regulatory source - 100 mg/kg bw/day rabbit oral 13-day - p.65
Regulatory source - 100 mg/kg bw/day dog oral 4-week - p.65
Regulatory source - 100 mg/kg bw/day dog oral 1 year - p.67
Regulatory source - 200 mg/kg bw/day rat oral 6 months - p.66
Regulatory source - 200 mg/kg bw/day dog oral Chronic - p.67
Regulatory source - 200 mg/kg bw/day rat oral 32-day - p.65
Regulatory source - 200 mg/kg bw/day dog oral 1-year - p.67
Regulatory source - 224 mg/kg bw/day rat - - - p.96
Regulatory source - 240 mg/kg bw/day mouse dermal 4-week - p.69
Regulatory source - 248 mg/kg bw/day - - - - p.94
Regulatory source - 250 mg/kg bw/d mouse oral 5d - p.26
Regulatory source - >300 mg/kg/day mouse oral 5d - p.26
Regulatory source - 300 mg/kg bw/d rat oral 9 days - p.36
Regulatory source - 300 mg/kg bw/day dog oral 4-week - p.65
Regulatory source - 300 mg/kg bw/day dog oral 1 year - p.67
Regulatory source - 353 mg/kg bw/day rat oral 13-week - p.68
Regulatory source - 500 mg/kg bw/day dog oral Chronic - p.67
Regulatory source - 500 mg/kg bw/day rat oral 6 months - p.66
Regulatory source - 500 mg/kg bw/day dog oral 1-year - p.67
Regulatory source - 625 mg/kg bw/day rat oral 13-week - p.68
Regulatory source - 761 mg/kg bw/day rat oral 3 months - p.66
Regulatory source - 761 mg/kg bw/day rat oral 13-week - p.66
Regulatory source - 770 mg/kg bw/day rat - - - p.96
Regulatory source - 1000 mg/kg bw/day rat oral 3 months - p.66
Regulatory source - 1000 mg/kg bw/day rabbit oral 13-day - p.65
Regulatory source - 1000 mg/kg bw/day rat - - - p.97
Regulatory source - 2000 mg/kg bw/day rat dermal 52-week - p.97
Regulatory source - 2000 mg/kg bw/day rat oral 1-month - p.65
Regulatory source - 2000 mg/kg bw/day rat oral 3 months - p.66
Regulatory source - 2000 mg/kg bw/day rat oral 4-week - p.67
Regulatory source - 2000 mg/kg bw/day rat oral 90-day - p.68
Regulatory source - 3009 mg/kg bw/day mouse - - - p.95
Regulatory source - 3081 mg/kg bw/day - oral 96-week - p.94
Regulatory source - 4294 mg/kg bw/day mouse oral 13-week - p.67
Regulatory source - 5375 mg/kg bw/day rat oral 13-week - p.68
Regulatory source - 5375 mg/kg bw/day - - - - p.68
Regulatory source carcinogenicity 2 % rat - 2-year carcinogenicity p.94
Regulatory source carcinogenicity 2.5 % rat oral 91-week carcinogenicity p.93
Regulatory source carcinogenicity 4 % rat oral 91-week carcinogenicity p.95
Regulatory source carcinogenicity 39 mg/kg bw/day rat - chronic carcinogenicity p.35
Regulatory source carcinogenicity 39 mg/kg bw/day rat - 91-week carcinogenicity p.35
Regulatory source carcinogenicity 49 mg/kg bw/day rat oral 13 weeks carcinogenicity p.37
Regulatory source carcinogenicity 49 mg/kg bw/day rat - 2-year carcinogenicity p.93
Regulatory source carcinogenicity 49 mg/kg bw/day rat - - carcinogenicity p.99
Regulatory source carcinogenicity 95 mg/kg bw/day rat dermal 2- year carcinogenicity p.35
Regulatory source carcinogenicity 95 mg/kg bw/day rat - 56-week carcinogenicity p.96
Regulatory source carcinogenicity 95 mg/kg bw/day rat oral 2-year carcinogenicity p.96
Regulatory source carcinogenicity 100 mg/kg bw/day rat dermal 2-year carcinogenicity p.94
Regulatory source carcinogenicity 100 mg/kg bw/day rat - 2-year carcinogenicity p.94
Regulatory source carcinogenicity 125 mg/kg bw/day - oral 2-year carcinogenicity p.95
Regulatory source carcinogenicity 125 mg/kg bw/day rat oral 91-week carcinogenicity p.95
Regulatory source carcinogenicity 224 mg/kg bw/day rat - - carcinogenicity p.102
Regulatory source carcinogenicity 250 mg/kg bw/day rat oral chronic carcinogenicity p.35
Regulatory source carcinogenicity 250 mg/kg bw/day rat oral 2-year carcinogenicity p.93
Regulatory source carcinogenicity 250 mg/kg bw/day rat - - carcinogenicity p.98
Regulatory source carcinogenicity 250 mg/kg bw/day mouse - 2-year carcinogenicity p.93
Regulatory source carcinogenicity 269 mg/kg bw/day rat - 2-year carcinogenicity p.93
Regulatory source carcinogenicity 269 mg/kg bw/day rat oral 91-week carcinogenicity p.93
Regulatory source carcinogenicity 395 mg/kg bw/day rat - 2-year carcinogenicity p.96
Regulatory source carcinogenicity 1000 mg/kg bw/day mouse oral Chronic carcinogenicity p.93
Regulatory source carcinogenicity 1000 mg/kg bw/day mouse - 2-year carcinogenicity p.93
Regulatory source carcinogenicity 1500 mg/kg bw/day - - 36 weeks carcinogenicity p.96
Regulatory source carcinogenicity 3009 mg/kg bw/day mouse - - carcinogenicity p.95
Regulatory source carcinogenicity 10000 ppm rat - 2-year carcinogenicity p.93
Regulatory source carcinogenicity 20000 ppm - oral 2-year carcinogenicity p.95
Regulatory source carcinogenicity 20000 ppm rat oral 2-year carcinogenicity p.96
Regulatory source carcinogenicity 20000 ppm - - 112-week carcinogenicity p.96
Regulatory source developmental toxicity 22.4 mg/kg bw/day rat oral 104-week developmental toxicity p.37
Regulatory source developmental toxicity 25 mg/kg/d rat - developmental developmental toxicity p.35
Regulatory source developmental toxicity 25 mg/kg bw/d rat - Developmental developmental toxicity p.37
Regulatory source developmental toxicity 25 mg/kg bw/d - - developmental developmental toxicity p.38
Regulatory source developmental toxicity 25 mg/kg bw/d rabbit - developmental developmental toxicity p.47
Regulatory source developmental toxicity =25 mg/kg bw/d rabbit oral developmental developmental toxicity p.47
Regulatory source developmental toxicity 25 mg/kg bw/day rat - developmental developmental toxicity p.31
Regulatory source developmental toxicity 25 mg/kg bw/d rat - 104-week developmental toxicity p.37
Regulatory source developmental toxicity 25 mg/kg bw/day - - developmental developmental toxicity p.76
Regulatory source developmental toxicity 100 mg/kg/d rat - developmental developmental toxicity p.35
Regulatory source developmental toxicity 100 mg/kg bw rat - Developmental developmental toxicity p.37
Regulatory source developmental toxicity 100 % rabbit oral developmental developmental toxicity p.47
Regulatory source developmental toxicity 150 mg/kg mouse - developmental developmental toxicity p.36
Regulatory source developmental toxicity 150 mg/kg bw/day rat oral Prenatal developmental toxicity p.73
Regulatory source developmental toxicity 150 mg/kg bw/day rat oral 9 days developmental toxicity p.74
Regulatory source developmental toxicity 250 mg/kg bw/day rabbit oral Prenatal developmental toxicity p.74
Regulatory source developmental toxicity 250 mg/kg bw/day - - developmental developmental toxicity p.76
Regulatory source developmental toxicity 300 mg/kg bw/day rat oral Prenatal developmental toxicity p.73
Regulatory source developmental toxicity 400 mg/ kg bw/ day mouse oral Prenatal developmental toxicity p.76
Regulatory source developmental toxicity 600 mg/kg bw/d mouse oral developmental developmental toxicity p.36
Regulatory source developmental toxicity 600 mg/kg bw/day rat oral Developmental developmental toxicity p.74
Regulatory source developmental toxicity 700 mg/kg bw/day rat oral Developmental developmental toxicity p.74
Regulatory source developmental toxicity 700 mg/kg bw/day rat oral Prenatal developmental toxicity p.73
Regulatory source developmental toxicity 750 mg/ kg bw/day rabbit oral Prenatal developmental toxicity p.74
Regulatory source developmental toxicity 1200 mg/kg bw/day rat oral Prenatal developmental toxicity p.74
Regulatory source developmental toxicity 1450 mg/kg bw/day mouse oral Prenatal developmental toxicity p.72
Regulatory source irritation 100 mg/kg bw/day rat dermal 21-day irritation p.69
Regulatory source irritation 1000 mg/kg bw/day rat dermal 21-day irritation p.69
Regulatory source repeated dose toxicity 2.5 % rat oral Sub-chronic repeated dose toxicity p.66
Regulatory source repeated dose toxicity 100 mg/kg bw/day rat oral 1 year repeated dose toxicity p.67
Regulatory source repeated dose toxicity 200 mg/kg bw/day rat oral Sub-acute repeated dose toxicity p.65
Regulatory source repeated dose toxicity 200 mg/kg bw/day rat oral 1-year repeated dose toxicity p.67
Regulatory source repeated dose toxicity 1865 mg/kg bw/day mouse dermal 4-week repeated dose toxicity p.69
Regulatory source repeated dose toxicity 4294 mg/kg bw/day mouse oral Sub-chronic repeated dose toxicity p.67
Regulatory source repeated dose toxicity 10000 mg/kg bw/day rat oral Sub-acute repeated dose toxicity p.65
Regulatory source reproductive toxicity 25 mg/kg bw/d mouse oral developmental reproductive toxicity p.50
Regulatory source reproductive toxicity 25 mg/kg bw/day rabbit - developmental reproductive toxicity p.31
Regulatory source reproductive toxicity 25 mg/kg/d rabbit - developmental reproductive toxicity p.31
Regulatory source reproductive toxicity 25 mg/kg/d rabbit oral developmental reproductive toxicity p.31
Regulatory source reproductive toxicity 25 mg/kg bw/day rat - developmental reproductive toxicity p.44
Regulatory source reproductive toxicity 35 mg/kg bw/d rat oral 2-year reproductive toxicity p.32
Regulatory source reproductive toxicity 35 mg/kg bw/day - - - reproductive toxicity p.70
Regulatory source reproductive toxicity 35 mg/kg bw/day rat oral - reproductive toxicity p.70
Regulatory source reproductive toxicity 39 mg/kg bw/d rat oral 2-year reproductive toxicity p.32
Regulatory source reproductive toxicity 92 mg/kg bw/day rat - chronic reproductive toxicity p.71
Regulatory source reproductive toxicity 92 mg/kg bw/day - - chronic reproductive toxicity p.71
Regulatory source reproductive toxicity 92 mg/kg bw/day rat oral chronic reproductive toxicity p.71
Regulatory source reproductive toxicity 100 mg/kg rabbit - chronic reproductive toxicity p.34
Regulatory source reproductive toxicity 100 mg/kg bw rat - developmental reproductive toxicity p.37
Regulatory source reproductive toxicity 100 mg/kg bw/day - - developmental reproductive toxicity p.75
Regulatory source reproductive toxicity 100 mg/kg bw/day rabbit oral Prenatal reproductive toxicity p.75
Regulatory source reproductive toxicity 100 mg/kg bw/day mouse oral Prenatal reproductive toxicity p.76
Regulatory source reproductive toxicity 250 mg/kg bw/day rabbit oral Prenatal reproductive toxicity p.75
Regulatory source reproductive toxicity 457 mg/kg rat - - reproductive toxicity p.33
Regulatory source reproductive toxicity 457 mg/kg bw/day - - - reproductive toxicity p.70
Regulatory source reproductive toxicity 457 mg/kg bw/day - oral - reproductive toxicity p.71
Regulatory source reproductive toxicity 490 mg/kg bw/day rat oral - reproductive toxicity p.70
Regulatory source reproductive toxicity 500 mg/kg bw/d - - chronic reproductive toxicity p.34
Regulatory source reproductive toxicity 500 mg/kg bw/day - - - reproductive toxicity p.75
Regulatory source reproductive toxicity 500 mg/kg bw/day rat oral chronic reproductive toxicity p.71
Regulatory source reproductive toxicity 1450 mg/kg bw/day mouse - - reproductive toxicity p.73
Regulatory source reproductive toxicity 2100 mg/kg bw/day mouse oral Developmental reproductive toxicity p.72
openFDA substances 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier D343Z75HT8 UNII - - - chemical -