NOAEL Studies Preservative

Bronopol NOAEL Studies

INCI: BRONOPOL

CAS: 52-51-7

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

ECHA 14 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ECHA LOAEL 32 mg/kg bw/day rat oral: drinking water - chronic toxicity: oral dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=64ba93f7-ee96-4fde-8152-432c2b7639e2_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=64ba93f7-ee96-4fde-8152-432c2b7639e2/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1976; basis=other:; key_result=false; entry_uuid=8776867a-f722-43ff-a65d-9896c5259620
ECHA LOAEL 30 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=0563d001-43ca-4878-8762-dc9da8af6b62_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=0563d001-43ca-4878-8762-dc9da8af6b62/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=2007; ReportDate=2007-08-29; basis=body weight and weight gain; key_result=false; entry_uuid=5430293e-7b64-47fc-b9e0-b85611fc6dcb
ECHA LOAEL 80 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=cbbd8bd3-f134-445c-86fc-ef57b1180440_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=cbbd8bd3-f134-445c-86fc-ef57b1180440/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1991; key_result=false; entry_uuid=a127140e-8053-4072-9b09-b1b7a39eea87
ECHA LOAEL 20 mg/kg bw/day dog oral: gavage - sub-chronic toxicity: oral dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=fd464039-b739-4769-aa92-92b653d9cc31_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=fd464039-b739-4769-aa92-92b653d9cc31/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1973; basis=clinical signs; key_result=false; entry_uuid=b239c166-3ba0-4917-9c95-04754d3be0de
ECHA NOAEL 80 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=c307ce9b-01ba-4b69-9c99-5fe403c49e87_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=c307ce9b-01ba-4b69-9c99-5fe403c49e87/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1995; basis=other:; key_result=false; entry_uuid=64a96da7-be5a-4811-9843-56ba7eaa9c00
ECHA NOAEL <=25 mg/kg bw/day rat oral: drinking water - two-generation reproductive toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=39ff1bab-5675-4dd5-8ca5-8f4b1a1f29b9_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=39ff1bab-5675-4dd5-8ca5-8f4b1a1f29b9/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1987; basis=other:; key_result=true; upper_value=25; entry_uuid=476efed8-2f67-4cbf-bb92-2644107cd66b
ECHA NOAEL 200 mg/kg bw/day rat oral: drinking water - two-generation reproductive toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=39ff1bab-5675-4dd5-8ca5-8f4b1a1f29b9_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=39ff1bab-5675-4dd5-8ca5-8f4b1a1f29b9/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1987; basis=reproductive performance; key_result=true; entry_uuid=425d9ab3-bcd7-4c3d-b559-6af06129aeb6
ECHA NOAEL 7 mg/kg bw/day rat oral: drinking water - chronic toxicity: oral dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=64ba93f7-ee96-4fde-8152-432c2b7639e2_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=64ba93f7-ee96-4fde-8152-432c2b7639e2/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1976; basis=other:; key_result=true; entry_uuid=94c8ee1e-f752-4652-a2b6-6aeba8d0ef2b
ECHA NOAEL 10 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=0563d001-43ca-4878-8762-dc9da8af6b62_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=0563d001-43ca-4878-8762-dc9da8af6b62/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=2007; ReportDate=2007-08-29; basis=other:; key_result=false; entry_uuid=f8c05edd-6139-496a-bbd8-681f8286f7ec
ECHA NOAEL <=20 mg/kg bw/day rat oral: gavage - sub-chronic toxicity: oral dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=a35a557b-af5c-4a73-822f-b2fca2dd15a4_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=a35a557b-af5c-4a73-822f-b2fca2dd15a4/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1973; basis=gross pathology; key_result=true; upper_value=20; entry_uuid=8b33ca23-7d1b-4750-aa9e-946c53da63df
ECHA NOAEL 100 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=5d140647-15f6-4de4-adda-0b3a8fc6bf41_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=5d140647-15f6-4de4-adda-0b3a8fc6bf41/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1993; key_result=false; entry_uuid=e44f1fc4-99e0-491c-8790-5dc629243fbc
ECHA NOAEL 40 mg/kg bw/day rat oral: gavage - one-generation reproductive toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=113d71f3-95f1-4b86-bb03-d9aac592b2e8_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=113d71f3-95f1-4b86-bb03-d9aac592b2e8/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1973; basis=reproductive performance; key_result=true; entry_uuid=02846427-925f-4166-a711-d01da3be67dc
ECHA NOAEL 50 mg/kg bw/day rat oral: drinking water - two-generation reproductive toxicity dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=7c6d339c-011a-45b6-a149-0690e81083a5_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=7c6d339c-011a-45b6-a149-0690e81083a5/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=2008; ReportDate=2008-03-13; basis=reproductive performance; key_result=false; entry_uuid=ca6f88d7-e24f-426b-abe7-25311aba2f64
ECHA NOAEL 8 mg/kg bw/day dog oral: gavage - sub-chronic toxicity: oral dossier=81cda80a-4c7b-4607-a16c-682a3631da5d.i6z; document=fd464039-b739-4769-aa92-92b653d9cc31_81cda80a-4c7b-4607-a16c-682a3631da5d.i6d; document_key=fd464039-b739-4769-aa92-92b653d9cc31/81cda80a-4c7b-4607-a16c-682a3631da5d; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1973; basis=clinical signs; key_result=true; entry_uuid=59ac2e94-6895-4cad-942c-1aea83086902
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=2162; Record_ID=acute_dermal_8; Data_Type=In Vivo; Formulation_ID=MIX8; Formulation_Name=Acticide LA 2605-F; Percent_Active_Ingredient=5.3; Mixture=Mixture; DTXSID=DTXSID8024652; 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/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute dermal EPA classification 4 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=2166; Record_ID=acute_dermal_368; Data_Type=In Vivo; Formulation_ID=MIX361; Formulation_Name=Preventol P 91; Percent_Active_Ingredient=9.97; Mixture=Mixture; DTXSID=DTXSID8024652; 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/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute dermal GHS classification 5 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=2168; Record_ID=acute_dermal_8; Data_Type=In Vivo; Formulation_ID=MIX8; Formulation_Name=Acticide LA 2605-F; Percent_Active_Ingredient=5.3; Mixture=Mixture; DTXSID=DTXSID8024652; 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/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute dermal LD50 >5000 mg/kg Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=2163; Record_ID=acute_dermal_406; Data_Type=In Vivo; Formulation_ID=MIX400; Formulation_Name=Rocima 586; Percent_Active_Ingredient=7.5; Mixture=Mixture; DTXSID=DTXSID8024652; 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/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute dermal LD50 >2000 mg/kg Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=2165; Record_ID=acute_dermal_8; Data_Type=In Vivo; Formulation_ID=MIX8; Formulation_Name=Acticide LA 2605-F; Percent_Active_Ingredient=5.3; Mixture=Mixture; DTXSID=DTXSID8024652; 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/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
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=4568; Record_ID=acute_inhalation_293; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX361; Formulation_Name=Preventol P 91; Percent_Active_Ingredient=9.97; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Rat Acute Inhalation Toxicity; Endpoint=EPA Classification; Response=3; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute inhalation EPA Classification 2 unitless - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=4570; Record_ID=acute_inhalation_29; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX8; Formulation_Name=Acticide LA 2605-F; Percent_Active_Ingredient=5.3; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Rat Acute Inhalation Toxicity; Endpoint=EPA Classification; Response=2; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute inhalation GHS Classification 4 unitless - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=4575; Record_ID=acute_inhalation_329; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX400; Formulation_Name=Rocima 586; Percent_Active_Ingredient=7.5; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Rat Acute Inhalation Toxicity; Endpoint=GHS Classification; Response=4; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute inhalation LC50 1.69 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=4572; Record_ID=acute_inhalation_329; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX400; Formulation_Name=Rocima 586; Percent_Active_Ingredient=7.5; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=1.69; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute inhalation LC50 0.21 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=4574; Record_ID=acute_inhalation_29; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX8; Formulation_Name=Acticide LA 2605-F; Percent_Active_Ingredient=5.3; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=0.21; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute inhalation LC50 >5 mg/L - Inhalation Duration=6 hr In Vivo; AcuteInhalNICEATM; Rat Acute Inhalation Toxicity sheet=Data; excel_row=4576; Record_ID=acute_inhalation_2996; Data_Type=In Vivo; Internal_Data_Source=AcuteInhalNICEATM; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=>; Response=5; Response_Unit=mg/L; Reference=ChemIDplus; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute inhalation LC50 range0.52 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=4577; Record_ID=acute_inhalation_293; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX361; Formulation_Name=Preventol P 91; Percent_Active_Ingredient=9.97; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=range; Response=>0.52 and <2.05; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE acute oral 5 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE acute oral EPA classification =2 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12189; row=13788; data_type=In Vivo; mixture=Mixture; formulation_id=MIX8; formulation_name=Acticide LA 2605-F; chemical_name=Bronopol; preferred_name=Bronopol; percent_active_ingredient=5.3; dtxsid=DTXSID8024652; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID8024652; source_file=acute_oral.xlsx
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_12959; row=13792; data_type=In Vivo; mixture=Mixture; formulation_id=MIX400; formulation_name=Rocima 586; chemical_name=Bronopol; preferred_name=Bronopol; percent_active_ingredient=7.5; dtxsid=DTXSID8024652; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID8024652; 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_12860; row=13789; data_type=In Vivo; mixture=Mixture; formulation_id=MIX361; formulation_name=Preventol P 91; chemical_name=Bronopol; preferred_name=Bronopol; percent_active_ingredient=9.97; dtxsid=DTXSID8024652; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID8024652; source_file=acute_oral.xlsx
NTP ICE acute oral LD50 =1030 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_12860; row=13786; data_type=In Vivo; mixture=Mixture; formulation_id=MIX361; formulation_name=Preventol P 91; chemical_name=Bronopol; preferred_name=Bronopol; percent_active_ingredient=9.97; dtxsid=DTXSID8024652; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID8024652; 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_12959; row=13787; data_type=In Vivo; mixture=Mixture; formulation_id=MIX400; formulation_name=Rocima 586; chemical_name=Bronopol; preferred_name=Bronopol; percent_active_ingredient=7.5; dtxsid=DTXSID8024652; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID8024652; source_file=acute_oral.xlsx
NTP ICE dart 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE dart LOEL 80 mg/kg bw/day Rabbit Oral - In Vivo; DART, In life observation sheet=Data; excel_row=123115; Record_ID=dart_8049; Data_Type=In Vivo; DTXSID=DTXSID8024652; Assay=DART, In life observation; Endpoint=LOEL; Response=80; Response_Unit=mg/kg/day; Species=Rabbit; Strain=New Zealand White; Sex=Female; Life_Stage=Adult; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C3540840;CUI;Sign or Symptom|UMLS;C0011135;CUI;Defecation; Reference=ToxRefDB v2 , ID = 6181; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE dart LOEL 80 mg/kg bw/day Rabbit Oral - In Vivo; DART, Developmental malformation sheet=Data; excel_row=123117; Record_ID=dart_8174; Data_Type=In Vivo; DTXSID=DTXSID8024652; Assay=DART, Developmental malformation; Endpoint=LOEL; Response=80; Response_Unit=mg/kg/day; Species=Rabbit; Strain=New Zealand White; Sex=Male/Female; Life_Stage=Fetal; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C0000768;CUI;Congenital Abnormality|UMLS;C0265509;CUI;Congenital anomaly of skeletal bone|UMLS;C1282719;CUI;Incomplete ossification; Reference=ToxRefDB v2 , ID = 6181; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE dart LOEL 40 mg/kg bw/day Rabbit Oral - In Vivo; DART, In life observation sheet=Data; excel_row=123118; Record_ID=dart_10214; Data_Type=In Vivo; DTXSID=DTXSID8024652; Assay=DART, In life observation; Endpoint=LOEL; Response=40; Response_Unit=mg/kg/day; Species=Rabbit; Strain=New Zealand White; Sex=Female; Life_Stage=Adult; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C0005910;CUI;Body Weight|UMLS;C3540840;CUI;Sign or Symptom|UMLS;C0005910;CUI;Body Weight; Reference=ToxRefDB v2 , ID = 6645; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE endocrine 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=5760; RecordID=ARPathway2016_1275; DatasetName=ARPathway2016; DTXSID=DTXSID8024652; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE eye irritation 1 endpoint
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=2447; Record_ID=eye_irritation_968; Data_Type=In Vivo; Formulation_ID=EyeIrritation6pack_PID822; Formulation_Name=Rocima 586; Percent_Active_Ingredient=7.5; Mixture=Mixture; DTXSID=DTXSID8024652; 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/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin irritation 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin irritation EPA classification 2 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=1643; Record_ID=skin_irritation_invivo_378; Data_Type=In Vivo; Formulation_ID=MIX361; Formulation_Name=Preventol P 91; Percent_Active_Ingredient=9.97; Mixture=Mixture; DTXSID=DTXSID8024652; 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/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin irritation EPA classification 1 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=1645; Record_ID=skin_irritation_invivo_892; Data_Type=In Vivo; Formulation_ID=MIX400; Formulation_Name=Rocima 586; Percent_Active_Ingredient=7.5; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=1; Response_Unit=Unitless; Species=Rabbit; Reported_Strain=New Zealand White; Strain=New Zealand White; Sex=Male/Female; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization 11 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin sensitization Concentration, 5% incidence of positive responses 2.114 % Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7758; Record_ID=skin_sensitization_invivo_1755; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Concentration, 5% incidence of positive responses; Response=2.114; Response_Unit=%; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1973; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Concentration, one positive response 0.4545 % Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7754; Record_ID=skin_sensitization_invivo_1755; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Concentration, one positive response; Response=0.4545; Response_Unit=%; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1973; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization GHS Classification 1 unitless Guinea pig Dermal - In Vivo; SkinSensitization6pack; Guinea Pig Maximization/Buehler sheet=Data_invivo; excel_row=730; Record_ID=skin_sensitization_invivo_25; Data_Type=In Vivo; Internal_Data_Source=SkinSensitization6pack; Formulation_ID=MIX8; Formulation_Name=Acticide LA 2605-F; Percent_Active_Ingredient=5.3; Mixture=Mixture; DTXSID=DTXSID8024652; Assay=Guinea Pig Maximization/Buehler; Endpoint=GHS Classification; Response=1; Response_Unit=Unitless; Species=Guinea pig; Route=Dermal; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Incidence of positive responses 0 % Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7744; Record_ID=skin_sensitization_invivo_1754; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=2.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Incidence of positive responses; Response=0; Response_Unit=%; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1974; 4459237; 10.1016/0015-6264(74)90367-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Incidence of positive responses 11.83 % Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7750; Record_ID=skin_sensitization_invivo_1755; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Incidence of positive responses; Response=11.83; Response_Unit=%; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1973; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Induction dose per skin area 1395 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7742; Record_ID=skin_sensitization_invivo_1754; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=2.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Induction dose per skin area; Response=1395; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1974; 4459237; 10.1016/0015-6264(74)90367-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Induction dose per skin area 3488 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7748; Record_ID=skin_sensitization_invivo_1755; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Induction dose per skin area; Response=3488; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1973; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Induction dose per skin area, 5% incidence of positive responses 1474 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7760; Record_ID=skin_sensitization_invivo_1755; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Induction dose per skin area, 5% incidence of positive responses; Response=1474; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1973; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Induction dose per skin area, one positive response 317 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7756; Record_ID=skin_sensitization_invivo_1755; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Induction dose per skin area, one positive response; Response=317; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1973; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Relative reliability score 2 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7747; Record_ID=skin_sensitization_invivo_1754; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=2.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Relative reliability score; Response=2; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1974; 4459237; 10.1016/0015-6264(74)90367-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
NTP ICE skin sensitization Relative reliability score 3 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=7762; Record_ID=skin_sensitization_invivo_1755; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID8024652; Assay=Human Repeat Insult Patch Test; Endpoint=Relative reliability score; Response=3; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Marzulli and Maibach 1973; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID8024652; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID8024652
EPA ToxRefDB v3 11 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EPA ToxRefDB v3 LEL =80 mg/kg bw/day rabbit (new zealand white; New Zealand White) oral 7 GD to 19 GD DEV study_id=6181; toxval_study_source_id=studyid6181_Adult_F0_F_systemic; toxval_effect_list=in life observation-clinical signs-defecation|in life observation-food consumption-food consumption|in life observation-body weight-body weight gain; dose_level=4; study_year=1991; study_citation=Irvine, L.F.H. 1991. Bronopol: Oral (Gavage) Rabbit Developmental Toxicity (Teratogenicity) study: Study No. BON/3/91. Prepared by Toxicol Laboratories Limited, Bromyard Road, Ledbury, Herefordshire, HR8 1LH, England.; dsstox_substance_id=DTXSID8024652; 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 =10 mg/kg bw/day rat (sprague dawley; Sprague Dawley) oral 0 week to 104 week CHR study_id=6183; toxval_study_source_id=studyid6183_Adult_F0_F_systemic; toxval_effect_list=in life observation-water consumption-water consumption|organ weight-liver-relative to body weight|urinalysis-volume-volume|in life observation-body weight-body weight gain|pathology gross-stomach-ulcer|in life observation-food consumption-food efficiency|organ weight-thyroid gland-absolute|pathology gross-stomach-thickened|pathology microscopic-salivary glands-dilatation|pathology microscopic-stomach-ulcer|pathology microscopic-kidney-glomerulonephropathy|urinalysis-occult blood-blood|pathology microscopic-stomach-hyperplasia|pathology gross-stomach-irregular surface|in life observation-clinical signs-fur (altered appearance)|pathology microscopic-salivary glands-metaplasia|pathology microscopic-lymph node-dilatation|pathology microscopic-salivary glands-atrophy|in life observation-mortality-mortality|in life observation-food consumption-food consumption|in life observation-body weight-body weight|pathology microscopic-stomach-squamous cell papilloma|organ weight-heart-absolute|pathology microscopic-salivary glands-inflammation|organ weight-kidney-relative to body weight|organ weight-kidney-absolute|organ weight-brain-relative to body weight|organ weight-adrenal gland-relative to body weight|organ weight-lung-relative to body weight|in life observation-clinical signs-frequent face washing; dose_level=1; study_year=1976; dsstox_substance_id=DTXSID8024652; admin_method=Water; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =4.27 mg/kg bw/day dog (beagle; beagle) oral 0 day to 28 day SAC study_id=6646; toxval_study_source_id=studyid6646_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-nose-inflammation|pathology microscopic-stomach-hypertrophy; dose_level=1; study_year=2006; study_citation=C Stewart. 2006. Bronopol: 28-Day Drinking Water Toxicity Study in Beagle Dogs. The Dow Chemical Company. MRID 47081001. Unpublished.; dsstox_substance_id=DTXSID8024652; admin_method=Water; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =4.1 mg/kg bw/day dog (beagle; beagle) oral 0 day to 28 day SAC study_id=6646; toxval_study_source_id=studyid6646_Adult_F0_M_systemic; toxval_effect_list=pathology microscopic-nose-inflammation|pathology microscopic-stomach-hypertrophy; dose_level=1; study_year=2006; study_citation=C Stewart. 2006. Bronopol: 28-Day Drinking Water Toxicity Study in Beagle Dogs. The Dow Chemical Company. MRID 47081001. Unpublished.; dsstox_substance_id=DTXSID8024652; admin_method=Water; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =150 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 10 weeks (premating) to 2 generation MGR study_id=6661; toxval_study_source_id=studyid6661_Adult Pregnancy_F0_F_reproductive; toxval_effect_list=reproductive performance-dystocia-dystocia; dose_level=3; study_year=2008; study_citation=EW Carney et al. 2008. Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats. The Dow Chemical Company. MRID 47455601. Unpublished.; dsstox_substance_id=DTXSID8024652; admin_method=Water; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LOAEL =40 mg/kg bw/day rat (sprague dawley; Sprague Dawley) oral 0 week to 104 week CHR study_id=6183; toxval_study_source_id=studyid6183_Adult_F0_F_systemic; toxval_effect_list=in life observation-water consumption-water consumption; dose_level=2; study_year=1976; dsstox_substance_id=DTXSID8024652; admin_method=Water; 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 rabbit (new zealand white; New Zealand White) oral 7 GD to 19 GD DEV study_id=6181; toxval_study_source_id=studyid6181_Adult_F0_F_systemic; toxval_effect_list=in life observation-clinical signs-defecation|in life observation-food consumption-food consumption|in life observation-body weight-body weight gain; dose_level=3; study_year=1991; study_citation=Irvine, L.F.H. 1991. Bronopol: Oral (Gavage) Rabbit Developmental Toxicity (Teratogenicity) study: Study No. BON/3/91. Prepared by Toxicol Laboratories Limited, Bromyard Road, Ledbury, Herefordshire, HR8 1LH, England.; dsstox_substance_id=DTXSID8024652; 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 =28 mg/kg bw/day rat (sprague dawley; sprague dawley) oral 6 GD to 15 GD DEV study_id=6182; toxval_study_source_id=studyid6182_Adult_F0_F_systemic; toxval_effect_list=in life observation-body weight-body weight gain; dose_level=2; study_year=1995; study_citation=Palmer, K. (1995) Bronopol: Oral (Gavage) Rat Developmental Toxicity study. Study No. BON/9/95. Unpublished.; dsstox_substance_id=DTXSID8024652; 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 >0 mg/kg bw/day rat (sprague dawley; Sprague Dawley) oral 0 week to 104 week CHR study_id=6183; toxval_study_source_id=studyid6183_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-stomach-squamous cell papilloma|in life observation-clinical signs-frequent face washing|organ weight-lung-relative to body weight|pathology microscopic-stomach-hyperplasia|in life observation-mortality-mortality|pathology microscopic-salivary glands-atrophy|pathology microscopic-lymph node-dilatation|organ weight-heart-absolute|pathology microscopic-salivary glands-inflammation|in life observation-food consumption-food consumption|in life observation-body weight-body weight|pathology microscopic-stomach-ulcer|organ weight-kidney-absolute|pathology microscopic-kidney-glomerulonephropathy|organ weight-kidney-relative to body weight|organ weight-adrenal gland-relative to body weight|organ weight-brain-relative to body weight|pathology microscopic-salivary glands-dilatation|urinalysis-volume-volume|pathology microscopic-salivary glands-metaplasia|in life observation-clinical signs-fur (altered appearance)|pathology gross-stomach-irregular surface|in life observation-water consumption-water consumption|organ weight-liver-relative to body weight|pathology gross-stomach-ulcer|in life observation-food consumption-food efficiency|in life observation-body weight-body weight gain|organ weight-thyroid gland-absolute|pathology gross-stomach-thickened|urinalysis-occult blood-blood; dose_level=0; study_year=1976; dsstox_substance_id=DTXSID8024652; admin_method=Water; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL =50 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 10 weeks (premating) to 2 generation MGR study_id=6661; toxval_study_source_id=studyid6661_Adult Pregnancy_F0_F_reproductive; toxval_effect_list=reproductive performance-dystocia-dystocia; dose_level=2; study_year=2008; study_citation=EW Carney et al. 2008. Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats. The Dow Chemical Company. MRID 47455601. Unpublished.; dsstox_substance_id=DTXSID8024652; admin_method=Water; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL =10 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 10 weeks (premating) to 2 generation MGR study_id=6661; toxval_study_source_id=studyid6661_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-stomach-erosion|pathology microscopic-liver-vacuolization|organ weight-thyroid gland-absolute|organ weight-kidney-relative to body weight|pathology microscopic-stomach-inflammation|in life observation-body weight-body weight gain|in life observation-food consumption-food consumption|organ weight-kidney-absolute|pathology microscopic-stomach-ulcer|organ weight-thyroid gland-relative to body weight|pathology microscopic-thyroid gland-dilatation|pathology microscopic-kidney-inflammation|in life observation-water consumption-water consumption|pathology microscopic-kidney-dilatation|pathology microscopic-kidney-degeneration; dose_level=1; study_year=2008; study_citation=EW Carney et al. 2008. Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats. The Dow Chemical Company. MRID 47455601. Unpublished.; dsstox_substance_id=DTXSID8024652; admin_method=Water; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxValDB GESTIS DNEL 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB GESTIS DNEL DNEL local =2.5 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_dup_-_15630330_15630331:-:--; 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_a3384d9f22eea33eaef7238dea5acda9
ToxValDB GESTIS DNEL DNEL systemic =3.5 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_dup_-_15630330_15630331:-:--; 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_724a399a54a42f894bfc19c1b3b518d1
ToxValDB HESS 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB HESS LOEL =90 mg/kg bw/day Rat oral short-term; 28 days short-term STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/60da0ddae4b0a676289dde66; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.nite.go.jp/en/chem/qsar/hess_update-e.html; TOXICOLOGICAL_EFFECT=Deaths|Clinical Observation: Locomotor activity decrease, Abnormal respiratory sound Deep respiration Pale skin Hypothermia Ptosis Salivation Rough fur|Functional Observational Battery: Righting reflex decrease, Hind limb grip strength decrease|Body Weight Changes: decrease|Urinalysis: Occult blood|Necropsy: Lung-Reddish area Glandular stomach-Reddish, mucosa|Histopathology: Forestomach-Squamous hyperplasia Glandular stomach-Hyperplasia, surface epithelium Glandular stomach-Necrosis Duodenum-Erosion Kidney-Hyperplasia,collecting tubular epithelium Kidney-Dilatation, tubular R Kidney-Basophlic tubule Urinary bladder-Hyperplasia, transitional cell, simple Thymus-Atrophy Testis-Hypospermatogenesis Testis-Hyperplasia, interstitial cell, diffuse Epididymis-Decrease, sperm Epididymis-Atrophy Liver-Necrosis, focal Liver-Congestion Trachea-Inflammation Lung-Inflammation; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|gross pathology|mortality/survival|neurobehavior|nonneoplastic histopathology|urinalysis; STUDY_GROUP=HESS_dup_-_15638878_15638879:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was manually checked; QC_STATUS=pass; SOURCE_HASH=ToxValhc_f178562583a27eb3a40eb8142ee23231
ToxValDB HESS NOEL =30 mg/kg bw/day Rat oral short-term; 28 days short-term STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/60da0ddae4b0a676289dde66; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.nite.go.jp/en/chem/qsar/hess_update-e.html; TOXICOLOGICAL_EFFECT=Necropsy: Lung-Reddish area|Histopathology: Lung-Inflammation; TOXICOLOGICAL_EFFECT_CATEGORY=gross pathology|nonneoplastic histopathology; STUDY_GROUP=HESS_dup_-_15638878_15638879:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_c1c7f5d8f73c85090637ff1ac5b5065b
ToxValDB HESS NOEL =10 mg/kg bw/day Rat oral short-term; 28 days short-term STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/60da0ddae4b0a676289dde66; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.nite.go.jp/en/chem/qsar/hess_update-e.html; TOXICOLOGICAL_EFFECT=Clinical Observation: Locomotor activity decrease, Abnormal respiratory sound, Deep respiration, Hypothermia; TOXICOLOGICAL_EFFECT_CATEGORY=clinical signs; STUDY_GROUP=HESS_dup_-_15638984_15638985:F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_c2ab08131d9fdf8757048abdd10ea5ab
ToxValDB ToxRefDB 10 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB ToxRefDB LEL =80 mg/kg bw/day Rabbit oral short-term (developmental); 13 days reproduction developmental LONG_REF=Irvine, L.F.H. 1991. Bronopol: Oral (Gavage) Rabbit Developmental Toxicity (Teratogenicity) study: Study No. BON/3/91. Prepared by Toxicol Laboratories Limited, Bromyard Road, Ledbury, Herefordshire, HR8 1LH, England.; TITLE=Bronopol: Oral (Gavage) Rabbit Developmental Toxicity (Teratogenicity) study; AUTHOR=Irvine, L.F.H; EXTERNAL_SOURCE_ID=6181; 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-defecation|systemic: in life observation-body weight-body weight gain|systemic: in life observation-food consumption-food consumption; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|food and/or water consumption; STUDY_GROUP=ToxRefDB_dup_-_15711178_15711179_15711180_15711181:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_96ac37723661fe93fd6910d8e6f434fe
ToxValDB ToxRefDB LEL =10 mg/kg bw/day Rat oral chronic; 104 weeks chronic EXTERNAL_SOURCE_ID=6183; 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=1976; ORIGINAL_YEAR=1976; TOXICOLOGICAL_EFFECT=systemic: in life observation-water consumption-water consumption|systemic: organ weight-liver-relative to body weight|systemic: pathology microscopic-lymph node-dilatation|systemic: pathology microscopic-salivary glands-dilatation|systemic: pathology microscopic-salivary glands-atrophy|systemic: in life observation-mortality-mortality|systemic: pathology microscopic-stomach-ulcer|systemic: urinalysis-volume-volume|systemic: in life observation-food consumption-food consumption|systemic: in life observation-body weight-body weight|systemic: pathology microscopic-kidney-glomerulonephropathy|systemic: organ weight-lung-relative to body weight|systemic: pathology microscopic-stomach-squamous cell papilloma|systemic: in life observation-body weight-body weight gain|systemic: pathology gross-stomach-ulcer|systemic: in life observation-food consumption-food efficiency|systemic: organ weight-heart-absolute|systemic: pathology microscopic-salivary glands-inflammation|systemic: in life observation-clinical signs-frequent face washing|systemic: organ weight-thyroid gland-absolute|systemic: organ weight-kidney-relative to body weight|systemic: urinalysis-occult blood-blood|systemic: organ weight-kidney-absolute|systemic: pathology microscopic-stomach-hyperplasia|systemic: pathology gross-stomach-irregular surface|systemic: organ weight-brain-relative to body weight|systemic: organ weight-adrenal gland-relative to body weight|systemic: in life observation-clinical signs-fur (altered appearance)|systemic: pathology gross-stomach-thickened|systemic: pathology microscopic-salivary glands-metaplasia; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|cancer|clinical signs|food and/or water consumption|gross pathology|mortality/survival|nonneoplastic histopathology|organ weight|urinalysis; STUDY_GROUP=ToxRefDB_dup_-_15711194_15711195_15711196:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_38b576ec1c523683fbb3e95486eb1205
ToxValDB ToxRefDB LEL =4.27 mg/kg bw/day Dog oral short-term; 28 days short-term LONG_REF=C Stewart. 2006. Bronopol: 28-Day Drinking Water Toxicity Study in Beagle Dogs. The Dow Chemical Company. MRID 47081001. Unpublished.; TITLE=Bronopol: 28-Day Drinking Water Toxicity Study in Beagle Dogs; AUTHOR=C Stewart; EXTERNAL_SOURCE_ID=6646; 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=2006; ORIGINAL_YEAR=2006; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-nose-inflammation|systemic: pathology microscopic-stomach-hypertrophy; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology; STUDY_GROUP=ToxRefDB:15712381:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_ccb091d622ddc491c116a83ec04b38be
ToxValDB ToxRefDB LEL =4.1 mg/kg bw/day Dog oral short-term; 28 days short-term LONG_REF=C Stewart. 2006. Bronopol: 28-Day Drinking Water Toxicity Study in Beagle Dogs. The Dow Chemical Company. MRID 47081001. Unpublished.; TITLE=Bronopol: 28-Day Drinking Water Toxicity Study in Beagle Dogs; AUTHOR=C Stewart; EXTERNAL_SOURCE_ID=6646; 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=2006; ORIGINAL_YEAR=2006; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-nose-inflammation|systemic: pathology microscopic-stomach-hypertrophy; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology; STUDY_GROUP=ToxRefDB:15712382:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_c7aaf85a053d3ac038bfdc3716a40e9a
ToxValDB ToxRefDB LEL =150 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=EW Carney et al. 2008. Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats. The Dow Chemical Company. MRID 47455601. Unpublished.; TITLE=Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats; AUTHOR=EW Carney et al; EXTERNAL_SOURCE_ID=6661; 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=2008; ORIGINAL_YEAR=2008; TOXICOLOGICAL_EFFECT=reproductive: reproductive performance-dystocia-dystocia; TOXICOLOGICAL_EFFECT_CATEGORY=reproduction; STUDY_GROUP=ToxRefDB_dup_-_15712391_15712392_15712393_15712394:F:F0adult-pregnancy; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_afbeca46974ffaec1849b5a29a2aaca1
ToxValDB ToxRefDB LOAEL =40 mg/kg bw/day Rat oral chronic; 104 weeks chronic EXTERNAL_SOURCE_ID=6183; 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=1976; ORIGINAL_YEAR=1976; TOXICOLOGICAL_EFFECT=systemic: in life observation-water consumption-water consumption; TOXICOLOGICAL_EFFECT_CATEGORY=food and/or water consumption; STUDY_GROUP=ToxRefDB_dup_-_15711194_15711195_15711196:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_6f036b03c4456a744637884fb902bcd9
ToxValDB ToxRefDB NEL =40 mg/kg bw/day Rabbit oral short-term (developmental); 13 days reproduction developmental LONG_REF=Irvine, L.F.H. 1991. Bronopol: Oral (Gavage) Rabbit Developmental Toxicity (Teratogenicity) study: Study No. BON/3/91. Prepared by Toxicol Laboratories Limited, Bromyard Road, Ledbury, Herefordshire, HR8 1LH, England.; TITLE=Bronopol: Oral (Gavage) Rabbit Developmental Toxicity (Teratogenicity) study; AUTHOR=Irvine, L.F.H; EXTERNAL_SOURCE_ID=6181; 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-defecation|systemic: in life observation-body weight-body weight gain|systemic: in life observation-food consumption-food consumption; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|food and/or water consumption; STUDY_GROUP=ToxRefDB_dup_-_15711178_15711179_15711180_15711181:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_4ca19431d4bc706c365276f6ef636c0c
ToxValDB ToxRefDB NEL =28 mg/kg bw/day Rat oral short-term (developmental); 10 days reproduction developmental LONG_REF=Palmer, K. (1995) Bronopol: Oral (Gavage) Rat Developmental Toxicity study. Study No. BON/9/95. Unpublished.; TITLE=Bronopol: Oral (Gavage) Rat Developmental Toxicity study; AUTHOR=Palmer, K; EXTERNAL_SOURCE_ID=6182; 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=1995; ORIGINAL_YEAR=1995; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ToxRefDB_dup_-_15711186_15711187_15711188_15711189:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_21a2dee30a1cde703da736e104966a9e
ToxValDB ToxRefDB NEL =50 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=EW Carney et al. 2008. Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats. The Dow Chemical Company. MRID 47455601. Unpublished.; TITLE=Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats; AUTHOR=EW Carney et al; EXTERNAL_SOURCE_ID=6661; 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=2008; ORIGINAL_YEAR=2008; TOXICOLOGICAL_EFFECT=reproductive: reproductive performance-dystocia-dystocia; TOXICOLOGICAL_EFFECT_CATEGORY=reproduction; STUDY_GROUP=ToxRefDB_dup_-_15712391_15712392_15712393_15712394:F:F0adult-pregnancy; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_79d674dc3b94d31b9f2fb3bf68db59f2
ToxValDB ToxRefDB NEL =10 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=EW Carney et al. 2008. Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats. The Dow Chemical Company. MRID 47455601. Unpublished.; TITLE=Bronopol: Two Generation Drinking Water Reproductive Toxicity Study in Crl:CD(SD) Rats; AUTHOR=EW Carney et al; EXTERNAL_SOURCE_ID=6661; 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=2008; ORIGINAL_YEAR=2008; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-stomach-inflammation|systemic: in life observation-body weight-body weight gain|systemic: organ weight-kidney-relative to body weight|systemic: pathology microscopic-stomach-erosion|systemic: in life observation-water consumption-water consumption|systemic: in life observation-food consumption-food consumption|systemic: organ weight-kidney-absolute|systemic: pathology microscopic-liver-vacuolization|systemic: pathology microscopic-stomach-ulcer|systemic: organ weight-thyroid gland-relative to body weight|systemic: pathology microscopic-thyroid gland-dilatation|systemic: pathology microscopic-kidney-dilatation|systemic: organ weight-thyroid gland-absolute|systemic: pathology microscopic-kidney-degeneration|systemic: pathology microscopic-kidney-inflammation; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|nonneoplastic histopathology|organ weight; STUDY_GROUP=ToxRefDB_dup_-_15712399_15712400_15712401_15712402:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_3a8ea8d75a0340ebcdfdaf218e41d21a
openFDA substances 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier 6PU1E16C9W UNII - - - chemical -