NOAEL Studies Cosmetic Ingredient

Allyl Phenoxyacetate NOAEL Studies

INCI: ALLYL PHENOXYACETATE

CAS: 7493-74-5

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

NTP ICE skin irritation 16 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin irritation Viability 55.4 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2760; Record_ID=skin_irritation_invitro_1187; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=55.4; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 56 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2781; Record_ID=skin_irritation_invitro_1200; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=56; Response_Unit=%; Reference=Katoh and Hata 2011; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 72 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2761; Record_ID=skin_irritation_invitro_1188; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=72; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 72.7 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2758; Record_ID=skin_irritation_invitro_1189; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=72.7; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 77 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2780; Record_ID=skin_irritation_invitro_1190; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=77; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 91.7 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2757; Record_ID=skin_irritation_invitro_1191; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=91.7; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 91.9 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2756; Record_ID=skin_irritation_invitro_1192; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=91.9; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 94.3 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2759; Record_ID=skin_irritation_invitro_1193; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=94.3; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 94.7 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2779; Record_ID=skin_irritation_invitro_1201; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=94.7; Response_Unit=%; Reference=Katoh and Hata 2011; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 95.46 % - Dermal - In Vitro; EpiDerm Irritation sheet=Data_invitro; excel_row=2787; Record_ID=skin_irritation_invitro_1194; Data_Type=In Vitro; Formulation_Name=allyl phenoxyacetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=EpiDerm Irritation; Endpoint=Viability; Response=95.46; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 96.3 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=2778; Record_ID=skin_irritation_invitro_1202; Data_Type=In Vitro; Formulation_Name=allyl phenoxy-acetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=96.3; Response_Unit=%; Reference=Katoh and Hata 2011; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 96.39 % - Dermal - In Vitro; EpiSkin Irritation sheet=Data_invitro; excel_row=2786; Record_ID=skin_irritation_invitro_1195; Data_Type=In Vitro; Formulation_Name=allyl phenoxyacetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=EpiSkin Irritation; Endpoint=Viability; Response=96.39; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 96.82 % - Dermal - In Vitro; EpiSkin Irritation sheet=Data_invitro; excel_row=2785; Record_ID=skin_irritation_invitro_1196; Data_Type=In Vitro; Formulation_Name=allyl phenoxyacetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=EpiSkin Irritation; Endpoint=Viability; Response=96.82; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 99.66 % - Dermal - In Vitro; EpiDerm Irritation sheet=Data_invitro; excel_row=2784; Record_ID=skin_irritation_invitro_1197; Data_Type=In Vitro; Formulation_Name=allyl phenoxyacetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=EpiDerm Irritation; Endpoint=Viability; Response=99.66; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 102.14 % - Dermal - In Vitro; EpiSkin Irritation sheet=Data_invitro; excel_row=2783; Record_ID=skin_irritation_invitro_1198; Data_Type=In Vitro; Formulation_Name=allyl phenoxyacetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=EpiSkin Irritation; Endpoint=Viability; Response=102.14; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin irritation Viability 105.57 % - Dermal - In Vitro; EpiDerm Irritation sheet=Data_invitro; excel_row=2782; Record_ID=skin_irritation_invitro_1199; Data_Type=In Vitro; Formulation_Name=allyl phenoxyacetate; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=EpiDerm Irritation; Endpoint=Viability; Response=105.57; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin sensitization 7 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin sensitization CV75 >1000 ug/mL - Dermal - In Vitro; CE_hCLAT2018; h-CLAT sheet=Data_invitro; excel_row=2439; Record_ID=skin_sensitization_invitro_590; Data_Type=In Vitro; Internal_Data_Source=CE_hCLAT2018; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=h-CLAT; Endpoint=CV75; Response_Modifier=>; Reported_Response_Modifier=>; Reported_Response=1000; Reported_Response_Unit=ug/mL; Response=1000; Response_Unit=ug/mL; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin sensitization EC1.5 404.9 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=6660; Record_ID=skin_sensitization_invitro_1576; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=404.94075659999999; Reported_Response_Unit=uM; Response=404.9; Response_Unit=uM; Reference=Natsch et al. 2015; 25338925; 10.1093/toxsci/kfu229; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin sensitization EC3 >2000 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=6661; Record_ID=skin_sensitization_invitro_1576; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=KeratinoSens; Endpoint=EC3; Response_Modifier=>; Reported_Response_Modifier=>; Reported_Response=2000; Reported_Response_Unit=uM; Response=2000; Response_Unit=uM; Reference=Natsch et al. 2015; 25338925; 10.1093/toxsci/kfu229; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin sensitization Imax 1.85 ratio - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=6663; Record_ID=skin_sensitization_invitro_1576; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=1.85; Reported_Response_Unit=Unitless; Response=1.85; Response_Unit=Ratio; Reference=Natsch et al. 2015; 25338925; 10.1093/toxsci/kfu229; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin sensitization Incidence of positive responses 0 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10013; Record_ID=skin_sensitization_invivo_2214; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=1.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=0; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1974: report to RIFM|Opdyke 1975; Not available; 10.1016/0015-6264(75)90184-4|Api et al. 2015; 25430073; 10.3109/15569527.2014.979425|Api et al. 2017; 28691948; 10.1097/der.0000000000000304; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin sensitization Induction dose per skin area 648 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10050; Record_ID=skin_sensitization_invivo_2214; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=1.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=648; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1974: report to RIFM|Opdyke 1975; Not available; 10.1016/0015-6264(75)90184-4|Api et al. 2015; 25430073; 10.3109/15569527.2014.979425|Api et al. 2017; 28691948; 10.1097/der.0000000000000304; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
NTP ICE skin sensitization Relative reliability score 3 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10018; Record_ID=skin_sensitization_invivo_2214; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=1.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID3064722; Assay=Human Maximization Test; Endpoint=Relative reliability score; Response=3; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Kligman 1974: report to RIFM|Opdyke 1975; Not available; 10.1016/0015-6264(75)90184-4|Api et al. 2015; 25430073; 10.3109/15569527.2014.979425|Api et al. 2017; 28691948; 10.1097/der.0000000000000304; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3064722
ECHA 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ECHA LOAEL =150 mg/kg bw/day Rat oral short-term; 2 weeks short-term QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7cbc8e4b0a7c65d227864; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/23017/7/6/2?documentUUID=a8496f63-c384-4c0a-a927-908a145ca783; YEAR=2016; ORIGINAL_YEAR=2016; TOXICOLOGICAL_EFFECT=liver: clinical biochemistry|gross pathology|haematology|histopathology: non-neoplastic|organ weights and organ / body weight ratios; TOXICOLOGICAL_EFFECT_CATEGORY=clinical chemistry|gross pathology|hematology|nonneoplastic histopathology|organ weight; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15839517_15839518:M/F:--; 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_d88c60ea2239c4a8a8b523f1c31127dc
ECHA NOAEL =50 mg/kg bw/day Rat oral short-term; 2 weeks short-term QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7cbc8e4b0a7c65d227864; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/23017/7/6/2?documentUUID=a8496f63-c384-4c0a-a927-908a145ca783; YEAR=2016; ORIGINAL_YEAR=2016; TOXICOLOGICAL_EFFECT=liver; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15839517_15839518:M/F:--; 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_f1e74cab128ce8a3bf36a07bb066ac1f
ECHA NOAEL >=150 mg/kg bw/day Rat oral - reproduction developmental QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eab5ae4b0a7c65d1b9d15; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/23017/7/9/2?documentUUID=a8496f63-c384-4c0a-a927-908a145ca783; YEAR=2016; ORIGINAL_YEAR=2016; STUDY_GROUP=ECHA IUCLID_dup_Toxicity Reproduction_15855474_15856287:M/F:P0-; 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_fd3626044f0ae6c4aef8f209fa949e09
ToxValDB GESTIS DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB GESTIS DNEL DNEL systemic =2.47 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:15629581:-:--; 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_3deec494fe5a0988a1895f92eee6cd96
openFDA substances 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier Q3P8UAF9WE UNII - - - chemical {"approval_status":null,"molecular_formula":"C11H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"Q3P8UAF9WE"}
openFDA substances FDA UNII substance identifier Q3P8UAF9WE UNII - - - chemical {"approval_status":null,"molecular_formula":"C11H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"Q3P8UAF9WE"}
openFDA substances FDA UNII substance identifier Q3P8UAF9WE UNII - - - chemical {"approval_status":null,"molecular_formula":"C11H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"Q3P8UAF9WE"}
openFDA substances FDA UNII substance identifier Q3P8UAF9WE UNII - - - chemical {"approval_status":null,"molecular_formula":"C11H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"Q3P8UAF9WE"}