NOAEL Studies Fragrance

Musk Ketone NOAEL Studies

INCI: MUSK KETONE

CAS: 81-14-1

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

COSMOS_DB 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
COSMOS_DB NOAEL 125 mg/kg bw/day rat oral 365 day Chronic US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS_DB NOAEL 10 mg/kg bw/day mouse oral 7 day Special Toxicology Study US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS_DB NOAEL 45 mg/kg bw/day rat oral 11 day Developmental US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS_DB NOAEL 20 mg/kg bw/day rat oral 7 day Special Toxicology Study US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
NTP_ICE_acute_oral 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_acute_oral LD50 >10000 mg/kg bw Rat (Male) oral acute Rat Acute Oral Toxicity record_id=acute_oral_10614; row=10403; data_type=In Vivo; mixture=Chemical; chemical_name=Musk ketone; preferred_name=Musk ketone; dtxsid=DTXSID6025690; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6025690; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID6025690; source_file=acute_oral.xlsx
NTP_ICE_skin_sensitization 5 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_skin_sensitization Incidence of positive responses 0 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10592; Record_ID=skin_sensitization_invivo_2328; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=3.2; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6025690; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=0; Response_Unit=%; Species=Human; Route=Dermal; Reference=Greif 1967; Not available; Not available|Opdyke 1975; Not available; 10.1016/0015-6264(75)90261-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6025690; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID6025690
NTP_ICE_skin_sensitization Induction dose per skin area 1986 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10589; Record_ID=skin_sensitization_invivo_2328; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=3.2; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6025690; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=1986; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Greif 1967; Not available; Not available|Opdyke 1975; Not available; 10.1016/0015-6264(75)90261-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6025690; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID6025690
NTP_ICE_skin_sensitization Induction dose per skin area 3240 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10621; Record_ID=skin_sensitization_invivo_2334; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6025690; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=3240; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1970: report to RIFM|Opdyke 1975; Not available; 10.1016/0015-6264(75)90261-9; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6025690; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID6025690
NTP_ICE_skin_sensitization Relative reliability score 2 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10620; Record_ID=skin_sensitization_invivo_2328; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=3.2; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6025690; Assay=Human Maximization Test; Endpoint=Relative reliability score; Response=2; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Greif 1967; Not available; Not available|Opdyke 1975; Not available; 10.1016/0015-6264(75)90261-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6025690; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID6025690
NTP_ICE_skin_sensitization Relative reliability score 3 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=10624; Record_ID=skin_sensitization_invivo_2334; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=5.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6025690; Assay=Human Maximization Test; Endpoint=Relative reliability score; Response=3; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Kligman 1970: report to RIFM|Opdyke 1975; Not available; 10.1016/0015-6264(75)90261-9; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6025690; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID6025690
ToxValDB_ECHA_IUCLID 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_ECHA_IUCLID NOAEL =45 mg/kg bw/day Rat oral - developmental QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eac7be4b0a7c65d1bf485; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24162/7/9/3?documentUUID=07970391-5fe1-453d-b9f7-015f19d90130; YEAR=2018; ORIGINAL_YEAR=2018; TOXICOLOGICAL_EFFECT=fetus: fetal/pup body weight changes; TOXICOLOGICAL_EFFECT_CATEGORY=development; STUDY_GROUP=ECHA IUCLID:15821051:-:-fetal; 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_a5e967554cfeb200b97c71a6d975416a
ToxValDB_ECHA_IUCLID NOAEL =15 mg/kg bw/day Rat oral - reproduction developmental QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eac7be4b0a7c65d1bf485; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24162/7/9/3?documentUUID=07970391-5fe1-453d-b9f7-015f19d90130; YEAR=2018; ORIGINAL_YEAR=2018; TOXICOLOGICAL_EFFECT=maternal: body weight and weight gain|maternal: clinical signs|maternal: food consumption and compound intake; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|food and/or water consumption; STUDY_GROUP=ECHA IUCLID:15822376:F:-maternal; 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_5dfdeb98c8adda8075a23986653311cc
ToxValDB_ECHA_IUCLID NOAEL =75 mg/kg bw/day Rat dermal subchronic; 90 days subchronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/67c61da4e4b096bca877682e; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24162/7/6/4?documentUUID=07970391-5fe1-453d-b9f7-015f19d90130; YEAR=2018; ORIGINAL_YEAR=2018; TOXICOLOGICAL_EFFECT=liver; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECHA IUCLID:15826236: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_ff8ab447f14e61b283cdbaf66f2cf86e
ToxValDB_GESTIS_DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_GESTIS_DNEL DNEL systemic =0.247 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:15633588:-:--; 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_c529b16b6edc692fd59608ad9e2381c5
openFDA substances 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier 483V3E1L6J UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H18N2O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"483V3E1L6J"}
openFDA substances FDA UNII substance identifier 483V3E1L6J UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H18N2O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"483V3E1L6J"}
openFDA substances FDA UNII substance identifier 483V3E1L6J UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H18N2O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"483V3E1L6J"}
openFDA substances FDA UNII substance identifier 483V3E1L6J UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H18N2O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"483V3E1L6J"}