estratetraenol
estra-1,3,5(10),16-tetraen-3-ol
Identification
| Name | estratetraenol |
| CAS Number | 1150-90-9 |
| FDA UNII | 4QD0FTG3VT |
| Molecular Formula | C18 H22 O |
| Molecular Weight | 254.37254000 |
| MDL Number | MFCD00198961 |
| Nikkaji Number | J131.272C |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 400.20 °C. @ 760.00 mm Hg (est) |
| Flash Point | 357.00 °F. TCC ( 180.60 °C. ) (est) |
| logP (o/w) | 5.720 (est) |
| Soluble in | water, 2.706 mg/L @ 25 °C (est) |
Cosmetic Information
| CosIng | cosmetic data |
| Cosmetic Uses | fragrance |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | cosmetic agents |
| Recommendation for estratetraenol usage levels up to | not for fragrance use. |
| Recommendation for estratetraenol flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
estra-1,3,5(10),16-tetraen-3-ol
estra-1(10),2,4,16-tetraen-3-ol
1,3,5,(10),16-
estratetraen-3-ol
(8S,9S,13R,14S)-13-
methyl-6,7,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-3-ol
PubMed:
Chemosensory communication of gender through two human steroids in a sexually dimorphic manner.
PubMed:
High fetal testosterone and sexually dimorphic cerebral networks in females.
PubMed:
Individual differences in sensitivity to the odor of 4,16-androstadien-3-one.
PubMed:
Context-dependent effects of steroid chemosignals on human physiology and mood.
PubMed:
Induction of rat liver microsomal epoxide hydrolase by its endogenous substrate 16 alpha, 17 alpha-epoxyestra-1,3,5-trien-3-ol.
PubMed:
Identification of estra-1,3,5(10),16-tetraen-3-ol (estratetraenol) from the urine of pregnant women (1).
PubMed:
[Biogenesis of estratetraenol in man].