estratetraenol, 1150-90-9

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CODE168721 CODE168721
Product(s):
1150-90-9 1,3,5(10)-16-Estratetraen-3-ol 95%
A steroid produced by females having pheromone activities.

CAS Number:	1150-90-9	3D/inchi
FDA UNII:	4QD0FTG3VT
Nikkaji Web:	J131.272C
MDL:	MFCD00198961
XlogP3-AA:	5.10 (est)
Molecular Weight:	254.37254000
Formula:	C18 H22 O
BioActivity Summary:	listing
NMR Predictor:	Predict (works with chrome, Edge or firefox)

Category:cosmetic agents

US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:

Google Scholar:	Search
Google Books:	Search
Google Scholar: with word "volatile"	Search
Google Scholar: with word "flavor"	Search
Google Scholar: with word "odor"	Search
Google Patents:	Search
US Patents:	Search
EU Patents:	Search
Pubchem Patents:	Search
PubMed:	Search
NCBI:	Search

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)

Organoleptic Properties:

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

CosIng:	cosmetic data
Cosmetic Uses:	fragrance

Suppliers:

BOC Sciences

For experimental / research use only.

1,3,5(10)-16-Estratetraen-3-ol 95%

Odor: characteristic

Use: A steroid produced by females having pheromone activities.

Carbosynth

For experimental / research use only.

Estratetraenol

Safety Information:


Hazards identification

Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements

Pictogram

Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

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.

Safety References:

EPI System: View

AIDS Citations:Search

Cancer Citations:Search

Toxicology Citations:Search

EPA ACToR:Toxicology Data

EPA Substance Registry Services (SRS):Registry

Laboratory Chemical Safety Summary :101988

National Institute of Allergy and Infectious Diseases:Data

(8S,9S,13R,14S)-13-methyl-6,7,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-3-ol

Chemidplus:0001150909

References:

	(8S,9S,13R,14S)-13-methyl-6,7,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-3-ol
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	101988
Pubchem (sid):	135058537

Other Information:

(IUPAC):	Atomic Weights of the Elements 2011 (pdf)
Videos:	The Periodic Table of Videos
tgsc:	Atomic Weights use for this web site
(IUPAC):	Periodic Table of the Elements
CHEBI:	View
CHEMBL:	View
HMDB (The Human Metabolome Database):	Search
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View
Wikipedia:	View

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

found in nature

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

Articles:

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].

Notes:

None found

estratetraenol estra-1,3,5(10),16-tetraen-3-ol

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Articles:

estratetraenol
estra-1,3,5(10),16-tetraen-3-ol