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A7883

Sigma-Aldrich

5α-Androst-16-en-3α-ol

Synonym(e):

Androstenol, 16-(5α)Androsten-3α-ol, 3α-Hydroxy-5α-androst-16-ene

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CHF 336.00

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10 MG
CHF 63.20
100 MG
CHF 336.00

About This Item

Empirische Formel (Hill-System):
C19H30O
CAS-Nummer:
1153-51-1
Molekulargewicht:
274.44
EG-Nummer:
214-573-1
MDL-Nummer:
MFCD00051224
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24891288
NACRES:
NA.77

CHF 63.20

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Biologische Quelle

synthetic (organic)

Qualitätsniveau

200

Assay

≥98% (TLC)

Form

powder

Arzneimittelkontrolle

regulated under CDSA - not available from Sigma-Aldrich Canada

Methode(n)

GC/MS: suitable

mp (Schmelzpunkt)

140-141 °C (lit.)

Löslichkeit

ethanol: 19.60-20.40 mg/mL, clear, colorless

Versandbedingung

ambient

Lagertemp.

room temp

SMILES String

C[C@]12CC[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC=C2

InChI

1S/C19H30O/c1-18-9-3-4-16(18)15-6-5-13-12-14(20)7-11-19(13,2)17(15)8-10-18/h3,9,13-17,20H,4-8,10-12H2,1-2H3/t13-,14+,15-,16-,17-,18-,19-/m0/s1

InChIKey

KRVXMNNRSSQZJP-PHFHYRSDSA-N

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Anwendung

5-α-androst-16-en-3-α-ol (androstenol) is an androgen believed to act as a pheromone. Androstenol has been used in a study to develop a combined gas chromatography/thermal conversion/isotope ratio mass spectrometry (GC/TC/IRMS) method for D/H ratio determination of endogenous urinary steroids.

Biochem./physiol. Wirkung

5alpha-androst-16-en-3alpha-ol (androstenol), is an androgen believed to act as a pheromone.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
0000403993
0000403991
0000403991
0000403993
0000388499

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Die Dokumentenbibliothek aufrufen

Jeremy Vincent et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 61(Pt 1), 156-159 (2006-03-02)
The constitutive androstane receptor (CAR) is a member of the nuclear receptor superfamily. In contrast to classical nuclear receptors, which possess small-molecule ligand-inducible activity, CAR exhibits constitutive transcriptional activity in the apparent absence of ligand. CAR is among the most
Guan Wang et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 870(2), 209-215 (2008-07-01)
A novel method using solid-phase extraction coupled with gas chromatography and flame ionization detector (FID)/electron impact mass spectrometry (EIMS) was developed for the determination of 5alpha-androst-16-en-3alpha-ol (androstenol), a steroidal compound belonging to the group of musk odorous 16-androstenes, in truffle
D Benton et al.
Biological psychology, 22(2), 141-147 (1986-04-01)
The hypothesis that 5-alpha-androst-16-en-3 alpha-ol increases the sexual arousal of the human female was examined. This substance is produced by the male and has been suggested to be a possible human pheromone. Groups of female subjects were asked to read
W D Booth
The Journal of endocrinology, 100(2), 195-202 (1984-02-01)
Submaxillary glands of mature Göttingen miniature pigs were examined for the presence of a sexual dimorphism. Gland weights, serous cell hypertrophy and total protein in the glands were much greater in male than female pigs. High concentrations of the pheromonal
[Synthesis of mammalian pheromone 5 alpha-androst-16-en-3-one and 5 alpha-Androst-16-en-3 alpha-ol].
G D Han et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 17(9), 696-698 (1982-09-01)
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