A7883
5α-雄甾-16-烯-3α-醇
synthetic (organic), ≥98% (TLC), androgen pheromone, powder
别名:
16-(5α)雄甾烯-3α-醇, 3α-羟基-5α-雄甾-16-烯
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关于此项目
经验公式（希尔记法）:
C19H30O
化学文摘社编号:
分子量:
274.44
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
214-573-1
MDL number:
产品名称
5α-雄甾-16-烯-3α-醇,
biological source
synthetic (organic)
Quality Level
assay
≥98% (TLC)
form
powder
drug control
regulated under CDSA - not available from Sigma-Aldrich Canada
technique(s)
GC/MS: suitable
mp
140-141 °C (lit.)
solubility
ethanol: 19.60-20.40 mg/mL, clear, colorless
shipped in
ambient
storage temp.
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
InChI key
KRVXMNNRSSQZJP-PHFHYRSDSA-N
Application
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 Actions
5alpha-androst-16-en-3alpha-ol (androstenol), is an androgen believed to act as a pheromone.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Thomas Piper et al.
Rapid communications in mass spectrometry : RCM, 23(13), 1917-1926 (2009-05-23)
The development and application of a combined gas chromatography/thermal conversion/isotope ratio mass spectrometry (GC/TC/IRMS) method for D/H ratio determination of endogenous urinary steroids are presented. The key element in sample preparation was the consecutive cleanup with high-performance liquid chromatography of
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
W D Booth
Journal of reproduction and fertility, 81(2), 427-431 (1987-11-01)
The pheromone binding protein 'pheromaxein' which binds the pheromonal 16-androstene steroids in the saliva of the male pig (boar), was degraded and lost its binding activity in saliva incubated in air for 72 h at 21 degrees C and 37
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| A7883-100MG | 04061832847580 |
| A7883-10MG | 04061833386552 |
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