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
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
产品名称
5α-雄甾-16-烯-3α-醇,
生物来源
synthetic (organic)
质量水平
方案
≥98% (TLC)
表单
powder
药品控制
regulated under CDSA - not available from Sigma-Aldrich Canada
技术
GC/MS: suitable
mp
140-141 °C (lit.)
溶解性
ethanol: 19.60-20.40 mg/mL, clear, colorless
运输
ambient
储存温度
room temp
SMILES字符串
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
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应用
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.
生化/生理作用
5alpha-androst-16-en-3alpha-ol (androstenol), is an androgen believed to act as a pheromone.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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
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
S Stefańczyk-Krzymowska et al.
Experimental physiology, 85(6), 801-809 (2001-02-24)
It is generally accepted that pheromones act by stimulating of the dendritic receptors of the olfactory neurones massed in the olfactory epithelium. This study was designed to ascertain whether it is possible for the boar pheromone androstenol (5alpha-androst-16-en-3-ol) to be
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
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
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