853904-64-0

Basic information

• Product Name: 3β-tert-ButyldiMethylsilyloxy-17-Methyl-5α-androstane-17β-ol-d5
• Synonyms: 3β-tert-ButyldiMethylsilyloxy-17-Methyl-5α-androstane-17β-ol-d5;(3β,5α,17β)-3-[[(1,1-DiMethylethyl)diMethylsilyl]oxy]-17-(Methyl-d3)-androstan-16,16-d2-17-ol;(3S,5S,8R,9S,10S,13S,14S,17S)-3-[tert-butyl(dimethyl)silyl]oxy-16,16-dideuterio-10,13-dimethyl-17-(trideuteriomethyl)-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol
• CAS NO: 853904-64-0
• Molecular Formula: C26H48O2Si
• Molecular Weight: 420.74362
• Product Categories: Intermediates & Fine Chemicals;Isotope Labelled Compounds;Metabolites & Impurities;Pharmaceuticals;Steroids
• Mol File: 853904-64-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3β-tert-ButyldiMethylsilyloxy-17-Methyl-5α-androstane-17β-ol-d5(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-tert-ButyldiMethylsilyloxy-17-Methyl-5α-androstane-17β-ol-d5(853904-64-0)
• EPA Substance Registry System: 3β-tert-ButyldiMethylsilyloxy-17-Methyl-5α-androstane-17β-ol-d5(853904-64-0)

Safety Data

• Hazardous Substances Data: 853904-64-0(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

A labelled protected metabolite of 17α-Methyltestosterone (M326400).

Upstream product

• 853904-63-9 16,16-dideuterio-O³-[(1,1-dimethylethyl)dimethylsilanyl] epiandrosterone 
• 15772-82-4 trideuteriomethyl-lithium 
• 481-29-8 Epiandrosterone 
• 57711-44-1 (3S,10S,13S)-3-((tert-butyldimethylsilyl)oxy)-10,13-dimethyl-1,2,3,4,7,8,9,10,11,12,13,14,15,16-tetradecahydro-17H-cyclopenta-[a]phenanthren-17-one 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 853904-67-3 16,16,20,20,20-pentadeuterio-3,17β-dihydroxy-17α-methyl-androst-2-ene-2-carboxylic acid methyl ester 
• 853904-65-1 16,16,20,20,20-pentadeuterio-17α-methyl-5α-androstan-3β,17β-diol 

Relevant articles and documents

First synthesis of a pentadeuterated 3′-hydroxystanozolol - An internal standard in doping analysis

The first synthesis of 16,16,20,20,20-pentadeuterio-3′- hydroxystanozolol (8) in 26% yield over nine steps is described using moderately priced starting materials and economic amounts of reagents. Compound 8 can be used as an internal standard in screening procedures for anabolic steroids as well as for the quantification of stanozolol metabolites via mass spectrometric techniques, such as LC-MS or gas chromatography-mass spectrometry (GC-MS).