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63-01-4

63-01-4 Structure

63-01-4 Structure
IdentificationBack Directory
[Name]

19-HYDROXYTESTOSTERONE-19-CME
[CAS]

63-01-4
[Synonyms]

16-hydroxytestosterone
16A-HYDROXYTESTOSTERONE
19-HYDROXYTESTOSTERONE-19-CME
4-Androstene-16α,17β-diol-3-one
4-Androstene-16ALPHA,17B-diol-3-one
16α,17β-Dihydroxyandrost-4-en-3-one
16A hydroxytestosterone--dea schedule*iii item
4-ANDROSTEN-17-BETA, 19-DIOL-3-ONE-19-CARBOXYMETHYLETHER
16α, 17β-Dihydroxyandrost-4-en-3-one, 4-Androstene-16α,17β-diol-3-one
(8R,9S,10R,13S,14S,16R,17R)-16,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
[Molecular Formula]

C19H28O3
[MDL Number]

MFCD00273183
[MOL File]

63-01-4.mol
[Molecular Weight]

304.43
Chemical PropertiesBack Directory
[Melting point ]

192-194 °C
[storage temp. ]

2-8°C
Hazard InformationBack Directory
[Uses]

16α-Hydroxytestosterone is an metabolite of Testosterone (T155000), the major circulating androgen. Testosterone was found to be metabolized by cytochrome P-450 to 16α-Hydroxytestosterone in rat liver .
[Definition]

ChEBI: 16alpha-hydroxytestosterone is a C19-steroid that is testosterone in which the hydrogen at the 16alpha position has been replaced by a hydroxy group. It has a role as an androgen. It is a 3-oxo-Delta(4) steroid, a 16alpha-hydroxy steroid, a 17beta-hydroxy steroid, a C19-steroid, an androstanoid, a diol and a secondary alcohol. It is functionally related to a testosterone.
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H312-H302-H332-H351-H361
[Precautionary statements ]

P280-P302+P352-P312-P322-P363-P501-P201-P202-P281-P308+P313-P405-P501-P264-P270-P301+P312-P330-P501-P201-P202-P281-P308+P313-P405-P501-P261-P271-P304+P340-P312
[Hazard Codes ]

Xn
[Risk Statements ]

61-40-20/21/22-63
[Safety Statements ]

53-22-36/37/39-36/37
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