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A2480

5α-Androstan-3β-ol

powder

Synonym(s):

3β-Hydroxy-5α-androstane

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About This Item

Empirical Formula (Hill Notation):
C19H32O
CAS Number:
Molecular Weight:
276.46
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
51111800
EC Number:
214-952-1
MDL number:
Form:
powder
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biological source

synthetic (organic)

sterility

non-sterile

form

powder

solubility

DMSO: soluble 14 mg/mL at ≤60 °C, H2O: insoluble

shipped in

ambient

storage temp.

room temp

SMILES string

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

InChI

1S/C19H32O/c1-18-9-3-4-16(18)15-6-5-13-12-14(20)7-11-19(13,2)17(15)8-10-18/h13-17,20H,3-12H2,1-2H3/t13-,14-,15-,16-,17-,18-,19-/m0/s1

InChI key

DJTOLSNIKJIDFF-LOVVWNRFSA-N

Application

5α-Androstan-3β-ol has been used as a cortisone analog to test its effect on the voltage-dependent potassium channel (Kv) current.[1]

Biochem/physiol Actions

mCAR (constitutive androstane receptor) inverse agonist; testosterone metabolite.

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This Item
A7755T8390E3375
form

powder

form

powder

form

powder

form

powder

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

solubility

DMSO: soluble 14 mg/mL at ≤60 °C, H2O: insoluble

solubility

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

solubility

ethanol: soluble 49-51 mg/mL, clear, colorless to faintly yellow

solubility

chloroform: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow

sterility

non-sterile

sterility

-

sterility

non-sterile

sterility

non-sterile

biological source

synthetic (organic)

biological source

-

biological source

-

biological source

synthetic (organic)

shipped in

ambient

shipped in

-

shipped in

ambient

shipped in

ambient


hcodes

Hazard Classifications

Aquatic Chronic 4

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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