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750026

Sigma-Aldrich

3α,5β-Tetrahydroaldosterone

≥98% (CP)

Synonym(s):

11β,18-Epoxy-3α,18,21-trihydroxy-5β-pregnan-20-one, 5β-Pregnan-11β,18-epoxy-3α,18,21-triol-20-one

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About This Item

Empirical Formula (Hill Notation):
C21H32O5
CAS Number:
Molecular Weight:
364.48
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.24

Quality Level

Assay

≥98% (CP)

form

powder

technique(s)

mass spectrometry (MS): suitable

storage temp.

−20°C

SMILES string

C[C@]12CC[C@@H](O)C[C@H]1CC[C@H]3[C@@H]4CC[C@H](C(=O)CO)[C@@]45C[C@H](O[C@@H]5O)[C@H]23

InChI

1S/C21H32O5/c1-20-7-6-12(23)8-11(20)2-3-13-14-4-5-15(16(24)10-22)21(14)9-17(18(13)20)26-19(21)25/h11-15,17-19,22-23,25H,2-10H2,1H3/t11-,12-,13+,14+,15-,17+,18-,19+,20+,21-/m1/s1

InChI key

JDEYOKPHRJVBQO-BMDKAXIVSA-N

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Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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G T Griffing et al.
Hypertension (Dallas, Tex. : 1979), 7(2), 178-181 (1985-03-01)
19-Nor-deoxycorticosterone (19-nor-DOC) is a human mineralocorticoid. The regulation of its secretion is poorly understood, as renin angiotensin II (ANG II) stimulation has minimal effects on 19-nor-DOC. This study sought to determine if ANG II inhibition would decrease 19-nor-DOC production. Six
S Ulick et al.
The Journal of clinical endocrinology and metabolism, 76(4), 873-878 (1993-04-01)
18-Hydroxycortisol and 18-oxocortisol have been isolated from the urine of patients with aldosterone producing adrenocortical adenomas, but not from those with idiopathic hyperaldosteronism associated with bilateral adrenal hyperplasia. These C-18 oxygenated cortisols are biosynthesized by the substitution of cortisol for
D Armanini et al.
Journal of endocrinological investigation, 19(9), 624-629 (1996-10-01)
The pathogenesis of pseudohyperaldosteronism from licorice has been evaluated in 6 male volunteers taking daily 7 g of a commercial preparation of licorice for 7 days, corresponding to an intake of 500 mg/day of glycyrrhizic acid. Pseudohyperaldosteronism was evident during
S A Latif et al.
Steroids, 49(6), 589-600 (1987-06-01)
Specific methods are described for the enzymatic synthesis of each of the six possible 3H-labeled Ring-A reduced metabolites of aldosterone (5 alpha- and 5 beta-DHAldo; 3 alpha,5 alpha-THAldo; 3 beta,5 alpha-THAldo; 3 alpha,5 beta-THAldo; and 3 beta,5 beta-THAldo; see footnote
D Rolland et al.
Annales de biologie clinique, 45(1), 70-73 (1987-01-01)
The authors describe a method of titration of tetrahydroaldosterone in the urine, requiring an internal non-radioactive standard. This method uses high performance liquid chromatography as a mean of isolating tetrahydroaldosterone (THAldo) and chromatography in gaseous phase as a method of

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