Skip to Content
Merck
CN
All Photos(1)

Documents

30830

Sigma-Aldrich

Dehydrocholic acid

≥99.0% (T)

Sign Into View Organizational & Contract Pricing

Synonym(s):
(5β)-3,7,12-Trioxocholan-24-oic acid, 3,7,12-Trioxo-5β-cholanic acid, 5β-Cholanic acid-3,5,12-trione
Empirical Formula (Hill Notation):
C24H34O5
CAS Number:
Molecular Weight:
402.52
Beilstein:
3226734
EC Number:
MDL number:
UNSPSC Code:
41141802
PubChem Substance ID:
NACRES:
NA.77

biological source

bovine bile
synthetic

Quality Level

description

anionic

Assay

≥99.0% (T)

form

powder

optical activity

[α]20/D +26±1°, c = 1% in ethanol

mp

238-240 °C

solubility

ethanol: 10 mg/mL, clear (hot)

functional group

carboxylic acid

SMILES string

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

InChI

1S/C24H34O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h13-14,16-18,22H,4-12H2,1-3H3,(H,28,29)/t13-,14+,16-,17+,18+,22+,23+,24-/m1/s1

InChI key

OHXPGWPVLFPUSM-KLRNGDHRSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Dehydrocholic acid was used to study the interaction of bile salts with copper ions in unbuffered systems.

Biochem/physiol Actions

Dehydrocholic acid is an oxidation product of cholic acid by chromic acid that is not present in physiological conditions. When used in animal experiments, it stimulates bile secretion.

Preparation Note

Dehydrocholic acid yields clear solution in hot ethanol at 10 mg/ml.

Other Notes

In the production of chenodeoxycholic acid by bioconversion

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

H. Sawada et al.
Adv. Biotechnol., [Proc. Int. Ferment. Symp.], 6th (1980) (C.Vezina,K.Singh eds., 3, 495-495 (1981)
R D Soloway et al.
The Journal of clinical investigation, 52(3), 715-724 (1973-03-01)
[24-(14)C]Dehydrocholic acid (triketo-5-beta-cholanoic acid) was synthesized from [24-(14)C]cholic acid, mixed with 200 mg of carrier, and administered intravenously to two patients with indwelling T tubes designed to permit bile sampling without interruption of the enterohepatic circulation. More than 80% of
G Feroci et al.
Journal of pharmaceutical sciences, 84(1), 119-125 (1995-01-01)
Interaction of bile salts with Cu2+ ions in unbuffered systems containing 0.15 M NaNO3 was followed by measuring polarographic limiting currents and half-wave potentials. Whereas taurocholate forms neither soluble complexes nor compounds of limited solubility, cholate, glycocholate, and dehydrocholate from
Paula V Messina et al.
Colloids and surfaces. B, Biointerfaces, 75(1), 34-41 (2009-09-08)
The physicochemical and elastic properties of Langmuir mixed monolayers composed by dehydrocholic acid (HDHC) and didodecyldimethylammonium bromide (DDAB) were evaluated. The experiments were performed with a constant surface pressure penetration Langmuir balance based on Axisymmetric Drop Shape Analysis (ADSA). The
W B Mors et al.
Phytochemistry, 55(6), 627-642 (2000-12-29)
The article surveys the substances identified in plants reputed to neutralize the effects of snake venoms. Protective activity of many of them against the lethal action of the venom of the jararaca (Bothrops jararaca) snake was confirmed by biological assays.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service