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D3875

Sigma-Aldrich

Sodium dehydrocholate

~95%

Synonym(s):

3,7,12-Trioxo-5β-cholanic acid sodium salt, Dehydrocholic acid sodium salt

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About This Item

Empirical Formula (Hill Notation):
C24H33NaO5
CAS Number:
145-41-5
Molecular Weight:
424.51
Beilstein:
4119624
EC Number:
205-652-1
MDL number:
MFCD00066411
UNSPSC Code:
12000000

description

anionic

Assay

~95%

SMILES string

[Na+].[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

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Storage Class Code

13 - Non Combustible Solids

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’.

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M K Mohanty et al.
Tropical gastroenterology : official journal of the Digestive Diseases Foundation, 31(3), 184-189 (2011-05-13)
Small ductules communicating with the bile ducts have been described at the porta hepatis in extrahepatic biliary atresia (EHBA) and these form the basis for hepatic portoenterostomy. The use of cholagogues like dehydrocholic acid (DHC) and ursodeoxycholic acid (UDCA) to
Ana I Prieto et al.
Journal of bacteriology, 191(11), 3615-3622 (2009-04-07)
A genetic screen for suppressors of bile sensitivity in DNA adenine methylase (dam) mutants of Salmonella enterica serovar Typhimurium yielded insertions in an uncharacterized locus homologous to the Escherichia coli asmA gene. Disruption of asmA suppressed bile sensitivity also in
Tao Huang et al.
Biotechnology and applied biochemistry, 42(Pt 1), 47-56 (2004-12-23)
A novel chemically modified insulin, -NB29-DHC-insulin (where DHC-insulin stands for dehydrocholyl-insulin), was prepared by covalent linkage of DHC (dehydrocholic acid) to the -amino group of LysB29 without any protecting agent and analysed by PAGE and reversed-phase HPLC. DHC-insulin was identified
Boqiao Sun et al.
Biotechnology and bioengineering, 110(1), 68-77 (2012-07-19)
Ursodeoxycholic acid (UDCA) is a bile acid of industrial interest as it is used as an agent for the treatment of primary sclerosing cholangitis and the medicamentous, non-surgical dissolution of gallstones. Currently, it is prepared industrially from cholic acid following
Amr Ali Mohamed et al.
Journal of colloid and interface science, 368(1), 625-628 (2011-12-14)
Two methods for the preparation of uniform dispersions of dehydrocholic acid of different morphologies are described. In the first case, the drug was dissolved in acetone and then re-precipitated by adding a non-solvent (either water or an aqueous stabilizer solution)
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