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Merck
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Key Documents

D3875

Sigma-Aldrich

Sodium dehydrocholate

~95%

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C24H33NaO5
Número CAS:
Peso molecular:
424.51
Beilstein:
4119624
Número CE:
Número MDL:
Código UNSPSC:
12000000

descrição

anionic

Ensaio

~95%

cadeia de caracteres SMILES

[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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Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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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
Yuji Sakai et al.
Hepato-gastroenterology, 55(81), 17-20 (2008-05-30)
The aim of this study was to investigate whether exogenous dehydrocholic acid (DHCA) was useful to enhance the delineation of anastomotic site. DHCA is a cholagogue which produces an immediate effect by acting directly on liver cells. Its choleretic effect
Paula V Messina et al.
Biophysical chemistry, 132(1), 39-46 (2007-10-31)
Bile acids (deoxycholic and dehydrocholic acids) spread mixed monolayers behavior at the air/water interface were studied as a function of subphase pH using a constant surface pressure penetration Langmuir balance based on the Axisymmetric Drop Shape Analysis (ADSA). We examined
What we counted.
Robert L Rosenthal
The American journal of cardiology, 111(7), 1073-1075 (2013-01-29)
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

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