D6750
Sodium deoxycholate
≥97% (titration)
Synonym(s):
3α,12α-Dihydroxy-5β-cholanic acid sodium salt, 7-Deoxycholic acid sodium salt, Desoxycholic acid sodium salt
About This Item
Recommended Products
biological source
bovine bile
Quality Level
description
anionic
Assay
≥97% (titration)
form
powder
mol wt
micellar avg mol wt 1200-5000
aggregation number
3-12
CMC
2-6 mM (20-25°C)
solubility
water: 50 mg/mL, clear, colorless to light yellow
HLB
16
functional group
carboxylic acid
shipped in
ambient
storage temp.
room temp
SMILES string
[Na+].[H][C@]12CC[C@@]3([H])[C@]4([H])CC[C@H]([C@H](C)CCC([O-])=O)[C@@]4(C)[C@@H](O)C[C@]3([H])[C@@]1(C)CC[C@@H](O)C2
InChI
1S/C24H40O4.Na/c1-14(4-9-22(27)28)18-7-8-19-17-6-5-15-12-16(25)10-11-23(15,2)20(17)13-21(26)24(18,19)3;/h14-21,25-26H,4-13H2,1-3H3,(H,27,28);/q;+1/p-1/t14-,15-,16-,17+,18-,19+,20+,21+,23+,24-;/m1./s1
InChI key
FHHPUSMSKHSNKW-SMOYURAASA-M
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General description
Moreover, Sodium Deoxycholate extends its utility to nucleic acid extraction from cells and tissues. By lysing cells and disrupting cellular structures, it facilitates the release and purification of nucleic acids, proving valuable in cell biology and biochemical research. Beyond these applications, its effectiveness in cell lysis processes positions it as a valuable tool for breaking down cells and releasing their contents, finding applications in diverse biological studies, encompassing microscopy, cell biology, and biochemical research.
Application
Biochem/physiol Actions
Features and Benefits
Other Notes
also commonly purchased with this product
comparable product
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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