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Merck
CN

86345

Sodium taurodeoxycholate hydrate

≥94.0% (TLC)

Synonym(s):

3α,12α-Dihydroxy-5β-cholan-24-oic acid N-(2-sulfoethyl)amide sodium salt, N-(Deoxycholyl)taurine sodium salt, Taurodeoxycholic acid sodium salt

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About This Item

Empirical Formula (Hill Notation):
C26H44NNaO6S · xH2O
CAS Number:
Molecular Weight:
521.69 (anhydrous basis)
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
3901204
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description

anionic

assay

≥94.0% (TLC)

optical activity

[α]20/D +33.5±1°, c = 2.5% in H2O

solubility

H2O: 0.1 g/mL, clear, colorless to very faintly yellow

SMILES string

[Na+].[H]O[H].[H][C@]12CC[C@@]3([H])[C@]4([H])CC[C@]([H])([C@H](C)CCC(=O)NCCS([O-])(=O)=O)[C@@]4(C)[C@@H](O)C[C@]3([H])[C@@]1(C)CC[C@@H](O)C2

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Other Notes

Mixed micelle component; Effect on hydrolysis of gangliosides, glycoproteins and neuraminyl-lactose by neuraminidase

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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D P Hajjar et al.
The Journal of biological chemistry, 258(1), 192-198 (1983-01-10)
We describe here an activable neutral cholesteryl esterase (EC 3.1.1.13) in arteries similar to the hormone-sensitive lipase of adipose tissue and adrenal cortex. Maximum enzyme activity in rabbit aorta was given by cholesteryl ester substrates dispersed as a mixed micelle
S Gatt et al.
The Biochemical journal, 193(1), 267-273 (1981-01-01)
Studies were done on the effect of bile salts on the rates of hydrolysis of the N-acetylneuraminyl linkages of several sialic acid-containing compounds by the neuraminidase of Clostridium perfringens. When GM3-ganglioside, two glycolipids (glycophorin and orosomucoid) and neuraminyl-lactose were used

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