Sodium taurocholate CAS#: 145-42-6

Sodium taurocholate Basic information

Product Name:

Sodium taurocholate

Synonyms:

2-([3-ALPHA,7-ALPHA,12-ALPHA-TRIHYDROXY-24-OXO-5-BETA-CHOLAN-24-YL]AMINO)ETHANESULFONIC ACID
ethanesulfonicacid,2-[[(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxy-24
monosodiumtaurocholicacid
n-choloyl-taurinsodiumsalt
taurocholatesodium
taurocholatesodiumsalt
5BETA-CHOLANIC ACID-3ALPHA,7ALPHA,12ALPHA-TRIOL 24-N-(2-SULFOETHYL) AMIDE SODIUM
5-BETA-CHOLANIC ACID-3-ALPHA, 7-ALPHA, 12-ALPHA-TRIOL N-(2-SULPHOETHYL)-AMIDE SODIUM SALT

CAS:

145-42-6

MF:

C26H44NNaO7S

MW:

537.68

EINECS:

205-653-7

Product Categories:

Bile Acids
Biochemistry
Steroids
145-42-6

Mol File:

145-42-6.mol

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Sodium taurocholate Chemical Properties

Melting point:: 230 °C
alpha: 23 º (c=3 H2O)
Density: 1.177 g/cm3(Temp: 22.5 °C)
refractive index: 23 ° (C=3, H2O)
Flash point:: 9℃
storage temp.: -20°C
solubility: H₂O: 0.5 M at 20 °C, clear, colorless to faintly yellow
form: Solid
color: Brown to greenish brown
PH: pH (30g/l, 25℃) : 4.5～7.5
Water Solubility: > 250 g/L (20 ºC)
Decomposition: 125°C
Merck: 14,9075
BRN: 3901620
LogP: 0.051 (est)
CAS DataBase Reference: 145-42-6(CAS DataBase Reference)
EPA Substance Registry System: Ethanesulfonic acid, 2-[[(3.alpha.,5.beta.,7.alpha.,12.alpha.)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino]-, monosodium salt (145-42-6)

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Safety Information

Risk Statements: 36/37/38
Safety Statements: 26-36/37/39-24/25
RIDADR: UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany: 3
RTECS: WX0400000
F: 3-10
HS Code: 29049090

MSDS

Language:English Provider:Sodium 2-[(3a,7a,12a-trihydroxy-24-oxo-5beta-cholan-24-yl)amino]ethanesulfonate

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Sodium taurocholate Usage And Synthesis

Chemical Properties

White to off-white powder

Uses

Sodium taurocholate is a detergent useful for the solubilization of lipids and membrane-bound proteins.

Uses

selectively activates retinoid X receptors (RXRs)

Definition

ChEBI: Sodium taurocholate is a bile salt. It contains a taurocholate.

Purification Methods

Purify it by recrystallisation and gel chromatography using Sephadex LH-20. [Beilstein 10 III 1655, 10 IV 2078.]

Sodium taurocholateSupplier

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