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GLYCODEOXYCHOLIC ACID SODIUM SALT

GLYCODEOXYCHOLIC ACID SODIUM SALT structure

GLYCODEOXYCHOLIC ACID SODIUM SALT 

structure
  • CAS No:

    16409-34-0

  • Formula:

    C26H43NO5.Na

  • Chemical Name:

    GLYCODEOXYCHOLIC ACID SODIUM SALT

  • Synonyms:

    GDCA;GDCA, SODIUM SALT;GLYCODEOXYCHOLIC ACID SODIUM SALT;5-BETA-CHOLANIC ACID-3-ALPHA, 12-ALPHA-DIOL N-(CARBOXYMETHYL)-AMIDE SODIUM SALT;5BETA-CHOLAN-24-OIC ACID N-[CARBOXYMETHYL]AMIDE-3ALPHA,12ALPHA-DIOL SODIUM SALT;3ALPHA,12ALPHA-DIHYDROXY-5BETA-CHOLAN-24-OIC ACID N-(CARBOXYMETHYL)-AMIDE SODIUM SALT;Glycodeoxycholic Acid, Sodiu;(SYNONYMS: SODIUM GLYCYLDEOXYCHOLATE)

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

Sodium deoxyglycolic acid is a kind of bile salt, and exists in bile in the form of combining with glycine or taurine to form glycodeoxycholic acid or sodium taurodeoxycholate. It is cholanoic acid that forms many organic compounds and stable molecular compounds.


ChEBI: Sodium glycodeoxycholate is a bile acid salt that is the sodium salt of glycodeoxycholic acid. It has a role as a human metabolite. It is a bile acid salt and an organic sodium salt. It contains a glycodeoxycholate.


Sodium glycodeoxycholate is a bile salt that can be used to form biomimicking environments.

GLYCODEOXYCHOLIC ACID SODIUM SALT Basic Attributes

472.61

471.29606772

240-455-4

White to Off-White

29221990

Characteristics

Solid

245-250 °C

water: 10mg/mL

4.8

Inert atmosphere,2-8°C

Safety Information

3

Xi

26-36

MB9670000

36/37/38

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

GLYCODEOXYCHOLIC ACID SODIUM SALT Use and Manufacturing

Sodium glycodeoxycholate has been used in a study to develop more similar mimetic intestinal fluids to physiological fluids than those developed by mixed bile salt systems (MBS). It has also been used in a study to investigate Ca2+buffering capability of bile salt micelles.

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