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16564-43-5

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16564-43-5 Usage

Chemical Properties

White to off-white powder

Uses

Different sources of media describe the Uses of 16564-43-5 differently. You can refer to the following data:
1. Glycochenodeoxycholic Acid Sodium Salt is a bile salt formed in the liver from chenodeoxycholate and glycine. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic.
2. Sodium glycochenodeoxycholate has been used in a study to assess the repair of DNA damage induced by bile salts. It has also been used in a study to investigate enterotoxin production by Clostridium perfringens type A in the presence of human bile salts.

Definition

ChEBI: A bile acid salt that is the sodium salt of glycochenodeoxycholic acid.

Purification Methods

Dissolve it in EtOH, filter it and concentrate it to crystallisation, and recrystallise from a little EtOH. It also recrystallises from EtOH/Et2O. [Beilstein 10 IV 1611.]

Check Digit Verification of cas no

The CAS Registry Mumber 16564-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,6 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16564-43:
(7*1)+(6*6)+(5*5)+(4*6)+(3*4)+(2*4)+(1*3)=115
115 % 10 = 5
So 16564-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C26H43NO5.Na/c1-15(4-7-22(30)27-14-23(31)32)18-5-6-19-24-20(9-11-26(18,19)3)25(2)10-8-17(28)12-16(25)13-21(24)29;/h15-21,24,28-29H,4-14H2,1-3H3,(H,27,30)(H,31,32);/t15-,16+,17-,18-,19+,20+,21-,24+,25+,26-;/m1./s1

16564-43-5 Well-known Company Product Price

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  • Sigma

  • (G0759)  Sodium glycochenodeoxycholate  ≥97% (HPLC)

  • 16564-43-5

  • G0759-25MG

  • 451.62CNY

  • Detail
  • Sigma

  • (G0759)  Sodium glycochenodeoxycholate  ≥97% (HPLC)

  • 16564-43-5

  • G0759-100MG

  • 558.09CNY

  • Detail
  • Sigma

  • (G0759)  Sodium glycochenodeoxycholate  ≥97% (HPLC)

  • 16564-43-5

  • G0759-500MG

  • 1,890.72CNY

  • Detail
  • Sigma

  • (G0759)  Sodium glycochenodeoxycholate  ≥97% (HPLC)

  • 16564-43-5

  • G0759-1G

  • 4,284.54CNY

  • Detail
  • Sigma

  • (G0759)  Sodium glycochenodeoxycholate  ≥97% (HPLC)

  • 16564-43-5

  • G0759-10G

  • 23,821.20CNY

  • Detail
  • Sigma

  • (G0759)  Sodium glycochenodeoxycholate  ≥97% (HPLC)

  • 16564-43-5

  • G0759-25G

  • 47,700.90CNY

  • Detail
  • Sigma

  • (50534)  Sodium glycochenodeoxycholate  ≥97.0% (TLC)

  • 16564-43-5

  • 50534-250MG

  • 1,084.59CNY

  • Detail
  • Sigma

  • (50534)  Sodium glycochenodeoxycholate  ≥97.0% (TLC)

  • 16564-43-5

  • 50534-1G

  • 4,290.39CNY

  • Detail

16564-43-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Glycochenodeoxycholic acid sodium

1.2 Other means of identification

Product number -
Other names N-(3α,7α-Dihydroxy-24-oxocholan-24-yl)glycine sodium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16564-43-5 SDS

16564-43-5Relevant articles and documents

Continuous flow synthesis and scale-up of glycine- and taurine-conjugated bile salts

Venturoni, Francesco,Gioiello, Antimo,Sardella, Roccaldo,Natalini, Benedetto,Pellicciari, Roberto

experimental part, p. 4109 - 4115 (2012/06/15)

A multi-gram scale protocol for the N-acyl amidation of bile acids with glycine and taurine has been successfully developed under continuous flow processing conditions. Selecting ursodeoxycholic acid (UDCA) as the model compound and N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) as the condensing agent, a modular mesoreactor assisted flow set-up was employed to significantly speed up the optimization of the reaction conditions and the flow scale-up synthesis. The results in terms of yield, in line purification, analysis, and implemented flow set-up for the reaction optimization and large scale production are reported and discussed.

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