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145-41-5

145-41-5

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145-41-5 Usage

Chemical Properties

mp >300°C

Uses

Different sources of media describe the Uses of 145-41-5 differently. You can refer to the following data:
1. glycopeptide antibiotic complex from Actinoplanes teichomyceticus, structurally related to vancomycin, comprised of 5 major components differentiated by a specific fatty acid moiety. It inhibits peptidoglycan synthesis in the cell wall of gram-positive ba
2. choleretic
3. Sodium Dehydrocholate is a compound used to study biliary excretion.

Brand name

Decholin Sodium (Bayer).

Check Digit Verification of cas no

The CAS Registry Mumber 145-41-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 145-41:
(5*1)+(4*4)+(3*5)+(2*4)+(1*1)=45
45 % 10 = 5
So 145-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H34O5.Na/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26;/h13-14,16-18,22H,4-12H2,1-3H3,(H,28,29);/q;+1/p-1/t13-,14+,16-,17+,18+,22+,23+,24-;/m1./s1

145-41-5 Well-known Company Product Price

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  • TCI America

  • (D0043)  Sodium Dehydrocholate  >98.0%(T)

  • 145-41-5

  • 25g

  • 820.00CNY

  • Detail

145-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium dehydrocholate

1.2 Other means of identification

Product number -
Other names biliton

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:145-41-5 SDS

145-41-5Synthetic route

C34H50O10

C34H50O10

diethyl (2R,3R)-tartrate
87-91-2

diethyl (2R,3R)-tartrate

3,7,12-trioxo-5β-cholan-24-oic acid ethyl ester
52718-49-7

3,7,12-trioxo-5β-cholan-24-oic acid ethyl ester

A

C28H35O10(3-)*3Na(1+)

C28H35O10(3-)*3Na(1+)

B

Biliton
145-41-5

Biliton

C

sodium L-tartrate
526-94-3, 868-18-8, 4504-50-1, 14475-11-7, 21106-15-0, 21348-52-7, 21595-79-9, 22476-77-3, 25817-08-7, 51307-92-7, 60131-40-0, 64183-71-7, 109175-69-1

sodium L-tartrate

Conditions
ConditionsYield
With methanol; sodium hydroxide; water
Biliton
145-41-5

Biliton

7,12-dioxolitocholic acid
517-33-9

7,12-dioxolitocholic acid

Conditions
ConditionsYield
With phosphate buffer; 3α-HSDH from Pseudomonas paucimobilis; NAD; iso-butanol In water at 22℃; for 48h;100%
With hydrogen; nickel In water at 30℃; for 2h; pH=8.8; ultrasound irradiation;80%
triphenylsulfonium 2-(4-chlorobutyryloxy)-1,1,3,3,3-pentafluoropropane-1-sulfonate
1126206-31-2

triphenylsulfonium 2-(4-chlorobutyryloxy)-1,1,3,3,3-pentafluoropropane-1-sulfonate

Biliton
145-41-5

Biliton

triphenylsulfonium 2-{4-[4-(10,13-dimethyl-3,7,12-trioxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanoyloxy]-butyryloxy}-1,1,3,3,3-pentafluoropropane-1-sulfonate

triphenylsulfonium 2-{4-[4-(10,13-dimethyl-3,7,12-trioxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanoyloxy]-butyryloxy}-1,1,3,3,3-pentafluoropropane-1-sulfonate

Conditions
ConditionsYield
With sodium iodide In N,N-dimethyl-formamide at 80℃; for 11h;50%
Biliton
145-41-5

Biliton

A

7,12-dioxolitocholic acid
517-33-9

7,12-dioxolitocholic acid

B

3β-hydroxy-7,12-diketo-5β-cholan-24-oic acid
3615-35-8

3β-hydroxy-7,12-diketo-5β-cholan-24-oic acid

Conditions
ConditionsYield
With malt extract; D-glucose; Collybia velutipes In water at 24℃; for 168h; Microbiological reaction;A 40%
B 20%
triphenylsulfonium 2-(2-chloroacetoxy)-1,1,3,3,3-pentafluoropropane-1-sulfonate
1126206-28-7

triphenylsulfonium 2-(2-chloroacetoxy)-1,1,3,3,3-pentafluoropropane-1-sulfonate

Biliton
145-41-5

Biliton

triphenylsulfonium 2-{4-[4-(10,13-dimethyl-3,7,12-trioxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanoyloxy]-acetoxy}-1,1,3,3,3-pentafluoropropane-1-sulfonate

triphenylsulfonium 2-{4-[4-(10,13-dimethyl-3,7,12-trioxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanoyloxy]-acetoxy}-1,1,3,3,3-pentafluoropropane-1-sulfonate

Conditions
ConditionsYield
With sodium iodide In N,N-dimethyl-formamide at 90℃; for 15h;24%
1-methylnicotinamide chloride
1005-24-9

1-methylnicotinamide chloride

Biliton
145-41-5

Biliton

C31H38N2O5

C31H38N2O5

Conditions
ConditionsYield
With potassium hydroxide for 12h; Ambient temperature;16.6%
Biliton
145-41-5

Biliton

erythromycin
114-07-8

erythromycin

C37H67NO13*C24H34O5

C37H67NO13*C24H34O5

Conditions
ConditionsYield
With phosphate buffer pH=5.5; ion pair formation;
Biliton
145-41-5

Biliton

methyl 3α-hydroxy-7,12-dioxo-5β-cholan-24-oate
10538-66-6

methyl 3α-hydroxy-7,12-dioxo-5β-cholan-24-oate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 40 percent / Collybia velutipes; glucose; malt extract / H2O / 168 h / 24 °C / Microbiological reaction
2: methanesulfonic acid; Na2SO4 / 0.03 h / Microwave irradiation
View Scheme
Multi-step reaction with 2 steps
1: 80 percent / H2 / Raney nickel / H2O / 2 h / 30 °C / pH 8.8 / ultrasound irradiation
2: methanesulfonic acid; Na2SO4 / 0.03 h / Microwave irradiation
View Scheme
Biliton
145-41-5

Biliton

methyl 3β-hydroxy-7,12-dioxo-5β-cholanate
81847-12-3

methyl 3β-hydroxy-7,12-dioxo-5β-cholanate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 20 percent / Collybia velutipes; glucose; malt extract / H2O / 168 h / 24 °C / Microbiological reaction
2: methanesulfonic acid; Na2SO4 / 0.03 h / Microwave irradiation
View Scheme
C28H35O10(3-)*3Na(1+)

C28H35O10(3-)*3Na(1+)

Biliton
145-41-5

Biliton

A

C32H42O15

C32H42O15

B

C32H42O15

C32H42O15

C

C28H38O10
623552-24-9

C28H38O10

D

dehydrocholic acid
81-23-2

dehydrocholic acid

Conditions
ConditionsYield
With sulfuric acid; water In ethyl acetate pH=1 - 5;

145-41-5Related news

The aggregation of Sodium dehydrocholate (cas 145-41-5) in water09/30/2019

We used a battery of different methods to study the association in aqueous sodium dehydrocholate (NaDHC) solutions. This salt associates by a stepwise mechanism. Below (9.64.2)104 moldm3 there is a molecular solution with some strongly insoluble dehydrocholic acid produced by hydrolysis. Between...detailed

145-41-5Relevant articles and documents

Platinum complexes containing chemically modified bile acids, having antitumor activity

-

Page/Page column 2-3; 6, (2010/02/11)

The present invention relates to platinum complexes containing bile acid derivatives having antitumor activity

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