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Sodium deoxycholate monohydrate

Original price was: $3,395.00.Current price is: $1,695.00.

Catalog Number: B2018527 (10 g)
Sodium deoxycholate monohydrate is a compound used in biochemical and molecular biology research to aid in protein extraction, solubilization, and cell lysis. It can also disrupt cell membranes to release proteins for analysis. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (2 votes)

Sodium deoxycholate monohydrate
Catalog number: B2018527
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 10 g
Molecular Weight or Concentration: 432.57 g/mol
Supplied as: Powder
Applications: a molecular tool for various biochemical applications
Storage: RT
Keywords: 3α,12α-Dihydroxy-5β-cholanic acid sodium salt, 7-Deoxycholic acid sodium salt, Desoxycholic acid sodium salt
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Dowling RH. Review: pathogenesis of gallstones Aliment Pharmacol Ther. 2000 May;14 Suppl 2:39-47.
2: Campanelli AR, Candeloro De Sanctis S, Giglio E, Scaramuzza L. A model for micellar aggregates of a bile salt: crystal structure of sodium taurodeoxycholate monohydrate J Lipid Res. 1987 May;28(5):483-9.
3: Tseng YJ, Kuo CT, Wang SY, Liao HW, Chen GY, Ku YL, Shao WC, Kuo CH. Metabolomic characterization of rhubarb species by capillary electrophoresis and ultra-high-pressure liquid chromatography Electrophoresis. 2013 Oct;34(19):2918-27.
4: Gupta SL, Higuchi WI, Ho NF. Cholesterol monohydrate dissolution rate studies in aqueous micellar sodium chenodeoxycholate solutions J Pharm Sci. 1985 Nov;74(11):1178-83.
5: Poša M, Bjedov S, Sebenji A, Sakač M. Wittig reaction (with ethylidene triphenylphosphorane) of oxo-hydroxy derivatives of 5β-cholanic acid: Hydrophobicity, haemolytic potential and capacity of derived ethylidene derivatives for solubilisation of cholesterol Steroids. 2014 Aug;86:16-25.
6: Salvioli G, Igimi H, Carey MC. Cholesterol gallstone dissolution in bile. Dissolution kinetics of crystalline cholesterol monohydrate by conjugated chenodeoxycholate-lecithin and conjugated ursodeoxycholate-lecithin mixtures: dissimilar phase equilibria and dissolution mechanisms J Lipid Res. 1983 Jun;24(6):701-20.
7: Igimi H, Carey MC. Cholesterol gallstone dissolution in bile: dissolution kinetics of crystalline (anhydrate and monohydrate) cholesterol with chenodeoxycholate, ursodeoxycholate, and their glycine and taurine conjugates J Lipid Res. 1981 Feb;22(2):254-70.
8: Rodríguez-Nogales A, Algieri F, Vezza T, Garrido-Mesa J, Molina-Tijeras JA, Rodríguez-Cabezas ME, Utrilla MP, Pischel I, Gálvez J. Calcium Pyruvate Exerts Beneficial Effects in an Experimental Model of Irritable Bowel Disease Induced by DCA in Rats Nutrients. 2019 Jan 10;11(1):140.
9: Park YH, Igimi H, Carey MC. The “mirroring” of gallstones: description of a novel silvering method to determine the surface area of an irregular object. In vitro demonstration that multiple gallstones from the same gallbladder dissolve in unsaturated “bile” at the same rate Gastroenterology. 1982 Nov;83(5):1071-8.
10: Polonini H, da Silva SL, Brandão MAF, Bauters T, De Moerloose B, Ferreira AO. Compatibility of Baclofen, Carvedilol, Hydrochlorothiazide, Mercaptopurine, Methadone Hydrochloride, Oseltamivir Phosphate, Phenobarbital, Propranolol Hydrochloride, Pyrazinamide, Sotalol Hydrochloride, Spironolactone, Tacrolimus Monohydrate, Ursodeoxycholic Acid, and Vancomycin Hydrochloride Oral Suspensions Compounded with SyrSpend SF pH4 Int J Pharm Compd. 2018 Nov-Dec;22(6):516-526.

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Additional Information

Weight 2.6 oz
Dimensions 3.3 × 1.2 × 1.2 in
5/5 - (2 votes)

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