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Home  > Taurohyodeoxycholic acid sodium salt hydrate

AE08162

110026-03-4 | Taurohyodeoxycholic acid sodium salt hydrate

Packsize Purity Availability Price Discounted Price    Quantity
1mg 95% in stock $15.00 $10.00 -   +
100mg 95% in stock $18.00 $12.00 -   +
1g 95% in stock $42.00 $29.00 -   +
5g 95% in stock $113.00 $79.00 -   +

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*All prices are in USD.

Description
Catalog Number: AE08162
Chemical Name: Taurohyodeoxycholic acid sodium salt hydrate
CAS Number: 110026-03-4
Molecular Formula: C26H46NNaO7S
Molecular Weight: 539.7007
MDL Number: MFCD09263185
SMILES: [Na]OS(=O)(=O)CCNC(=O)CC[C@H]([C@H]1CC[C@@H]2[C@]1(C)[C@@H](O)C[C@H]1[C@H]2CC[C@H]2[C@]1(C)CC[C@H](C2)O)C.O

 

Upstream Synthesis Route
  • Sodium taurodeoxycholate monohydrate, a derivative of the naturally occurring bile salt taurodeoxycholic acid, serves as a valuable reagent in chemical synthesis. This compound, due to its unique properties, finds widespread application in various synthetic procedures within the realm of organic chemistry.One of the prominent utilizations of sodium taurodeoxycholate monohydrate is as a chiral selector in chromatographic separations. Its ability to interact selectively with enantiomers enables the resolution of racemic mixtures, crucial in the production of optically pure compounds. Furthermore, in the synthesis of pharmaceuticals, this compound plays a pivotal role in the preparation of drug molecules with specific stereochemical configurations.In addition to its chiral recognition properties, sodium taurodeoxycholate monohydrate also functions as a surfactant in various chemical reactions. By lowering interfacial tension, it enhances the solubilization and dispersion of hydrophobic compounds in aqueous solutions. This attribute is particularly beneficial in formulations requiring emulsification or micelle formation, facilitating efficient chemical transformations.Moreover, the amphiphilic nature of sodium taurodeoxycholate monohydrate makes it an effective solubilizing agent for poorly water-soluble compounds. By forming stable complexes with hydrophobic molecules, it improves their dissolution rates and bioavailability, essential considerations in the development of pharmaceutical formulations.Overall, the multifaceted role of sodium taurodeoxycholate monohydrate in chemical synthesis underscores its significance as a versatile reagent with diverse applications across different sectors of the chemical industry.
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