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Ursodeoxycholylcysteic Acid CAS NO 119059-81-3
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CAS No.:119059-81-3
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Ursodeoxycholylcysteic Acid is a chemically modified bile acid derivative, synthesized from ursodeoxycholic acid. This compound is valued for its role as a key intermediate in advanced pharmaceutical research and development, particularly for creating novel therapeutic agents. It is primarily utilized by research institutions and pharmaceutical companies focused on hepatobiliary and metabolic disease treatments, as well as in the synthesis of specialized biochemical probes.
Application
- Pharmaceutical Intermediate: A critical building block in the synthesis of novel bile acid-based drugs and prodrugs targeting liver and intestinal diseases.
- Biochemical Research: Used as a reference standard or reagent in metabolic pathway studies, particularly those involving bile acid conjugation and transport.
- Probe Development: Serves as a precursor for developing fluorescent or radiolabeled probes to study bile acid receptor interactions and cellular uptake mechanisms.
- Academic & Contract Research: Employed in university and CRO laboratories for investigating cholestasis, gallstone dissolution, and related metabolic disorders.
Basic Information
| Product Name | Ursodeoxycholylcysteic Acid |
| CAS No. | 119059-81-3 |
| Molecular Formula | C₂₇H₄₅NO₇S |
| Molecular Weight | 527.71 g/mol |
| Synonyms | 3α,7β-Dihydroxy-5β-cholan-24-oyl-L-cysteic Acid; Ursodeoxycholyl-L-cysteic Acid; UDCA-Cysteic Acid; N-[(3α,5β,7β)-3,7-Dihydroxy-24-oxocholan-24-yl]-L-cysteic Acid; Ursodeoxycholic Acid Cysteic Acid Conjugate; Tauroursodeoxycholic Acid Sulfonate Analog; Bile Acid-Cysteic Acid Conjugate |
| EINECS | Contact for details |
Quality Control
Our Ursodeoxycholylcysteic Acid is produced under strict quality management protocols to ensure high purity and batch-to-batch consistency, suitable for research and development purposes. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to cGMP principles where applicable, and specifications can be aligned with client requirements for advanced pharmaceutical applications.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); ensure the container is sealed tightly after each use to minimize exposure to atmospheric humidity. For long-term storage, consider desiccants or an inert atmosphere.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 95.0% |
| Related Substances (HPLC) | Total impurities ≤ 3.0% |
| Water Content (KF) | ≤ 5.0% |
| Residue on Ignition | ≤ 0.5% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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