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Ursodeoxycholic Acid Impurity 1

SZ目录编号 SZ-U003015
CAS 号 139265-35-3
分子式 C23H38O5
分子量 394.6
投资状态 Custom Synthesis


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SynZeal will update these details as per new development or finding in product specification without further noticed.

化学名称: (R)-3-((3R,5S,7S,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)butanoic acid

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: C[C@@]([C@]1([H])C[C@@H]2O)(CC[C@@H](O)C1)[C@]3([H])[C@]2([H])[C@@](CC[C@]4([H])[C@H](C)CC(O)=O)([H])[C@]4(C)[C@@H](O)C3

Ursodeoxycholic Acid Impurity 1 is chemically (R)-3-((3R,5S,7S,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)butanoic acid. Ursodeoxycholic Acid Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Ursodeoxycholic Acid Impurity 1 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Ursodeoxycholic.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

A validated RP-HPLC method for quantitative determination of related impurities of ursodeoxycholic acid (API) by refractive index detection
Ashok Peepliwal, C.G.Bonde, K.G.Bothara
Journal of Pharmaceutical and Biomedical Analysis Volume 54, Issue 4, 25 March 2011, Pages 845-849
 
Determination of Chenodeoxycholic Acid in Pharmaceutical Preparations of Ursodeoxycholic Acid by High Performance Liquid Chromatography with Coulometric Electrochemical Detection
E. Bousquet, N. A. Santagati & S. Tirendi
Journal of Liquid Chromatography & Related Technologies  Volume 20, 1997 - Issue 5 Pages 757-770
 
Validated High-performance Liquid Chromatography Method for Degradation Study of Ursodeoxycholic Acid and Silymarin
Imran A. Sheikh, Manoj Charde , Abhilasha Mittal
International Journal of Pharmaceutical & Biological Archives 2018; 9(3):73-77

  • We need to receive valid purchase order with Bill to & Ship to address.
  • The quotation ID needs to be mentioned in the purchase order.
  • You will receive order confirmation prior to dispatch which need to be verified for any error in product, pack size, prices.

Delivery time:
  • In Stock product will dispatch in 24 h after receipt of purchase order. It usually take 2-3 days to receive products in India and 5-6 working days for export customer depending on destination.
  • The custom synthesis products would be dispatched as per quoted timeline.

Shipping:
  • There will be 100 USD towards logistic charges per shipment if we used our FedEx. There will not be any charge if we use your FedEx/DHL Account. Depending on part shipment logistic charges will be added.
  • For countries dispatch by courier is not allowed where product would be dispatched in cargo mode as per agreed Inco term.

Additional Charges:
  • Controlled substance charges need to follow as per quotation. The specific inputs are required for controlled substance because regulatory status will differ based on destination.
  • Cold Shipment Charges needs to be considered as per quotation.
  • For ice pack there are no additional charges.

Technical Queries:
  • All technical queries need to raise within 15 days of product receipt. Thereafter it will be our resolved at our discretion.

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