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Pazopanib Impurity 7

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SZ目录编号 SZ-P013012
CAS 号 1414375-50-0
分子式 C21H23N7O3S
分子量 453.5
投资状态 Custom Synthesis


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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

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

化学名称: 5-((4-((2,3-Dimethyl-2H-indazol-6-yl)(methyl)amino)pyrimidin-2-yl)amino)-2-(hydroxymethyl)benzenesulfonamide

异名: GSK 1268997

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: NS(C1=C(C=CC(NC2=NC=CC(N(C)C3=CC4=NN(C)C(C)=C4C=C3)=N2)=C1)CO)(=O)=O

Pazopanib Impurity 7 is chemically 5-((4-((2,3-Dimethyl-2H-indazol-6-yl)(methyl)amino)pyrimidin-2-yl)amino)-2-(hydroxymethyl)benzenesulfonamide. It is also known as GSK 1268997. Pazopanib Impurity 7 is supplied with detailed characterization data compliant with regulatory guideline. Pazopanib Impurity 7 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 Pazopanib.

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.

Analytical control of process impurities in Pazopanib hydrochloride by impurity fate mapping
Yan Li 1, David Q Liu, Shawn Yang, Ravinder Sudini, Michael A McGuire, Dharmesh S Bhanushali, Alireza S Kord
J Pharm Biomed Anal. 2010 Aug 1;52(4):493-507.
 
Determination and characterization of process impurities in pazopanib hydrochloride drug substance
musty sharada, ravichandra babu
Int J Pharm Pharm Sci, Vol 8, Issue 4, 97-102
 
Characterization of forced degradation products of pazopanib hydrochloride by UHPLC‐Q‐TOF/MS and in silico toxicity prediction
Prinesh N. Patel  Pradipbhai D. Kalariya  Mahesh Sharma  Prabha Garg  M. V. N Kumar Talluri  S. Gananadhamu  R. Srinivas
Journal of mass spectrometry Volume50, Issue7 July 2015 Pages 918-928
 
Development and validation of a stability indicating RP-HPLC method for the determination of Pazopanib in bulk drug and its pharmaceutical dosage form
Kishore Kumar Reddy Y, J. Raveendra Reddy and N. Devanna
J. Chem. Pharm. Res., 2015, 7(9):127-132
 
Validated RP-HPLC Method Development of Pazopanib in Bulk and its Pharmaceutical Dosage Form
Kiran Kumar Buralla, and Varadarajan Parthasarathy
Pharmaceutical Methods,2020,11,1,21-24.

  • We need to receive valid purchase order with Bill to & Ship to address.
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  • 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.

Reach to Us:
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  • For specific purpose, there are below e-mail address to be used.
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