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.
Nome Químico: (E)-1-((3-(6-(3-oxobut-1-en-1-yl)pyridin-2-yl)-3-(p-tolyl)oxiran-2-yl)methyl)pyrrolidine 1-oxide
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: [O-][N+]1(CC2OC2(C3=CC=C(C)C=C3)C4=NC(/C=C/C(C)=O)=CC=C4)CCCC1
Acrivastine Impurity 1 is chemically (E)-1-((3-(6-(3-oxobut-1-en-1-yl)pyridin-2-yl)-3-(p-tolyl)oxiran-2-yl)methyl)pyrrolidine 1-oxide. Acrivastine Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Acrivastine 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 Acrivastine.
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.
Development and validation of a rapid stability indicating HPLC-method using monolithic stationary phase and two spectrophotometric methods for determination of antihistaminic acrivastine in capsules
By Gouda, Ayman A.; Hashem, Hisham; Jira, Thomas
From Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy (2014), 130, 480-487