Loratadine EP Impurity C

Loratadine EP Impurity C is chemically Ethyl 4-(4,8-dichloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidine-1-carboxylate (as per EP). It is also known as Loratadine USP Related Compound G ; 4-Chloro Loratadine. Loratadine EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Loratadine EP Impurity C 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 Loratadine.

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.

LC determination of loratadine and related impurities
F.J. Rupe´rez, H. Ferna´ndez, C. Barbas
Journal of Pharmaceutical and Biomedical Analysis 29 (2002) 35–41
 
Measurement and Correlation of Solubility of Loratadine in Different Pure Solvents and Binary Mixtures
Xiujuan Yang,† Shui Wang,† and Jidong Wang
J. Chem. Eng. Data 2017, 62, 1, 391–397

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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.

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• 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.
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• 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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