Chlorphenamine EP Impurity A Price & Suppliers in India
CAS: 1246816-57-8Safety Information
Research Use Only
This substance is for laboratory research and analytical use only. Not for human or animal consumption.
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AboutChlorphenamine EP Impurity A
Chlorphenamine EP Impurity A is a specialized chemical entity utilized primarily as a reference standard in pharmaceutical quality control laboratories. It is chemically defined as a specific byproduct or degradation product associated with the synthesis or storage of Chlorphenamine Maleate, a widely used antihistamine.
In the Indian pharmaceutical sector, this impurity standard is critical for manufacturers exporting to regulated markets like the EU. It enables analytical chemists to perform precise impurity profiling during stability studies and batch release testing, ensuring that the final drug product meets stringent safety and purity specifications defined by international pharmacopeias.
When procuring this material, buyers should prioritize suppliers who provide a comprehensive Certificate of Analysis (CoA) and clear traceability to international standards. Given its high sensitivity and low usage volume, it is typically sourced in milligram quantities and requires strict adherence to cold-chain storage protocols to maintain chemical integrity.
Applications & Industries
Price in IndiaChlorphenamine EP Impurity A
Chlorphenamine EP Impurity A pricing in India depends on grade, order quantity, and delivery location, and it moves with market conditions — so a single fixed price is rarely accurate for a specific requirement.
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Frequently Asked Questions
What is the price of Chlorphenamine EP Impurity A in India?
Chlorphenamine EP Impurity A prices in India vary by grade, order quantity and delivery location, and move with market conditions. To get the current price for your requirement, submit an enquiry on Chemical Dekho and receive verified quotes from suppliers and manufacturers within 24 hours.
Is this product suitable for clinical use?
No, this is an analytical reference standard intended strictly for laboratory research and quality control purposes.
Does this come with a Certificate of Analysis?
Yes, all our impurity standards are provided with a full CoA detailing purity, method of analysis, and structural confirmation.
How should I store this impurity?
It should be stored in a freezer at -20°C, protected from light and moisture, to prevent degradation.
Can this be used for routine manufacturing?
No, it is used for analytical testing to monitor the quality of the manufacturing process, not as a raw material in production.
Is this compliant with Indian Pharmacopoeia standards?
This is specifically an EP (European Pharmacopoeia) impurity standard, which is widely accepted for international quality compliance in India.
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