Harmful if swallowed
This substance may cause skin and eye irritation. Handle with appropriate laboratory safety equipment.
Eyes: Rinse cautiously with water for several minutes.
Skin: Wash with plenty of soap and water.
Amlodipine EP Impurity G (CAS 43067-01-2) is a specific degradation product or synthetic byproduct associated with the manufacturing of Amlodipine, a widely used calcium channel blocker. In the pharmaceutical industry, this compound is classified as a reference standard, critical for validating the safety and efficacy of final drug formulations.
In the Indian pharmaceutical landscape, which serves as a global hub for generic drug manufacturing, the demand for high-quality impurity standards is significant. Indian manufacturers utilize this compound to perform rigorous impurity profiling as mandated by CDSCO and international regulatory bodies like the USFDA and EMA, ensuring that Amlodipine APIs meet strict purity specifications.
Procurement of this chemical requires careful attention to the Certificate of Analysis (CoA) and the availability of supporting documentation such as NMR, Mass Spectrometry, and HPLC chromatograms. Buyers should source from reputable suppliers who provide stable, well-characterized batches to ensure reproducibility in analytical testing.
Amlodipine EP Impurity G 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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Amlodipine EP Impurity G 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.
No, this is an analytical reference standard intended for laboratory research and quality control use only.
Yes, every batch is supplied with a comprehensive CoA including HPLC, NMR, and Mass Spectrometry data.
It is recommended to store the product at -20°C in a light-protected container to maintain chemical stability.
Yes, it is widely used by Indian pharmaceutical QC labs to comply with EP and USP monograph testing requirements.
Short-term exposure during transit is acceptable, but long-term storage must be under refrigerated or frozen conditions.
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