Alfuzosin EP Impurity F Price & Suppliers in India
CAS: 19216-53-6Safety Information
Harmful if swallowed
This substance may cause irritation to the skin, eyes, and respiratory tract. Handle with appropriate laboratory safety equipment.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
AboutAlfuzosin EP Impurity F
Alfuzosin EP Impurity F (CAS 19216-53-6) is a specific chemical impurity associated with the synthesis and degradation of Alfuzosin, a medication used to treat benign prostatic hyperplasia. In the pharmaceutical industry, this compound is classified as a reference standard, critical for ensuring the safety and efficacy of final drug products.
In the Indian pharmaceutical market, this impurity is primarily sourced by API manufacturers and contract research organizations (CROs) to comply with stringent pharmacopeial standards (EP/USP). It is utilized during the validation of analytical methods to ensure that drug batches meet regulatory requirements for purity and impurity limits set by the CDSCO and international bodies.
When procuring this chemical, buyers should prioritize suppliers who provide a comprehensive Certificate of Analysis (CoA) including HPLC, NMR, and Mass Spectrometry data. Due to its nature as a high-value analytical reagent, it is typically supplied in small, high-purity quantities and requires precise storage conditions to maintain chemical integrity.
Applications & Industries
Price in IndiaAlfuzosin EP Impurity F
Alfuzosin EP Impurity F 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 Alfuzosin EP Impurity F in India?
Alfuzosin EP Impurity F 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 impurity certified for regulatory filing?
Yes, it is intended for use as a reference standard in analytical method validation.
What documentation is provided with the order?
Each shipment includes a Certificate of Analysis (CoA) and MSDS.
How is the purity verified?
Purity is typically verified via HPLC and structural confirmation via NMR/Mass Spec.
Can this be used for clinical trials?
It is a chemical reagent for analytical testing, not for direct clinical administration.
What is the typical lead time in India?
Stock items are usually dispatched within 2-3 business days.
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