Toxic and Irritant
Harmful if swallowed, in contact with skin, or if inhaled. Causes skin and serious eye irritation.
Eyes: Rinse cautiously with water for several minutes; seek medical attention.
Skin: Wash with plenty of soap and water; remove contaminated clothing.
Bupivacaine EP Impurity F, chemically known as 2,6-xylidine hydrochloride, is a critical chemical entity in the pharmaceutical sector. It serves as a vital reference standard for manufacturers to ensure compliance with European Pharmacopoeia (EP) standards during the production of Bupivacaine and related amide-type local anesthetics.
In the Indian market, this chemical is highly sought after by pharmaceutical R&D facilities and contract manufacturing organizations (CMOs) located in hubs like Hyderabad, Ahmedabad, and Mumbai. It is essential for conducting impurity profiling and method validation, ensuring that final drug products meet stringent regulatory requirements for safety and efficacy.
Procurement of this impurity requires careful attention to purity levels and documentation. Buyers should prioritize suppliers who provide a comprehensive Certificate of Analysis (CoA) and adhere to global quality standards. Given its sensitive nature, it is typically sourced in smaller, high-purity quantities for analytical use rather than bulk industrial volumes.
Bupivacaine 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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Bupivacaine 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.
No, this is an analytical impurity standard intended for laboratory and R&D use only.
Yes, all our batches are supplied with a detailed CoA including HPLC purity and impurity profile.
It is primarily used as a reference standard for Bupivacaine impurity testing in pharmaceutical quality control.
It should be stored in a cool, dry, and dark environment, preferably in a temperature-controlled facility.
Yes, we can supply in larger drum quantities upon request for validated manufacturing processes.
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