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Epalrestat (CAS No.: 82159-09-9)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Epalrestat, 82159-09-9.
We offer the product Epalrestat, 82159-09-9 from our manufacturer / supplier / principals for your Research and Development / Evaluation or Commercial requirements, based on the product's availability from our network. We can also offer Epalrestat, 82159-09-9 intermediates with the supportive technical package required for evaluation.
We respect our customer's requirements of strict regulatory compliance and specification needs by offering the API - Active Pharmaceutical Ingredients and intermediates transparently while offering easy access to manufacturer / supplier / principals with affordable and high-quality raw materials.
If you are looking for the API -Active Pharmaceutical Ingredients Epalrestat, 82159-09-9 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

82159-09-9

Chemical Name:

Epalrestat;(E,E)-2-[5-(2-Methyl-3-phenyl-prop-2-enylidene)-4-oxo-2-sulfanylidene-thiazo lidin-3-yl]acetic acid, Epalrestat (CAS No.: 82159-09-9)

Pharmacopeia:

JP, CP, In House

Manufacturer Certificate:

GMP, cGMP, WHO GMP, ISO Certified

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

(E,E)-2-[5-(2-Methyl-3-phenyl-prop-2-enylidene)-4-oxo-2-sulfanylidene-thiazo lidin-3-yl]acetic acid, Epalrestat (CAS No.: 82159-09-9)

Molecular Formula

C15H13NO3S2

Molecular Weight

319.39

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Availability

FOR R&D PURPOSE

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Manufacturer Documentation / Approvals :

TDP

Products protected by valid patents from a manufacturer are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use from a manufacturer in accordance with 35 USC 271 +A13(1)
Products falling in to controlled substance category / list of schedule drugs shall be exported directly from the manufacturer principals only against receipt of original import permission issued by concerned authorities of the importing country.
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