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Zanamivir (CAS No.: 139110-80-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Zanamivir, 139110-80-8.
We offer the product Zanamivir, 139110-80-8 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 Zanamivir, 139110-80-8 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 Zanamivir, 139110-80-8 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

139110-80-8

Chemical Name:

(2R,3R,4S)-3-Acetamido-4-(diaminomethylideneamino)-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid, Zanamivir (CAS No.: 139110-80-8)

Manufacturer Certificate:

cGMP, WHO GMP, ISO Certified

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

(2R,3R,4S)-3-Acetamido-4-(diaminomethylideneamino)-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid, Zanamivir (CAS No.: 139110-80-8)

Molecular Formula

C12H20N4O7

Molecular Weight

332.31

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
N-Acetylneuraminic acid	131-48-6	View \| Inquire
1H-Pyrazole-1-carboxamidine hydrochloride	4023-02-3	View \| Inquire

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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