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5-Fluorouracil (CAS No.: 51-21-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product 5-Fluorouracil, 51-21-8.
We offer the product 5-Fluorouracil, 51-21-8 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 5-Fluorouracil, 51-21-8 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 5-Fluorouracil, 51-21-8 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

51-21-8

Chemical Name:

Fluorouracil;5-Fluoro-2,4(1H,3H)-pyrimidinedione; 5-Fluoro-2,4-pyrimidinedione; 5-Fluoropyrimidine-2,4-dione, 5-Fluorouracil (CAS No.: 51-21-8)

Pharmacopeia:

USP, BP

Manufacturer Certificate:

GMP, cGMP, WHO GMP

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Fluorouracil;5-Fluoro-2,4(1H,3H)-pyrimidinedione; 5-Fluoro-2,4-pyrimidinedione; 5-Fluoropyrimidine-2,4-dione, 5-Fluorouracil (CAS No.: 51-21-8)

Molecular Formula

C4H3FN2O2

Molecular Weight

130.08

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

The list of intermediates for 5-Fluorouracil (CAS No.: 51-21-8) will be updated soon.

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Manufacturer Documentation / Approvals :

EDMF	CEP / COS	DMF (OPEN PART)

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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