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Capecitabine (CAS No.: 154361-50-9;158798-73-3)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Capecitabine, 154361-50-9;158798-73-3.
We offer the product Capecitabine, 154361-50-9;158798-73-3 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 Capecitabine, 154361-50-9;158798-73-3 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 Capecitabine, 154361-50-9;158798-73-3 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

154361-50-9;158798-73-3

Chemical Name:

Pentyl [1-(3,4-dihydroxy-5-methyl-oxolan-2-yl)-5-fluoro-2-oxo-pyrimidin-4-yl]aminoformate; Xeloda, Capecitabine (CAS No.: 154361-50-9;158798-73-3)

Pharmacopeia:

USP, EP, IP

Manufacturer Certificate:

GMP, GMP - SFDA, cGMP, EUGMP, WHO GMP, USFDA, Cofepris Mexico

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Pentyl [1-(3,4-dihydroxy-5-methyl-oxolan-2-yl)-5-fluoro-2-oxo-pyrimidin-4-yl]aminoformate; Xeloda;158798-73-3, Capecitabine (CAS No.: 154361-50-9;158798-73-3)

Molecular Formula

C15H22FN3O6

Molecular Weight

359.35

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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Description:

Capecitabine is a chemotherapy drug that is given as a treatment for some types of cancer, including advanced bowel cancer or breast cancer.

Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS	DMF (OPEN PART)	TDP	DMF - CTD

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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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