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Granisetron hydrochloride (CAS No.: 107007-99-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Granisetron hydrochloride, 107007-99-8.
We offer the product Granisetron hydrochloride, 107007-99-8 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 Granisetron hydrochloride, 107007-99-8 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.
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CAS number:

107007-99-8

Chemical Name:

1-methyl-n-(9-methyl-9-azabicyclo(3.3.1)non-3-yl)-1h-indazole-3-carboxamid, Granisetron hydrochloride (CAS No.: 107007-99-8)

Pharmacopeia:

USP, EP, BP, CP

Manufacturer Certificate:

GMP, GMP - SFDA, cGMP, ISO Certified, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

endo-1-methyl-n-(9-methyl-9-azabicyclo(3.3.1)non-3-yl)-1h-indazole-3-carboxa, Granisetron hydrochloride (CAS No.: 107007-99-8)

Molecular Formula

C18H25ClN4O

Molecular Weight

348.87

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
Endo-3-amine-9-methyl-9-azabicyclo[3,3,1]nonane	76272-56-5	View \| Inquire
1-Methylindazole-3-carboxylic acid	50890-83-0	View \| Inquire

Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS	PMDA - JAPAN	DMF - CANADA	TGA - AUSTRALIA	DMF (OPEN PART)	TDP	DMF - CTD

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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