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Galanthamine hydrobromide (CAS No.: 1953-04-4 [69353-21-5])

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Galanthamine hydrobromide, 1953-04-4 [69353-21-5].
We offer the product Galanthamine hydrobromide, 1953-04-4 [69353-21-5] 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 Galanthamine hydrobromide, 1953-04-4 [69353-21-5] 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 Galanthamine hydrobromide, 1953-04-4 [69353-21-5] manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

1953-04-4 [69353-21-5]

Chemical Name:

Galanthamine hydrobromide; Galantamine hydrobromide, Galanthamine hydrobromide (CAS No.: 1953-04-4 [69353-21-5])

Pharmacopeia:

USP

Manufacturer Certificate:

cGMP, EUGMP, WHO GMP, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Galanthamine hydrobromide, Galanthamine hydrobromide (CAS No.: 1953-04-4 [69353-21-5])

Molecular Formula

C17H21NO3.HBr;C17H22BrNO3

Molecular Weight

368.27

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

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Manufacturer Documentation / Approvals :

USDMF	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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