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Rivastigmine tartrate (CAS No.: 129101-54-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Rivastigmine tartrate, 129101-54-8.
We offer the product Rivastigmine tartrate, 129101-54-8 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 Rivastigmine tartrate, 129101-54-8 intermediates with the supportive technical package required for evaluation.
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CAS number:

129101-54-8

Chemical Name:

(S)-N-Ethyl-3-[(1-dimethylamino)ethyl]-N-methylphenylcarbamate hydrogen tartrate, Rivastigmine tartrate, Rivastigmine tartrate (CAS No.: 129101-54-8)

Pharmacopeia:

USP, EP, In House

Manufacturer Certificate:

GMP, cGMP, EUGMP, WHO GMP, ISO Certified, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

(S)-N-Ethyl-3-[(1-dimethylamino)ethyl]-N-methylphenylcarbamate hydrogen tartrate, Rivastigmine tartrate, Rivastigmine tartrate (CAS No.: 129101-54-8)

Molecular Formula

C14H22N2O2.C4H6O6

Molecular Weight

400.43

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
3-[(1S)-1-(Dimethylaminoethyl)]phenol	139306-10-8	View \| Inquire
3-(1-(Dimethylamino)ethyl]phenol	105601-04-5	View \| Inquire
Ethylmethyl-carbamic chloride	42252-34-6	View \| Inquire
Ethylmethyl-carbamic chloride	42252-34-6	View \| Inquire
Bis(4-nitrophenyl) carbonate	5070-13-3	View \| Inquire

Manufacturer Documentation / Approvals :

EDMF	DMF (OPEN PART)	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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