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Domperidone maleate (CAS No.: 99497-03-7 (83898-65-1))

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Domperidone maleate, 99497-03-7 (83898-65-1).
We offer the product Domperidone maleate, 99497-03-7 (83898-65-1) 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 Domperidone maleate, 99497-03-7 (83898-65-1) intermediates with the supportive technical package required for evaluation.
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CAS number:

99497-03-7 (83898-65-1)

Chemical Name:

5-chloro-1-[1-[3-(2-oxo-1,3-dihydrobenzoimidazol-1-yl)propyl]-4-piperidyl]-1,3-dihydrobenzoimidazol-2-one maleate, Domperidone maleate, Domperidone maleate (CAS No.: 99497-03-7 (83898-65-1))

Pharmacopeia:

EP, IP, BP

Manufacturer Certificate:

GMP, Factory GMP, GMP - SFDA, cGMP, Product GMP, EUGMP, WHO GMP, ISO Certified, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

2H-Benzimidazol-2-one, 5-chloro-1-(1-(3-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl)-4-piperidinyl)-1,3-dihydro-, (Z)-2-butenedioate, Domperidone maleate, Domperidone maleate (CAS No.: 99497-03-7 (83898-65-1))

Molecular Formula

C26H28ClN5O6

Molecular Weight

541.98

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Comments

REGULATORY APPROVALS : EU Compliant

Product Name	CAS No.
1-(3-Chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one	62780-89-6	View \| Inquire
5-Chloro-1-(4-piperidyl)-2-benzimidazolinone	53786-28-0	View \| Inquire

Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS	DMF - CANADA	DMF (OPEN PART)	DMF (CLOSED PART)	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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