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Levosulpiride (CAS No.: 23672-07-3)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Levosulpiride, 23672-07-3.
We offer the product Levosulpiride, 23672-07-3 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 Levosulpiride, 23672-07-3 intermediates with the supportive technical package required for evaluation.
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CAS number:

23672-07-3

Chemical Name:

Levosulpiride, (S)-(-)-Sulpiride; (S)-5-Aminosulfonyl-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide, Levosulpiride (CAS No.: 23672-07-3)

Pharmacopeia:

In House

Manufacturer Certificate:

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

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Levosulpiride, (S)-(-)-Sulpiride; (S)-5-Aminosulfonyl-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide, Levosulpiride (CAS No.: 23672-07-3)

Molecular Formula

C15H23N3O4S

Molecular Weight

341.43

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Comments

It is an atypical neuroleptic and a prokinetic agent. Levosulpiride is also claimed to have mood elevating properties.

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o-Anisic acid	579-75-9	View \| Inquire
(S)-2-(Aminomethyl)-1-ethylpyrrolidine	22795-99-9	View \| Inquire
2-Methoxy-5-sulfamoylbenzoic acid	22117-85-7	View \| Inquire
Methyl 2-methoxy-5-sulfamoylbenzoate	33045-52-2	View \| Inquire

Description:

Levosulpiride is a substituted benzamide antipsychotic, reported to be a selective antagonist of dopamine D2 receptor activity on both central and peripheral levels.

Manufacturer Documentation / Approvals :

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