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Racecadotril (CAS No.: 81110-73-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Racecadotril, 81110-73-8.
We offer the product Racecadotril, 81110-73-8 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 Racecadotril, 81110-73-8 intermediates with the supportive technical package required for evaluation.
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CAS number:

81110-73-8

Chemical Name:

N-[2-[(Acetylthio)methyl]-1-oxo-3-phenylpropyl]-glycine phenylmethyl ester; Acetorphan; Tiorfan, Racecadotril, Racecadotril (CAS No.: 81110-73-8)

Pharmacopeia:

USP, EP, BP, In House

Manufacturer Certificate:

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

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

N-[2-[(Acetylthio)methyl]-1-oxo-3-phenylpropyl]-glycine phenylmethyl ester; Acetorphan; Tiorfan, Racecadotril, Racecadotril (CAS No.: 81110-73-8)

Molecular Formula

C21H23NO4S

Molecular Weight

385.48

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Availability

FOR R&D PORPOSE

Comments

Unlike other opioid medications used to treat diarrhea, which reduce intestinal motility, racecadotril has an antisecretory effect—it reduces the secretion of water and electrolytes into the intestine.

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Description:

Racecadotril, also known as acetorphan, is an antidiarrheal drug which acts as a peripherally acting enkephalinase inhibitor.

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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