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Darifenacin (CAS No.: 133099-04-4)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Darifenacin, 133099-04-4.
We offer the product Darifenacin, 133099-04-4 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 Darifenacin, 133099-04-4 intermediates with the supportive technical package required for evaluation.
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CAS number:

133099-04-4

Chemical Name:

2-[1-[2-(2,3-Dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-di(phenyl)acetamide,Darifenacin, Darifenacin (CAS No.: 133099-04-4)

Manufacturer Certificate:

GMP, WHO GMP, ISO Certified

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

2-[1-[2-(2,3-Dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-di(phenyl)acetamide, Darifenacin, Darifenacin (CAS No.: 133099-04-4)

Molecular Formula

C28H30N2O2

Molecular Weight

426.55

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Availability

FOR R&D PORPOSE

Product Name	CAS No.
(S)-alpha,alpha-Diphenyl-3-pyrrolidineacetamide	133099-11-3	View \| Inquire
2,3-Dihydrobenzofuranyl-5-acetic acid	69999-16-2	View \| Inquire
5-(2-Bromoethyl)-2,3-dihydrobenzofuran	127264-14-6	View \| Inquire
Difenyl[(S)-Pyrrolidine-3-Yl]Acetonitrilhydrobromide	194602-27-2	View \| Inquire
3-(S)-(+)-(1-Carbamoyl-1,1-diphenylmethyl)pyrroloidine-L-(+)-tartarate	134002-26-9	View \| Inquire
5-(2-chloroethyl)-2,3-dihydrobenzofuran	943034-50-2	View \| Inquire
2,3-Dihydrobenzofuran	496-16-2	View \| Inquire

Description:

Darifenacin is a medication used to treat urinary incontinence.

Manufacturer Documentation / Approvals :

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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