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Torasemide (CAS No.: 56211-40-6)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Torasemide, 56211-40-6.
We offer the product Torasemide, 56211-40-6 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 Torasemide, 56211-40-6 intermediates with the supportive technical package required for evaluation.
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CAS number:

56211-40-6

Chemical Name:

Torasemide, 1-[4-(3-Methylphenyl)aminopyridin-3-yl]sulfonyl-3-propan-2-yl-urea, Torasemide (CAS No.: 56211-40-6)

Pharmacopeia:

USP, EP

Manufacturer Certificate:

GMP, GMP - SFDA, cGMP, EUGMP, WHO GMP, ISO Certified, USFDA, Cofepris Mexico

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Torsemide ; Torasemide, 1-[4-(3-Methylphenyl)aminopyridin-3-yl]sulfonyl-3-propan-2-yl-urea, Torasemide (CAS No.: 56211-40-6)

Molecular Formula

C16H20N4O3S

Molecular Weight

348.42

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
4-Hydroxypyridine-3-sulfonic acid	51498-37-4	View \| Inquire
4-Chloro-3-pyridinesulfonamide	33263-43-3	View \| Inquire
4-Chloro-3-pyridinesulfonamide	33263-43-3	View \| Inquire
4-(3'-Methylphenyl)amino-3-pyridinesulfonamide	72811-73-5	View \| Inquire
4-Hydroxypyridine	626-64-2	View \| Inquire

Description:

Torsemide or Torasemide is a pyridine-sulfonyl urea type loop diuretic mainly used in the management of edema associated with congestive heart failure. Torsemide is also used at low doses for the management of hypertension.

Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS	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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