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Bendroflumethiazide (CAS No.: 73-48-3)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Bendroflumethiazide, 73-48-3.
We offer the product Bendroflumethiazide, 73-48-3 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 Bendroflumethiazide, 73-48-3 intermediates with the supportive technical package required for evaluation.
We respect our customer's requirements of strict regulatory compliance and specification needs by offering the API - Active Pharmaceutical Ingredients and intermediates transparently while offering easy access to manufacturer / supplier / principals with affordable and high-quality raw materials.
If you are looking for the API -Active Pharmaceutical Ingredients Bendroflumethiazide, 73-48-3 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

73-48-3

Chemical Name:

3-Benzyl-3,4-dihydro-6-(trifluoromethy)-2H-1,2,4-benzothiadiazine-7-sulfonamide-1,1-dioxide, Bendroflumethiazide (CAS No.: 73-48-3)

Pharmacopeia:

USP, EP, BP

Manufacturer Certificate:

ISO Certified

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

3-Benzyl-3,4-dihydro-6-(trifluoromethy)-2H-1,2,4-benzothiadiazine-7-sulfonamide-1,1-dioxide, Bendroflumethiazide (CAS No.: 73-48-3)

Molecular Formula

C15H14F3N3O4S2

Molecular Weight

421.41

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

The list of intermediates for Bendroflumethiazide (CAS No.: 73-48-3) will be updated soon.

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Manufacturer Documentation / Approvals :

USDMF

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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