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Eosin Disodium FRP (CAS No.: 17372-87-1)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Eosin Disodium FRP, 17372-87-1.
We offer the product Eosin Disodium FRP, 17372-87-1 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 Eosin Disodium FRP, 17372-87-1 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 Eosin Disodium FRP, 17372-87-1 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

17372-87-1

Chemical Name:

Acid Red 87, Eosin Disodium FRP (CAS No.: 17372-87-1)

Manufacturer Certificate:

GMP, WHO GMP

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

2',4',5',7'-Tetrabromofluorescein disodium salt, Eosin Disodium FRP (CAS No.: 17372-87-1)

Molecular Formula

C20H6Br4Na2O5

Molecular Weight

691.86

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

The list of intermediates for Eosin Disodium FRP (CAS No.: 17372-87-1) will be updated soon.

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Manufacturer Documentation / Approvals :

USDMF	DMF (OPEN PART)	DMF (CLOSED PART)	DMF - CTD

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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