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Loxoprofen sodium (CAS No.: 80382-23-6)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Loxoprofen sodium, 80382-23-6.
We offer the product Loxoprofen sodium, 80382-23-6 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 Loxoprofen sodium, 80382-23-6 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 Loxoprofen sodium, 80382-23-6 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

80382-23-6

Chemical Name:

Sodium 2-[4-(2-Oxocyclopentyl-1-methyl)phenyl]propionate dihydrate, Loxoprofen sodium (CAS No.: 80382-23-6)

Pharmacopeia:

Manufacturer Certificate:

GMP, cGMP

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Sodium 2-[4-(2-Oxocyclopentyl-1-methyl)phenyl]propionate dihydrate, Loxoprofen sodium (CAS No.: 80382-23-6)

Molecular Formula

C15H17NaO3.2(H2O)

Molecular Weight

304.32

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
2-{4-[(2-Oxocyclopentyl)methyl]phenyl}propanoic acid	68767-14-6	View \| Inquire
2-(4-Bromomethyl)phenylpropionic acid	111128-12-2	View \| Inquire
Methyl 2-oxocyclopentanecarboxylate, 95%	10472-24-9	View \| Inquire
DL-2-Phenylpropionic acid	492-37-5	View \| Inquire

Manufacturer Documentation / Approvals :

EDMF	CEP / COS

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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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