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Estradiol (CAS No.: 50-28-2)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Estradiol, 50-28-2.
We offer the product Estradiol, 50-28-2 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 Estradiol, 50-28-2 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.
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CAS number:

50-28-2

Chemical Name:

1,3,5-Estratriene-3,17beta-diol; 17beta-Estradiol; 3,17beta-Dihydroxy-1,3,5(10)-estratriene; Dihydrofolliculin , Estradiol (CAS No.: 50-28-2)

Pharmacopeia:

USP, EP, BP, CP

Manufacturer Certificate:

GMP, Factory GMP, cGMP, EUGMP, WHO GMP, ISO Certified

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

1,3,5-Estratriene-3,17beta-diol; 17beta-Estradiol; 3,17beta-Dihydroxy-1,3,5(10)-estratriene; Dihydrofolliculin , Estradiol (CAS No.: 50-28-2)

Molecular Formula

C18H24O2

Molecular Weight

272.38

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

The list of intermediates for Estradiol (CAS No.: 50-28-2) will be updated soon.

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Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS	DMF - CANADA	DMF (OPEN PART)	TDP	JDMF	DCGI

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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