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Estradiol valerate (CAS No.: 979-32-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Estradiol valerate, 979-32-8.
We offer the product Estradiol valerate, 979-32-8 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 valerate, 979-32-8 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 Estradiol valerate, 979-32-8 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

979-32-8

Chemical Name:

Estradiol valerate, Estradiol valerate (CAS No.: 979-32-8)

Pharmacopeia:

USP

Manufacturer Certificate:

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

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

3,5(10)-triene-3,17-diol(17-beta)-estra-17-pentanoate;atladiol;b-estradiol17-valerate;deladiol;delahormoneunimatic;delestrogen;delestrogen4x;dura-estradiol, Estradiol valerate (CAS No.: 979-32-8)

Molecular Formula

C23H32O3

Molecular Weight

356.5

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

The list of intermediates for Estradiol valerate (CAS No.: 979-32-8) will be updated soon.

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Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS	DMF (OPEN PART)	DMF (CLOSED PART)	TDP	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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