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Misoprostol (CAS No.: 59122-46-2 (62015-39-8))

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Misoprostol, 59122-46-2 (62015-39-8).
We offer the product Misoprostol, 59122-46-2 (62015-39-8) 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 Misoprostol, 59122-46-2 (62015-39-8) 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 Misoprostol, 59122-46-2 (62015-39-8) manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

59122-46-2 (62015-39-8)

Chemical Name:

(11alpha,13E)-(+)-11alpha,16-Dihydroxy-16-methyl-9-oxoprost-13E-en-1-oic acid methyl ester, Misoprostol (CAS No.: 59122-46-2 (62015-39-8))

Pharmacopeia:

USP, EP, IP

Manufacturer Certificate:

cGMP, WHO GMP, ISO Certified, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

(11alpha,13E)-(+)-11alpha,16-Dihydroxy-16-methyl-9-oxoprost-13E-en-1-oic acid methyl ester, Misoprostol (CAS No.: 59122-46-2 (62015-39-8))

Molecular Formula

C22H38O5

Molecular Weight

382.54

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

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1-Octyn-4-ol, 4-methyl	22128-43-4	View \| Inquire
((S)-oct-1-yn-3-yloxy)trimethylsilane	62555-05-9	View \| Inquire

Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS	MHRA - UK	TDP	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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