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Tiaprost (CAS No.: 71116-82-0)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Tiaprost, 71116-82-0.
We offer the product Tiaprost, 71116-82-0 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 Tiaprost, 71116-82-0 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 Tiaprost, 71116-82-0 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

71116-82-0

Chemical Name:

7-[3,5-Dihydroxy-2-[3-hydroxy-4-(3-thienyloxy)-1-butenyl]cyclopentyl]-5-heptenoic acid, Tiaprost (CAS No.: 71116-82-0)

Manufacturer Certificate:

cGMP, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

7-[3,5-Dihydroxy-2-[3-hydroxy-4-(3-thienyloxy)-1-butenyl]cyclopentyl]-5-heptenoic acid, Tiaprost (CAS No.: 71116-82-0)

Molecular Formula

C20H28O6S

Molecular Weight

396.50

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Availability

R&D

Product Name	CAS No.
[1,1'-Biphenyl]-4-carboxylic acid, hexahydro-2-oxo-4-[3-oxo-4-(3-thienyloxy)-1-butenyl]-2H-cyclopenta[b]	63150-91-4	View \| Inquire
TIP	62401-58-5	View \| Inquire

Manufacturer Documentation / Approvals :

TDP

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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