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Lomitapide (CAS No.: 182431-12-5)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Lomitapide, 182431-12-5.
We offer the product Lomitapide, 182431-12-5 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 Lomitapide, 182431-12-5 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:

182431-12-5

Chemical Name:

Lomitapide, Lomitapide (CAS No.: 182431-12-5)

Manufacturer Certificate:

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

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

N-(2,2,2-Trifluoroethyl)-9-(4-[4-[4'-(trifluoromethyl)[1,1'-biphenyl]-2-carboxamido]piperidin-1-yl]butyl)-9H-fluorene-9-carboxamide, Lomitapide (CAS No.: 182431-12-5)

Molecular Formula

C39H37F6N3O2

Molecular Weight

693.73

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
4-(Trifluoromethyl)-2'-biphenylcarboxylic acid	84392-17-6	View \| Inquire
1-benzylpiperidin-4-amine	303779-73-9	View \| Inquire
N-4-Piperidinyl-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamide	182439-41-4	View \| Inquire
9-Carboxyfluorene	1989-33-9	View \| Inquire
2,2,2-Trifluoroethylamine hydrochloride	373-88-6	View \| Inquire
methyl 9-(4-bromobutyl)-9H-fluorene-9-carboxylate	182438-97-7	View \| Inquire

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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