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Cilastatin (CAS No.: 82009-34-5)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Cilastatin, 82009-34-5.
We offer the product Cilastatin, 82009-34-5 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 Cilastatin, 82009-34-5 intermediates with the supportive technical package required for evaluation.
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CAS number:

82009-34-5

Chemical Name:

Cilastatin; (Z)-7-[(2S)-2-Amino-3-hydroxy-3-oxopropyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopropanecarbonyl]amino]hept-2-enoic acid, Cilastatin (CAS No.: 82009-34-5)

Pharmacopeia:

USP, In House

Manufacturer Certificate:

cGMP, WHO GMP, ISO Certified

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

(Z)-7-[(2S)-2-Amino-3-hydroxy-3-oxopropyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopropanecarbonyl]amino]hept-2-enoic acid, Cilastatin (CAS No.: 82009-34-5)

Molecular Formula

C16H26N2O5S

Molecular Weight

358.45

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
Ethyl 7-chloro-2-oxoheptanoate	78834-75-0	View \| Inquire
(S)-(+)-2,2-Dimethylcyclopropanecarboxamide	75885-58-4	View \| Inquire
(Z)-7-[(2S)-2-Amino-3-hydroxy-3-oxopropyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopropanecarbonyl]amino]hept-2-enoic acid	82009-34-5	View \| Inquire
(S)-(+)-2,2-Dimethylcyclopropanecarboxylic acid	14590-53-5	View \| Inquire
7-Chloro-2-[[[(1S)-2,2-dimethylcyclopropyl]carbonyl]amino]-2-heptenoic acid	877674-77-6	View \| Inquire

Manufacturer Documentation / Approvals :

USDMF	EDMF	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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