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1,3-Dimethylpiperidin-4-one (CAS No.: 4629-80-5)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product CAS No.: 4629-80-5.
We offer the product CAS No.: 4629-80-5 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 other required upstream or downstream intermediates with the supportive technical package for evaluation based on the customer's request.
We respect our customer's requirements of strict regulatory compliance and specification needs by offering the intermediates transparently while offering easy access to manufacturer / supplier / principals with affordable and high-quality raw material intermediates.
If you are looking for any upstream or downstream intermediates concerning CAS No.: 4629-80-5, please feel free to email us. Based on your specific request, we will source the right manufacturer / supplier / principals who is reliable and meets your required quality standard requirements.

CAS number:

4629-80-5

Chemical Name:

1,3-Dimethylpiperidin-4-one, 1,3-Dimethylpiperidin-4-one (CAS No.: 4629-80-5)

Pharmacopeia:

In House

Manufacturer Certificate:

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

Application:

For R&D Purpose

Properties
Related API's

Synonym

1,3-Dimethyl-4-piperidinone, 1,3-Dimethylpiperidin-4-one (CAS No.: 4629-80-5)

Molecular Formula

C7H13NO

Molecular Weight

127.18

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

The details in this section shall be updated soon.

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Manufacturer Documentation / Approvals :

TDP	ICH

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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