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Closantel Base (CAS No.: 57808-65-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Closantel Base, 57808-65-8.
We offer the product Closantel Base, 57808-65-8 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 Closantel Base, 57808-65-8 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 Closantel Base, 57808-65-8 manufacturer supplier who is reliable and meets your required quality standard requirements in the first place, you are at the right place!

CAS number:

57808-65-8

Chemical Name:

N-[5-Chloro-4-[(chlorophenyl)cyannomethyl]-2-methylphenyl]-2-hydroxy-3,5-diiodobenzamid,Closantel base,Closantel sodium BP VET, Closantel Base (CAS No.: 57808-65-8)

Manufacturer Certificate:

GMP, ISO Certified

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Closantel,N-[5-Chloro-4-[(chlorophenyl)cyannomethyl]-2-methylphenyl]-2-hydroxy-3,5-diiodobenzamid,Closantel base,Closantel sodium BP VET, Closantel Base (CAS No.: 57808-65-8)

Molecular Formula

C22H14Cl2I2N2O2

Molecular Weight

663.08

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
2-(4-Amino-2-chloro-5-methylphenyl)-2-(4-chlorophenyl)acetonitrile	61437-85-2	View \| Inquire
3,5-Diiodosalicylic acid	133-91-5	View \| Inquire

Manufacturer Documentation / Approvals :

EDMF

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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