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Penicillin G Benzathine (CAS No.: 1538-09-6)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Penicillin G Benzathine, 1538-09-6.
We offer the product Penicillin G Benzathine, 1538-09-6 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 Penicillin G Benzathine, 1538-09-6 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:

1538-09-6

Chemical Name:

N,N'-Dibenzylethylethylenediamine Bis(benzylpenicillin); (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid with N,N'-Dibenzylethylenediamine (2:1) , Penicillin G Benzathine (CAS No.: 1538-09-6)

Pharmacopeia:

USP, EP

Manufacturer Certificate:

GMP

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

N,N'-Dibenzylethylethylenediamine Bis(benzylpenicillin); (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid with N,N'-Dibenzylethylenediamine (2:1) , Penicillin G Benzathine (CAS No.: 1538-09-6)

Molecular Formula

C16H20N2.2(C16H18N2O4S)

Molecular Weight

909.13

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
N,N'-Dibenzylethylenediamine	140-28-3	View \| Inquire

Manufacturer Documentation / Approvals :

CEP / COS

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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