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7β-(5-carboxy-5-oxopentanamido)cephalosporanic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28242-83-3

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28242-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28242-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,4 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28242-83:
(7*2)+(6*8)+(5*2)+(4*4)+(3*2)+(2*8)+(1*3)=113
113 % 10 = 3
So 28242-83-3 is a valid CAS Registry Number.

28242-83-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7β-(5-carboxy-5-oxopentanamido)cephalosporanic acid

1.2 Other means of identification

Product number -
Other names 7-(5-Oxoadipamido)cephalosporansaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:28242-83-3 SDS

28242-83-3Upstream product

28242-83-3Relevant academic research and scientific papers

One-pot conversion of cephalosporin C to 7-aminocephalosporanic acid in the absence of hydrogen peroxide

Lopez-Gallego, Fernando,Batencor, Lorena,Hidalgo, Aurelio,Mateo, Cesar,Fernandez-Lafuente, Roberto,Guisan, Jose M.

, p. 1804 - 1810 (2005)

The main drawback in the production of 7-aminocephalosporanic acid (7-ACA) at the industrial level is the inactivation of the enzymes implicated in the process due to the presence of hydrogen peroxide during the reaction. As an alternative, we have developed the conversion of cephalosporin C to 7-ACA in a single reactor without the presence of hydrogen peroxide during the reaction, achieving more than 80% yield. In order to develop this process, D-amino acid oxidase (DAAO) was co-immobilized with catalase (CAT), which is able to fully eliminate in situ the hydrogen peroxide formed by the neighbouring DAAO molecules. Thus, the product of the reaction is only α-ketoadipyl-7-ACA. This system prevents the inactivation of the oxidase by hydrogen peroxide, solving the main problem of the enzymatic process. Moreover, we have found that α-ketoadipyl-7-ACA is recognized as a substrate by glutaryl acylase (GAC) and hydrolyzed as long as glutaric acid is absent from the reaction medium (because it is able to inhibit the hydrolysis). The low stability of α-ketoadipyl-7-ACA justifies the use of a single reactor, in which glutaryl acylase is already present when this substrate is generated. Thus, the whole process may (and must) be performed in a single step, and in the absence of hydrogen peroxide that could affect the stabilities of the involved enzymes.

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