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L-Alanine, N-acetyl, 4-nitrophenyl ester is a chemical compound derived from the amino acid L-alanine. It is formed by the esterification of L-alanine with N-acetyl and 4-nitrophenol. L-Alanine, N-acetyl-, 4-nitrophenyl ester is often used as a substrate in enzymatic assays, particularly for the determination of enzyme activity in various biological systems. The 4-nitrophenyl group serves as a chromophore, allowing for the colorimetric detection of the reaction progress. When the enzyme cleaves the ester bond, the 4-nitrophenol is released, and its absorbance can be measured at 400 nm, providing a quantitative measure of the enzyme's activity. L-Alanine, N-acetyl-, 4-nitrophenyl ester is also used in the study of esterases and lipases, which are enzymes that catalyze the hydrolysis of esters.

5013-08-1

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5013-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5013-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,1 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5013-08:
(6*5)+(5*0)+(4*1)+(3*3)+(2*0)+(1*8)=51
51 % 10 = 1
So 5013-08-1 is a valid CAS Registry Number.

5013-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-α-Acetyl-L-alanine p-nitrophenyl ester

1.2 Other means of identification

Product number -
Other names Ac-L-Ala-ONP

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:5013-08-1 SDS

5013-08-1Relevant academic research and scientific papers

Preparation of N-acetyl, tert-butyl amide derivatives of the 20 natural amino acids

Ekkati,Campanali,Abouelatta,Shamoun,Kalapugama,Kelley,Kodanko, Jeremy J.

scheme or table, p. 747 - 751 (2010/08/05)

N-Acetyl-AA(amino acid)-NHtBu derivatives of all 20 naturally occurring amino acids have been synthesized. Syntheses were performed via solution-phase methodology with yields that allow for access to gram quantities of substrates, in most cases. Syntheses include the coupling of a hindered amine, tert-butylamine, with each amino acid, either directly or in two steps using an activated ester isolated as an intermediate. The introduction of protecting groups was necessary in some cases. The development of synthetic sequences to access challenging substrates, such as the one derived from asparagine, are discussed.

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