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Isohistidine is a non-proteinogenic amino acid, which means it is not commonly found in proteins. It is an isomer of histidine, differing in the position of the imidazole ring's attachment to the side chain. Isohistidine is formed through the deamination of histidine, a process that can occur during food processing or cooking. It is not an essential amino acid for humans, as it can be synthesized from histidine. Isohistidine has been studied for its potential role in various biological processes, including its involvement in the Maillard reaction, which is a series of chemical reactions between amino acids and reducing sugars that contribute to the browning of cooked food and the formation of flavor compounds. While it is not a significant component of human nutrition, understanding isohistidine's formation and properties can provide insights into the chemistry of food and the potential effects of dietary components on health.

501-32-6

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501-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501-32-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 501-32:
(5*5)+(4*0)+(3*1)+(2*3)+(1*2)=36
36 % 10 = 6
So 501-32-6 is a valid CAS Registry Number.

501-32-6SDS

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 2-amino-3-imidazol-1-yl-propionic acid

1.2 Other means of identification

Product number -
Other names α-AMINO-1H-IMIDAZOLE-1-PROPANOIC ACID

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:501-32-6 SDS

501-32-6Downstream Products

501-32-6Relevant academic research and scientific papers

THE REACTION OF IMIDAZOLE WITH 2-PHENYL,4-CHLOROMETHYLENE-OXAZOL-5-ONE

Bish, Christopher J.,Jones, John H.

, p. 679 - 680 (2007/10/02)

The displacement of chlorine from 2-phenyl,4-chloromethylene-oxazol-5-one by imidazole does not lead to carbon-carbon bond formation as previously reported, but involves attack by nitrogen leading to 2-phenyl,4-(imidazol-1-yl)methylene-oxazol-5-one.

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