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2,5-dimethyl-3-(E-1-propenyl)pyrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55138-77-7

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55138-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55138-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,3 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55138-77:
(7*5)+(6*5)+(5*1)+(4*3)+(3*8)+(2*7)+(1*7)=127
127 % 10 = 7
So 55138-77-7 is a valid CAS Registry Number.

55138-77-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethyl-3-(E-1-propenyl)pyrazine

1.2 Other means of identification

Product number -
Other names -

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:55138-77-7 SDS

55138-77-7Downstream Products

55138-77-7Relevant academic research and scientific papers

Impact of the N-terminal amino acid on the formation of pyrazines from peptides in maillard model systems

Van Lancker, Fien,Adams, An,De Kimpe, Norbert

scheme or table, p. 4697 - 4708 (2012/08/27)

Only a minor part of Maillard reaction studies in the literature focused on the reaction between carbohydrates and peptides. Therefore, in continuation of a previous study in which the influence of the peptide C-terminal amino acid was investigated, this study focused on the influence of the peptide N-terminal amino acid on the production of pyrazines in model reactions of glucose, methylglyoxal, or glyoxal. Nine different dipeptides and three tripeptides were selected. It was shown that the structure of the N-terminal amino acid is determinative for the overall pyrazine production. Especially, the production of 2,5(6)-dimethylpyrazine and trimethylpyrazine was low in the case of proline, valine, or leucine at the N-terminus, whereas it was very high for glycine, alanine, or serine. In contrast to the alkyl-substituted pyrazines, unsubstituted pyrazine was always produced more in the case of experiments with free amino acids. It is clear that different mechanisms must be responsible for this observation. This study clearly illustrates the capability of peptides to produce flavor compounds such as pyrazines.

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