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Details

Stereochemistry ACHIRAL
Molecular Formula C7H10N2
Molecular Weight 122.1677
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3,5-TRIMETHYLPYRAZINE

SMILES

CC1=NC(C)=C(C)N=C1

InChI

InChIKey=IAEGWXHKWJGQAZ-UHFFFAOYSA-N
InChI=1S/C7H10N2/c1-5-4-8-6(2)7(3)9-5/h4H,1-3H3

HIDE SMILES / InChI

Molecular Formula C7H10N2
Molecular Weight 122.1677
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Alkylpyrazines and other volatiles in cocoa liquors at pH 5 to 8, by Selected Ion Flow Tube-Mass Spectrometry (SIFT-MS).
2010-05-25
Application of supercritical CO(2) extraction for the elimination of odorant volatile compounds from winemaking inactive dry yeast preparation.
2010-03-24
Selectivity and efficiency of different reversed-phase and mixed-mode sorbents to preconcentrate and isolate aroma molecules.
2010-03-05
Formation of pyrazines in Maillard model systems of lysine-containing dipeptides.
2010-02-24
Syntheses, structures, and photoluminescence of a series of silver(I) sulfonates with pyrazine derivatives.
2009-10-14
Development of a GC x GC-TOFMS method using SPME to determine volatile compounds in cacao beans.
2009-07
Two volatiles from the venom gland of the Samsum ant, Pachycondyla sennaarensis.
2009-07
Identification of chemicals emitted by calling males of the Sapote fruit fly, Anastrepha serpentina.
2009-05
Approaches to wine aroma: C1 transfer during the reaction between diacetyl and cysteine.
2008-04
Suppression of blood lipid concentrations by volatile Maillard reaction products.
2008-01-24
Degradation of 2,5-dimethylpyrazine by Rhodococcus erythropolis strain DP-45 isolated from a waste gas treatment plant of a fishmeal processing company.
2007-10
Solitary foraging in the ancestral South American ant, Pogonomyrmex vermiculatus. Is it due to constraints in the production or perception of trail pheromones?
2007-02
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.
2007-01-24
Tetramethylpyrazine production from glucose by a newly isolated Bacillus mutant.
2006-12
Effect of citric acid and glycine addition on acrylamide and flavor in a potato model system.
2006-08-09
Characterization of aroma compounds of chinese "Wuliangye" and "Jiannanchun" liquors by aroma extract dilution analysis.
2006-04-05
Determination of the 2H/1H and 15N/14N ratios of Alkylpyrazines from coffee beans (Coffea arabica L. and Coffea canephoravar. robusta) by isotope ratio mass spectrometry.
2005-10-05
Effects of water content on volatile generation and peptide degradation in the maillard reaction of glycine, diglycine, and triglycine.
2005-08-10
Reactivity of epicatechin in aqueous glycine and glucose maillard reaction models: quenching of C2, C3, and C4 sugar fragments.
2005-05-18
Aroma compounds in sweet whey powder.
2004-12
Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning.
2004-05-12
[Chemical profiles of methylpyrazines contained in commercially available natto].
2004-01
Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction.
2003-05-21
Mechanisms responsible for the in vitro relaxation of ligustrazine on porcine left anterior descending coronary artery.
2003-05-16
Purine metabolizing capability of Enterobacter agglomerans affects volatiles production and attractiveness to Mexican fruit fly.
2002-08
Identification of aroma compounds in Parmigiano-Reggiano cheese by gas chromatography/olfactometry.
2002-06
Use of gas chromatography-olfactometry to identify key odorant compounds in dark chocolate. Comparison of samples before and after conching.
2002-04-10
Amelioratory effect of barley tea drinking on blood fluidity.
2002-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:07:43 GMT 2025
Edited
by admin
on Mon Mar 31 18:07:43 GMT 2025
Record UNII
Q8PR0W8TIT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3,5-TRIMETHYLPYRAZINE
FCC   FHFI  
Systematic Name English
2,3,5-TRIMETHYLPYRAZINE [FCC]
Preferred Name English
FEMA NO. 3244
Code English
2,3,5-TRIMETHYLPYRAZINE [FHFI]
Common Name English
PYRAZINE, 2,3,5-TRIMETHYL-
Systematic Name English
TRIMETHYLPYRAZINE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2,3,5-TRIMETHYLPYRAZINE
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
Code System Code Type Description
WIKIPEDIA
2,3,5-Trimethylpyrazine
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
PUBCHEM
26808
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
ECHA (EC/EINECS)
238-712-0
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
FDA UNII
Q8PR0W8TIT
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
EVMPD
SUB185037
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
SMS_ID
100000170869
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
JECFA MONOGRAPH
838
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
EPA CompTox
DTXSID1047075
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY
CAS
14667-55-1
Created by admin on Mon Mar 31 18:07:43 GMT 2025 , Edited by admin on Mon Mar 31 18:07:43 GMT 2025
PRIMARY