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Details

Stereochemistry ACHIRAL
Molecular Formula C6H8N2
Molecular Weight 108.1411
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-DIMETHYLPYRAZINE

SMILES

CC1=CN=CC(C)=N1

InChI

InChIKey=HJFZAYHYIWGLNL-UHFFFAOYSA-N
InChI=1S/C6H8N2/c1-5-3-7-4-6(2)8-5/h3-4H,1-2H3

HIDE SMILES / InChI

Molecular Formula C6H8N2
Molecular Weight 108.1411
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Temporal changes of flavour and texture in cooked bologna type sausages as affected by fat and salt content.
2010-07
Alkylpyrazines and other volatiles in cocoa liquors at pH 5 to 8, by Selected Ion Flow Tube-Mass Spectrometry (SIFT-MS).
2010-05-25
Bioconversion of 2,6-dimethylpyridine to 6-methylpicolinic acid by Exophiala dermatitidis (Kano) de Hoog DA5501 cells grown on n-dodecane.
2010-04
Coffee aroma--statistical analysis of compositional data.
2009-12-15
Poly[[bis-(μ(2)-6-methyl-pyrazin-2-carboxyl-ato-κN,O:N)copper(II)] dihydrate].
2009-10-23
Syntheses, structures, and photoluminescence of a series of silver(I) sulfonates with pyrazine derivatives.
2009-10-14
Characterization of fish sauce aroma-impact compounds using GC-MS, SPME-Osme-GCO, and Stevens' power law exponents.
2008-05
Bis(2,6-dimethyl-pyrazine-κN)diiodidozinc(II).
2008-03-05
Suppression of blood lipid concentrations by volatile Maillard reaction products.
2008-01-24
Competition between photochemistry and energy transfer in UV-excited diazabenzenes. 4. UV photodissociation of 2,3-, 2,5-, and 2,6-dimethylpyrazine.
2007-12-27
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
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
Aroma compounds in sweet whey powder.
2004-12
Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning.
2004-05-12
Lanthanide(III)/actinide(III) differentiation in coordination of azine molecules to tris(cyclopentadienyl) complexes of cerium and uranium.
2004-02-21
[Chemical profiles of methylpyrazines contained in commercially available natto].
2004-01
Mechanisms responsible for the in vitro relaxation of ligustrazine on porcine left anterior descending coronary artery.
2003-05-16
Identification of aroma compounds in Parmigiano-Reggiano cheese by gas chromatography/olfactometry.
2002-06
Effects of carnosine on volatile generation from Maillard reaction of ribose and cysteine.
2002-04-10
Comparison of stochastic modelling of the intakes of intentionally added flavouring substances with theoretical added maximum daily intakes (TAMDI) and maximized survey-derived daily intakes (MSDI).
2002-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:39:28 GMT 2025
Edited
by admin
on Mon Mar 31 18:39:28 GMT 2025
Record UNII
N77Q72C9I3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DIMETHYLPYRAZINE
FCC   FHFI  
Systematic Name English
FEMA NO. 3273
Preferred Name English
2,6-DIMETHYLPYRAZINE [FCC]
Common Name English
2,6-DIMETHYLPYRAZINE [FHFI]
Common Name English
3,5-DIMETHYLPYRAZINE
Systematic Name English
PYRAZINE, 2,6-DIMETHYL-
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2,6-DIMETHYLPYRAZINE
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
Code System Code Type Description
FDA UNII
N77Q72C9I3
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
JECFA MONOGRAPH
842
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
CAS
108-50-9
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
MESH
C075524
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID5047619
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-589-4
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
PUBCHEM
7938
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY