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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
Effects of carnosine on volatile generation from Maillard reaction of ribose and cysteine.
2002 Apr 10
Identification of aroma compounds in Parmigiano-Reggiano cheese by gas chromatography/olfactometry.
2002 Jun
Mechanisms responsible for the in vitro relaxation of ligustrazine on porcine left anterior descending coronary artery.
2003 May 16
Aroma compounds in sweet whey powder.
2004 Dec
Lanthanide(III)/actinide(III) differentiation in coordination of azine molecules to tris(cyclopentadienyl) complexes of cerium and uranium.
2004 Feb 21
[Chemical profiles of methylpyrazines contained in commercially available natto].
2004 Jan
Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning.
2004 May 12
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 Oct 5
Characterization of aroma compounds of chinese "Wuliangye" and "Jiannanchun" liquors by aroma extract dilution analysis.
2006 Apr 5
Competition between photochemistry and energy transfer in UV-excited diazabenzenes. 4. UV photodissociation of 2,3-, 2,5-, and 2,6-dimethylpyrazine.
2007 Dec 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 Oct
Bis(2,6-dimethyl-pyrazine-κN)diiodidozinc(II).
2008 Mar 5
Characterization of fish sauce aroma-impact compounds using GC-MS, SPME-Osme-GCO, and Stevens' power law exponents.
2008 May
Suppression of blood lipid concentrations by volatile Maillard reaction products.
2008 Nov-Dec
Coffee aroma--statistical analysis of compositional data.
2009 Dec 15
Syntheses, structures, and photoluminescence of a series of silver(I) sulfonates with pyrazine derivatives.
2009 Oct 14
Poly[[bis-(μ(2)-6-methyl-pyrazin-2-carboxyl-ato-κN,O:N)copper(II)] dihydrate].
2009 Oct 23
Bioconversion of 2,6-dimethylpyridine to 6-methylpicolinic acid by Exophiala dermatitidis (Kano) de Hoog DA5501 cells grown on n-dodecane.
2010 Apr
Alkylpyrazines and other volatiles in cocoa liquors at pH 5 to 8, by Selected Ion Flow Tube-Mass Spectrometry (SIFT-MS).
2010 Jan-Feb
Temporal changes of flavour and texture in cooked bologna type sausages as affected by fat and salt content.
2010 Jul
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:01:14 GMT 2023
Edited
by admin
on Fri Dec 15 17:01:14 GMT 2023
Record UNII
N77Q72C9I3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DIMETHYLPYRAZINE
FCC   FHFI  
Systematic Name English
2,6-DIMETHYLPYRAZINE [FCC]
Common Name English
2,6-DIMETHYLPYRAZINE [FHFI]
Common Name English
3,5-DIMETHYLPYRAZINE
Systematic Name English
FEMA NO. 3273
Code English
PYRAZINE, 2,6-DIMETHYL-
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2,6-DIMETHYLPYRAZINE
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
Code System Code Type Description
FDA UNII
N77Q72C9I3
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
PRIMARY
JECFA MONOGRAPH
842
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
PRIMARY
CAS
108-50-9
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
PRIMARY
MESH
C075524
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID5047619
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-589-4
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
PRIMARY
PUBCHEM
7938
Created by admin on Fri Dec 15 17:01:14 GMT 2023 , Edited by admin on Fri Dec 15 17:01:14 GMT 2023
PRIMARY