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Details

Stereochemistry ACHIRAL
Molecular Formula C7H6N2O4
Molecular Weight 182.1335
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,5-DINITROTOLUENE

SMILES

CC1=CC(=CC(=C1)[N+]([O-])=O)[N+]([O-])=O

InChI

InChIKey=RUIFULUFLANOCI-UHFFFAOYSA-N
InChI=1S/C7H6N2O4/c1-5-2-6(8(10)11)4-7(3-5)9(12)13/h2-4H,1H3

HIDE SMILES / InChI

Molecular Formula C7H6N2O4
Molecular Weight 182.1335
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemical signatures of TNT-filled land mines.
2001 May 10
Characterization and origin identification of 2,4,6-trinitrotoluene through its by-product isomers by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry.
2002 Feb 8
Nephrotoxicity and nephrocarcinogenicity of dinitrotoluene: new aspects to be considered.
2002 Jul-Sep
The response of adult rat sertoli cells, immortalized by a temperature-sensitive mutant of SV40, to 1,2-dinitrobenzene, 1,3-dinitrobenzene, 2,4-dinitrotoluene, 3,4-dinitrotoluene, and cadmium.
2003 Apr
Exposure to nitroaromatic explosives and health effects during disposal of military waste.
2003 Jul
TNT biotransformation and detoxification by a Pseudomonas aeruginosa strain.
2003 Oct
Use of poultry litter for biodegradation of soil contaminated with 2,4- and 2,6-dinitrotoluene.
2004 Dec 10
Characterization of a gene cluster encoding the maleylacetate reductase from Ralstonia eutropha 335T, an enzyme recruited for growth with 4-fluorobenzoate.
2004 Feb
Anaerobic biotransformation of dinitrotoluene isomers by Lactococcus lactis subsp. lactis strain 27 isolated from earthworm intestine.
2005 Sep
Fluorescence of aromatic amines and their fluorescamine derivatives for detection of explosive vapors.
2006 Sep
Recovery of nitrotoluenes from wastewater by solvent extraction enhanced with salting-out effect.
2007 Aug 17
Transport mechanisms for the uptake of organic compounds by rice (Oryza sativa) roots.
2007 Jul
Gas phase detection of explosives such as 2,4,6-trinitrotoluene by molecularly imprinted polymers.
2007 May 15
A review on slurry bioreactors for bioremediation of soils and sediments.
2008 Feb 29
Acute toxicity of 2,4,6-trinitrotoluene, 2,4-dinitrotoluene, and 2,6-dinitrotoluene in the adult bullfrog (Lithobates catesbeiana).
2008 Jun
Decomposition of nitrotoluenes from trinitrotoluene manufacturing process by Electro-Fenton oxidation.
2008 Jun
Electrochemical destruction of dinitrotoluene isomers and 2,4,6-trinitrotoluene in spent acid from toluene nitration process.
2009 Jan 30
Assessing TNT and DNT groundwater contamination by compound-specific isotope analysis and 3H-3He groundwater dating: a case study in Portugal.
2009 Oct
Fluorescence-based sensing of 2,4,6-trinitrotoluene (TNT) using a multi-channeled poly(methyl methacrylate) (PMMA) microimmunosensor.
2010
Detection of explosive vapors with a charge transfer molecule: self-assembly assisted morphology tuning and enhancement in sensing efficiency.
2010 Feb 14
Simultaneous Raman spectroscopy-laser-induced breakdown spectroscopy for instant standoff analysis of explosives using a mobile integrated sensor platform.
2010 Feb 15
Shewanella spp. genomic evolution for a cold marine lifestyle and in-situ explosive biodegradation.
2010 Feb 8
Engineering a novel self-powering electrochemical biosensor.
2010 Sep
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:11:31 GMT 2023
Edited
by admin
on Fri Dec 15 19:11:31 GMT 2023
Record UNII
B651857LG8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,5-DINITROTOLUENE
HSDB  
Systematic Name English
NSC-87348
Code English
5-METHYL-1,3-DINITROBENZENE
Systematic Name English
DINITROTOLUENE, 3,5-
Systematic Name English
BENZENE, 1-METHYL-3,5-DINITRO-
Systematic Name English
3,5-DINITROTOLUENE [HSDB]
Common Name English
TOLUENE, 3,5-DINITRO-
Systematic Name English
1-METHYL-3,5-DINITROBENZENE
Systematic Name English
3,5-DINITROTOLUENE [IARC]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
210-566-2
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
EPA CompTox
DTXSID40210803
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
PUBCHEM
12067
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
HSDB
6463
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
NSC
87348
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
FDA UNII
B651857LG8
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
CAS
618-85-9
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY