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Details

Stereochemistry ACHIRAL
Molecular Formula C7H5N3O6
Molecular Weight 227.1311
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4,6-TRINITROTOLUENE

SMILES

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

InChI

InChIKey=SPSSULHKWOKEEL-UHFFFAOYSA-N
InChI=1S/C7H5N3O6/c1-4-6(9(13)14)2-5(8(11)12)3-7(4)10(15)16/h2-3H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Explosive biodegradation in soil slurry batch reactors amended with exogenous microorganisms.
2001
Effect of photosensitizer riboflavin on the fate of 2,4,6-trinitrotoluene in a freshwater environment.
2001 Aug
Electrochemical treatment of 2,4,6-trinitrotoluene and related compounds.
2001 Jan 15
Biotransformation and partial mineralization of the explosive 2,4,6-trinitrotoluene (TNT) by rhizobia.
2001 Jun
Polymorphism in 2,4,6-trinitrotoluene crystallized from solution.
2001 Mar 14
Fluorescence quenching as an indirect detection method for nitrated explosives.
2001 May 1
Methemoglobin formation in human erythrocytes by nitroaromatic explosives.
2001 Nov-Dec
Screening method for nitroaromatic compounds in water based on solid-phase microextraction and infrared spectroscopy.
2001 Sep 1
Short pulse laser mass spectrometry of nitrotoluenes: ionization and fragmentation behavior.
2002
Biotransformation of 2,4,6-trinitrotoluene in a continuous-flow Anabaena sp. system.
2002 Apr
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
On-line coupling of supercritical fluid extraction with high-performance liquid chromatography for the determination of explosives in vapour phases.
2002 Jul 19
Evaluation of tissue and cellular biomarkers to assess 2,4,6-trinitrotoluene (TNT) exposure in earthworms: effects-based assessment in laboratory studies using Eisenia andrei.
2002 Jul-Aug
[The retrospective survey of malignant tumor in weapon workers exposed to 2,4,6-trinitrotoluene].
2002 Jun
Demonstration of four immunoassay formats using the array biosensor.
2002 Mar 1
Selective functionalisation of TNT for sensitive detection by SERRS.
2002 Mar 21
Coupled abiotic-biotic mineralization of 2,4,6-trinitrotoluene (TNT).
2002 May-Jun
Detection of 2,4,6-trinitrotoluene in seawater using a reversed-displacement immunosensor.
2002 Nov 1
Reactivity of partially reduced arylhydroxylamine and nitrosoarene metabolites of 2,4,6-trinitrotoluene (TNT) toward biomass and humic acids.
2002 Oct 15
Alkali hydrolysis of trinitrotoluene.
2002 Spring
Biodegradation of the energetic compound TNT through a multiple-stage treatment approach.
2003
Exposure to nitroaromatic explosives and health effects during disposal of military waste.
2003 Jul
2,4,6-Trinitrotoluene detection using recombinant antibodies.
2003 Jun
Potassium ferrate [Fe(VI)] does not mediate self-sterilization of a surrogate Mars soil.
2003 Mar 6
HPLC-MS investigations of acidic contaminants in ammunition wastes using volatile ion-pairing reagents (VIP-LC-MS).
2004 Feb
Express analysis of explosives, chemical warfare agents and drugs with multicapillary column gas chromatography and ion mobility increment spectrometry.
2004 Feb 5
Diversity of contaminant reduction reactions by zerovalent iron: role of the reductate.
2004 Jan 1
Use of reversed-phase high-performance liquid chromatography-diode array detection for complete separation of 2,4,6-trinitrotoluene metabolites and EPA Method 8330 explosives: influence of temperature and an ion-pair reagent.
2004 Jan 2
Patents
Name Type Language
2,4,6-TRINITROTOLUENE
MI  
Systematic Name English
TRINITROTOLUENE, 2,4,6-
Systematic Name English
TNT
Common Name English
SYM-TRINITROTOLUENE
Common Name English
1-METHYL-2,4,6-TRINITROBENZENE
Systematic Name English
2,4,6-TRINITROTOLUENE [IARC]
Common Name English
NSC-36949
Code English
2,4,6-TNT
Common Name English
2,4,6-TRINITROTOLUENE [MI]
Common Name English
TRINITROTOLUENE [HSDB]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-289-6
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
CHEBI
46053
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
WIKIPEDIA
TNT
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
DRUG BANK
DB01676
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
CAS
118-96-7
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
HSDB
1146
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
MERCK INDEX
m11172
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID7024372
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
FDA UNII
H43RF5TRM5
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
NSC
36949
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY
PUBCHEM
8376
Created by admin on Fri Dec 15 18:58:59 GMT 2023 , Edited by admin on Fri Dec 15 18:58:59 GMT 2023
PRIMARY