Page last updated: 2024-11-05

4-amino-2,6-dinitrotoluene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

4-amino-2,6-dinitrotoluene : An amino-nitrotoluene that is 2,6-dinitrotoluene substituted at position 4 by an amino group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID29574
CHEBI ID77424
SCHEMBL ID314000
MeSH IDM0108047

Synonyms (49)

Synonym
p-toluidine,5-dinitro-
19406-51-0
4-amino-2,6-dinitrotoluene
4-methyl-3,5-dinitrobenzenamine
3,5-dinitro-4-methylaniline
nsc-25010
nsc25010
2,6-dinitro-4-aminotoluene
4-amino-1-methyl-2,6-dinitrobenzene
nsc55353
nsc-55353
p-toluidine, 3,5-dinitro-
benzenamine, 4-methyl-3,5-dinitro-
4-methyl-3,5-dinitroaniline
STK313330
benzenamine,5-dinitro-
3,5-dinitro-p-toluidine
brn 2462150
benzenamine, 3,5-dinitro-4-methyl-
ai3-23207
ccris 5190
nsc 25010
AC-10512
AKOS000310028
unii-vgf967ajx2
vgf967ajx2 ,
4-toluenamine, 2,6-dinitro-
58449-89-1
4-methyl-3,5-dinitro-aniline
A813697
4-methyl-3,5-dinitro-phenylamine
FT-0637844
4-methyl-3,5-dinitrophenylamine
BBL023069
SCHEMBL314000
4-adnt
CHEBI:77424
4-methyl-3,5-dinitroaniline #
4-amino-2,6-dinitrotoluene, vial of 100 mg, analytical standard
DTXSID8074312
4-amino-2,6-dinitrotoluene (3,5-dinitro-4-methylaniline)
(4-methyl-3,5-dinitrophenyl)amine
VS-07320
Q27105069
mfcd00033978
153919-64-3
1-amino-3,5-dinitro-4-methylbenzene
EN300-183718
CS-0237441

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"2,4,6-Trinitrotoluene (TNT) and compounds associated with its production are toxic and phototoxic to a wide range of biota."( Phototoxicology. 3. Comparative toxicity of trinitrotoluene and aminodinitrotoluenes to Daphnia magna, Dugesia dorotocephala, and sheep erythrocytes.
Balbach, H; Davenport, R; Johnson, LR; Schaeffer, DJ, 1994
)
0.29
"A pond in an industrial area in Sweden was selected to study adverse effects on salmon alevins from 2,4,6-trinitrotoluene (TNT)-contaminated water."( Toxicity and accumulation of trinitrotoluene (TNT) and its metabolites in Atlantic salmon alevins exposed to an industrially polluted water.
Berglind, R; Brännäs, E; Leffler, P; Ragnvaldsson, D; Wingfors, H, 2014
)
0.4

Dosage Studied

ExcerptRelevanceReference
" Based on the slopes of the dose-response lines, the nuv coexposure and dark toxic mechanisms of action for TNT, 2A, and 4A appeared to be similar."( Phototoxicology. 2. Near-ultraviolet light enhancement of Microtox assays of trinitrotoluene and aminodinitrotoluenes.
Balbach, H; Davenport, R; Johnson, LR; Schaeffer, DJ, 1994
)
0.29
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
explosiveA substance capable of undergoing rapid and highly exothermic decomposition.
fungal xenobiotic metaboliteAny fungal metabolite produced by metabolism of a xenobiotic compound in fungi.
marine metaboliteAny metabolite produced during a metabolic reaction in marine macro- and microorganisms.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
amino-nitrotolueneA nitrotoluene carrying at least one amino group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (1)

PathwayProteinsCompounds
2,4,6-trinitrotoluene degradation39

Research

Studies (32)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (15.63)18.7374
1990's7 (21.88)18.2507
2000's9 (28.13)29.6817
2010's10 (31.25)24.3611
2020's1 (3.13)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 25.65

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index25.65 (24.57)
Research Supply Index3.58 (2.92)
Research Growth Index4.67 (4.65)
Search Engine Demand Index29.12 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (25.65)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other35 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]