File:Trinitrotoluene_v2.svg · Wikimedia Commons · See Wikimedia Commons
Also known as 2,4,6-TNT, α-TNT, s-trinitrotoluene, Tritol, Trotyl, 2,4,6-trinitrotoluene, 1-methyl-2,4,6-trinitrotoluene, sym-trinitrotoluene
thumb|Trinitrotoluene spin view
OverviewAI-generated
Trinitrotoluene, also identified by the IUPAC name 2-methyl-1,3,5-trinitrobenzene, is a chemical compound with the formula C₇H₅N₃O₆. It has a mass of 227.018 and a density of 1600. The substance exhibits a melting point of 176 and a boiling point of 160. Its vapor pressure is 0.0002, and its solubility is 0.01. The ionization energy is 10.59, and the explosive velocity is 6900.
Chemical properties include an xlogp of 1.6, a tpsa of 137, and a charge of 0. The molecule contains 0 hydrogen bond donors and 6 hydrogen bond acceptors. Safety data indicates a time-weighted average exposure limit of 1.5 and an immediately dangerous to life or health level of 500. The compound is associated with 7529 PubMed entries and is referenced by 1,220 other encyclopedia articles.
Synthesized by Vinony from 27 facts across 4 sources: Wikidata, PubChem, PubMed, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.
Chemical data
- Formula
- C7H5N3O6
- Molecular weight
- 227.13 g/mol
- IUPAC name
- 2-methyl-1,3,5-trinitrobenzene
- SMILES
- CC1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]
- InChIKey
- SPSSULHKWOKEEL-UHFFFAOYSA-N
- XLogP
- 1.6
- Polar surface area
- 137 Ų
- H-bond donors
- 0
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Research
7,529 papers- TNT biotransformation: when chemistry confronts mineralization.ReviewApplied microbiology and biotechnology · 2007Smets BF, Yin H, Esteve-Nuñez ADOI: 10.1007/s00253-007-1008-7
- Dendroremediation of trinitrotoluene (TNT). Part 1: Literature overview and research concept.ReviewEnvironmental science and pollution research international · 2004Schoenmuth BW, Pestemer WDOI: 10.1007/BF02979637
- Common explosives (TNT, RDX, HMX) and their fate in the environment: Emphasizing bioremediation.ReviewChemosphere · 2017Chatterjee S, Deb U, Datta S et al.DOI: 10.1016/j.chemosphere.2017.06.008
- 2,4,6-trinitrotoluene (TNT) degradation by Indiicoccus explosivorum (S5-TSA-19).Archives of microbiology · 2022Lamba J, Anand S, Dutta J et al.DOI: 10.1007/s00203-022-03057-8
- Genotoxicity and potential carcinogenicity of 2,4,6-TNT trinitrotoluene: structural and toxicological considerations.ReviewReviews on environmental health · 2006Bolt HM, Degen GH, Dorn SB et al.DOI: 10.1515/reveh.2006.21.4.217
- Synthesis of 2,4,6-Trinitrotoluene (TNT) Using Flow Chemistry.Molecules (Basel, Switzerland) · 2020Kyprianou D, Berglund M, Emma G et al.DOI: 10.3390/molecules25163586
- 2,4,6-TRINITROTOLUENE (TNT).American Industrial Hygiene Association journal · 1964NEWMAN BLDOI: 10.1080/00028896409342634
- Oxygen-insensitive nitroreductase bacteria-mediated degradation of TNT and proteomic analysis.Environmental science and pollution research international · 2023Yin ML, Zhao SP, Lai JL et al.DOI: 10.1007/s11356-023-30568-8
via PubMed
~17 min read
Encyclopedic overview
16 sectionsContents
- History
- Preparation
- Applications
- Explosive character
- Energy content
- Detection
- Safety and toxicity
- Pink and red water
- Ecological impact
- Aqueous solubility
- Soil adsorption
- Chemical breakdown
- Biodegradation
- See also
- References
- External links
thumb|Trinitrotoluene spin view
Trinitrotoluene ( ), more commonly known as TNT (and more specifically 2,4,6-trinitrotoluene, and by its preferred IUPAC name 2-methyl-1,3,5-trinitrobenzene), is a chemical compound with the formula . TNT is occasionally used as a reagent in chemical synthesis, but it is best known as an explosive material with convenient handling properties. The explosive yield of TNT is considered to be the standard comparative convention of bombs and asteroid impacts. In chemistry, TNT is used to generate charge transfer salts.
Excerpted from Wikipedia’s “TNT” article, available under the CC BY-SA 4.0 licence.
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