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Names | |||
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Preferred IUPAC name
2-Methyl-1,3,5-trinitrobenzene[1] | |||
Other names
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Identifiers | |||
3D model (JSmol)
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Abbreviations | TNT | ||
ChEMBL | |||
ChemSpider | |||
DrugBank | |||
ECHA InfoCard | 100.003.900 | ||
EC Number |
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KEGG | |||
PubChem CID
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RTECS number |
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UNII | |||
UN number | 0209 – Dry or wetted with < 30% water 0388, 0389 – Mixtures with trinitrobenzene, hexanitrostilbene | ||
CompTox Dashboard (EPA)
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Properties | |||
C7H5N3O6 | |||
Molar mass | 227.132 g·mol−1 | ||
Appearance | Pale yellow solid. Loose "needles", flakes or prills before melt-casting. A solid block after being poured into a casing. | ||
Density | 1.654 g/cm3 | ||
Melting point | 80.35 °C (176.63 °F; 353.50 K) | ||
Boiling point | 240.0 °C (464.0 °F; 513.1 K) (decomposes)[2] | ||
0.13 g/L (20 °C) | |||
Solubility in ether, acetone, benzene, pyridine | soluble | ||
Vapor pressure | 0.0002 mmHg (20°C)[3] | ||
Explosive data | |||
Shock sensitivity | Insensitive | ||
Friction sensitivity | Insensitive to 353 N | ||
Detonation velocity | 6900 m/s | ||
RE factor | 1.00 | ||
Hazards | |||
GHS labelling: | |||
Danger | |||
H201, H301, H311, H331, H373, H411 | |||
P210, P273, P309+P311, P370+P380, P373, P501 | |||
NFPA 704 (fire diamond) | |||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
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795 mg/kg (rat, oral) 660 mg/kg (mouse, oral)[4] | ||
LDLo (lowest published)
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500 mg/kg (rabbit, oral) 1850 mg/kg (cat, oral)[4] | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible)
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TWA 1.5 mg/m3 [skin][3] | ||
REL (Recommended)
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TWA 0.5 mg/m3 [skin][3] | ||
IDLH (Immediate danger)
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500 mg/m3[3] | ||
Safety data sheet (SDS) | ICSC 0967 | ||
Related compounds | |||
Related compounds
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picric acid hexanitrobenzene 2,4-Dinitrotoluene | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Trinitrotoluene (/ˌtraɪˌnaɪtroʊˈtɒljuiːn/),[5][6] more commonly known as TNT (and more specifically 2,4,6-trinitrotoluene, and by its preferred IUPAC name 2-methyl-1,3,5-trinitrobenzene),[1] is a chemical compound with the formula C6H2(NO2)3CH3. 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.