Names | |
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Preferred IUPAC name
Methyl(2,4,6-trinitrophenyl)nitramide | |
Other names
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.006.848 |
PubChem CID
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RTECS number |
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UNII | |
UN number | 0208 |
CompTox Dashboard (EPA)
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Properties | |
C7H5N5O8 | |
Molar mass | 287.144 g·mol−1 |
Appearance | Yellow crystalline solid |
Odor | Odorless |
Density | 1.73 g/cm3 |
Melting point | 129.5 °C (265.1 °F; 402.6 K) |
Boiling point | 187 °C (369 °F; 460 K) decomposes |
Virtually insoluble | |
Vapor pressure | <1 mmHg (20°C)[1] |
Explosive data | |
Shock sensitivity | Sensitive |
Friction sensitivity | Sensitive |
Detonation velocity | 7,570 m/s (24,836 f/s) |
RE factor | 1.25 |
Hazards | |
Lethal dose or concentration (LD, LC): | |
LDLo (lowest published)
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5000 mg/kg (dog, subcutaneous)[2] |
NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 1.5 mg/m3 [skin][1] |
REL (Recommended)
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TWA 1.5 mg/m3 [skin][1] |
IDLH (Immediate danger)
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750 mg/m3[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2,4,6-Trinitrophenylmethylnitramine or tetryl (C7H5N5O8) is an explosive compound used to make detonators and explosive booster charges.
Tetryl is a nitramine booster explosive, though its use has been largely superseded by RDX. Tetryl is a sensitive secondary high explosive used as a booster, a small charge placed next to the detonator in order to propagate detonation into the main explosive charge.