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2.4.6- trinitrophenyl methylnitramine

Trimethyl benzene 2.4.6- Trinitrophenol, see Picric acid 2.4.6- Trinitrophenyl-methylnitramine, see Tetryl CT... [Pg.384]

Meiayaku (Army), Sanshoki (Navy ) or Mechiru Nitroamin. Tetryl or 2,4,6-Trinitrophenyl-methylnitramine,... [Pg.487]

Tetryl. Tetryl or 2,4,6-trinitrophenyl methylnitramine, 3, was frequently used as a base charge in blasting caps, as the booster explosive in high-explosive shells, and as an ingredient of binary explosives. Tetryl is now replaced by PETN or RDX. Tetryl is a very toxic chemical [4-6],... [Pg.441]

Shah MM and Spain JC, Elimination of nitrite from the explosive 2,4,6-trinitrophenyl-methylnitramine (tetryl) catalyzed by ferredoxin NADP oxidoreductase from spinach, Biochem. Biophys. Res. Commun., 220, 563, 1996. [Pg.225]

TETRYL (NO,),C,H,N(NOJ CH, 2,4.6 Trinitrophenyl methylnitramin e N-Mcthyl N-2,4,64etra nitro> aniline Nitramine Tctralite Oxidicabte materials Explodes ... [Pg.230]

Synonym(s) 2,4,6-trinitrophenyl-N-methylnitramine N-methyl-N,2,4,6-tetranitrobenzenamine N-picryl-N-methyl-nitr amine tetralit tetralite tetril tetryl trinitrophenyl-methylnitramine nitramine CE HSDB 1994... [Pg.47]

PICRYLNITROMETHYLA. nNE TETRALIT TETRALITE N,2,4,5-TETR. NITRO-N-METHYLANIL-INE TETRIL 2,4,6-TETRYL TRINITROPHENYL-METHYLNITRAMINE 2,4,6-TRlNITROPHENYLMETH-YLNITR. MINE 2,4,6-TRINITROPHENYL-N-METHYL-NITR. MINE... [Pg.1326]

N, 2,3,4-Tetranitro-N-methylaniline (2,3,4-trinitrophenyl-N-methylnitramine), mp 122.5° prepd by the nitration of 2,3,5-trinitro-N-niethyl-aniline with nitric acid (concn unspecified)... [Pg.119]

Synonyms BRN 0964788 CCRIS 3143 CE EINECS 207-531-9 7V-Methyl-2,4,6-tetranitro-aniline -Methyl-iV,2,4,6-tetranitrobenzenaniine Nitramine NSC 2166 Picrylmethyl-nitramine Picrylnitromethylamine Tetralit Tetralite Tetril 2,4,6-Tetryl Trinitrophenylmethyl-nitramine Trinitrophenyl-7V-methylnitramine 2,4,6-Trinitrophenylmethylnitramine 2,4,6-Trinitro-phenyl-A7methylnitramine UN 0208. [Pg.1046]

Trinitrophenol, see Picric acid Trinitrophenylmethylnitramine, see Tetryl Trinitrophenyl-fV-methylnitramine, see Tetryl... [Pg.1513]

Trinitrophenyl-fV-methylnitramine, see Tetryl Trinitrotoluene, see 2,4,6-Trinitrotoluene s/m-Trinitrotoluene, see 2,4,6-Trinitrotoluene Trinitrotoluol, see 2,4,6-Trinitrotoluene a-Trinitrotoluol, see 2,4,6-Trinitrotoluene... [Pg.1513]

Agency for Toxic Substances and Disease Registry (ATSDR) Toxicological Profile for Tetryl (2,4,6 Trinitrophenyl-N-Methylnitramine) pp 1-100. US Department of Health and Human Services, Public Health Service, 1995... [Pg.669]

Teflon AF amorphous Teflon or copolymer of PTFE and 2,2-bis(trifluoro-methy l)-4,5-difluoro-1,3-dioxide Teryl 2,4,6-trinitrophenyl-iV-methylnitramine TFA trifluoroacetic acid TGF temperature gradient focusing TGGE temperature gradient gel electrophoresis Ti titanium... [Pg.484]

Tetryl is a synthetic substance that was used to make explosives, mostly during World War I and World War II. It is no longer manufactured or used in the United States. The chemical name for tetryl is N-methyl-N,2,4,6-tetranitroaniline. Other commonly used names are 2,4,6-trinitrophenyl-N-methylnitramine, nitramine, tetralite, and tetril. Stocks of tetryl are found in storage at military installations and are being destroyed by the Department of Defense. Tetryl was frequently manufactured as pellets or powder. Under certain manufacturing conditions, it could exist in the air as a dust. Tetryl is a yellow, crystal-like solid at room temperature. It dissolves slightly in... [Pg.13]

N,2,4,5-Tetranitro-N-methylamline (2,4,5-trinitrophenyl-N-methylnitramine), needles from nitric acid-, mp 143.5° prepd by nitration of 2,4,5-trinitro-N-methylaniline, or by the action of 90% nitric acid on 2,4,5-trinitro-N,N-dimethylaniline (Refs 1 3) 2,3,4,6-Tetranitro-N-methylanilme, mp 127° prepd by the action of sulfuric acid on N,2,4,5-tetranitro-N-methylaniline (Refs 2 3)... [Pg.120]

Dye intermediates were early on adapted to the production of explosives. While most modern explosives are aromatic nitro compounds, ancillary products incorporate amino groups. Of interest here are two tetranitroanilines. Tetryl (2,4,6-trinitrophenyl-A-methylnitramine, or A,2,4,6-tetranitro-iV-methylaniline) (40) is employed as a booster for TNT. It can be made from V-methylaniline (39), or the cheaper V,V-dimethylaniline (32), since the latter loses one methyl group on oxidation. An alternative route, introduced in World War II, starts with conversion of dinitrochlorobenzene into dinitro-lV-methylaniline, which is then nitrated. The explosive tetrotyl is 70% tetryl and 30% TNT. [Pg.32]

Figure 3. Chemical structure of nitroglycerine (NG), dinitrotoluene (DNT), trinitrotoluene (TNT), pentanerythritoltetranitrate (PETN), cyclotrimethylenetrinitramine (RDX), and trinitrophenyl-n-methylnitramine (Tetryl). Open structures (two on left) are more likely to decompose compared with closed aromatic ring structures. Figure 3. Chemical structure of nitroglycerine (NG), dinitrotoluene (DNT), trinitrotoluene (TNT), pentanerythritoltetranitrate (PETN), cyclotrimethylenetrinitramine (RDX), and trinitrophenyl-n-methylnitramine (Tetryl). Open structures (two on left) are more likely to decompose compared with closed aromatic ring structures.
TRINITROPHENYLMETHYLNITRAMINE or 2,4,6-TRINITROPHENYL-iV-METHYLNITRAMINE (479-45-8) A powerful oxidizer and heat-, friction-, and shock-sensitive high explosive. Explodes in elevated temperatures above approximately 482°F/250°C. The reaction may take about 0.1 second, but this material can explode after a delayed period in lower temperatures (16.6 minutes at 320°F/160°C). Ignition or explosion on contact with reducing agents, combustible materials, fuels, hydrocarbons, hydrazine, powdered metals, organic substances, trinitrogen difluoride. [Pg.1203]

Synonyms/Trade Names N-Methyl-N,2,4,6-tetranitroaniline Nitramine 2,4,6-Tetryl 2,4,6-Trinitrophenyl-N-methylnitramine ... [Pg.305]

OtherNames Aniline,A -methyl-M2,4,6-tetranitro- 2,4,6,A-Tetranitro-A-methylaniline 2,4,6-Tetryl 2,4,6-Trinitro-N-methyl-A-nitroaniline 2,4,6-Trinitrophenyl-A-methylnitramine 2,4,6-Trinitro-phenylmethylnitroamine CE A-Methyl-A,2,4,6-tetranitroaniline A-Methyl-A-picrylnitramine A-Picryl-A-methylnitramine NSC 2166 Nitramine Nitramine (indicator) Picrylmethylnitra-mine Picrylnitromethylamine Tetralit Tetralite Tetril Tetryl CA Index Name Benzenamine, A-methyl-A,2,4,6-tetranitro-CAS Registry Number 479-45-8 Merck Index Number 6573 Chemical Structure... [Pg.264]

See other pages where 2.4.6- trinitrophenyl methylnitramine is mentioned: [Pg.258]    [Pg.384]    [Pg.75]    [Pg.75]    [Pg.174]    [Pg.174]    [Pg.409]    [Pg.258]    [Pg.174]    [Pg.174]    [Pg.174]    [Pg.614]    [Pg.258]    [Pg.384]    [Pg.75]    [Pg.75]    [Pg.174]    [Pg.174]    [Pg.409]    [Pg.258]    [Pg.174]    [Pg.174]    [Pg.174]    [Pg.614]    [Pg.332]    [Pg.1924]    [Pg.747]    [Pg.2]    [Pg.68]    [Pg.1057]    [Pg.694]    [Pg.699]   
See also in sourсe #XX -- [ Pg.668 ]



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2.4.6- Trinitrophenyl-N-methylnitramine

Methylnitramine

Trinitrophenyl

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