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Tetralit = Tetryl

TETRILE, Tetranitrometilanilina, Trinitrofenil-metilnitroammine o Tetralite (Tetryl, Amer and CE, British). It is described in Belgrano (Ref 31, pp 272-75). He lists its uses in Gt-Britain and the USA but says nothing about its uses in Italy. In Ref 28, p 349 it is stated that it is used as a component of some expl mixtures, as with TNT, such as Tetritol... [Pg.443]

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]

Tetraleno, see Tetrachloroethylene Tetralex, see Tetrachloroethylene Tetralit, see Tetryl Tetralite, see Tetryl... [Pg.1511]

Prepn of Tetryl (or Tetralite) was first described by van Romburgh in RecTravChim 2, p 108. Quoted from Marshall 1 (Ref 11, p 274)... [Pg.143]

Tetryl is a widely-used explosive. It is also known under the names of Pyronite, Tetrylit, Tetralite, Tetralita. In England it has been known for some time as Composition Exploding—CE. The incorrect name—tetranitromethylaniline—may sometimes be encountered in the literature. [Pg.40]

Tetralite. Ital for Tetryl. See in Vol 7, II79-L and in this Vol under Tetryl ... [Pg.568]

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]

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]

Beilstein Handbook Reference) Aniline, N-methyl-N,2,4,6-tetranitro- Benzenamine, N-methyl-N,2.4,6-tetranitro- BRN 0964788 CCRIS 3143 CE EINECS 207-531-9 HSDB 2857 N-Methyl-N-picryl-nitramine N-Methyl-N,2,4,6-tetranitroaniline N-Methyl-N-2,4,6-letranitrobenzenamine Nitramine NSC 2166 Picryimethylnitramine N-Picryl-N-methyInitramine Pic-rylnitromethylamine Tetralite Tetril Tetryl 2,4,6-Tetryl ... [Pg.614]

Among the booster explosives, we find trinitrophenylmethylnitramine, commonly called tetryl or tetralite. An outstanding example of an alkylated compound in the field of flavors is vanillin. Alkylation plays a striking part in the preparation of hypnotics, e.g., barbital (Veronal), pheno-barbital (Luminal), and Amytal, rendering them lipoid-soluble. [Pg.806]

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 Tetralit = Tetryl is mentioned: [Pg.45]    [Pg.1039]    [Pg.45]    [Pg.1039]    [Pg.300]    [Pg.373]    [Pg.374]    [Pg.175]    [Pg.386]    [Pg.1225]    [Pg.1228]    [Pg.373]    [Pg.374]    [Pg.132]   
See also in sourсe #XX -- [ Pg.311 ]




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