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Tetryl

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789: 294: 191: 627: 24: 742:. It is detonated by friction, shock, or spark. It remains stable at all temperatures which may be encountered in storage. It is generally used in the form of pressed pellets, and has been approved as the standard bursting charge for small-caliber projectiles, since it gives much better fragmentation than TNT. It has an 766:
The most toxic ordnance compounds, tetryl and 1,3,5-TNB, are also the most degradable. Therefore, these chemicals are expected to be short-lived in nature, and environmental impacts would not be expected in areas that are not currently subject to chronic inputs of these chemicals. Tetryl decomposes
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and acidified to pH < 3. All samples expected to contain tetryl should not be exposed to temperatures above room temperature. In addition, degradation products of tetryl appear as a shoulder on the 2,4,6-TNT peak. Peak heights rather than peak areas should be used when tetryl is present in
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Epidemiological data shows that tetryl has most effect on the skin, acting as a strong irritant. Symptoms of skin sensitization such as dermatitis, itch, erythema, etc. may occur. Tetryl can also affect mucous membranes, the upper respiratory tract, and possibly the liver.
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Although tetryl is among the most toxic explosive compounds, it is very short-lived. This combined with the fact that the health impacts of this compound are largely unstudied, not much is known about any health problems that this compound may cause.
128: 714:. 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. 926: 904: 567: 640: 1017: 1033: 1025: 958:“A Military Guide to Terrorism in the 21st Century.” August 2003. P. 171. U.S. Army Training and Doctrine Command, Fort Leavenworth, Kansas. 730:
and other solvents. When tetryl is heated, it first melts, then decomposes and explodes. It burns readily and is more easily detonated than
343: 812:. Tetryl is no longer manufactured or used in the United States, but can still be found in legacy munitions such as the 1001: 308: 945: 647: 635: 264: 808:
and later conflicts. Tetryl is usually used on its own, though can sometimes be found in compositions such as
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Tetryl is a yellow crystalline solid powder material, practically insoluble in water but soluble in
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of 23,600–23,900 feet per second (7200–7300 m/s). Tetryl is the basis for the service tetryl
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CDC - Documentation for Immediately Dangerous To Life or Health Concentrations (IDLHs)
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InChI=1S/C7H5N5O8/c1-8(12(19)20)7-5(10(15)16)2-4(9(13)14)3-6(7)11(17)18/h2-3H,1H3
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concentrations that are significant relative to the concentration of 2,4,6-TNT.
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InChI=1/C7H5N5O8/c1-8(12(19)20)7-5(10(15)16)2-4(9(13)14)3-6(7)11(17)18/h2-3H,1H3
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shells (dating from circa 1945) showing color code for tetryl filling
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Except where otherwise noted, data are given for materials in their
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booster explosive, though its use has been largely superseded by
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Immediately Dangerous to Life or Health Concentrations (IDLH)
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http://smallwarsjournal.com/documents/terrorismhandbook.pdf
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is included in the cap to ensure detonation of tetryl.
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necessary for positive detonation of TNT. A mixture of
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National Institute for Occupational Safety and Health
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National Institute for Occupational Safety and Health
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Occupational Safety and Health Guideline for Tetryl
456:187 °C (369 °F; 460 K) decomposes 1040: 1018:Agency for Toxic Substances and Disease Registry 211: 1034:Occupational Safety & Health Administration 103: 983:CDC - NIOSH Pocket Guide to Chemical Hazards 446:129.5 °C (265.1 °F; 402.6 K) 292: 189: 167: 247: 899:NIOSH Pocket Guide to Chemical Hazards. 787: 940: 938: 936: 761: 288: 1041: 894: 892: 890: 888: 717: 180: 320:Key: AGUIVNYEYSCPNI-UHFFFAOYSA-N 147: 41:Methyl(2,4,6-trinitrophenyl)nitramide 933: 828:Tetryl is produced by slowly mixing 885: 660:2,4,6-Trinitrophenylmethylnitramine 330:Key: AGUIVNYEYSCPNI-UHFFFAOYAF 202: 13: 843: 14: 1065: 1007: 625: 384: 378: 351:CN(c1c(cc(cc1(=O))(=O))(=O))(=O) 22: 621:(at 25 °C , 100 kPa). 562:5000 mg/kg (dog, subcutaneous) 79:,2,4,6-tetranitrophenyl-1-amine 976: 965: 952: 911: 800:Tetryl was used mainly during 738:, being about as sensitive as 390: 372: 1: 996:, New York: Wiley-VCH, 1996. 878: 823: 572:(US health exposure limits): 7: 856: 544:or concentration (LD, LC): 10: 1070: 783: 615: 566: 540: 535: 482: 416:Yellow crystalline solid 359: 339: 304: 87: 47: 35: 30: 21: 962:. Accessed May 11, 2010. 792:Cross-sectional view of 69:,2,4,6-tetranitroaniline 994:Explosives Engineering 797: 695:compound used to make 794:Oerlikon 20 mm cannon 791: 53:Nitramine (incorrect) 946:"Booster Explosives" 762:Environmental Effect 499:Friction sensitivity 468:Virtually insoluble 37:Preferred IUPAC name 1049:Explosive chemicals 836:in the presence of 718:Chemical properties 509:Detonation velocity 463:Solubility in water 408: g·mol 18: 1028:2009-02-27 at the 832:with concentrated 798: 756:potassium chlorate 744:explosive velocity 648:Infobox references 607:(Immediate danger) 478:<1 mmHg (20°C) 16: 992:Cooper, Paul W., 752:mercury fulminate 701:explosive booster 656:Chemical compound 654: 653: 489:Shock sensitivity 273:CompTox Dashboard 129:Interactive image 1061: 985: 980: 974: 969: 963: 956: 950: 949: 942: 931: 930: 915: 909: 908: 896: 863:Hexanitrobenzene 732:ammonium picrate 638: 632: 629: 628: 556:lowest published 407: 392: 386: 380: 374: 367:Chemical formula 297: 296: 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231:BY6300000 56:Tetralite 1026:Archived 929:(NIOSH). 919:"Tetryl" 907:(NIOSH). 857:See also 818:landmine 810:tetrytol 769:methanol 691:) is an 536:Hazards 517:(24,836 105:479-45-8 75:-Methyl- 65:-Methyl- 901:"#0607" 784:History 728:benzene 724:acetone 641:what is 639: ( 432:Density 406:287.144 200:PubChem 17:Tetryl 1014:Tetryl 1000:  664:tetryl 636:verify 633:  513:7,570 344:SMILES 59:Tetril 31:Names 569:NIOSH 531:1.25 309:InChI 213:10178 140:ChEBI 118:JSmol 998:ISBN 804:and 754:and 699:and 605:IDLH 422:Odor 265:0208 240:UNII 169:9770 814:M14 736:TNT 734:or 712:RDX 662:or 592:REL 579:PEL 519:f/s 515:m/s 278:EPA 203:CID 1045:: 1032:, 1016:, 935:^ 925:. 921:. 903:. 887:^ 840:. 820:. 806:II 726:, 552:Lo 550:LD 521:) 948:. 689:8 686:O 683:5 680:N 677:5 674:H 671:7 668:C 666:( 631:Y 558:) 554:( 394:8 391:O 388:5 385:N 382:5 379:H 376:7 373:C 280:) 276:( 120:) 77:N 73:N 67:N 63:N

Index


Preferred IUPAC name
CAS Number
479-45-8
JSmol
Interactive image
ChEBI
CHEBI:28950
ChemSpider
9770
ECHA InfoCard
100.006.848
Edit this at Wikidata
PubChem
10178
RTECS number
UNII
GJ18911991
UN number
0208
CompTox Dashboard
DTXSID7047770
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Odor
Density
Melting point

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