| 词条 | HBT (explosive) |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 412683567 | ImageFile = HBT.png | ImageFile_Ref = {{chemboximage|correct|??}} | ImageSize = 121 | ImageName = Skeletal formula of a minor tautomer of HBT | IUPACName = N,N'-Bis-(1H-tetrazol-5-yl)-hydrazine | OtherNames = 1,2-Ditetrazolylhydrazine 5,5'-Hydrazinebistetrazole |Section1={{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = 74999-19-2 | PubChem = 144703 | ChemSpiderID = 127666 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | SMILES = N(Nc1nn[nH]n1)c1nn[nH]n1 | SMILES1 = N(NC1=NNN=N1)C1=NNN=N1 | SMILES2 = C1(NNC2=NN=NN2)=NN=NN1 | StdInChI = 1S/C2H4N10/c3(1-5-9-10-6-1)4-2-7-11-12-8-2/h(H2,3,5,6,9,10)(H2,4,7,8,11,12) | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = KOVNXYJOKSNDJA-UHFFFAOYSA-N | StdInChIKey_Ref = {{stdinchicitecite|correct|chemspider}} }} |Section2={{Chembox Properties | C=2 | H=4 | N=10 | Density = 2.327 g cm−3 }} }} HBT is a bistetrazole.[1] It is an explosive approximately as powerful as HMX or CL-20, but it releases less toxic reaction products when detonated: ammonia and hydrogen cyanide. When combined with ADN or AN oxidizers, the amount of HCN produced by a deflagration may be reduced. The compound is thus considered by its advocates to be a more environmentally friendly explosive than traditional nitroamine-based explosives. References1. ^{{cite journal| journal = Chem. Mater. |doi=10.1021/cm703657k |year= 2008 |title= Bistetrazoles: Nitrogen-Rich, High-Performing, Insensitive Energetic Compounds| author=Thomas M. Klapötke and Carles Miró Sabaté |url=http://pubs.acs.org/cgi-bin/sample.cgi/cmatex/asap/html/cm703657k.html| volume = 20| issue = 11| pages = 3629–3637}} See also
3 : Explosive chemicals|Hydrazines|Tetrazoles |
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