| Names | |
|---|---|
| Preferred IUPAC name Butane-1,2,4-triyl trinitrate | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.026.998 |
| EC Number |
|
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C4H7N3O9 | |
| Molar mass | 241.11 g/mol |
| Density | 1.52 g/cm3 |
| Melting point | −27 °C |
| Boiling point | 230 °C (446 °F; 503 K) (explosion temperature) |
| Hazards | |
| GHS labelling: [1] | |
| | |
| Danger | |
| H200, H300, H310, H330, H373, H411 | |
| P201, P202, P260, P262, P264, P270, P271, P273, P280, P281, P284, P301+P316, P302+P352, P304+P340, P316, P319, P320, P321, P330, P361+P364, P372, P373, P380, P391, P401, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
1,2,4-Butanetriol trinitrate (BTTN), also called butanetriol trinitrate, is an important military propellant. It is a colorless to brown explosive liquid. [2]
BTTN is used as a propellant in virtually all single-stage missiles used by the United States, including the Hellfire. [3] It is less volatile, less sensitive to shock, and more thermally stable than nitroglycerine, [4] for which it is a promising replacement. [5]
BTTN as a propellant is often used in a mixture with nitroglycerin. [4] The mixture can be made by co-nitration of butanetriol and glycerol. [6] BTTN is also used as a plasticizer in some nitrocellulose-based propellants. [7]
BTTN is manufactured by nitration of 1,2,4-butanetriol. [8] Biotechnological manufacture of butanetriol is under intensive research. [9]