Nitroglycerin
Appearance
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| Names | |
|---|---|
| IUPAC name
1,2,3-Trinitroxypropane | |
| Seestematic IUPAC name
2,3-Bis(nitrooxy)propyl nitrate | |
| Ither names
1,3-Dinitrooxypropan-2-yl nitrate Propane-1,2,3-triyl trinitrate | |
| Identifiers | |
3D model (JSmol) |
|
| 1802063 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| EC Nummer | 200-240-8 |
| Gmelin Reference | 165859 |
| KEGG | |
| MeSH | Nitroglycerin |
PubChem CID |
|
| UNII | |
| UN nummer | 0143, 0144, 1204, 3064, 3319 |
| |
| |
| Properties | |
| C3H5N3O9 | |
| Molar mass | 227.09 g·mol−1 |
| Appearance | Colourless liquid |
| Density | 1.6 g cm−3 (at 15 °C) |
| Meltin pynt | 14 °C (57 °F; 287 K) |
| Bylin pynt | 50 °C (122 °F; 323 K) |
| slichtly[1] | |
| Solubility | acetone, ether, benzene, alcohol[1] |
| log P | 2.154 |
| Structur | |
| Tetragonal at C1, C2, an C3 Trigonal planar at N7, N8, an N9 | |
| Molecular shape | Tetrahedral at C1, C2, an C3 Dihedral at N7, N8, and N9 |
| Thermochemistry | |
| Std enthalpy o formation ΔfH |
−370 kJ mol−1 |
| Std enthalpy o combustion ΔcH |
−1.529 MJ mol−1 |
| Pharmacology | |
| Intravenous, Oral, Sublingual, Topical, Transdermal | |
| Pharmacokinetics: | |
| <1% | |
| Hepatic | |
| 3 min | |
| Legal status |
|
| Explosive data | |
| Shock sensitivity | Heich |
| Friction sensitivity | Heich |
| RE factor | 1.50 |
| Hazards | |
| EU clessification | |
| R-phrases | R3, R12, R26/27/28, R33, R51/53 |
| S-phrases | (S1/2), S33, S35, S36/37, S45, S53, S61 |
| NFPA 704 | |
Except whaur itherwise notit, data are gien for materials in thair staundart state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Nitroglycerin (NG), forby kent as nitroglycerine, trinitroglycerin, trinitroglycerine, or nitro, or mair correctly as glyceryl trinitrate, or mair formally as 1,2,3-trinitroxypropane, is a hivy, colourless, ily, explosive liquid maist commonly produced bi treatin glycerol wi white fumin nitric acid unner condeetions appropriate tae the formation o the nitric acid ester.
References
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