Centralite
Centralite[1] | |
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IUPAC name 1,3-diethyl-1,3-diphenylurea | |
Other names Ethyl centralite | |
Identifiers | |
CAS number | 85-98-3 |
PubChem | 6828 |
ChemSpider | 6567 |
Jmol-3D images | Image 1 |
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Properties | |
Molar mass | 268.3535 |
Appearance | White to light grey crystalline powder |
Density | 0.8/cm3 |
Solubility in water | Insoluble |
Solubility | Acetone, ethanol and benzene |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
Centralite (empirical formula: C17H20N2O) is a gunshot residue also known as ethyl centralite. Its IUPAC name is 1,3-diethyl-1,3-diphenylurea. Ethyl centralite is insoluble in water, but is soluble in acetone, ethanol and benzene. It is mainly used as a burning rate moderator and stabilizer for smokeless powder, and also a plasticizer for celluloid.
Naming
The term "Centralite" was originally applied to dimethyldiphenylurea developed about 1906 at the German Central War Laboratory Zentralstelle fuer Wissenschaftlichtechnische Untersuchungen in Neubabelsberg as a deterrent coating for smokeless powder in military rifle cartridges. Thereafter, all hydrocarbon-substituted symmetrical diphenyl urea compounds used as smokeless powder deterrents (or moderants) were called centralites after the laboratory. The preferred ethyl centralite became known as Centralite No. 1 and the original methyl centralite was identified as Centralite No. 2. Butyl centralite was also used as a celluloid plasticizer.[2][3]
Notes
- ↑ Centralite - Compound Summary, PubChem.
- ↑ Davis, Tenny L. The Chemistry of Powder & Explosives (1943) pages 317-320
- ↑ Davis, William C., Jr. Handloading National Rifle Association of America (1981) p.30
References
- Davis, Tenney L. (1943). The Chemistry of Powder & Explosives (Angriff Press [1992] ed.). John Wiley & Sons Inc. ISBN 0-913022-00-4.
- Davis, William C., Jr. (1981). Handloading. National Rifle Association of America. ISBN 0-935998-34-9.