Thiocarbanilide
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| Names | |
|---|---|
| IUPAC name
N,N’-Diphenylthiourea | |
| Other names
sym-diphenylthiourea, diphenylthiourea, 1,3-diphenyl-2-thiourea, DPTU, 1,3-diphenylthiourea, sulfocarbanilide | |
| Identifiers | |
| 102-08-9 | |
| 3D model (Jmol) | Interactive image |
| ChEMBL | ChEMBL275260 |
| ChemSpider | 610932 |
| ECHA InfoCard | 100.002.732 |
| PubChem | 700999 |
| UNII | 9YCB5VR86Z |
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| Properties | |
| C13H12N2S | |
| Molar mass | 228.312 g/mol |
| Appearance | White powder |
| Density | 1.32 g/cm3 |
| Melting point | 154.5 °C (310.1 °F; 427.6 K) |
| Boiling point | decomposes |
| slightly soluble in water | |
| Solubility | very soluble in ethanol, diethyl ether, chloroform[1] |
| Hazards | |
| NFPA 704 | |
| Flash point | 164.7 °C (328.5 °F; 437.8 K) |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Thiocarbanilide is an organic chemical compound with the formula (C6H5NH)2CS. This white solid is a derivative of thiourea. It is prepared by the reaction of aniline and carbon disulfide.
Uses
Thiocarbanilide is commonly used as a vulcanization accelerator for rubber,[2] and as a stabilizer for PVC and PVDC.
Reactions
Thiocarbanilide reacts with phosphorus pentachloride or hydrochloric acid, dilute sulfuric acid, acetic anhydride or iodine to produce phenyl isothiocyanate.
Toxicology
Oral, rat: LD50 = 50 mg/kg.
References
- ↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, pp. 3–242, ISBN 0-8493-0594-2
- ↑ Hans-Wilhelm Engels, Herrmann-Josef Weidenhaupt, Manfred Pieroth, Werner Hofmann, Karl-Hans Menting, Thomas Mergenhagen, Ralf Schmoll, Stefan Uhrlandt "Rubber, 4. Chemicals and Additives" in Ullmann's Encyclopedia of Industrial Chemistry 2004, Wiley-VCH, Weinheim. doi:10.1002/14356007.a23_365.pub2
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