| IUPAC name
| Other names
Cyanamide calcium salt
|Molar mass||80.102 g/mol|
|Appearance||White solid (Often gray or black from impurities)|
|Melting point||1,340 °C (2,440 °F; 1,610 K)|
|Solubility||Insoluble in organic solvents|
|Vapor pressure||~0 mmHg|
Std enthalpy of
|Safety data sheet||Sigma-Aldrich|
| Calcium carbide|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Calcium cyanamide is an inorganic compound with the formula CaCN2, widely used as fertilizer in agriculture.
Hydrolysis of CaCN2 will yield cyanamide, as well as ammonia.
- CaCN2 + H2O + CO2 → CaCO3 + H2NCN
- CaCN2 + 3 H2O → 2 NH3 + CaCO3
Fusing calcium cyanamide with sodium carbonate will give sodium cyanide.
- CaCN2 + Na2CO3 + 2C → 2 NaCN + CaO + 2 CO
Calcium cyanamide is a white (gray or black if impure) solid, which reacts with water.
Calcium cyanamide is sold as fertilizer. In some places it's hard to find, as the compounds readily hydrolyzes in the presence of moisture, and water-sensitive materials are generally not sold in most stores.
It can also be bought from chemical suppliers.
- 3 CO(NH2)2 → 3 HOCN + NH3
- CaO + 2 HOCN → Ca(OCN)2 + H2O
- Ca(OCN)2 → CaCN2 + CO2
Calcium cyanamide is obtained industrially by heating calcium carbide powder at 1,000 °C, usually in an electric furnace, while injecting nitrogen gas over the hot carbide, which is recirculated. The reaction takes several hours for completion.
Another route involves heating calcium cyanide with nitrogen gas at 600 °C for at least one hour.
Reducing calcium nitride with carbon at 800-900 °C in a nitrogen atmosphere will also give calcium cyanamide.
Since calcium cyanamide reacts with oxygen at high temperatures, all of these routes must be done in low of oxygen environment, and an inert gas is used.
Calcium cyanamide is harmful and should be handled with care.
It is known to cause alcohol intolerance, before or after the consumption of alcohol.
In closed containers, away from moisture.
Can be dumped in the ground.
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- Franck, H.; Heimann, H.; Angewandte Chemie; vol. 44; (1931); p. 372 - 378
- Krase, H. J.; Jee, J. Y.; Journal of the American Chemical Society; vol. 46; (1924); p. 1358 - 1366
- Franklin; Journal of the American Chemical Society; vol. 44; (1922); p. 504
- Patent; Caro; Frank; DE467479; Fortschr. Teerfarbenfabr. Verw. Industriezweige; vol. 16; p. 283