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| Names | |||
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IUPAC name
2-Cyanoguanidine
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| Other names
Cyanoguanidine, dicyanodiamide, N-cyanoguanidine, 1-cyanoguanidine, Guanidine-1-carbonitrile, dicyandiamin, Didin, DCD, Dicy
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| Identifiers | |||
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3D model (JSmol)
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| ChemSpider | |||
| ECHA InfoCard | 100.006.649 | ||
| EC Number | 207-312-8 | ||
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PubChem CID
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| RTECS number | ME9950000 | ||
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| Properties | |||
| C2H4N4 | |||
| Molar mass | 84.08 g/mol | ||
| Appearance | White crystals | ||
| Density | 1.400 g/cm3 | ||
| Melting point | 209.5 °C (409.1 °F; 482.6 K) | ||
| Boiling point | 252 °C (486 °F; 525 K) | ||
| 41.3 g/l | |||
| log P | -0.52 | ||
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Henry's law
constant (kH) |
2.25·10−10 atm.m3/mol | ||
| -44.55·10−6 cm3/mol | |||
| Hazards | |||
| Main hazards | harmful (Xn) | ||
| R-phrases (outdated) | R20/21/22 | ||
| S-phrases (outdated) | S24/25 | ||
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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 | |||
2-Cyanoguanidine is a nitrile derived from guanidine. It is a dimer of cyanamide, from which it can be prepared. 2-Cyanoguanidine is a colourless solid that is soluble in water, acetone, and alcohol, but not nonpolar organic solvents.
2-Cyanoguanidine is produced by treating cyanamide with base. It is produced in soil by decomposition of cyanamide. A variety of useful compounds are produced from 2-cyanoguanidine, guanidines and melamine. It is also used as a slow fertilizer. Formerly, it was used as a fuel in some explosives. It is used in the adhesive industry as a curing agent for epoxies.
There are two tautomeric forms, differing in the protonation and bonding of the nitrogen to which the nitrile group is attached.
2-Cyanoguanidine can also exist in a zwitterionic form via a formal acid–base reaction among the nitrogens.
Loss of ammonia (NH3) from the zwitterionic form, followed by deprotonation of the remaining central nitrogen atom, gives the dicyanamide anion, [N(CN)2]−.