Cyclododecane

Cyclododecane
Skeletal formula of cyclododecane
Ball-and-stick model of the cyclododecane molecule
Names
IUPAC name
cyclododecane
Identifiers
294-62-2 N
ChemSpider 8911 YesY
Jmol interactive 3D Image
PubChem 9268
Properties
C12H24
Molar mass 168.319
Appearance white waxy solid
Density 0.79 g/cm3
Melting point 60.8 °C (141.4 °F; 333.9 K)
Boiling point 244 °C (471 °F; 517 K)
Hazards
Flash point 87.6 °C (189.7 °F; 360.8 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Cyclododecane is an organic compound with the chemical formula (CH2)12. It is a waxy white solid that is soluble in nonpolar organic solvents.

Uses

It is a precursor to laurolactam, a precursor to the polymer Nylon-12.[1]

Cyclododecane is also an intermediate in production of flame retardants, detergents, and other chemicals.

Cyclododecane is also used as a volatile binding medium, a temporary binder for sealing and conservation of friable and structurally weak materials, e.g. during excavation and transport of archaeological objects and in art restoration, e.g. to protect water-sensitive parts during cleaning. Due to its relatively slow evaporation in comparison with other volatile binding mediums the layer can last for several weeks. Very pure material has to be used so it does not leave any residue. Cyclododecane can be applied in molten state or dissolved in a nonpolar organic solvent. Other volatile binding mediums in use are camphene, tricyclene and with some limits menthol.

Environmental considerations

Cyclododecane is persistent in the environment, as it does not biodegrade easily. Cyclododecane is lipophilic, usually present in the environment as adsorbed on the surface of soil particles. It has the potential to bioaccumulate. Concentrations above 1 mg/L are toxic to aquatic life.[2]

References

  1. Schiffer, T.; Oenbrink, G. "Cyclododecanol, Cyclododecanone, and Laurolactam" in Ullman’s Encyclopedia of Industrial Chemistry: Wiley-VCH, 2009. doi:10.1002/14356007.a08_201.pub2
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