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Octyl cyanoacrylate

From Wikipedia, the free encyclopedia
Octyl cyanoacrylate
Skeletal formula
Space-filling model of the octyl cyanoacrylate molecule
Names
Preferred IUPAC name
Octyl 2-cyanoprop-2-enoate
Other names
Octyl 2-cyanopropenoate
Octyl 2-cyanoacrylate
Ocrylate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.027.045 Edit this at Wikidata
UNII
  • InChI=1S/C12H19NO2/c1-3-4-5-6-7-8-9-15-12(14)11(2)10-13/h2-9H2,1H3 checkY
    Key: RPQUGMLCZLGZTG-UHFFFAOYSA-N checkY
  • InChI=1/C12H19NO2/c1-3-4-5-6-7-8-9-15-12(14)11(2)10-13/h2-9H2,1H3
    Key: RPQUGMLCZLGZTG-UHFFFAOYAE
  • N#CC(C(OCCCCCCCC)=O)=C
Properties
C12H19NO2
Molar mass 209.289 g·mol−1
Appearance Colorless liquid
Density 1.0±0.1 g/cm3
Boiling point 297.6±23.0 °C
Reacts
Hazards
Flash point 137.2±9.4 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Octyl cyanoacrylate (OCA), a cyanoacrylate ester, is an octyl ester of 2-cyano-2-propenoic acid. It is a clear colorless liquid with a sharp, irritating odor. Its chief use is as the main component of medical cyanoacrylate glues.

In medical and veterinary applications, OCA, n-butyl cyanoacrylate (n-BCA) and isobutyl cyanoacrylate (ICA) are commonly used. They provide rapid wound closure,[1] are bacteriostatic, and their use is usually painless.[citation needed] Butyl esters provide a stronger bond, but the glue is rigid. The octyl ester, while providing weaker bond, is more flexible. Blends of OCA and n-BCA are available which offer both flexibility and a strong bond.

It polymerizes rapidly in presence of moisture.

Heating to higher temperatures causes pyrolysis and depolymerization of the cured glue, producing gaseous products strongly irritating to the lungs and eyes.

References

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  1. ^ Singer, A. J.; McClain, S. A.; Katz, A. (2004). "A porcine epistaxis model: hemostatic effects of octylcyanoacrylate". Otolaryngology–Head and Neck Surgery. 130 (5): 553–557. doi:10.1016/j.otohns.2003.09.035. PMID 15138419.

See also

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