French
DeutschEthylidene norbornene
 | |
| Names | |
|---|---|
| Other names 2-ethylidene-5-norbornene | |
| Identifiers | |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| Properties | |
| C9H12 | |
| Molar mass | 120.195 g·mol−1 |
| Appearance | colorless liquid |
| Density | 0.893 g/mL |
| Melting point | −80 °C (−112 °F; 193 K) |
| Boiling point | 146 °C (295 °F; 419 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Ethylidene norbornene (ENB) is an organic compound that consists of an ethylidene (CH3C(H)=) group attached to norbornene. It is a colorless liquid. The molecule consists of two sites of unsaturation. The compound consists of E- and Z-stereoisomers, but the mixtures are typically not separated.
Preparation and use
[edit]It is prepared by isomerization of vinyl norbornene, which in turn is obtained by the Diels-Alder reaction of butadiene and cyclopentadiene.[1]
It is a monomer that used in the production of the commercial polymer EPDM. Only the ring alkene participates in the copolymerization. The exocyclic double bond (the ethylidene group) undergoes sulfur vulcanization.
Safety
[edit]Its LD50 (intravenous, rabbit) ranges from 0.09 (male rabbit) to 0.11 ml/kg (female). It is also a neurotoxin.[2]
References
[edit]- ^ Behr, Arno (2000). "Organometallic Compounds and Homogeneous Catalysis". Ullmann's Encyclopedia of Industrial Chemistry. p. 10. doi:10.1002/14356007.a18_215. ISBN 3527306730.
- ^ Ballantyne, Bryan; Myers, Roy C.; Klonne, Dennis R. (1997). "Comparative acute toxicity and primary irritancy of the ethylidene and vinyl isomers of norbornene". Journal of Applied Toxicology. 17 (4): 211–221. doi:10.1002/(SICI)1099-1263(199707)17:4<211::AID-JAT430>3.0.CO;2-X. PMID 9285533. S2CID 21154862.