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Chemical compound From Wikipedia, the free encyclopedia
4-Vinylcyclohexene dioxide (VCD) is an organic compound that contains two epoxide functional groups. It is industrially used as a crosslinking agent for the production of epoxy resins.[5][6] It is a colourless liquid. It is an intermediate for synthesis of organic compounds.[2]
Names | |
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IUPAC name
3-Oxiranyl-7-oxabicyclo[4.1.0]heptane | |
Other names
1,2-Epoxy-4-(epoxyethyl)cyclohexane 4-Vinylcyclohexene diepoxide | |
Identifiers | |
3D model (JSmol) |
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Abbreviations | VCD |
ECHA InfoCard | 100.003.126 |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C8H12O2 | |
Molar mass | 140.182 g·mol−1 |
Appearance | Colorless liquid[1] |
Density | 1.09 g·cm−3[2][3] |
Melting point | −108.9 °C (−164.0 °F; 164.2 K)[4] |
Boiling point | 227 °C (441 °F; 500 K)[4] |
Vapor pressure | 13 Pa (20 °C)[4] |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards |
Toxic |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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4-Vinylcyclohexene dioxide is prepared by epoxidation of 4-vinylcyclohexene with peroxybenzoic acid.[5] Its viscosity is 15 mPa·s.[5]
4-Vinylcyclohexene dioxide, like other volatile epoxides, is classified as an alkylating agent.[5] VCD has toxic effects on fertility. It is a killer of oocytes, eggs in a female's ovaries, in immature ovarian follicles in mice and rats.[7][8][9]
In pest control, it has been used as an ovotoxic agent for reducing rat fertility.[10]
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