4-Vinylpyridine
Names | |
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Preferred IUPAC name
4-Ethenylpyridine | |
Identifiers | |
3D model (JSmol)
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104506 | |
ChemSpider | |
ECHA InfoCard | 100.002.593 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C7H7N | |
Molar mass | 105.140 g·mol−1 |
Appearance | colorless liquid |
Density | 0.988 g/cm3 |
Boiling point | 62–65 °C (144–149 °F; 335–338 K) 15 mmHg |
Hazards | |
GHS labelling: | |
Signal word
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Danger |
H226, H301, H314, H315, H317, H319, H330, H334, H411 | |
P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P272, P273, P280, P284, P285, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P304+P341, P305+P351+P338, P310, P320, P321, P330, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P370+P378, P391, P403+P233, P403+P235, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
4-Vinylpyridine is an organic compound with the formula CH2CHC5H4N. It is a derivative of pyridine with a vinyl group in the 4-position. It is a colorless liquid, although impure samples are often brown. It is a monomeric precursor to specialty polymers. 4-Vinylpyridine is prepared by the condensation of 4-methylpyridine and formaldehyde.[1]
See also[]
References[]
- ^ Shimizu, Shinkichi; Watanabe, Nanao; Kataoka, Toshiaki; Shoji, Takayuki; Abe, Nobuyuki; Morishita, Sinji; Ichimura, Hisao (2007). "Pyridine and Pyridine Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_399.
Categories:
- Pyridines
- Monomers
- Vinyl compounds