4-Vinylpyridine

4-Vinylpyridine
Names
Preferred IUPAC name
4-Ethenylpyridine
Other names
4-VP
Identifiers
CAS Number
  • 100-43-6
3D model (JSmol)
  • Interactive image
Beilstein Reference
104506
ChemSpider
  • 7221
ECHA InfoCard 100.002.593 Edit this at Wikidata
EC Number
  • 202-852-0
PubChem CID
  • 7502
UNII
  • I56G67XM8D
CompTox Dashboard (EPA)
  • DTXSID0051499 Edit this at Wikidata
InChI
  • InChI=1S/C7H7N/c1-2-7-3-5-8-6-4-7/h2-6H,1H2
    Key: KFDVPJUYSDEJTH-UHFFFAOYSA-N
  • C=CC1=CC=NC=C1
Properties
Chemical formula
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:
Pictograms
GHS02: FlammableGHS05: CorrosiveGHS06: ToxicGHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard
Danger
Hazard statements
H226, H301, H314, H315, H317, H319, H330, H334, H411
Precautionary statements
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
Chemical compound

4-Vinylpyridine (4-VP) 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]

4-VP is sometimes used in biochemistry to alkylate protein cysteine residues. When compared to other alkylation agents, such as iodoacetamide, acrylamide, and N-ethylmaleimide, 4-VP is less reactive, meaning the completion rate of cysteine alkylation is lower, but it also yields fewer side reactions.[2] For some uses, such as during mass spectrometry measurements, 4-VP might be better because it is basic and can thus be protonated, adding net charge.[3]

See also

References

  1. ^ 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. ISBN 978-3527306732.
  2. ^ Suttapitugsakul, Suttipong; Xiao, Haopeng; Smeekens, Johanna; Wu, Ronghu (2017). "Evaluation and optimization of reduction and alkylation methods to maximize peptide identification with MS-based proteomics". Molecular BioSystems. 13 (12): 2574–2582. doi:10.1039/C7MB00393E. ISSN 1742-206X. PMC 5698164. PMID 29019370.
  3. ^ Sechi, Salvatore; Chait, Brian T. (1998-12-01). "Modification of Cysteine Residues by Alkylation. A Tool in Peptide Mapping and Protein Identification". Analytical Chemistry. 70 (24): 5150–5158. doi:10.1021/ac9806005. ISSN 0003-2700. PMID 9868912.