Encyclopedia

1-hexene

Also found in: Wikipedia.

1-hexene

[¦wən ′hek‚sēn]
(organic chemistry)
CH3(CH2)3HC:CH2 Colorless, olefinic hydrocarbon boiling at 64°C; soluble in alcohol, acetone, ether, and hydrocarbons, insoluble in water; used as a chemical intermediate and for resins, drugs, and insecticides. Also known as hexylene.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
Mentioned in
References in periodicals archive
[56] studied low-temperature branching mechanisms for alkenes and developed a kinetic model for n-hexene (1-hexene, trans-2-hexene, and trans-3-hexene) isomers.
Browse the full Alpha Olefins Market by product type 1-Butene, 1-Hexene, 1-Octene, 1-Decene, 1-Dodecene and Others; by application Polyethylene, Detergent Alcohol, Synthetic lubricant and Others - Market Growth, Future Prospects and Competitive Analysis, 2016 2024 report at http://www.credenceresearch.com/report/alpha-olefins-market
mPE1 and mPE2 are based on 1-hexene comonomers produced from different metallocene systems by Braskem.
Molecular orbital data for 1-hexene. Double-ionization threshold = 25.22 eV from CCSD(T)/cc-pV(T+d)Z (to singlet dication).
In this study, we propose a novel way to detect typical breath gases of lung cancer: benzene ([C.sub.6][H.sub.6]), styrene ([C.sub.8][H.sub.8]), isoprene ([C.sub.5][H.sub.8]), and 1-hexene ([C.sub.6][H.sub.12]) by theory computation [23, 24].
2l) 1-hexene, IR (KBr): 3080 (=CH), 1642 (C=C), 912 (OOP =CH), 1H-NMR (CDCl3): 0.90 (3H, t, J= 8.0 Hz, CH3); 1.07 (2H, m, CH2); 1.50 (2H, m, CH2); 2.06 (2H, td, J= 7.1 Hz, 6.2 Hz, CH2); 4.92 (1H, dd, J= 10.0 Hz, J= 2.1 Hz, CH); 4.96 (1H, dd, J= 16.8, J=2.1 Hz, CH); 5.80 (1H, ddt, J= 16.8 Hz, J= 10.0 Hz, J= 6.2 Hz, CH); 13C-NMR (CDCl3): 14.0, 22.4, 31.3, 33.7, 114.2, 139.2.
Other compounds, such as octane, heptane, 2,4-dimethylpentane, 2,2-dimethylpentane, 1,4-diethylbenzene, 2-methylhexane, 3-methylhexane, 1-hexene are clearly targeted in operations of distillation, while nonane, dodecane, cis-2-butene may come from the cracking, distillation, and/or catalytic dehydrogenation operations.
Copyright © 2003-2025 Farlex, Inc Disclaimer
All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. This information should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional.