1-Butene
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| Names | |||
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| Preferred IUPAC name But-1-ene[1] | |||
| Other names Ethylethylene 1-Butylene α-Butylene | |||
| Identifiers | |||
CAS Number |
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3D model (JSmol) |
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Beilstein Reference | 1098262 | ||
| ChEBI |
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| ChEMBL |
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| ChemSpider |
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| ECHA InfoCard | 100.003.137  | ||
| EC Number |
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Gmelin Reference | 25205 | ||
PubChem CID |
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| UNII |
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| UN number | 1012 | ||
CompTox Dashboard (EPA) |
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InChI
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| Properties | |||
Chemical formula | C4H8 | ||
| Molar mass | 56.108 g·mol−1 | ||
| Appearance | Colorless Gas | ||
| Odor | slightly aromatic | ||
| Density | 0.62 g/cm3 | ||
| Melting point | −185.3 °C (−301.5 °F; 87.8 K) | ||
| Boiling point | −6.47 °C (20.35 °F; 266.68 K) | ||
| 0.221 g/100 mL | |||
| Solubility | soluble in alcohol, ether, benzene | ||
Refractive index (nD) | 1.3962 | ||
| Viscosity | 7.76 Pa | ||
| Hazards | |||
| GHS labelling: | |||
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| Danger | |||
| H220, H221, H280 | |||
| P210, P377, P381, P403, P410+P403 | |||
| NFPA 704 (fire diamond) |  1 4 0 | ||
| Flash point | −79 °C; −110 °F; 194 K | ||
Autoignition temperature | 385 °C (725 °F; 658 K) | ||
| Explosive limits | 1.6-10% | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  N verify (what is  Y N ?) Infobox references | |||
Chemical compound
1-Butene (IUPAC name: But-1-ene, also known as 1-butylene) is the organic compound with the formula CH3CH2CH=CH2. It is a colorless gas. But-1-ene is an alkene easily condensed to give a colorless liquid. It is classified as a linear alpha-olefin (terminal alkene).[2] It is one of the isomers of butene (butylene). It is a precursor to diverse products.
Reactions
Polymerization of but-1-ene gives polybutylene, which is used to make piping for domestic plumbing.[3] Another application is as a comonomer in the production of certain kinds of polyethylene, such as linear low-density polyethylene (LLDPE).[4] It has also been used as a precursor to polypropylene resins, butylene oxide, and butanone.[5]
Manufacturing
But-1-ene is produced by separation from crude C4 refinery streams and by ethylene dimerization. The former affords a mixture of 1-and 2-butenes, while the latter affords only the terminal alkene.[6] It is distilled to give a very high purity product. An estimated 12 billion kilograms were produced in 2011.[7]
References
- ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 17, 61, 374. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
- ^ "1-BUTENE". chemicalland21.com. Retrieved 22 April 2018.
- ^ Whiteley, Kenneth S.; Heggs, T. Geoffrey; Koch, Hartmut; Mawer, Ralph L.; Immel, Wolfgang (2000). "Polyolefins". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a21_487. ISBN 978-3527306732.
- ^ Chum, P. Steve; Swogger, Kurt W. (2008). "Olefin polymer technologies—History and Recent Progress at the Dow Chemical Company". Progress in Polymer Science. 33 (8): 797–819. doi:10.1016/j.progpolymsci.2008.05.003.
- ^ "1-Butene product overview". shell.com. Archived from the original on 2012-02-10. Retrieved 22 April 2018.
- ^ "Alphabutol process - Big Chemical Encyclopedia". chempedia.info. Archived from the original on 2017-12-08. Retrieved 22 April 2018.
- ^ Geilen, Frank M.A.; Stochniol, Guido; Peitz, Stephan; Schulte-Koerne, Ekkehard (2014). "Butenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_483.pub3. ISBN 978-3527306732.
- v
- t
- e
- Dehydrohalogenation from haloalkane
- Dehydration reaction from alcohol
- Semihydrogenation from alkyne
- Bamford–Stevens reaction
- Barton–Kellogg reaction
- Boord olefin synthesis
- Chugaev elimination
- Cope reaction
- Corey–Winter olefin synthesis
- Grieco elimination
- Hofmann elimination
- Horner–Wadsworth–Emmons reaction
- Hydrazone iodination
- Julia olefination
- Kauffmann olefination
- McMurry reaction
- Peterson olefination
- Ramberg–Bäcklund reaction
- Shapiro reaction
- Takai olefination
- Wittig reaction
- Olefin metathesis
- Ene reaction
- Cope rearrangement
