heptene
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{{Distinguish|heptane|heptyne}}
{{Chembox
| Watchedfields = changed
| verifiedrevid = 447805155
| Name = 1-Heptene
| ImageFile = N-heptene structure.svg
| ImageSize =
| PIN = Hept-1-ene
| OtherNames =
|Section1={{Chembox Identifiers
| index1_label = 1-heptene
| index2_label = 2-heptene
| index3_label = 3-heptene
| index4_label = cis-2-
| index5_label = trans-2-
| CASNo1 = 592-76-7
| CASNo1_Ref = {{cascite|correct|CAS}}
| CASNo2 = 592-77-8
| CASNo3 = 592-78-9
| EC_number2 = 209-768-3
| EC_number3 = 209-769-9
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = O748KJ11V7
| UNNumber = 2278
| PubChem1 = 11610
| PubChem2 = 11611
| PubChem3 = 11612
| PubChem4 = 643836
| PubChem5 = 639662
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 11121
| InChI1_Ref = {{stdinchicite|correct|chemspider}}
| InChI1 = 1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3
| InChIKey1_Ref = {{stdinchicite|correct|chemspider}}
| InChIKey1 = ZGEGCLOFRBLKSE-UHFFFAOYSA-N
| SMILES1 = C=CCCCCC
| InChI3=1S/C7H14/c1-3-5-7-6-4-2/h5,7H,3-4,6H2,1-2H3
| InChIKey3 = WZHKDGJSXCTSCK-UHFFFAOYSA-N
| SMILES3 = CCCC=CCC
| InChI4=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3-
| InChIKey4 = OTTZHAVKAVGASB-HYXAFXHYSA-N
| SMILES4 = CCCC/C=C\C
| InChI5=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+
| InChIKey5 = OTTZHAVKAVGASB-HWKANZROSA-N
| SMILES5 = CCCC/C=C/C
}}
|Section2={{Chembox Properties
| Properties_ref = [http://www.sigmaaldrich.com/catalog/product/aldrich/h3208?lang=en®ion=US 1-Heptene] at Sigma-Aldrich
| C=7 | H=14
| Appearance = Colorless liquid
| Density = 0.697 g/mL
| MeltingPtC = -119
| BoilingPtC = 94
| Solubility =
}}
|Section3={{Chembox Hazards
| MainHazards =
| FlashPtC = -9
| AutoignitionPtC =
| GHSPictograms = {{GHS02}}{{GHS08}}{{GHS09}}
| GHSSignalWord = Danger
| HPhrases = {{H-phrases|225|304|410}}
| PPhrases = {{P-phrases|210|233|240|241|242|243|273|280|301+310|303+361+353|331|370+378|391|403+235|405|501}}
}}
}}
Heptene is a higher olefin, or alkene with the formula C7H14.
The commercial product is a liquid that is a mixture of isomers. It is used as an additive in lubricants, as a catalyst, and as a surfactant. This chemical is also known as heptylene.
{{Gallery |mode=packed |align=center
|File:vapor_pressure_chart.svg|A log-lin vapor pressure chart of Heptene compared with various liquids
}}
References
{{reflist}}
Further reading
- Carl Schaschke, 2014, [https://ebookcentral-proquest-com.ezproxy2.library.usyd.edu.au/lib/usyd/detail.action?docID=1591060 A Dictionary of Chemical Engineering], Oxford University Press.
- G. I. Nikishin, Yu. N. Ogibin & L. Kh. Rakhmatullina, 1975, ‘[https://link-springer-com.ezproxy2.library.usyd.edu.au/content/pdf/10.1007/BF00929657.pdf Peroxydisulfate-initiated reactions of 1-heptene with acetic and propionic acids]’, Bulletin of the Academy of Sciences of the USSR, Division of chemical science, volume 23, pages1479–1483
- Yu. D. Shenin, T. V. Kotenko & A. N. Egorenkova, Nystatin. IV. 1969, [https://link-springer-com.ezproxy2.library.usyd.edu.au/content/pdf/10.1007/BF00759817.pdf The heptaene component of samples of nystatin-nursimicin], Pharmaceutical Chemistry Journal volume 3, pages 631–634
- Nicholas E. Leadbeater, Cynthia B. McGowan, 2013, [https://www-taylorfrancis-com.ezproxy2.library.usyd.edu.au/books/9780429108303/chapters/10.1201/b14645-6 Experiment 2: Second-Order Elimination Reaction Preparation of Heptene from 2-Bromoheptane], Laboratory Experiments Using Microwave Heating, chapter 3
- E. S. Mortikov, M. I. Rozengart & B. A. Kazanskii, 1968, [https://link-springer-com.ezproxy2.library.usyd.edu.au/content/pdf/10.1007/BF00914644.pdf Dehydrocyclization of n-heptenes under conditions of a pulsed system and in the usual flow-type setup], Bulletin of the Academy of Sciences of the USSR, Division of chemical science volume 17, pages95–98(1968)
{{Alkenes}}
{{Hydrides by group}}
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