1-chlorohexane
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | 1-chlorohexane | |||||||||||||||
other names |
Hexyl chloride |
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Molecular formula | C 6 H 13 Cl | |||||||||||||||
Brief description |
colorless liquid with an aromatic odor |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 120.62 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
0.88 g cm −3 |
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Melting point |
−94 ° C |
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boiling point |
135 ° C |
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Vapor pressure |
6.65 hPa (15 ° C) |
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solubility | ||||||||||||||||
Refractive index |
1.419 (20 ° C) |
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safety instructions | ||||||||||||||||
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Toxicological data | ||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
1-Chlorhexane is a chemical compound of chlorine from the group of aliphatic , unsaturated halogenated hydrocarbons .
Extraction and presentation
1-Chlorhexane can be obtained by reacting hexyl alcohol with hydrochloric acid or thionyl chloride .
properties
1-chlorohexane is a colorless liquid with an aromatic odor that is very sparingly soluble in water.
use
1-Fluorohexane can be obtained by reacting 1-chlorohexane with potassium fluoride in ethylene glycol , and 2-phenylhexane by reacting with benzene and aluminum trichloride .
safety instructions
The vapors of 1-chlorohexane can form an explosive mixture with air ( flash point 26 ° C, ignition temperature 204 ° C).
Individual evidence
- ↑ a b c d e f g h i j k Entry on 1-chlorohexane in the GESTIS substance database of the IFA , accessed on January 8, 2020(JavaScript required) .
- ↑ David R. Lide: CRC Handbook of Chemistry and Physics A Ready-reference Book of Chemical and Physical Data . CRC Press, 1995, ISBN 978-0-8493-0595-5 , pp. 112 ( limited preview in Google Book search).
- ↑ Data sheet 1-chlorohexane, 99% from Sigma-Aldrich , accessed on October 28, 2018 ( PDF ).
- ↑ Data sheet 1-chlorohexane (PDF) from Merck , accessed on October 28, 2018.
- ^ H. Altenburg, I. Bang, K. Bartelt, Fr. Baum, C. Brahm, W. Cramer, K. Dieterich, R. Ditmar, M. Dohrn, H. Einbeck, H. Euler, ES Faust, C. Funk, O. v. Fürth, O. Gerngroß: Biochemisches Handlexikon 1st volume, 1st half carbon, hydrocarbons, alcohols of the aliphatic series, phenols . Springer-Verlag, 2013, ISBN 978-3-642-90817-0 , pp. 95 ( limited preview in Google Book search).
- ↑ VK Ahluwalia, R. Aggarwal, VK Ahluwalia: Comprehensive Practical Organic Chemistry: Preparations And Quantitative Analysis . 2000, ISBN 81-7371-475-4 , pp. 16 ( limited preview in Google Book search).
- ^ Houben-Weyl Methods of Organic Chemistry Vol. V / 3, 4th Edition Fluorine and Chlorine Compounds . Georg Thieme Verlag, 2014, ISBN 3-13-179994-3 , p. 153 ( limited preview in Google Book search).
- ^ Marye Anne Fox, James K. Whitesell: Organic Chemistry . Jones & Bartlett Learning, 2004, ISBN 978-0-7637-2197-8 , pp. 530 ( limited preview in Google Book search).