1-chloropentane
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | 1-chloropentane | |||||||||||||||
other names |
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Molecular formula | C 5 H 11 Cl | |||||||||||||||
Brief description |
colorless liquid with a sweet odor |
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properties | ||||||||||||||||
Molar mass | 106.60 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
0.88 g cm −3 |
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Melting point |
−99 ° C |
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boiling point |
108 ° C |
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Vapor pressure |
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solubility |
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Refractive index |
1.4115 (20 ° C, 589 nm) |
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safety instructions | ||||||||||||||||
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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-chloropentane is a chemical compound from the group of aliphatic saturated halogenated hydrocarbons .
Extraction and presentation
1-chloropentane can be obtained by reacting 1-pentanol with hydrochloric acid . The reaction of pentane with chlorine is also possible, the isomeric 2-chloropentane and 3-chloropentane also being formed.
properties
1-chloropentane is a volatile, colorless liquid with a sweetish odor that is sparingly soluble in water. The normal pressure boiling point is 107.8 ° C. According to August, the vapor pressure function results from lg (P) = −A / T + B ( P in Torr, T in K) with A = 1892 and B = 7.8573 in the temperature range from 10 ° C to 50 ° C. It decomposes slowly in the presence of oxygen when heated, but even at normal temperature when exposed to light, which can produce hydrogen chloride , phosgene and dioxin .
Safety-related parameters
1-chloropentane forms highly flammable vapor-air mixtures. The compound has a flash point at 3 ° C. The explosion range is between 1.4% by volume (60 g / m 3 ) as the lower explosion limit (LEL) and 8.6% by volume (380 g / m 3 ) as the upper explosion limit (UEL). The ignition temperature is 255 ° C. The substance therefore falls into temperature class T3.
use
1-chloropentane is used as a solvent , as a reference substance for gas chromatography , for soil disinfection and the synthesis of other pentyl halides. Hexanenitrile can be obtained by reaction with sodium cyanide .
Individual evidence
- ↑ a b c d e f g h i j k l m n o p Entry for CAS no. 543-59-9 in the GESTIS substance database of the IFA , accessed on June 10, 2017(JavaScript required) .
- ^ Richard J. Lewis, Sr .: Hawley's Condensed Chemical Dictionary . 15th edition. Wiley-Interscience, 2007, ISBN 978-0-471-76865-4 (English).
- ↑ a b c David R. Lide (Ed.): CRC Handbook of Chemistry and Physics . 90th edition. CRC Press, 2009, ISBN 978-1-4200-9084-0 .
- ↑ Data sheet 1-chloropentane (PDF) from Merck , accessed on January 2, 2012.
- ↑ Entry on 1-chloropentane in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
- ↑ PS Kalsi: Organic Tractions Stereochemistry and Mechanism Through Solved problem . New Age International, 2006, ISBN 978-81-224-1766-1 ( page 191 in the Google book search).
- ↑ a b J. C. Rintelen, JH Saylor, PM Gross: The Densities and Vapor Pressures of Some Alkylbenzenes, Aliphatic Ketones and n-Amyl Chloride . In: Journal of the American Chemical Society . tape 59 , no. 6 , 1937, pp. 1129–1130 , doi : 10.1021 / ja01285a050 .
- ↑ a b c E. Brandes, W. Möller: Safety-related parameters. Volume 1: Flammable Liquids and Gases. Wirtschaftsverlag NW - Verlag für neue Wissenschaft, Bremerhaven 2003.
- ↑ Michael B. Smith: Organic Synthesis . Academic Press, 2016, ISBN 978-0-12-800807-2 , pp. 548 ( limited preview in Google Book search).
- ↑ J. Org. Chem., 1960, 25 (2), pp 257-258