1-dodecanol
Structural formula | ||||||||||||||||||||||
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General | ||||||||||||||||||||||
Surname | 1-dodecanol | |||||||||||||||||||||
other names |
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Molecular formula | C 12 H 26 O | |||||||||||||||||||||
Brief description |
white, pasty solid with a characteristic odor |
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properties | ||||||||||||||||||||||
Molar mass | 186.34 g mol −1 | |||||||||||||||||||||
Physical state |
firmly |
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density |
0.83 g cm −3 |
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Melting point |
24 ° C |
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boiling point |
261 ° C |
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Vapor pressure |
1.69 Pa (30 ° C) |
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solubility |
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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 . |
Dodecanol , also 1-dodecanol , dodecan-1-ol or trivial lauryl alcohol , belongs to the homologous series of alcohols and is hydrophobic or lipophilic . Dodecanol is solid, colorless and does not dissolve in water. The common name is lauryl alcohol, whose root word -lauryl- is also used for esters of dodecanol.
Occurrence
Dodecanol occurs naturally in the essential oil of Hyperici flos recens (fresh St. John's wort flowers) and Hyperici herba ( St. John's wort ).
Extraction and presentation
Dodecanol can be obtained from methyl isobutyl ketone .
use
It is used in the manufacture of surfactants and in pharmacology . It is also a component of cooling lubricants in metal processing.
Individual evidence
- ↑ Entry on LAURYL ALCOHOL in the CosIng database of the EU Commission, accessed on January 14, 2020.
- ↑ a b c d e f g h Entry on 1-dodecanol in the GESTIS substance database of the IFA , accessed on January 14, 2020(JavaScript required) .
- ↑ Entry on dodecan-1-ol. In: Römpp Online . Georg Thieme Verlag, accessed on December 28, 2014.
- ↑ Data sheet 1-Dodecanol from AlfaAesar, accessed on February 9, 2009 ( PDF )(JavaScript required) .
- ↑ Rudolf Hänsel, Konstantin Keller, Horst Rimpler, Georg Schneider: Hager's handbook of pharmaceutical practice, drugs E-O . Springer-Verlag, 2013, ISBN 978-3-642-57993-6 , pp. 482 ( limited preview in Google Book search).
- ↑ Xueru Sheng, Ning Li, Guangyi Li, Wentao Wang, Aiqin Wang, Y. and Cong, Xiaodong Wang, Tao Zhang: Direct Synthesis of Renewable Dodecanol and Dodecane with Methyl Isobutyl Ketone over Dual-Bed Catalyst Systems. In: ChemSusChem. 10, 2017, p. 825, doi : 10.1002 / cssc.201601563 .
- ↑ Werner Baumann, Bettina Herberg-Liedtke: Chemicals in metal processing Data and facts on environmental protection . Springer-Verlag, 2013, ISBN 978-3-642-61004-2 , p. 398 ( limited preview in Google Book search).