1-dodecanol

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Structural formula
Structural formula of dodecan-1-ol
General
Surname 1-dodecanol
other names
  • Lauryl alcohol
  • 1-dodecanol
  • Dodecan-1-ol
  • LAURYL ALCOHOL ( INCI )
Molecular formula C 12 H 26 O
Brief description

white, pasty solid with a characteristic odor

External identifiers / databases
CAS number 112-53-8
EC number 203-982-0
ECHA InfoCard 100.003.620
PubChem 8193
ChemSpider 7901
DrugBank DB06894
Wikidata Q161617
properties
Molar mass 186.34 g mol −1
Physical state

firmly

density

0.83 g cm −3

Melting point

24 ° C

boiling point

261 ° C

Vapor pressure

1.69 Pa (30 ° C)

solubility
safety instructions
GHS labeling of hazardous substances
07 - Warning 09 - Dangerous for the environment

Caution

H and P phrases H: 319-410
P: 273-305 + 351 + 338
Toxicological data

> 12800 mg kg −1 ( LD 50ratoral )

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

  1. Entry on LAURYL ALCOHOL in the CosIng database of the EU Commission, accessed on January 14, 2020.
  2. 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) .
  3. Entry on dodecan-1-ol. In: Römpp Online . Georg Thieme Verlag, accessed on December 28, 2014.
  4. Data sheet 1-Dodecanol from AlfaAesar, accessed on February 9, 2009 ( PDF )(JavaScript required) .
  5. 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).
  6. 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 .
  7. 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).