2-butyloctanol

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Structural formula
Structural formula of 2-butyloctanol
Simplified structural formula without stereochemistry
General
Surname 2-butyloctanol
other names
  • 2-butyloctan-1-ol
  • 2-butyl-1-octanol
  • ( RS ) -2-butyloctan-1-ol
  • ( RS ) -2-butyl-1-octanol
  • (±) -2-butyloctan-1-ol
  • (±) -2-butyl-1-octanol
Molecular formula C 12 H 26 O
Brief description

colorless liquid

External identifiers / databases
CAS number 3913-02-8
EC number 223-470-0
ECHA InfoCard 100.021.337
PubChem 19800
Wikidata Q27157606
properties
Molar mass 186.33 g mol −1
Physical state

liquid

density

0.83 g cm −3 (racemate)

Melting point

<−30 ° C

boiling point

145–149 ° C (racemate)

Vapor pressure

0.081 hPa (37.8 ° C) (racemate)

solubility

practically insoluble in water (<1 mg l −1 at 23 ° C)

Refractive index

1.4435 (20 ° C) (racemate)

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

Caution

H and P phrases H: 410
P: 273-391-501
Toxicological data

13 g kg −1 ( LD 50ratoral )

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

2-Butyloctanol is a fully synthetic, branched primary alcohol . It is of little importance as a solvent . Most of it is chemically processed. The technical product is a 1: 1 mixture ( racemate ) of two isomeric forms:

  • ( R ) -2-butyloctanol and
  • ( S ) -2-butyloctanol.

Occurrence

Safflower ( Carthamus tinctorius ), inflorescence

2-Butyloctanol occurs naturally in safflower oil from safflower , tobacco smoke , Changium smyrnioides , real hops , Lonicera japonica and Portulaca oleracea .

Extraction and presentation

2-Butyloctanol can be obtained by condensation from 1-hexanol and a catalyst .

properties

2-Butyloctanol is a flammable, hardly ignitable, colorless liquid that is practically insoluble in water.

use

2-Butyloctanol is used as an intermediate in the production of other chemical compounds, such as 2-butyl-1-octyl methacrylate (BOMA) and 3,5,5-trimethyl-1-hexyl methacrylate (TMHMA), and as a solvent.

Individual evidence

  1. a b c d e f Entry on 2-butyloctanol in the GESTIS substance database of the IFA , accessed on June 28, 2017(JavaScript required) .
  2. a b c d e data sheet 2-butyl-1-octanol, 95% from Sigma-Aldrich , accessed on June 28, 2017 ( PDF ).
  3. Michael Ash: Handbook of Green Chemicals . Synapse Info Resources, 2004, ISBN 978-1-890595-79-1 , pp. 1306 ( limited preview in Google Book search).
  4. Shmuel Yannai: Dictionary of Food Compounds with CD-ROM, Second Edition . CRC Press, 2012, ISBN 978-1-4200-8351-4 , pp. 201 ( limited preview in Google Book search).
  5. Sabine Krist: Lexicon of vegetable fats and oils . Springer-Verlag, 2012, ISBN 978-3-7091-1005-8 , pp. 208 ( limited preview in Google Book search).
  6. Roger A. Jenkins, Bruce Tomkins, Michael R. Guerin: The Chemistry of Environmental Tobacco Smoke Composition and Measurement, Second Edition . CRC Press, 2000, ISBN 978-1-56670-509-7 , pp. 30 ( limited preview in Google Book search).
  7. ^ Dictionary of Organic Compounds: Sixth Edition: Second Supplement . Taylor & Francis, S. 76 ( limited preview in Google Book search).
  8. ^ Paul N. Rylander: Organic Syntheses with Noble Metal Catalysts . Elsevier, 2012, ISBN 978-0-323-16261-6 , pp. 209 ( limited preview in Google Book search).