Basic information Description References Safety Related Supplier
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D(+)-2-Octanol

Basic information Description References Safety Related Supplier
D(+)-2-Octanol Basic information
D(+)-2-Octanol Chemical Properties
  • Melting point:-61.15°C (estimate)
  • alpha 9.5 º (neat)
  • Boiling point:175 °C(lit.)
  • Density 0.822 g/mL at 25 °C(lit.)
  • refractive index n20/D 1.426(lit.)
  • Flash point:160 °F
  • storage temp. Store below +30°C.
  • solubility 1.28g/l
  • pka15.44±0.20(Predicted)
  • explosive limit0.8%(V)
  • optical activity[α]20/D +9.5°, neat
  • Water Solubility 1 g/L (20 ºC)
  • Merck 14,6752
  • BRN 1719323
  • Stability:Stable. Combustible. Incompatible with strong oxidizing agents
  • InChIKeySJWFXCIHNDVPSH-QMMMGPOBSA-N
  • CAS DataBase Reference6169-06-8(CAS DataBase Reference)
  • NIST Chemistry Reference2-Octanol, (S)-(6169-06-8)
  • EPA Substance Registry System2-Octanol, (2S)- (6169-06-8)
Safety Information
  • Hazard Codes Xi
  • Risk Statements 36/37/38
  • Safety Statements 26-36-37/39
  • WGK Germany 3
  • TSCA Yes
  • HS Code 29051620
MSDS
D(+)-2-Octanol Usage And Synthesis
  • Description2-Octanol is a fatty alcohol. It is directly produced from vegetal chemistry. In industry, it is produced by a cracking process from castor oil.
    2-octanol is mainly used as a raw material to produce caproic acid, an intermediate in flavor. It is used as a green solvent for various resins intended for paints and coatings or adhesives sectors.  It can be employed as a defoamer in different processes, as an additive for lubricants, and as a solvent in rare minerals extraction. In coal industry, it is used as floatation agent and as a frother in mineral flotation. As an intermediate, 2-octanol can be used in synthesis of a wide range of plasticizers, esters, and surfactants, which include alcohol alkoxylates and sulfates for detergency and personal care markets; adipates, aebacates, palmitates, stearates for applications in cosmetic, paints and coatings, plastic, paper, textile, etc…; phthalates; acrylates and maleates for coatings and adhesives markets; salicylate, myristate, méthoxycinnamate for application in fragrances.
  • References[1] https://en.wikipedia.org/wiki/2-Octanol
    [2] Robert A. Levis (2016) Hawley's Condensed Chemical Dictionary
    [3] http://www.castoroil.in/castor/castor_seed/castor_oil/2_octanol/2_octanol.html
  • Chemical PropertiesColorless to light yellow liqui
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