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Home > Encyclopedia > D(+)-2-Octanol

D(+)-2-Octanol

D(+)-2-Octanol structure

D(+)-2-Octanol 

structure
  • CAS No:

    6169-06-8

  • Formula:

    C8H18O

  • Chemical Name:

    D(+)-2-Octanol

  • Synonyms:

    (s)-2-octano;(S)-octan-2-ol;D(+)-2-OCTANOL;D-2-OCTANOL;(S)-(+)-2-HYDROXYOCTANE;(S)-2-HYDROXYOCTANE;(S)-(+)-2-OCTANOL;(S)-2-OCTANOL

  • Categories:

    Food Additives  >  Food Flavorings

Description

Colorless to light yellow liqui


(2S)-octan-2-ol is an octan-2-ol. It is an enantiomer of a (2R)-octan-2-ol.


2-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.

D(+)-2-Octanol Basic Attributes

130.23

130.23

1719323

228-213-6

2855UV552L

TSCA listed

Colorless to Almost colorless

29051620

Characteristics

20.23000

2.9

0.822 g/mL at 25 °C (lit.)

-61.15°C (estimate)

175 °C (lit.)

71ºC

n20/D1.426(lit.)

1 g/L (20 ºC)

Keep away from heat, sparks, and flame. Keep away from sources of ignition. Store in a tightly closed container. Store in a cool

at 1.00 % in dipropylene glycol. mushroom oily fatty creamy grape

15.44±0.20(Predicted)

Sealed in dry,Room Temperature

Safety Information

I; II; III

NONH for all modes of transport

3

Xi

26-36-37/39

Xi

Stable. Combustible. Incompatible with strong oxidizing agents

P261-P305 + P351 + P338

36/37/38

|Warning|H315 (86.67%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 45 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

D(+)-2-Octanol Use and Manufacturing

Uses

Used in paint, enamel, perfume, organic synthesis and anti-foaming agent. 1. Used in the manufacture of plasticizers, synthetic fiber oils, defoamers, mining flotation agents, pesticide emulsifiers and spices, and can also be used as a solvent for oils and waxes. Used as a solvent for nitro spray paint and enamel, it can improve ductility, gloss and fluidity. It is also used as a fiber wetting agent, brake oil, anti-emulsifier and raw material for plasticizers and fragrances. In addition, 2-octanol is still used to adjust the viscosity of urea-formaldehyde resin. 2. Esterification with phthalic anhydride to produce di-secondary octyl phthalate, which is an excellent plasticizer for polyvinyl chloride plastics. 2-octanol is also used as synthetic fiber oil, defoamer and surface active It can also be used as a raw material for flotation agents and pesticide emulsifiers used in coal mines, and also as a solvent for oils and waxes.


(S)-(+)-2-Octanol is used as chiral compounds.


(S)-(+)-2-Octanol can be used:To prepare the solution of 5-(benzyloxy)-isophthalic acid derivative, which is used as a 2D chiral self-assembly system comprising pyrolytic graphite.As a chiral template in the study of enantioselective glycidol esterification.As a starting material for the preparation of (+)-(S)-2-octyI tosylate, an intermediate used to prepare ()-(R)-2-halo and azido octanes.

2-Octanol, (2S)-: ACTIVE

Fatty Acyls [FA] -> Fatty alcohols [FA05]

Computed Properties

Molecular Weight:130.23
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:130.135765193
Monoisotopic Mass:130.135765193
Topological Polar Surface Area:20.2
Heavy Atom Count:9
Complexity:52.5
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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