Basic information Safety Supplier Related

Isodecanol

Basic information Safety Supplier Related

Isodecanol Basic information

Product Name:
Isodecanol
Synonyms:
  • DECANOL MIXTURE OF ISOMERS
  • isodecyl
  • isodecylalcohol(mixedisomers)
  • 8-Methylnonane-1-ol
  • Isodesyl alcohol
  • 8-methylnonan-1-ol
  • DECANOL-ISOMERENGEMISCH
  • Isodecanol
CAS:
25339-17-7
MF:
C10H22O
MW:
158.28
EINECS:
246-869-1
Mol File:
25339-17-7.mol
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Isodecanol Chemical Properties

Melting point:
-60°C
Boiling point:
215-225 °C
Density 
0.838 g/mL at 20 °C
refractive index 
n20/D 1.440
Flash point:
95 °C
storage temp. 
Refrigerator
solubility 
Benzene (Sparingly), Chloroform (Slightly)
form 
Oil
color 
Colourless
Odor
Weak alcoholic.
LogP
3.740 (est)
EPA Substance Registry System
Isodecanol (25339-17-7)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26-36
RIDADR 
3082
RTECS 
NR0960000
HazardClass 
9
PackingGroup 
III
Hazardous Substances Data
25339-17-7(Hazardous Substances Data)

MSDS

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Isodecanol Usage And Synthesis

Chemical Properties

Colorless liquid.Insoluble in water. Combustible.

Uses

Antifoaming agent in textile processing.

Uses

Isodecanol is a useful component for anti-wear lubricating oil.

Definition

Mixed isomers.

Production Methods

Isodecyl alcohol, or the C10 oxo alcohols, are made in the oxo process by reacting nonenes with carbon monoxide and hydrogen in the presence of a catalyst, followed by hydrogenation. The commercial product typically consists of trimethyl-1-heptanols and dimethyl-1-octanols; the composition and CAS registry number depend on the olefin feedstock.

Production Methods

Isodecyl alcohols are a mixture of alcohols produced by the oxo process in which undecenes are reacted with carbon monoxide and hydrogen in the presence of a catalyst, followed by hydrogenation . They are also prepared by other processes, including the Ziegler process that involves oxidation of trialklylaluminum compounds. Two of the major isomers found in the commercial product are trimethyl- 1-nonanols and dimethyl-1-decanols; the composition andCAS registry number depend on the olefin feedstock. These alcohols are used in producing phthalates and in detergents.

General Description

Colorless liquid with a mild alcohol odor. Floats on water.

Reactivity Profile

Isodecanol attacks plastics. REF [Handling Chemicals Safely, 1980. p. 236]. Acetyl bromide reacts violently with alcohols or water, [Merck 11th ed., 1989]. Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: An explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid, [Chem. Eng. News 45(43):73(1967); J, Org. Chem. 28:1893(1963)]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous-carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites, [NFPA 491 M, 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].

Health Hazard

Direct contact with skin can produce irritation.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Isodecanol Preparation Products And Raw materials

Preparation Products

IsodecanolSupplier

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