Basic information Safety Supplier Related

2,6-DIMETHYLOCTANE

Basic information Safety Supplier Related

2,6-DIMETHYLOCTANE Basic information

Product Name:
2,6-DIMETHYLOCTANE
Synonyms:
  • 2,6-DIMETHYLOCTANE
  • dimethyloctane
  • Octane, 2,6-dimethyl-
  • octane,2,6-dimethyl-
  • tetrahydrocitronellene
  • 2,6-DIMETHYLOCTANE 95+%
  • 2,6-Dimethyloctane >
  • 2,6-Dimethyloctane in isooctane
CAS:
2051-30-1
MF:
C10H22
MW:
142.28
Mol File:
2051-30-1.mol
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2,6-DIMETHYLOCTANE Chemical Properties

Melting point:
-53.15°C
Boiling point:
158°C
Density 
0,73 g/cm3
refractive index 
1.3990-1.4130
Flash point:
34°C
form 
clear liquid
color 
Colorless to Almost colorless
Water Solubility 
89.16ug/L(temperature not stated)
LogP
5.490 (est)
CAS DataBase Reference
2051-30-1(CAS DataBase Reference)
EPA Substance Registry System
Octane, 2,6-dimethyl- (2051-30-1)
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Safety Information

Risk Statements 
10
Safety Statements 
16
RIDADR 
3295
HS Code 
2901.10.5000
HazardClass 
3
PackingGroup 
III
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2,6-DIMETHYLOCTANE Usage And Synthesis

Chemical Properties

2,6-Dimethyloctane is a colourless, transparent liquid compound with a density of 0.73 g/mL3, a boiling point of 158° C, a flash point of 34 °C, soluble in ethanol and stored at room temperature.

Uses

2,6-Dimethyloctane is used as a diesel fuel additive and as a chemical reaction reagent or product. Optically active 6-chloro-2,6-dimethyloctane is capable of being reduced to 2,6-dimethyloctane in alkali metal solutions in liquid ammonia, and its primary configuration remains unchanged[1-2].

Uses

Myrcane is a useful synthetic intermediate. It was used to synthesize alcohols via C-H hydroxylation of alicyclic and aliphatics compounds.

References

[1] NOAH I. TRACY. Hydrogenated monoterpenes as diesel fuel additives[J]. Fuel, 2009. DOI:10.1016/j.fuel.2009.02.002.
[2] P. E. VERKADE  B. M W  K D Vries. Reactions of aliphatic halides with solutions of alkali metals in liquid ammonia: III. The reduction of optically active 6‐chloro‐2,6‐dimethyloctane to the corresponding hydrocarbon[J]. Recueil des Travaux Chimiques des Pays-Bas, 2010. DOI:10.1002/RECL.19640830406.

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