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113666-64-1

113666-64-1 Structure

113666-64-1 Structure
IdentificationBack Directory
[Name]

2-UNDECANOL
[CAS]

113666-64-1
[Synonyms]

FEMA 3246
2-UNDECANOL
DL-2-UNDECANOL
METHYL NONYL CARBINOL
[EINECS(EC#)]

216-722-6
[Molecular Formula]

C11H24O
[MDL Number]

MFCD00021958
[MOL File]

113666-64-1.mol
[Molecular Weight]

172.31
Chemical PropertiesBack Directory
[Melting point ]

2-3 °C
[Boiling point ]

130-131 °C28 mm Hg(lit.)
[density ]

0.828 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.437(lit.)
[Fp ]

226 °F
[storage temp. ]

Refrigerator
[solubility ]

Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Sparingly)
[form ]

Oil
[color ]

Colourless
[Odor]

Fatty-oily-fruity odour with a relatively refreshing, almost citrusy note.
[JECFA Number]

297
Safety DataBack Directory
[Hazard Codes ]

Xi,N
[Risk Statements ]

36/37/38-51/53
[Safety Statements ]

26-36-61
[RIDADR ]

UN 3082 9/PG 3
[WGK Germany ]

2
Hazard InformationBack Directory
[Chemical Properties]

Colorless liquid. Insoluble in water; soluble in alcohol and ether. Combustible.
[Uses]

2-Undecanol is a useful chemical reagent. It is reported that 2-Undecanol can be converted into aldehyde or ketone under mild conditions in the presence of a copper-based catalyst.
[Uses]

Antifoaming agent, intermediate, perfume fixatives, plasticizer.
[Application]

2-Undecanol finds limited use in flavour compositions, often in imitation Coconut, sometimes traces in Rum or Brandy flavours. Its taste is more pleasant than its odour, the fatty notes apparently subdued, and the fruity, nutty, sweeter notes enhanced at concentrations around 10 ppm.
[Definition]

ChEBI: Undecan-2-ol is a fatty alcohol that is undecane carrying a single hydroxy substituent at position 2. It has a role as a plant metabolite. It derives from a hydride of an undecane.
[Production Methods]

2-Undecanol is produced 1) by hydrogenation of Methyl nonyl ketone. 2) from Decanoic acid and Acetic acid by heating their vapours over Thorium oxide at about 450 ℃. The resulting ketone is subsequently hydrogenated to the alcohol.
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