| Identification | More | [Name]
3-NONANOL | [CAS]
624-51-1 | [Synonyms]
3-NONANOL
3-NONYL ALCOHOL
ETHYL HEXYL CARBINEL
ETHYL HEXYL CARBINOL
ETHYL-N-HEXYLCARBINOL
HEXYL ETHYL CARBINOL
N-HEXYLETHYLCARBINOL
nonan-3-ol
3-Nonanol,98%
DL-3-NONANOL | [EINECS(EC#)]
210-850-6 | [Molecular Formula]
C9H20O | [MDL Number]
MFCD00014411 | [Molecular Weight]
144.25 | [MOL File]
624-51-1.mol |
| Chemical Properties | Back Directory | [Melting point ]
22°C | [Boiling point ]
192-194 °C(lit.) | [density ]
0.824 g/mL at 20 °C(lit.)
| [refractive index ]
n20/D 1.431
| [Fp ]
79°C | [storage temp. ]
Store below +30°C. | [solubility ]
Very slightly soluble in water, soluble in alcohol and oils. | [pka]
15.44±0.20(Predicted) | [Odor]
at 100.00 %. spice herbal oily | [Odor Type]
herbal | [Water Solubility ]
288.4mg/L(temperature not stated) | [BRN ]
1719453 | [LogP]
3.230 (est) | [CAS DataBase Reference]
624-51-1(CAS DataBase Reference) | [EPA Substance Registry System]
3-Nonanol (624-51-1) |
| Safety Data | Back Directory | [Hazard Codes ]
N | [Risk Statements ]
R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [RIDADR ]
UN 3082 9/PG 3 | [WGK Germany ]
3 | [TSCA ]
Yes | [HS Code ]
2905 19 00 |
| Hazard Information | Back Directory | [Uses]
3-nonanol has been used in perfume
compositions mainly because it was inexpensive, derived from a large-scale manufactured industrial chemical, but it has also
served as intermediate in the manufacture of
a number of new perfume chemicals, including
the hydroxylated alcohols for Lavender and
Jasmin type odors.
As long as this material is available at a
very low cost, it can probably find use in
low-cost detergent perfumes, etc. as supporting note for fresh-herbaceous fragrances, for
odor power and in fantasy fragrances. | [Definition]
ChEBI:3-Nonanol is an aliphatic alcohol. | [Production Methods]
3-nonanol can be produced by hydrogenation of Ethyl hexyl
ketone.
It can also be prepared by reduction of
Hexyl vinyl carbinol. |
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