| Identification | Back Directory | [Name]
8-Methylnonanal | [CAS]
3085-26-5 | [Synonyms]
Isodecaldehyde
8-Methylnonanal
8-methylnonan-1-al
Nonanal, 8-methyl- | [Molecular Formula]
C10H20O | [MDL Number]
MFCD22581580 | [MOL File]
3085-26-5.mol | [Molecular Weight]
156.27 |
| Chemical Properties | Back Directory | [Definition]
Mixed isomers. | [Appearance]
Liquid. Insoluble in
water. Combustible. | [Boiling point ]
203.5±8.0 °C(Predicted) | [density ]
0.816±0.06 g/cm3(Predicted) | [FEMA ]
4803 | 8-METHYLNONANAL | [storage temp. ]
Hygroscopic, Refrigerator, under inert atmosphere | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Oil | [color ]
Clear Colourless | [Odor]
at 1.00 % in dipropylene glycol. citrus floral green waxy milky | [Odor Type]
citrus | [JECFA Number]
2239 | [EPA Substance Registry System]
Nonanal, 8-methyl- (3085-26-5) |
| Hazard Information | Back Directory | [Chemical Properties]
Liquid. Insoluble in
water. Combustible. | [Uses]
A flavor compound from orange essence oil. | [General Description]
Colorless liquid with a fruity odor. Floats on water. | [Reactivity Profile]
8-Methylnonanal is an aldehyde. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. | [Health Hazard]
Low general toxicity. Liquid may irritate eyes and skin. |
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