

Available forms:Colorless liquid
pd_proNo:478632-60da749d-0eb5-4188-9502-ce2647e959b3
pd_productuse:
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Preparation |
By oxidation of isoamyl alcohol. |
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Air & Water Reactions |
Highly flammable. |
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Reactivity Profile |
Isovaleraldehyde 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. |
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Health Hazard |
Inhalation causes chest discomfort, nausea, vomiting, and headache. Contact of liquid with eyes or skin causes irritation. Ingestion causes irritation of mouth and stomach. |
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Definition |
ChEBI: A methylbutanal that is butanal substituted by a methyl group at position 3. It occurs as a volatile constituent in olives. |
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General Description |
Colorless liquid with a weak suffocating odor. Floats on water. Produces an irritating vapor. |
InChI:InChI=1/C5H10O/c1-5(2)3-4-6/h4-5H,3H2,1-2H3
Nickel(II)-Schiff base-triphenylphosphin...
The effect of cationic surfactant cetylt...
Oxidation of isoamyl alcohol was carried...
A series of square planar nickel(II) com...
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Iron(III)-Schiff base-triphenylphosphine...
The catalytic properties of water-solubl...
The hydroformylation of olefins in the p...
Isoamyl alcohol oxidase (IAAOD) was puri...
The aerobic oxidations of aliphatic and ...
Kinetic studies in homogenous Ru(III) ca...
The controlled oxidation of the aliphati...
The diphosphine-ruthenium complex, [Ru(d...
4-Hydroxypyridinium chlorochromate funct...
The selective oxidation of alcohols to c...
i-Amyl alcohol
1-Phenylethanol
isovaleraldehyde
| Conditions | Yield |
|---|---|
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With
aluminium triisopentylate; acetophenone;
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i-Amyl alcohol
aluminium triisopentylate
acetophenone
1-Phenylethanol
isovaleraldehyde
| Conditions | Yield |
|---|---|
|
pentyl alcohol of fermentation;
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2,2-dimethyl-oxetane
N-Formylpiperidine
2-methylpropylmagnesium chloride
3-methylbutyric acid
4-methyl-2-pentanone
1,5,1',5'-tetramethyl-2,2'-diphenyl-1,2,1',2'-tetrahydro-4,4'-(3-methyl-butane-1,1-diyl)-bis-pyrazol-3-one
ethyl-6-isobutyl-2-methyl-4-oxocyclohex-2-ene-1-carboxylate
cyclohexyl-(3-methyl-butylidene)-amine
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