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Isobutyraldehyde is the chemical compound with the formula (CH 3) 2 CHCHO. It is an aldehyde, isomeric with n-butyraldehyde (butanal). [1] Isobutyraldehyde is made, often as a side-product, by the hydroformylation of propene. Its odour is described as that of wet cereal or straw. It undergoes the Cannizaro reaction even though it has alpha ...
Butyraldehyde undergoes reactions typical of alkyl aldehydes, and these define many of the uses of this compound.Important reactions include hydrogenation to the alcohol, oxidation to the acid, and base-catalyzed condensation.
Isobutyric acid is manufactured by the oxidation of isobutyraldehyde, which is a byproduct of the hydroformylation of propylene. [7]It can also be prepared by the high pressure hydrocarboxylation (Koch reaction) from propylene: [7]
2,4,6-Triisobutyl-1,3,5-trioxane Acid-catalyzed cyclic trimerization of Isovaleraldehyde gives 2,4,6-Triisobutyl- 1,3,5-trioxane [68165-40-2]. This is a flavouring agent that can be used in confectionary, tobacco, and other foodstuffs, toothpastes and the like. [ 8 ]
[1] It is produced by the condensation reaction of isobutyraldehyde and two equivalents of urea: (CH 3) 2 CHCHO + 2 OC(NH 2) 2 → (CH 3) 2 CHCH{NHC(O)NH 2} 2 + H 2 O. The controlled-release process is the reverse of the above reaction, which only occurs after the IBDU dissolves.
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Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH 3) 2 CHCH 2 OH (sometimes represented as i-BuOH). This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters.