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Butyraldehyde, also known as butanal, is an organic compound with the formula CH3(CH2)2CHO. It is a colorless flammable liquid with an unpleasant smell, and it is produced by hydroformylation of propylene or catalytic dehydrogenation of butanol.
Butanal is a member of the class of butanals that consists of propane bearing a formyl substituent at the 1-position. The parent of the class of butanals. It has a role as a biomarker, an Escherichia coli metabolite and a mouse metabolite. ChEBI.
Learn about butanal, a colorless flammable liquid with a strong odor, and its applications in chemical syntheses. Find out how butanal is produced by hydroformylation of propene, and how it undergoes hydrogenation, oxidation, addition and condensation reactions.
Butyraldehyde, also known as butanal, is an organic aldehyde with a fruity smell and various applications. Learn how it is made, what it is used for, and how to handle it safely.
Butanal is an organic compound with the formula C4H8O and the IUPAC name butyraldehyde. It has a CAS registry number of 123-72-8 and a molecular weight of 72.1057.
ChemSpider record containing structure, synonyms, properties, vendors and database links for Butyraldehyde, 123-72-8, Butanal
Butanal is used in the manufacture of rubber accelerators, synthetic resins, solvents, and plasticizers. n -Butyraldehyde is used as an intermediate in the manufacturing of plasticizers, alcohols, solvents, and polymers (such as 2-ethylhexanol, n -butanol, trimethylolpropane, n -butyric acid, polyvinyl butyral, and methyl amyl ketone).
Butanal is a chemical compound with the formula C4H8O and the IUPAC name butyraldehyde. It has a mass spectrum, a chemical structure, and other data available from NIST sources.
The IUPAC name for butyraldehyde is butanal, which reflects its position in the aldehyde naming convention. Butyraldehyde is commonly used as a solvent and as an intermediate in the production of other chemicals, such as butyric acid and butyl alcohol.
Butyraldehyde is produced almost exclusively by the hydroformylation of propylene:. CH 3 CH=CH 2 + H 2 + CO → CH 3 CH 2 CH 2 CHO. Traditionally, hydroformylation was catalyzed by cobalt carbonyl but rhodium complexes are more common. The dominant technology involves the use of rhodium catalysts derived from the water-soluble ligand tppts.An aqueous solution of the rhodium catalyst converts ...