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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

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Additional information

Studies on major metabolic pathways of 2-methylbutanal could not be identified. But it is assumed that the metabolism is similar to other aldehydes. In general, aldehydes are primarily oxidized to the corresponding carboxylic acid. Subsequently, they follow the metabolic pathways of this carboxylic acid.

 

In the study located (Roberts 1991), the deformylation reaction resulting in olefin formation of C3 to C5 aldehydes was investigated using a reconstituted system of different cytochrom P-450 isozymes. This reaction is not a major metabolic pathway of 2-methylbutyraldehyde.

In order to achieve deformylation and formation of the corresponding olefin, branching at theα-carbon atom was required. Activity increased with increasing branching (trimethylacetaldehyde > 2-methylbutyraldehyde > butyraldehyde).