Although biodegradation data specific to 2-methyl-1-butanol are unavailable, analogy to similar aliphatic alcohols suggests that 2-methyl-1-butanol will readily biodegrade. Hence it is indicated by cyclohexanecarboxylate. The alcoholic part is indicated by 'ethyl'. The acid part of the ester is derived from the cyclohexanecarboxylic acid. Methyl n-butyrate may also undergo direct photolysis in the environment since this compound contains a functional group that typically absorbs light greater than 290 nm(4). Note that the functional group is not the part of parent chain. Based upon an estimated Koc values of 15 and 120, 2-methyl-1-butanol is expected to leach readily in soil(2,SRC); however, the importance of leaching may be lessened by relatively rapid, concurrent biodegradation(SRC). (1) Bidleman TF; Environ Sci Technol 22: 361-367 (1988) (2) Yaws CL; Handbook of Vapor Pressure. 100-102 °C Alfa Aesar: 102-103 °C Food and Agriculture Organization of the United Nations Methyl butanoate: 100-103 °C OU Chemical Safety Data (No longer updated) More details: 100-102 °C Alfa Aesar L04250: 102-103 °C (Literature) LabNetwork LN00221925 102.3 °C FooDB FDB012084: 102-103 °C Sigma-Aldrich SIAL-19358 Compound-25 * The main functional group is ester. Functional groups will undergo the same type of reactions ... then write “ether.” For example, ethyl methyl ether is the ether that has an ethyl group and a methyl group on either side of the oxygen ... formate” instead of “methanoate,” “propionate” instead of “propanoate,” and “butyrate” instead of “butanoate. * The complete name is: methyl butanoate.
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