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Formate ( name: methanoate) is the of . Formate is an () or its derivatives such as of . The salts and esters are generally colorless.


Fundamentals
When dissolved in water, formic acid converts to formate:
Formate is a planar anion. The two oxygen atoms are equivalent and bear a partial negative charge. The remaining C-H bond is not acidic.


Biochemistry
Formate is a common C-1 source in living systems. It is formed from many precursors including , , and . It provides a C-1 source in the biosynthesis of some . Formate (or formic acid) is invoked as a leaving group in the of some . These conversions are catalyzed by using O2 as the oxidant. Specific conversions include to and to .

Formate is reversibly oxidized by the enzyme formate dehydrogenase from gigas:


Formate esters
Formate esters have the formula HCOOR (alternative way of writing formula ROC(O)H or RO2CH). Many form spontaneously when alcohols dissolve in formic acid. Some formate esters arise by the addition of formic acid to alkenes.

An important formate ester is , which is produced as an intermediate en route to . and react in the presence of a strong base, such as :

Hydrolysis of methyl formate gives formic acid and regenerates methanol:
In laboratory, formate esters can be used to produce pure carbon monoxide. Formic acid is used for many applications in industry.

Formate esters often are fragrant or have distinctive odors. Compared to the more common acetate esters, formate esters are less commonly used commercially because they are less stable. Ethyl formate is found in some confectionaries.


Formate salts
Formate salts have the formula M(O2CH)(H2O) x. Such salts are prone to decarboxylation. For example, hydrated decarboxylates at about 200 °C with reduction of the Ni2+ to finely powdered nickel metal:

Such fine powders are useful as catalysts.


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