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Carbonyls can be in reactions using compounds such as reagents, , or . Carbonyls also may be alkylated by as in . Carbonyls are also the prototypical groups with reactivity (e.g. the where an carbon in with the carbonyl is alkylated instead of the carbonyl itself).

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Calcium Carbonate is reported as an ingredient of Carbocal D in the following countries:

A carbonyl group characterizes the following types of compounds:

In , a carbonyl group is a composed of a to an atom: C=O. It is common to several classes of organic compounds, as part of many larger functional groups. A compound containing a carbonyl group is often referred to as a carbonyl compound.

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A special group of carbonyl compounds are 1,3-dicarbonyl compounds that have acidic protons in the central methylene unit. Examples are , and .

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They are usually dark gray to dark brown

In case of multiple carbonyl types in one molecule, one can expect the most electrophilic carbonyl carbon to react first. and react fastest, followed by and . react much more slowly and are almost completely unreactive due to resonance of the amide nitrogen towards the carbonyl group. This reactivity difference allows when a reactant contains multiple carbonyl groups. An instructive example is found in the last part of the of by in 1979:

The term carbonyl can also refer to  as a  in an  or  complex (a , e.g. ).

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Carbocal D is a preparation of calcium and Vitamin D. Carbocal D is used to assist the development and maintenance of healthy bones and teeth.


Since α,β-unsaturated compounds are electrophiles, many α,β-unsaturated carbonyl compounds are toxic, mutagenic and carcinogenic. can attack the β carbon and thus be . However, the endogenous scavenger compound naturally protects from toxic electrophiles in the body. Some drugs (amifostine, ) containing thiol group may protect biomolecules from such harmful alkylation