Ketone

Acetone, the simplest ketone

In organic chemistry, a ketone /ˈkiːtoʊn/ is an organic compound with the structure R−C(=O)−R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group −C(=O)− (a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' is methyl), with the formula (CH₃)₂CO. Many ketones are of great importance in biology and industry. Examples include many sugars (ketoses), many steroids (e.g., testosterone), and the solvent acetone.^[1]

Nomenclature and etymology

The word ketone is derived from Aketon, an old German word for acetone.^[2]^[3]

According to the rules of IUPAC nomenclature, ketone names are derived by changing the suffix -ane of the parent alkane to -anone. Typically, the position of the carbonyl group is denoted by a number, but traditional nonsystematic names are still generally used for the most important ketones, for example acetone and benzophenone. These nonsystematic names are considered retained IUPAC names,^[4] although some introductory chemistry textbooks use systematic names such as "2-propanone" or "propan-2-one" for the simplest ketone (C H₃−C(=O)−CH₃) instead of "acetone".

The derived names of ketones are obtained by writing separately the names of the two alkyl groups attached to the carbonyl group, followed by "ketone" as a separate word. Traditionally the names of the alkyl groups were written in order of increasing complexity, for example methyl ethyl ketone. However, according to the rules of IUPAC nomenclature, the alkyl groups are written alphabetically, for example ethyl methyl ketone. When the two alkyl groups are the same, the prefix "di-" is added before the name of alkyl group. The positions of other groups are indicated by Greek letters, the α-carbon being the atom adjacent to carbonyl group.

Although used infrequently, oxo is the IUPAC nomenclature for the oxo group (=O) and used as prefix when the ketone does not have the highest priority. Other prefixes, however, are also used. For some common chemicals (mainly in biochemistry), keto refer to the ketone functional group.

Structure and bonding

Representative ketones, from the left: acetone, a common solvent; oxaloacetate, an intermediate in the metabolism of sugars; acetylacetone in its (mono) enol form (the enol highlighted in blue); cyclohexanone, precursor to nylon; muscone, an animal scent; and tetracycline, an antibiotic

The ketone carbon is often described as sp² hybridized, a description that includes both their electronic and molecular structure. Ketones are trigonal planar around the ketonic carbon, with C–C–O and C–C–C bond angles of approximately 120°. Ketones differ from aldehydes in that the carbonyl group (C=O) is bonded to two carbons within a carbon skeleton. In aldehydes, the carbonyl is bonded to one carbon and one hydrogen and are located at the ends of carbon chains. Ketones are also distinct from other carbonyl-containing functional groups, such as carboxylic acids, esters and amides.^[5]

The carbonyl group is polar because the electronegativity of the oxygen is greater than that for carbon. Thus, ketones are nucleophilic at oxygen and electrophilic at carbon. Because the carbonyl group interacts with water by hydrogen bonding, ketones are typically more soluble in water than the related methylene compounds. Ketones are hydrogen-bond acceptors. Ketones are not usually hydrogen-bond donors and cannot hydrogen-bond to themselves. Because of their inability to serve both as hydrogen-bond donors and acceptors, ketones tend not to "self-associate" and are more volatile than alcohols and carboxylic acids of comparable molecular weights. These factors relate to the pervasiveness of ketones in perfumery and as solvents.

Classes of ketones

Ketones are classified on the basis of their substituents. One broad classification subdivides ketones into symmetrical and unsymmetrical derivatives, depending on the equivalency of the two organic substituents attached to the carbonyl center. Acetone and benzophenone ((C₆H₅)₂CO) are symmetrical ketones. Acetophenone (C₆H₅C(O)CH₃) is an unsymmetrical ketone.

Diketones

Many kinds of diketones are known, some with unusual properties. The simplest is diacetyl (CH₃C(O)C(O)CH₃), once used as butter-flavoring in popcorn. Acetylacetone (pentane-2,4-dione) is virtually a misnomer (inappropriate name) because this species exists mainly as the monoenol CH₃C(O)CH=C(OH)CH₃. Its enolate is a common ligand in coordination chemistry.

Unsaturated ketones

Ketones containing alkene and alkyne units are often called unsaturated ketones. A widely used member of this class of compounds is methyl vinyl ketone, CH₃C(O)CH=CH₂, a α,β-unsaturated carbonyl compound.

Cyclic ketones

Many ketones are cyclic. The simplest class have the formula (CH₂)_nCO, where n varies from 2 for cyclopropanone ((CH₂)₂CO) to the tens. Larger derivatives exist. Cyclohexanone ((CH₂)₅CO), a symmetrical cyclic ketone, is an important intermediate in the production of nylon. Isophorone, derived from acetone, is an unsaturated, asymmetrical ketone that is the precursor to other polymers. Muscone, 3-methylpentadecanone, is an animal pheromone. Another cyclic ketone is cyclobutanone, having the formula (CH₂)₃CO.

Characterization

An aldehyde differs from a ketone in that it has a hydrogen atom attached to its carbonyl group, making aldehydes easier to oxidize. Ketones do not have a hydrogen atom bonded to the carbonyl group, and are therefore more resistant to oxidation. They are oxidized only by powerful oxidizing agents which have the ability to cleave carbon–carbon bonds.

Spectroscopy

Ketones (and aldehydes) absorb strongly in the infra-red spectrum near 1750 cm⁻¹, which is assigned to ν_C=O ("carbonyl stretching frequency"). The energy of the peak is lower for aryl and unsaturated ketones.^[6]

Whereas ¹H NMR spectroscopy is generally not useful for establishing the presence of a ketone, ¹³C NMR spectra exhibit signals somewhat downfield of 200 ppm depending on structure. Such signals are typically weak due to the absence of nuclear Overhauser effects. Since aldehydes resonate at similar chemical shifts, multiple resonance experiments are employed to definitively distinguish aldehydes and ketones.

Qualitative organic tests

Ketones give positive results in Brady's test, the reaction with 2,4-dinitrophenylhydrazine to give the corresponding hydrazone. Ketones may be distinguished from aldehydes by giving a negative result with Tollens' reagent or with Fehling's solution. Methyl ketones give positive results for the iodoform test.^[7] Ketones also give positive results when treated with m-dinitrobenzene in presence of dilute sodium hydroxide to give violet coloration.

Synthesis

Many methods exist for the preparation of ketones in industrial scale and academic laboratories. Ketones are also produced in various ways by organisms; see the section on biochemistry below.

In industry, the most important method probably involves oxidation of hydrocarbons, often with air. For example, a billion kilograms of cyclohexanone are produced annually by aerobic oxidation of cyclohexane. Acetone is prepared by air-oxidation of cumene.

For specialized or small scale organic synthetic applications, ketones are often prepared by oxidation of secondary alcohols:

R₂CH(OH) + "O" → R₂C=O + H₂O

Typical strong oxidants (source of "O" in the above reaction) include potassium permanganate or a Cr(VI) compound. Milder conditions make use of the Dess–Martin periodinane or the Moffatt–Swern methods.

Many other methods have been developed, examples include:^[8]

By geminal halide hydrolysis.^[9]
By hydration of alkynes.^[10] Such processes occur via enols and require the presence of an acid and mercury(II) sulfate (HgSO₄). Subsequent enol–keto tautomerization gives a ketone. This reaction always produces a ketone, even with a terminal alkyne, the only exception being the hydration of acetylene, which produces acetaldehyde.
From Weinreb Amides using stoichiometric organometallic reagents.
aryl ketones can be prepared in the Friedel–Crafts acylation,^[11] the related Houben–Hoesch reaction,^[12] and the Fries rearrangement.^[10]
Ozonolysis, and related dihydroxylation/oxidative sequences, cleave alkenes to give aldehydes or ketones, depending on alkene substitution pattern.^[13]
From peroxides (Kornblum–DeLaMare rearrangement).
Cyclization of dicarboxylic acids (Ruzicka cyclization)
hydrolysis of salts of secondary nitro compounds ( Nef reaction^[14])
Alkylation of thioester with organozinc compounds (Fukuyama coupling).
Alkylation of acid chloride with organocadmium compounds or organocopper compounds.
The Dakin–West reaction provides an efficient method for preparation of certain methyl ketones from carboxylic acids.^[15]
Ketones can be prepared by the reaction of Grignard reagents with nitriles, followed by hydrolysis.^[16]
By decarboxylation of carboxylic anhydride.
Ketones can be prepared from haloketones in reductive dehalogenation of halo ketones.
In ketonic decarboxylation symmetrical ketones are prepared from carboxylic acids.^[10]^[17]
Hydrolysis of unsaturated secondary amides,^[18] β-Keto acid esters,^[10] or β-diketones (the acetoacetic ester synthesis).
Acid-catalysed rearrangement of 1,2-diols,^[10] or Criegee oxidation of the same.

Reactions

Keto-enol tautomerization

Ketones that have at least one alpha-hydrogen, undergo keto-enol tautomerization; the tautomer is an enol. Tautomerization is catalyzed by both acids and bases. Usually, the keto form is more stable than the enol. This equilibrium allows ketones to be prepared via the hydration of alkynes.

Acid/base properties of ketones

C−H bonds adjacent to the carbonyl in ketones are more acidic pK_a ≈ 20) than the C−H bonds in alkane (pK_a ≈ 50). This difference reflects resonance stabilization of the enolate ion that is formed upon deprotonation. The relative acidity of the α-hydrogen is important in the enolization reactions of ketones and other carbonyl compounds. The acidity of the α-hydrogen also allows ketones and other carbonyl compounds to react as nucleophiles at that position, with either stoichiometric and catalytic base. Using very strong bases like lithium diisopropylamide (LDA, pK_a of conjugate acid ~36) under non-equilibrating conditions (–78 °C, 1.1 equiv LDA in THF, ketone added to base), the less-substituted kinetic enolate is generated selectively, while conditions that allow for equilibration (higher temperature, base added to ketone, using weak or insoluble bases, e.g., CH₃CH₂ONa in CH₃CH₂OH, or NaH) provides the more-substituted thermodynamic enolate.

Ketones are also weak bases, undergoing protonation on the carbonyl oxygen in the presence of Brønsted acids. Ketonium ions (i.e., protonated ketones) are strong acids, with pK_a values estimated to be somewhere between –5 and –7.^[19]^[20] Although acids encountered in organic chemistry are seldom strong enough to fully protonate ketones, the formation of equilibrium concentrations of protonated ketones is nevertheless an important step in the mechanisms of many common organic reactions, like the formation of an acetal, for example. Acids as weak as pyridinium cation (as found in pyridinium tosylate) with a pK_a of 5.2 are able to serve as catalysts in this context, despite the highly unfavorable equilibrium constant for protonation (K_eq < 10⁻¹⁰).

Nucleophilic additions

An important set of reactions follow from the susceptibility of the carbonyl carbon toward nucleophilic addition and the tendency for the enolates to add to electrophiles. Nucleophilic additions include in approximate order of their generality:^[8]

With water (hydration) gives geminal diols, which are usually not formed in appreciable (or observable) amounts
With an acetylide to give the α-hydroxyalkyne
With ammonia or a primary amine gives an imine
With secondary amine gives an enamine
With Grignard and organolithium reagents to give, after aqueous workup, a tertiary alcohol
With an alcohols or alkoxides to gives the hemiketal or its conjugate base. With a diol to the ketal. This reaction is employed to protect ketones.
With sodium amide resulting in C–C bond cleavage with formation of the amide RCONH₂ and the alkane or arene R'H, a reaction called the Haller–Bauer reaction.^[21]

Oxidation

Ketones are cleaved by strong oxidizing agents and at elevated temperatures. Their oxidation involves carbon–carbon bond cleavage to afford a mixture of carboxylic acids having lesser number of carbon atoms than the parent ketone.

Other reactions

Electrophilic addition, reaction with an electrophile gives a resonance stabilized cation
With phosphonium ylides in the Wittig reaction to give the alkenes
With thiols to give the thioacetal
With hydrazine or 1-disubstituted derivatives of hydrazine to give hydrazones.
With a metal hydride gives a metal alkoxide salt, hydrolysis of which gives the alcohol, an example of ketone reduction
With halogens to form an α-haloketone, a reaction that proceeds via an enol (see Haloform reaction)
With heavy water to give an α-deuterated ketone
Fragmentation in photochemical Norrish reaction
Reaction of 1,4-aminodiketones to oxazoles by dehydration in the Robinson–Gabriel synthesis
In the case of aryl–alkyl ketones, with sulfur and an amine give amides in the Willgerodt reaction
With hydroxylamine to produce oximes
With reducing agents to form secondary alcohols
With peroxy acids to form esters in the Baeyer–Villiger oxidation

Biochemistry

Ketones do not appear in standard amino acids, nucleic acids, nor lipids. The formation of organic compounds in photosynthesis occurs via the ketone ribulose-1,5-bisphosphate. Many sugars are ketones, known collectively as ketoses. The best known ketose is fructose; it mostly exists as a cyclic hemiketal, which masks the ketone functional group. Fatty acid synthesis proceeds via ketones. Acetoacetate is an intermediate in the Krebs cycle which releases energy from sugars and carbohydrates.^[22]

In medicine, acetone, acetoacetate, and beta-hydroxybutyrate are collectively called ketone bodies, generated from carbohydrates, fatty acids, and amino acids in most vertebrates, including humans. Ketone bodies are elevated in the blood (ketosis) after fasting, including a night of sleep; in both blood and urine in starvation; in hypoglycemia, due to causes other than hyperinsulinism; in various inborn errors of metabolism, and intentionally induced via a ketogenic diet, and in ketoacidosis (usually due to diabetes mellitus). Although ketoacidosis is characteristic of decompensated or untreated type 1 diabetes, ketosis or even ketoacidosis can occur in type 2 diabetes in some circumstances as well.

Applications

Ketones are produced on massive scales in industry as solvents, polymer precursors, and pharmaceuticals. In terms of scale, the most important ketones are acetone, methylethyl ketone, and cyclohexanone.^[23] They are also common in biochemistry, but less so than in organic chemistry in general. The combustion of hydrocarbons is an uncontrolled oxidation process that gives ketones as well as many other types of compounds.

Toxicity

Although it is difficult to generalize on the toxicity of such a broad class of compounds, simple ketones are, in general, not highly toxic. This characteristic is one reason for their popularity as solvents. Exceptions to this rule are the unsaturated ketones such as methyl vinyl ketone with LD₅₀ of 7 mg/kg (oral).^[23]

References

^ Raymond, Kenneth W. (2010). General Organic and Biological Chemistry (3rd ed.). Wiley. p. 297.
^ Harper, Douglas. "ketone". Online Etymology Dictionary.
^ The word "ketone" was coined in 1848 by the German chemist Leopold Gmelin. See: Leopold Gmelin, ed., Handbuch der organischen Chemie: Organische Chemie im Allgemeinen … (Handbook of organic chemistry: Organic chemistry in general … ), 4th ed., (Heidelberg, (Germany): Karl Winter, 1848), volume 1, p. 40. From page 40: "Zu diesen Syndesmiden scheinen auch diejenigen Verbindungen zu gehören, die als Acetone im Allegemeinen (Ketone?) bezeichnet werden." (To these syndesmides*, those compounds also seem to belong, which are designated as acetones in general (ketones?).") [*Note: In 1844, the French chemist Auguste Laurent suggested a new nomenclature for organic compounds. One of his new classes of compounds was "syndesmides", which were compounds formed by the combination of two or more simpler organic molecules (from the Greek σύνδεσμος (syndesmos, union) + -ide (indicating a group of related compounds)). For example, acetone could be formed by the dry distillation of metal acetates, so acetone was the syndesmide of two acetate ions. See: Laurent, Auguste (1844) "Classification chimique," Comptes rendus, 19 : 1089–1100 ; see especially p. 1097.
^ List of retained IUPAC names retained IUPAC names Link Archived 9 July 2023 at the Wayback Machine
^ McMurry, John E. (1992), Organic Chemistry (3rd ed.), Belmont: Wadsworth, ISBN 0-534-16218-5
^ Smith, Brian (November 2018). "The C=O Bond, Part VIII: Review". Spectroscopy. November 2018. 33: 24–29. Archived from the original on 13 February 2024. Retrieved 12 February 2024.
^ Mendham, J.; Denney, R. C.; Barnes, J. D.; Thomas, M. J. K. (2000), Vogel's Quantitative Chemical Analysis (6th ed.), New York: Prentice Hall, ISBN 0-582-22628-7
^ ^a ^b Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
^ Marvel, C. S.; Sperry, W. M. (1928). "Benzophenone". Organic Syntheses. 8: 26. doi:10.15227/orgsyn.008.0026.
^ ^a ^b ^c ^d ^e Furniss, Brian; Hannaford, Antony; Smith, Peter; Tatchell, Austin (1996). Vogel's Textbook of Practical Organic Chemistry (5th ed.). London: Longman Science & Technical. pp. 612–623, 976–977, 982–983. ISBN 9780582462366.
^ Allen, C. F. H.; Barker, W. E. (1932). "Desoxybenzoin". Organic Syntheses. 12: 16. doi:10.15227/orgsyn.012.0016.
^ Gulati, K. C.; Seth, S.R.; Venkataraman, K. (1935). "Phloroacetophenone". Organic Syntheses. 15: 70. doi:10.15227/orgsyn.015.0070.
^ Tietze, Lutz F.; Bratz, Matthias (1993). "Dialkyl Mesoxalates by Ozonolysis of Dialkyl Benzalmalonates: Dimethyl Mesoxalate". Organic Syntheses. 71: 214. doi:10.15227/orgsyn.071.0214.
^ Heinzelman, R. V. (1955). "o-Methoxyphenylacetone". Organic Syntheses. 35: 74. doi:10.15227/orgsyn.035.0074.
^ Wiley, Richard H.; Borum, O. H. (1953). "3-Acetamido-2-butanone". Organic Syntheses. 33: 1. doi:10.15227/orgsyn.033.0001.
^ Moffett, R. B.; Shriner, R. L. (1941). "ω-Methoxyacetophenone". Organic Syntheses. 21: 79. doi:10.15227/orgsyn.021.0079.
^ Thorpe, J. F.; Kon, G. A. R. (1925). "Cyclopentanone". Organic Syntheses. 5: 37. doi:10.15227/orgsyn.005.0037.
^ Herbst, R. M.; Shemin, D. (1939). "Phenylpyruvic acid". Organic Syntheses. 19: 77. doi:10.15227/orgsyn.019.0077.
^ Evans, David A. (4 November 2005). "Evans pKa table" (PDF). Evans group website. Archived from the original (PDF) on 19 June 2018. Retrieved 14 June 2018.
^ Smith, Michael B. (2013). March's Advanced Organic Chemistry (7th ed.). Hoboken, N.J.: Wiley. pp. 314–315. ISBN 978-0-470-46259-1.
^ Haller–Bauer Reaction. homeip.net
^ Nelson, D. L.; Cox, M. M. (2000) Lehninger, Principles of Biochemistry. 3rd Ed. Worth Publishing: New York. ISBN 1-57259-153-6.
^ ^a ^b Siegel, Hardo; Eggersdorfer, Manfred (2000). "Ketones". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a15077 (inactive 11 September 2024). ISBN 9783527306732.{{cite book}}: CS1 maint: DOI inactive as of September 2024 (link)

External links

Media related to Ketones at Wikimedia Commons

[raymond2010-1] Raymond, Kenneth W. (2010). General Organic and Biological Chemistry (3rd ed.). Wiley. p. 297.

[2] Harper, Douglas. "ketone". Online Etymology Dictionary.

[3] The word "ketone" was coined in 1848 by the German chemist Leopold Gmelin. See: Leopold Gmelin, ed., Handbuch der organischen Chemie: Organische Chemie im Allgemeinen … (Handbook of organic chemistry: Organic chemistry in general … ), 4th ed., (Heidelberg, (Germany): Karl Winter, 1848), volume 1, p. 40. From page 40: "Zu diesen Syndesmiden scheinen auch diejenigen Verbindungen zu gehören, die als Acetone im Allegemeinen (Ketone?) bezeichnet werden." (To these syndesmides*, those compounds also seem to belong, which are designated as acetones in general (ketones?).") [*Note: In 1844, the French chemist Auguste Laurent suggested a new nomenclature for organic compounds. One of his new classes of compounds was "syndesmides", which were compounds formed by the combination of two or more simpler organic molecules (from the Greek σύνδεσμος (syndesmos, union) + -ide (indicating a group of related compounds)). For example, acetone could be formed by the dry distillation of metal acetates, so acetone was the syndesmide of two acetate ions. See: Laurent, Auguste (1844) "Classification chimique," Comptes rendus, 19 : 1089–1100 ; see especially p. 1097.

[4] List of retained IUPAC names retained IUPAC names Link Archived 9 July 2023 at the Wayback Machine

[5] McMurry, John E. (1992), Organic Chemistry (3rd ed.), Belmont: Wadsworth, ISBN 0-534-16218-5

[6] Smith, Brian (November 2018). "The C=O Bond, Part VIII: Review". Spectroscopy. November 2018. 33: 24–29. Archived from the original on 13 February 2024. Retrieved 12 February 2024.

[7] Mendham, J.; Denney, R. C.; Barnes, J. D.; Thomas, M. J. K. (2000), Vogel's Quantitative Chemical Analysis (6th ed.), New York: Prentice Hall, ISBN 0-582-22628-7

[March-8] Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1

[9] Marvel, C. S.; Sperry, W. M. (1928). "Benzophenone". Organic Syntheses. 8: 26. doi:10.15227/orgsyn.008.0026.

[Vogel-10] Furniss, Brian; Hannaford, Antony; Smith, Peter; Tatchell, Austin (1996). Vogel's Textbook of Practical Organic Chemistry (5th ed.). London: Longman Science & Technical. pp. 612–623, 976–977, 982–983. ISBN 9780582462366.

[Friedel-11] Allen, C. F. H.; Barker, W. E. (1932). "Desoxybenzoin". Organic Syntheses. 12: 16. doi:10.15227/orgsyn.012.0016.

[12] Gulati, K. C.; Seth, S.R.; Venkataraman, K. (1935). "Phloroacetophenone". Organic Syntheses. 15: 70. doi:10.15227/orgsyn.015.0070.

[13] Tietze, Lutz F.; Bratz, Matthias (1993). "Dialkyl Mesoxalates by Ozonolysis of Dialkyl Benzalmalonates: Dimethyl Mesoxalate". Organic Syntheses. 71: 214. doi:10.15227/orgsyn.071.0214.

[14] Heinzelman, R. V. (1955). "o-Methoxyphenylacetone". Organic Syntheses. 35: 74. doi:10.15227/orgsyn.035.0074.

[15] Wiley, Richard H.; Borum, O. H. (1953). "3-Acetamido-2-butanone". Organic Syntheses. 33: 1. doi:10.15227/orgsyn.033.0001.

[16] Moffett, R. B.; Shriner, R. L. (1941). "ω-Methoxyacetophenone". Organic Syntheses. 21: 79. doi:10.15227/orgsyn.021.0079.

[17] Thorpe, J. F.; Kon, G. A. R. (1925). "Cyclopentanone". Organic Syntheses. 5: 37. doi:10.15227/orgsyn.005.0037.

[18] Herbst, R. M.; Shemin, D. (1939). "Phenylpyruvic acid". Organic Syntheses. 19: 77. doi:10.15227/orgsyn.019.0077.

[19] Evans, David A. (4 November 2005). "Evans pKa table" (PDF). Evans group website. Archived from the original (PDF) on 19 June 2018. Retrieved 14 June 2018.

[20] Smith, Michael B. (2013). March's Advanced Organic Chemistry (7th ed.). Hoboken, N.J.: Wiley. pp. 314–315. ISBN 978-0-470-46259-1.

[21] Haller–Bauer Reaction. homeip.net

[22] Nelson, D. L.; Cox, M. M. (2000) Lehninger, Principles of Biochemistry. 3rd Ed. Worth Publishing: New York. ISBN 1-57259-153-6.

[Ullmann-23] Siegel, Hardo; Eggersdorfer, Manfred (2000). "Ketones". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a15077 (inactive 11 September 2024). ISBN 9783527306732.{{cite book}}: CS1 maint: DOI inactive as of September 2024 (link)

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v t e Organic chemistry affixes
Carbon-based	-ane (alkane) -ene (alkene) -ine (unsaturated hydrocarbon) -yne (alkyne) alk- (nonaromatic hydrocarbon) ar- (aromatic) cyclo- (cyclic)
Oxygen-based	-al (aldehyde) -oate (ester) -oic acid (carboxylic acid) -ol (alcohol) -one (ketone) -ose (sugar)
Nitrogen-based	-ine (alkaloid) aza- (N replaces C)
Sulfur-based	thio- (S replaces O)
Counting axial atoms	meth- (1) eth- (2) prop- (3) but- (4) (and the rest are ordinary Greek/Latin prefixes)
Other	-ase (enzyme) -yl (radical)

v t e Isomerases: intramolecular oxidoreductases (EC 5.3)
5.3.1: Aldoses/Ketoses	Triosephosphate isomerase Ribose-5-phosphate isomerase Mannose phosphate isomerase Glucose isomerase
5.3.2: Keto/Enol	Phenylpyruvate tautomerase Oxaloacetate tautomerase 4-Oxalocrotonate tautomerase
5.3.3: C = C	Steroid D-isomerase Isopentenyl-diphosphate delta isomerase Vinylacetyl-CoA D-isomerase Muconolactone D-isomerase Cholestenol Delta-isomerase (EBP) Methylitaconate D-isomerase Aconitate Delta-isomerase Enoyl CoA isomerase Prostaglandin-A1 Delta-isomerase 5-carboxymethyl-2-hydroxymuconate D-isomerase Isopiperitenone D-isomerase L-dopachrome isomerase Polyenoic fatty acid isomerase
5.3.4: S-S	Protein disulfide-isomerase (PDIA3)
5.3.99: other	Prostaglandin D2 synthase/Prostaglandin-D synthase Prostaglandin E synthase Prostacyclin synthase Thromboxane-A synthase

v t e Transferases: acyltransferases (EC 2.3)
2.3.1: other than amino-acyl groups	acetyltransferases: Acetyl-Coenzyme A acetyltransferase N-Acetylglutamate synthase Choline acetyltransferase Dihydrolipoyl transacetylase Acetyl-CoA C-acyltransferase Beta-galactoside transacetylase Chloramphenicol acetyltransferase N-acetyltransferase Serotonin N-acetyl transferase HGSNAT ARD1A Histone acetyltransferase P300/CBP NAT2 palmitoyltransferases: Carnitine O-palmitoyltransferase CPT1 CPT2 Serine C-palmitoyltransferase SPTLC1 SPTLC2 other: Acyltransferase like 2 Aminolevulinic acid synthase Beta-ketoacyl-ACP synthase Glyceronephosphate O-acyltransferase Lecithin—cholesterol acyltransferase Glycerol-3-phosphate O-acyltransferase 1-acylglycerol-3-phosphate O-acyltransferase 2-acylglycerol-3-phosphate O-acyltransferase ABHD5
2.3.2: Aminoacyltransferases	Gamma-glutamyl transpeptidase Peptidyl transferase Transglutaminase Tissue transglutaminase Keratinocyte transglutaminase Factor XIII
2.3.3: converted into alkyl on transfer	Citrate synthase Decylcitrate synthase Citrate (Re)-synthase Decylhomocitrate synthase 2-methylcitrate synthase 2-ethylmalate synthase 3-ethylmalate synthase ATP citrate lyase Malate synthase HMG-CoA synthase HMGCS2 2-hydroxyglutarate synthase 3-propylmalate synthase 2-isopropylmalate synthase Homocitrate synthase Sulfoacetaldehyde acetyltransferase

v t e Transferase: nitrogenous groups (EC 2.6)
2.6.1: Transaminases	Aspartate transaminase GOT1 GOT2 Alanine transaminase GABA transaminase Tyrosine aminotransferase Kynurenine—oxoglutarate transaminase Ornithine aminotransferase Branched-chain amino acid aminotransferase Alanine—glyoxylate transaminase AGXT
2.6.3: Oximinotransferases	Oximinotransferase
2.6.99: Other	Pyridoxine 5'-phosphate synthase

v t e Transferases: sulfur-containing group (EC 2.8)
2.8.1: Sulfurtransferases	Thiosulfate sulfurtransferase Rhodanese 3-mercaptopyruvate sulfurtransferase thiosulfate—thiol sulfurtransferase tRNA sulfurtransferase thiosulfate—dithiol sulfurtransferase biotin synthase cysteine desulfurase lipoyl synthase molybdenum cofactor sulfurtransferase thiazole synthase molybdopterin synthase sulfurtransferase molybdopterin synthase tRNA-uridine 2-sulfurtransferase () tRNA-5-taurinomethyluridine 2-sulfurtransferase () tRNA-5-methyluridine⁵⁴ 2-sulfurtransferase () L-aspartate semialdehyde sulfurtransferase ()
2.8.2: Sulfotransferases	aryl sulfotransferase amine sulfotransferase estrone sulfotransferase chondroitin 4-sulfotransferase choline sulfotransferase UDP-N-acetylgalactosamine-4-sulfate sulfotransferase heparan sulfate-glucosamine N-sulfotransferase tyrosine-ester sulfotransferase Renilla-luciferin sulfotransferase galactosylceramide sulfotransferase psychosine sulfotransferase bile salt sulfotransferase steroid sulfotransferase thiol sulfotransferase chondroitin 6-sulfotransferase cortisol sulfotransferase triglucosylalkylacylglycerol sulfotransferase protein-tyrosine sulfotransferase keratan sulfotransferase aryl-sulfate sulfotransferase (heparan sulfate)-glucosamine 3-sulfotransferase 1 desulfoglucosinolate sulfotransferase flavonol 3-sulfotransferase quercetin-3-sulfate 3′-sulfotransferase quercetin-3-sulfate 4′-sulfotransferase quercetin-3,3′-bissulfate 7-sulfotransferase (heparan sulfate)-glucosamine 3-sulfotransferase 2 (heparan sulfate)-glucosamine 3-sulfotransferase 3 petromyzonol sulfotransferase scymnol sulfotransferase N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase glycochenodeoxycholate sulfotransferase dermatan 4-sulfotransferase desulfo-A47934 sulfotransferase () trehalose 2-sulfotransferase () aliphatic desulfoglucosinolate sulfotransferase () hydroxyjasmonate sulfotransferase () ω-hydroxy-β-dihydromenaquinone-9 sulfotransferase (*) Alcohol sulfotransferase Tyrosylprotein sulfotransferase
2.8.3: CoA-transferases	Propionate CoA-transferase oxalate CoA-transferase malonate CoA-transferase 3-oxoacid CoA-transferase 3-oxoadipate CoA-transferase succinyl-CoA—Dcitramalate CoA-transferase acetate CoA-transferase butyrate—acetoacetate CoA-transferase citrate CoA-transferase citramalate CoA-transferase glutaconate CoA-transferase succinate—hydroxymethylglutarate CoA-transferase 5-hydroxypentanoate CoA-transferase succinyl-CoA:(R)-benzylsuccinate CoA-transferase formyl-CoA transferase cinnamoyl-CoA:phenyllactate CoA-transferase succinyl-CoA:acetate CoA-transferase () CoA:oxalate CoA-transferase () succinyl-CoA—D-citramalate CoA-transferase () L-carnitine CoA-transferase () succinyl-CoA—L-malate CoA-transferase () caffeate CoA-transferase () (R)-2-hydroxy-4-methylpentanoate CoA-transferase () bile acid CoA-transferase () succinyl-CoA:mesaconate CoA transferase (*)
2.8.4: Alkylthio	2.8.4: Coenzyme-B sulfoethylthiotransferase arsenate-mycothiol transferase tRNA-2-methylthio-N⁶-dimethylallyladenosine synthase () [ribosomal protein S12] (aspartate⁸⁹-C³)-methylthiotransferase () tRNA (N⁶-L-threonylcarbamoyladenosine³⁷-C²)-methylthiotransferase (*)
2.8.5:	2.8.5: S-sulfo-L-cysteine synthase (3-phospho-L-serine-dependent) () L-cysteine S-thiosulfotransferase ()