Ketones spices

Organic compounds with both ends of carbonyl connected with the hydrocarbon are called ketone. When the hydrocarbon group connected to both ends of the carbonyl group is aliphatic hydrocarbyl group, the compound belongs to aliphatic ketone; when there is at least one end of the carbonyl group connected with aromatic hydrocarbon group, the compound is called aromatic ketone. According to the number of carbonyl groups contained in the molecule, ketones can be divided into monoketone and diketones. Saturated monoaldehyde and ketone having the same number of carbon atoms are isomers with each other.
There are nearly 100 kinds of ketones spices with the chemical properties being generally stable but with varying degree of color change. Among them, aliphatic ketone has strong aroma with some individual species being used in only a small amount in the formulation of daily flavor. Aromatic ketones are only used in small quantities in individual flavors. Among those cyclic ketones consisting of 5 or 6 carbons or multiple carbons, widely used varieties include ionone, methyl ionone and damascone. Macrocyclic ketone containing more than 15 carbons is a composition of the natural animal spices. However, owning to the high price of synthetic products, it is only used at high-grade perfume fragrance.

Lower aliphatic ketones (both hydrocarbon groups are aliphatic hydrocarbons) are liquid of special odor smell. High-grade ketones are more fragrant, being easily soluble in water, ether and ethanol. With the increase in carbon number, they have decreased solubility but increased viscosity. Ketones of more than six carbon atoms are generally insoluble in water; higher aliphatic ketones are solids; aromatic ketones (both hydrocarbon groups are aromatic) are mostly solids. The simplest mono-ketone is acetone; the simplest mono-aromatic ketone is benzophenone. Lower ketone has a lower boiling point than alcohol of similar relative molecular mass, which is mainly due to hydrogen bonds can’t form between ketone molecules, thus having no association effect. But the boiling point of the higher ketone is gradually close to that of the alcohol of similar relative molecular mass.

Ketone has relatively active chemical activity, this is because the carbon-oxygen double bond of carbonyl group contains one α bond and one π bond, being an unsaturated polar bond. The oxygen atom has a stronger negative charge than the carbon, thus strongly attracting electron, enhancing the density of the electronic cloud around the oxygen atom while carbon atom has lower electronic cloud density, thus leading to a certain polarity with carbon atoms become positive carbon and oxygen atoms become negative oxygen ions. Compare those two, the former one is more active than the latter one, and is susceptible to the attack of nucleophilic reagents carrying charges or lone electron pair, inducing the occurrence of addition reaction, so the addition of ketones is mostly nucleophilic addition. For example, ketone and nucleophiles such as HCN, NH2OH and NH2NH2 can easily have additions reaction and these addition reactions are mostly reversible.

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Structure Chemical Name CAS MF
Vanillylidenacetone Vanillylidenacetone 1080-12-2 C11H12O3
Indole-3-acetone Indole-3-acetone 1201-26-9 C11H11NO
3-TETRADECANONE 3-TETRADECANONE 629-23-2 C14H28O
2-methylcyclopentenone 2-methylcyclopentenone 1120-73-6 C6H8O
DIHYDRO-BETA-IONONE DIHYDRO-BETA-IONONE 17283-81-7 C13H22O
CARVONE CARVONE 99-49-0 C10H14O
4'-Chloro-2-phenylacetophenone 4'-Chloro-2-phenylacetophenone 1889-71-0 C14H11ClO
3,4-(METHYLENEDIOXY)BENZYLIDENEACETONE 3,4-(METHYLENEDIOXY)BENZYLIDENEACETONE 3160-37-0 C11H10O3
4-ETHYLPHENYLACETONE 4-ETHYLPHENYLACETONE 75251-24-0 C11H14O
3-ethyl-2-hydroxy-4-methylcyclopent-2-en-1-one 3-ethyl-2-hydroxy-4-methylcyclopent-2-en-1-one 42348-12-9 C8H12O2
(Z)-beta-damascone (Z)-beta-damascone 23726-92-3 C13H20O
N-TETRADECANOPHENONE N-TETRADECANOPHENONE 4497-05-6 C20H32O
4'-METHOXY-2-PHENYLACETOPHENONE 4'-METHOXY-2-PHENYLACETOPHENONE 1023-17-2 C15H14O2
Zearalenone Zearalenone 17924-92-4 C18H22O5
2,6-DICHLOROPHENYLACETONE 2,6-DICHLOROPHENYLACETONE 93457-06-8 C9H8Cl2O
14-HEPTACOSANONE 14-HEPTACOSANONE 542-50-7 C27H54O
DIHYDO-ALPHA-IONONE DIHYDO-ALPHA-IONONE 31499-72-6 C13H22O
(2,4-Dimethoxyphenyl)acetone (2,4-Dimethoxyphenyl)acetone 831-29-8 C11H14O3
2-Cyclohexen-1-one, 2-hydroxy- 2-Cyclohexen-1-one, 2-hydroxy- 10316-66-2 C6H8O2
4,4-DIPHENYL-2-BUTANONE 4,4-DIPHENYL-2-BUTANONE 5409-60-9 C16H16O
3,4-dihydroxyphenylacetone 3,4-dihydroxyphenylacetone 2503-44-8 C9H10O3
3-HEPTYLDIHYDRO-5-METHYL-2(3H)-FURANONE 3-HEPTYLDIHYDRO-5-METHYL-2(3H)-FURANONE 40923-64-6 C12H22O2
DAMASCONE DAMASCONE 23726-91-2 C13H20O
(3-(TRIFLUOROMETHOXY)PHENYL)ACETONE (3-(TRIFLUOROMETHOXY)PHENYL)ACETONE 42823-09-6 C9H10F3N5O.ClH
4-HYDROXY-3-METHOXYPHENYLACETONE 4-HYDROXY-3-METHOXYPHENYLACETONE 2503-46-0 C10H12O3
2-CHLORO-6-FLUOROPHENYLACETONE 2-CHLORO-6-FLUOROPHENYLACETONE 93839-16-8 C9H8ClFO
4'-AMINOBUTYROPHENONE 4'-AMINOBUTYROPHENONE 1688-71-7 C10H13NO
4'-METHYL-2-PHENYLACETOPHENONE 4'-METHYL-2-PHENYLACETOPHENONE 2001-28-7 C15H14O
5-HYDROXY-2-DECENOIC ACID LACTONE 5-HYDROXY-2-DECENOIC ACID LACTONE 16400-72-9 C12H20O2
2,5-DIMETHYLPHENYLACETONE 2,5-DIMETHYLPHENYLACETONE 53291-89-7 C11H14O
3,4,5-TRIMETHOXYPHENYLACETONE 3,4,5-TRIMETHOXYPHENYLACETONE 16603-18-2 C12H16O4
2-BROMO-1-(3-BROMOPHENYL)-1-PROPANONE 2-BROMO-1-(3-BROMOPHENYL)-1-PROPANONE 76650-08-3 C9H8Br2O
5-ethyl-2-hydroxy-3-methylcyclopent-2-en-1-one 5-ethyl-2-hydroxy-3-methylcyclopent-2-en-1-one 53263-58-4 C8H12O2
Delta Damascone Delta Damascone 57378-68-4 C13H20O
hydroxypentanone,3-hydroxy-2-pentanone hydroxypentanone,3-hydroxy-2-pentanone 3142-66-3 C5H10O2
NOOTKATONE(SG) NOOTKATONE(SG)
PIPERONYL METHYL KETONE PIPERONYL METHYL KETONE 4676-39-5 C10H10O3
Prohydrojasmon Prohydrojasmon 158474-72-7 C15H26O3
(4-CARBOXYPHENYL)ACETONE (4-CARBOXYPHENYL)ACETONE 15482-54-9 C10H10O3
Bicyclohomofarnesal Bicyclohomofarnesal 3243-36-5 C16H26O
3-METHYLPHENYLACETONE 3-METHYLPHENYLACETONE 18826-61-4 C10H12O
BACCARTOL BACCARTOL 68916-62-1
4-Hydroxybenzylideneacetone 4-Hydroxybenzylideneacetone 3160-35-8 C10H10O2
4-NITROPHENYLACETONE 4-NITROPHENYLACETONE 5332-96-7 C9H9NO3
3-(hydroxymethyl)heptan-2-one 3-(hydroxymethyl)heptan-2-one 65405-68-7 C8H16O2
2-Mercapto-1-phenylethanone 2-Mercapto-1-phenylethanone C8H8OS
2,6-DIFLUOROPHENYLACETONE 2,6-DIFLUOROPHENYLACETONE 101712-20-3 C9H8F2O
ISOLONGIFOLANONE ISOLONGIFOLANONE 29461-14-1 C15H24O
methylheptenone methylheptenone 409-02-9 C8H14O
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