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Cycloalkenes, Food Additives


Cyclic compounds (31)
Six-membered rings (24)
Cyclohexenes (22)
Ketones (11)
Cosmetics chemicals (9)
Perfume ingredients (8)
Alkenes (6)
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Alcohols (4)
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Cyclopentenes (2)
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Four-membered rings (1)
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Terpenes and terpenoids (1)
Thiols (1)


Sigma Aldrich (19)
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Dipentene (7705-14-8, 9003-73-0, 8008-56-8, 65996-98-7, 8008-57-9, 138-86-3, 8028-38-4, 0008008-57-9)  
limonene  ·  (+)-limonene  ·  limonene, (S)-isomer
Limonene is a clear, colorless liquid hydrocarbon classified as a cyclic monoterpene, and is the major component in oil of citrus fruit peels. The D-isomer occurring more commonly in nature as the fragrance of oranges is a flavoring agent in food manufacturing. It is also used in chemical synthesis as a precursor to carvone and as a renewables-based solvent in cleaning products.
benzene (71-43-2, 26181-88-4, 8030-30-6, 71-43-2, 1076-43-3)  
Benzol  ·  Benzole  ·  Cyclohexatriene
Benzene is an important organic chemical compound with the chemical formula C6H6. The benzene molecule is composed of six carbon atoms joined in a ring with one hydrogen atom attached to each. As it contains only carbon and hydrogen atoms, benzene is classed as a hydrocarbon.
D-Limonene (5989-27-5, 68606-81-5, 5989-27-5, 65996-98-7)  
limonene  ·  dipentene  ·  (+)-limonene
ALPHA-PINENE (80-56-8, 2437-95-8, 25766-18-1, 67762-73-6, 7785-70-8)  
Wilt Pruf  ·  alpha-pinene, pinene  ·  2-pinene
α-Pinene is an organic compound of the terpene class, one of two isomers of pinene. It is an alkene and it contains a reactive four-membered ring. It is found in the oils of many species of many coniferous trees, notably the pine.
ISOPHORONE (78-59-1)  
Isophorone is an α,β-unsaturated cyclic ketone. It is a colorless liquid with a characteristic peppermint-like odor, although commercial samples can appear yellowish. Used as a solvent and as a precursor to polymers, it is produced on a large scale industrially.
beta-carotene (7235-40-7)  
beta Carotene  ·  Betacarotene  ·  Solatene
β-Carotene is an organic, strongly colored red-orange pigment abundant in plants and fruits. It is a member of the carotenes, which are terpenoids (isoprenoids), synthesized biochemically from eight isoprene units and thus having 40 carbons. Among the carotenes, β-carotene is distinguished by having beta-rings at both ends of the molecule.
alpha-TERPINEOL (8000-41-7, 10482-56-1, 68797-63-7, 2438-12-2, 98-55-5)  
alpha-terpineol, sodium salt  ·  1-alpha-terpineol  ·  D-alpha-terpineol
Terpineol is a monoterpene alcohol that has been isolated from a variety of sources such as cajuput oil, pine oil, and petitgrain oil. There are four isomers, alpha-, beta-, gamma-terpineol, and terpinen-4-ol. beta- and gamma-terpineol differ only by the location of the double bond.
trans-jasmone (6261-18-3, 488-10-8)  
jasmone  ·  cis-jasmone  ·  (Z)-3-methyl-2-(2-pentenyl)-2-cyclopenten-1-one
Jasmone is an organic compound, which is a volatile portion of the oil from jasmine flowers. It is a colorless to pale yellow liquid. Jasmone can exist in two isomeric forms with differing geometry around the pentenyl double bond, cis-jasmone and trans-jasmone.
NOOTKATONE (4674-50-4, 28834-25-5)  
nootkatone, (4R-(4alpha,4aalpha,6beta))-isomer
Nootkatone is a natural organic compound and is the most important and expensive aromatic of grapefruit. It is a sesquiterpene and a ketone. Nootkatone was previously thought to be one of the main chemical components of the smell and flavour of grapefruits.
Astaxanthin (472-61-7)  
astaxanthine  ·  E-astaxanthin
Astaxanthin is a keto-carotenoid. It belongs to a larger class of chemical compounds known as terpenes (in Asthaxanthin's case, a tetraterpenoid); terpenes are built from five carbon precursors; isopentenyl diphosphate (or IPP) and dimethylallyl diphosphate (or DMAPP). Astaxanthin is classified as a xanthophyll (originally derived from a word meaning "yellow leaves" since yellow plant leaf pigments were the first recognized of the xanthophyll family of carotenoids), but currently employed to describe carotenoid compounds that have oxygen-containing moities, hydroxyl (-OH) or ketone (C=O), such as zeaxanthin and canthaxanthin.
ALPHA-PHELLANDRENE (4221-98-1, 1329-99-3, 99-83-2, 34448-33-4)  
alpha phellandrene, (S+)-isomer  ·  alpha phellandrene, (R)-isomer  ·  5-isopropyl-2-methyl-1,3-cyclohexadiene
Phellandrene is the name for a pair of organic compounds that have a similar molecular structure and similar chemical properties. α-Phellandrene and β-phellandrene are cyclic monoterpenes and are double-bond isomers. In α-phellandrene, both double bonds are endocyclic and in β-phellandrene, one of them is exocyclic.
beta-terpinene  ·  1,4-p-menthadiene  ·  gamma-terpinene
The terpinenes are a group of isomeric hydrocarbons that are classified as terpenes. They each have the same molecular formula and carbon framework, but they differ in the position of carbon-carbon double bonds. α-Terpinene has been isolated from cardamom and marjoram oils, and from other natural sources.
CARVEOL (2102-59-2, 99-48-9)  
Carveol is a natural unsaturated, monocyclic monoterpenoid alcohol that is a constituent of spearmint essential oil in the form of cis-(−)-carveol. It is a colorless fluid soluble in oils, but insoluble in water and has an odor and flavor that resemble those of spearmint and caraway. Consequently, it is used as a fragrance in cosmetics and as a flavor additive in the food industry.
(-)-Limonene (5989-54-8)  
limonene  ·  dipentene  ·  (+)-limonene
Lutein (127-40-2)  
Lutein G  ·  Lutein F  ·  beta,epsilon-Carotene-3, 3'-Diol, (3R,3'R,6'S)-
Xanthophylls (originally phylloxanthins) are yellow pigments that occur widely in nature and form one of two major divisions of the carotenoid group; the other division is formed by the carotenes. The name is from Greek xanthos (ξανθός, "yellow") and phyllon (φύλλον, "leaf"), due to their formation of the yellow band seen in early chromatography of leaf pigments.
Perilla alcohol (536-59-4)  
perillyl alcohol  ·  (-)-p-mentha-1,8-dien-7-ol  ·  dihydrocuminyl alcohol
Perillyl alcohol (IUPAC name: [4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol) and its precursor limonene are naturally occurring monocyclic terpenes derived from the mevalonate pathway in plants. Perillyl alcohol can be found in the essential oils of various plants, such as lavender, lemongrass, sage, and peppermint. It has a number of manufacturing, household, and medical applications.
Damascenone (23696-85-7, 23726-93-4)  
Damascenones are a series of closely related chemical compounds that are components of a variety of essential oils. The damascenones belong to a family of chemicals known as rose ketones, which also includes damascones and ionones. beta-Damascenone is a major contributor to the aroma of roses, despite its very low concentration, and is an important fragrance chemical used in perfumery.
PERILLALDEHYDE (2111-75-3)  
perilla aldehyde  ·  4-mentha-1,8-dien-7-al  ·  perillaldehyde, (+)-isomer
Perillaldehyde, or perilla aldehyde, is a natural organic compound found most abundantly in the annual herb perilla, but also in a wide variety of other plants and essential oils. It is a monoterpenoid containing an aldehyde functional group. Perillaldehyde, or volatile oils from perilla that are rich in perillaldehyde, are used as food additives for flavoring and in perfumery to add spiciness.
LEVOMENOL (515-69-5, 23089-26-1)  
bisabolol  ·  bisabolol, (-)-isomer  ·  (+)-4-epi-alpha-bisabolol
Bisabolol, or more formally α-(−)-bisabolol or also known as levomenol, is a natural monocyclic sesquiterpene alcohol. It is a colorless viscous oil that is the primary constituent of the essential oil from German chamomile (Matricaria recutita) and Myoporum crassifolium. It is poorly soluble in water and glycerin, but soluble in ethanol.
Canthaxanthin (514-78-3)  
Canthaxanthine  ·  Roxanthin Red 10  ·  Orobronze
Canthaxanthin  ( listen) is a keto-carotenoid pigment widely distributed in nature. Carotenoids belong to a larger class of phytochemicals known as terpenoids. The chemical formula of canthaxanthin is C40H52O2.
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