Chemical Formula: C12H20O2

Chemical Formula C12H20O2

Found 233 metabolite its formula value is C12H20O2

Geranyl acetate

Geranyl acetate, food grade (71\\% geranyl acetate, 29\\% citronellyl acetate)

C12H20O2 (196.14632200000003)


Geranyl acetate is a clear colorless liquid with an odor of lavender. (NTP, 1992) Geranyl acetate is a monoterpenoid that is the acetate ester derivative of geraniol. It has a role as a plant metabolite. It is an acetate ester and a monoterpenoid. It is functionally related to a geraniol. Geranyl acetate is a natural product found in Nepeta nepetella, Xylopia sericea, and other organisms with data available. See also: Lemon oil, cold pressed (part of); Coriander Oil (part of); Java citronella oil (part of). Neryl acetate is found in cardamom. Neryl acetate is found in citrus, kumquat and pummelo peel oils, ginger, cardamon, clary sage, myrtle leaf and myrtle berries. Neryl acetate is a flavouring agent A monoterpenoid that is the acetate ester derivative of geraniol. Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent[1]. Geranyl acetate can induces cell apoptosis[2]. Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent[1]. Geranyl acetate can induces cell apoptosis[2].

   

(-)-Bornyl acetate

(1S,2R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetic acid

C12H20O2 (196.14632200000003)


(-)-Bornyl acetate is isolated from Blumea balsamifera, Jasonia sp., Salvia fruticosa, carrot, rosemary, sage and lavender oil. (-)-Bornyl acetate is a flavouring agent [CCD]. Isolated from Blumea balsamifera, Jasonia species, Salvia fruticosa, carrot, rosemary, sage and lavender oil. Flavouring agent [CCD] (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].

   

(-)-Linalyl acetate

(+-)-3,7-Dimethylocta-1,6-dien-3-yl acetic acid

C12H20O2 (196.14632200000003)


Linalyl acetate belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. The biosynthesis of monoterpenes is known to occur mainly through the methyl-eritritol-phosphate (MEP) pathway in the plastids. Geranyl diphosphate (GPP) is a key intermediate in the biosynthesis of monoterpenes. Linalyl acetate occurs naturally and is found in many flowers and spices. It can be isolated from numerous plants and essential oils, such as clary sage, lavender, lemon, cardamom. It is also one of the principal components of the essential oils of bergamot and lavender. Chemically, it is the acetate ester of linalool, and the two often occur in conjunction. Linalyl acetate is a flavouring ingredient and it tastes similar to how it smells, with a pleasant fruity odor reminiscent of bergamot mint oil. It is found in Eau de Cologne mint. As a volatile terpene, linalyl acetate is also combustible. Linalyl acetate, also known as (-)-linalyl acetic acid, is a member of the class of compounds known as acyclic monoterpenoids. Acyclic monoterpenoids are monoterpenes that do not contain a cycle. Thus, linalyl acetate is considered to be an isoprenoid lipid molecule. Linalyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Linalyl acetate can be found in cornmint and peppermint, which makes linalyl acetate a potential biomarker for the consumption of these food products. Linalyl acetate is a naturally occurring phytochemical found in many flowers and spice plants. It is one of the principal components of the essential oils of bergamot and lavender. Chemically, it is the acetate ester of linalool, and the two often occur in conjunction . Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1]. Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1].

   

Ethyl 2Z,4E-decadienoic acid

(2E,4Z)-2,4-Decadienoic acid, ethyl ester

C12H20O2 (196.14632200000003)


Constituent of odoriferous principle of Bartlett pearsand is) also present in fresh apple, Vitis subspecies, quince and spineless monkey orange (Strychnos madagasc). Flavouring agent. Pear ester is found in pomes, fruits, and pear. Ethyl 2Z,4E-decadienoic acid is a flavouring material.

   

alpha-Terpineol acetate

2-(4-methylcyclohex-3-en-1-yl)propan-2-yl acetate

C12H20O2 (196.14632200000003)


alpha-Terpineol acetate, also known as a-terpineol acetic acid or p-menth-1-en-8-yl acetate, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. alpha-Terpineol acetate is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2]. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2].

   

beta-Terpinyl acetate

Cyclohexanol, 1-methyl-4-(1-methylethenyl)-, 1-acetate

C12H20O2 (196.14632200000003)


   

gamma-Terpinyl acetate

Cyclohexanol, 1-methyl-4-(1-methylethylidene)-, 1-acetate

C12H20O2 (196.14632200000003)


   

Allyl 3-cyclohexylpropionate

2-Propenyl 3-cyclohexylpropanoic acid

C12H20O2 (196.14632200000003)


Pineapple flavourant. Pineapple flavourant

   

Fenchyl acetate

(1S,2S,4R)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-yl acetic acid

C12H20O2 (196.14632200000003)


(-)-alpha-Fenchyl acetate is a flavouring ingredient, together with stereoisomers. Flavouring ingredient, together with stereoisomers Same as: D09740

   

Linalyl acetate

3,7-Dimethyl-3-acetate(3R)-1,6-octadien-3-ol

C12H20O2 (196.14632200000003)


Linalyl acetate, also known as 3,7-dimethylocta-1,6-dien-3-yl acetate, is a monoterpenoid that is the acetate ester of linalool. It forms a principal component of the essential oils from bergamot and lavender. It is an acetate ester and a monoterpenoid that derives from linalool. Linalyl acetate is isolated from numerous plants and essential oils, e.g. clary sage, lavender, lemon etc., and it is used as a flavouring ingredient. Synthetic linalyl acetate is sometimes used as an adulterant in essential oils to make them more marketable. Isolated from numerous plants and essential oils, e.g. clary sage, lavender, lemon etc. Flavouring ingredient Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1]. Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1].

   

Dihydro-5-(2-octenyl)-2(3H)-furanone

6-Dodecenyl-laquo gammaraquo -lactone

C12H20O2 (196.14632200000003)


Dihydro-5-(2-octenyl)-2(3H)-furanone is found in milk and milk products. Dihydro-5-(2-octenyl)-2(3H)-furanone is isolated from butterfat. Dihydro-5-(2-octenyl)-2(3H)-furanone is a flavouring ingredien Isolated from butterfat. Flavouring ingredient. Dihydro-5-(2-octenyl)-2(3H)-furanone is found in milk and milk products.

   

Yuzu lactone

(10E)-1-oxacyclotridec-10-en-2-one

C12H20O2 (196.14632200000003)


Yuzu lactone is found in citrus. Yuzu lactone is a constituent of Citrus junos (yuzu). Constituent of Citrus junos (yuzu). Yuzu lactone is found in citrus.

   

6-Heptyl-5,6-dihydro-2H-pyran-2-one

6-Heptyl-5,6-dihydro-2H-pyran-2-one

C12H20O2 (196.14632200000003)


(±)-6-Heptyl-5,6-dihydro-2H-pyran-2-one is a flavouring ingredient. It is used as a food additive .

   

Dihydrocarveol acetate

2-Methyl-5-(prop-1-en-2-yl)cyclohexyl acetic acid

C12H20O2 (196.14632200000003)


Flavouring ingredient. Dihydrocarveol acetate is found in many foods, some of which are caraway, wild celery, spearmint, and anise. Dihydrocarveol acetate is found in anise. Dihydrocarveol acetate is a flavouring ingredient.

   

(S)-Santolina acetate

3-Ethenyl-2,5-dimethylhex-4-en-2-yl acetic acid

C12H20O2 (196.14632200000003)


(S)-Santolina acetate is a constituent of Artemisia vulgaris (mugwort). Constituent of Artemisia vulgaris (mugwort)

   

Artemisia alcohol acetate

3,3,6-Trimethylhepta-1,5-dien-4-yl acetic acid

C12H20O2 (196.14632200000003)


Artemisia alcohol acetate is from Artemisia specie From Artemisia subspecies

   

Methyl 2-undecynoate

2-Undecynoic acid, methyl ester

C12H20O2 (196.14632200000003)


Methyl 2-undecynoate is a flavouring ingredien Flavouring ingredient

   

cis-3-Hexenyl trans-4-hexenoate

(3Z)-Hex-3-en-1-yl (4E)-hex-4-enoic acid

C12H20O2 (196.14632200000003)


cis-3-Hexenyl trans-4-hexenoate is found in herbs and spices. cis-3-Hexenyl trans-4-hexenoate is a constituent of Spanish oregano (Coridothymus capitatus) Constituent of Spanish oregano (Coridothymus capitatus). cis-3-Hexenyl trans-4-hexenoate is found in herbs and spices.

   

alpha-Campholene acetate

2-(2,2,3-Trimethylcyclopent-3-en-1-yl)ethyl acetic acid

C12H20O2 (196.14632200000003)


xi-Campholene acetate is found in fruits. xi-Campholene acetate is a flavouring ingredient. alpha-Campholene acetate is a constituent of Juniperus communis (juniper It is used as a food additive .

   

(Z)-4-Hydroxy-6-dodecenoic acid lactone

(Z)-6-Dodecenyl-laquo gammaraquo -lactone

C12H20O2 (196.14632200000003)


(Z)-4-Hydroxy-6-dodecenoic acid lactone is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]")

   

(3R,3aR,7aS)-3-Butylhexahydro-1(3H)-isobenzofuranone

(3xi,3ax,7ax)-3-Butylhexahydro-1(3H)-isobenzofuranone

C12H20O2 (196.14632200000003)


(3xi,3ax,7ax)-3-Butylhexahydro-1(3H)-isobenzofuranone is found in green vegetables. (3xi,3ax,7ax)-3-Butylhexahydro-1(3H)-isobenzofuranone is a constituent of Apium graveolens, and black salsify (Scorzonera hispanica). Constituent of Apium graveolens, and black salsify (Scorzonera hispanica). (3xi,3ax,7ax)-3-Butylhexahydro-1(3H)-isobenzofuranone is found in green vegetables.

   

p-Menth-1-en-9-ol acetate

3-Cyclohexene-1-ethanol, beta,4-dimethyl-, acetate

C12H20O2 (196.14632200000003)


p-Menth-1-en-9-ol acetate is found in mandarin orange (clementine, tangerine). p-Menth-1-en-9-ol acetate is a flavouring ingredient. Flavouring ingredient. p-Menth-1-en-9-ol acetate is found in spearmint.

   

cis-3-Hexenyl cis-3-hexenoate

(3Z)-3-Hexen-1-yl ester(3Z)-3-hexenoic acid

C12H20O2 (196.14632200000003)


cis-3-Hexenyl cis-3-hexenoate is a flavouring ingredient. Flavouring ingredient

   

cis-3-Hexenyl trans-2-hexenoate

Hex-cis-3-enyl hex-trans-2-enoic acid

C12H20O2 (196.14632200000003)


Cis-3-hexenyl trans-2-hexenoate, also known as (3z)-3-hexenyl (2e)-2-hexenoate or fema 3928, is a member of the class of compounds known as fatty acid esters. Fatty acid esters are carboxylic ester derivatives of a fatty acid. Thus, cis-3-hexenyl trans-2-hexenoate is considered to be a fatty ester lipid molecule. Cis-3-hexenyl trans-2-hexenoate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Cis-3-hexenyl trans-2-hexenoate has a fruity, green, and pear taste. cis-3-Hexenyl trans-2-hexenoate is a flavouring ingredient.

   

Isopulegol acetate

Cyclohexanol,5-methyl-2-(1-methylethenyl)-, 1-acetate, (1R,2S,5R)-

C12H20O2 (196.14632200000003)


Isopulegol acetate is found in peppermint. Isopulegol acetate is a flavouring agent. Flavouring agent. (-)-Isopulegol acetate is found in peppermint.

   

3,7-Dimethyl-2,6-octadien-1-ylacetate

3,7-Dimethylocta-2,6-dien-1-yl acetic acid

C12H20O2 (196.14632200000003)


3,7-Dimethyl-2,6-octadien-1-ylacetate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol.

   

Dodecadienoic acid

dodeca-2,4-dienoic acid

C12H20O2 (196.14632200000003)


Dodecadienoic acid, also known as dodecadienoate, is a member of the class of compounds known as medium-chain fatty acids. Medium-chain fatty acids are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. Dodecadienoic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Dodecadienoic acid can be found in common buckwheat and dandelion, which makes dodecadienoic acid a potential biomarker for the consumption of these food products.

   

cis-Sabinene hydrate acetate

(2R,5S)-2-methyl-5-(propan-2-yl)bicyclo[3.1.0]hexan-2-yl acetate

C12H20O2 (196.14632200000003)


Cis-sabinene hydrate acetate is also known as cis-sabinene hydric acid acetic acid. Cis-sabinene hydrate acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Cis-sabinene hydrate acetate can be found in sweet marjoram, which makes cis-sabinene hydrate acetate a potential biomarker for the consumption of this food product.

   

alpha-Fenchyl acetate

1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl acetate

C12H20O2 (196.14632200000003)


Fenchyl acetate, also known as fenchyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Fenchyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Fenchyl acetate is a sweet, citrus, and fir tasting compound found in sweet basil, which makes fenchyl acetate a potential biomarker for the consumption of this food product.

   

Bornyl acetate

(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl acetate

C12H20O2 (196.14632200000003)


Bornyl acetate, also known as bornyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Bornyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Bornyl acetate is a camphor, cedar, and herbal tasting compound and can be found in a number of food items such as nutmeg, rosemary, spearmint, and sunflower, which makes bornyl acetate a potential biomarker for the consumption of these food products. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

(±)-Isobornyl acetate

(1S,2S,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetic acid

C12H20O2 (196.14632200000003)


Flavour and fragrance ingredient [CCD]. (±)-Isobornyl acetate is found in spearmint and rosemary.

   

7-Acetoxy-7-methyl-3-methylene-1-octene

2-methyl-6-methylideneoct-7-en-2-yl acetate

C12H20O2 (196.14632200000003)


7-acetoxy-7-methyl-3-methylene-1-octene is a member of the class of compounds known as carboxylic acid esters. Carboxylic acid esters are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group). 7-acetoxy-7-methyl-3-methylene-1-octene is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). 7-acetoxy-7-methyl-3-methylene-1-octene is a bergamot, citrus, and floral tasting compound found in pot marjoram, which makes 7-acetoxy-7-methyl-3-methylene-1-octene a potential biomarker for the consumption of this food product.

   

(+)-beta-Fenchyl acetate

(1R,2S,4S)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-yl acetic acid

C12H20O2 (196.14632200000003)


(+)-beta-fenchyl acetate, also known as (+)-beta-fenchyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other (+)-beta-fenchyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (+)-beta-fenchyl acetate can be found in fennel, which makes (+)-beta-fenchyl acetate a potential biomarker for the consumption of this food product. (+)-beta-fenchyl acetate, also known as (+)-β-fenchyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other (+)-beta-fenchyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (+)-beta-fenchyl acetate can be found in fennel, which makes (+)-beta-fenchyl acetate a potential biomarker for the consumption of this food product.

   

trans-Acetate-1-methyl-2-(1-methylethenyl)-cyclobutaneethanol

trans-Acetate-1-methyl-2-(1-methylethenyl)-cyclobutaneethanol

C12H20O2 (196.14632200000003)


   

lavandulyl acetate

(-)-dihydrocarvyl acetate

C12H20O2 (196.14632200000003)


   
   

beta-Isocyclolavandulyl acetate

beta-Isocyclolavandulyl acetate

C12H20O2 (196.14632200000003)


   

Bornylacetate

(+)-Bornyl acetate

C12H20O2 (196.14632200000003)


Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

neryl acetate

acetic acid geranyl ester

C12H20O2 (196.14632200000003)


Found in citrus, kumquat and pummelo peel oils, ginger, cardamon, clary sage, myrtle leaf and myrtle berries. Flavouring agent Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent[1]. Geranyl acetate can induces cell apoptosis[2]. Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent[1]. Geranyl acetate can induces cell apoptosis[2]. Neryl acetate is a chemical compound isolated from citrus oils[1]. Neryl acetate is a chemical compound isolated from citrus oils[1].

   

pichtosin

(1S,2R,4S)-(-)-Bornyl acetate

C12H20O2 (196.14632200000003)


Flavour and fragrance ingredient [CCD]. (±)-Isobornyl acetate is found in spearmint and rosemary. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].

   

alpha-Fenchyl acetate

1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl acetate

C12H20O2 (196.14632200000003)


Fenchyl acetate, also known as fenchyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Fenchyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Fenchyl acetate is a sweet, citrus, and fir tasting compound found in sweet basil, which makes fenchyl acetate a potential biomarker for the consumption of this food product.

   
   
   
   

2,6-Dimethyl-2,6-octadien-8-yl acetate

2,6-Dimethyl-2,6-octadien-8-yl acetate

C12H20O2 (196.14632200000003)


   

Ethyl chrysanthemate

Chrysanthemic Acid, Ethyl Ester

C12H20O2 (196.14632200000003)


D010575 - Pesticides > D007306 - Insecticides > D011722 - Pyrethrins

   

[2,2-dimethyl-3-(prop-1-en-2-yl)cyclobutyl]methyl acetate

[2,2-dimethyl-3-(prop-1-en-2-yl)cyclobutyl]methyl acetate

C12H20O2 (196.14632200000003)


   

(ent-4alpha)-4-Hydroxy-11,12,13-trinor-7-eudesmanone

(ent-4alpha)-4-Hydroxy-11,12,13-trinor-7-eudesmanone

C12H20O2 (196.14632200000003)


   
   

thymohydroquinone dimethyl ether

thymohydroquinone dimethyl ether

C12H20O2 (196.14632200000003)


   

1-(2-Acetoxyethyl)-2-isopropenyl-1-methylcyclobutane

1-(2-Acetoxyethyl)-2-isopropenyl-1-methylcyclobutane

C12H20O2 (196.14632200000003)


   
   

Aleprylic acid

7-(2-cyclopenten-1-yl)heptanoic acid

C12H20O2 (196.14632200000003)


   
   

3,4-Di-1-butenyltetrahydro-2-furanol

3,4-Di-1-butenyltetrahydro-2-furanol

C12H20O2 (196.14632200000003)


   

9-hydroxy-8-methylundeca-4,6-dien-3-one

9-hydroxy-8-methylundeca-4,6-dien-3-one

C12H20O2 (196.14632200000003)


   
   

(+)-3,4,5-Trimethyl-5-pentyl-5H-furan-2-one

(+)-3,4,5-Trimethyl-5-pentyl-5H-furan-2-one

C12H20O2 (196.14632200000003)


   

Ethyl 3,7-dimethylocta-2,6-dienoate

Ethyl 3,7-dimethylocta-2,6-dienoate

C12H20O2 (196.14632200000003)


   
   
   
   

Oxacyclododec-9-en-2-one, 12-methyl-, (9E)-

Oxacyclododec-9-en-2-one, 12-methyl-, (9E)-

C12H20O2 (196.14632200000003)


   
   
   

11,12,13-trinoreudesm-5-en-7beta,6alpha-diol

11,12,13-trinoreudesm-5-en-7beta,6alpha-diol

C12H20O2 (196.14632200000003)


   
   
   
   

4-hydroxy-5,10-dimethyl-octahydro-azulen-8-one|jasonone

4-hydroxy-5,10-dimethyl-octahydro-azulen-8-one|jasonone

C12H20O2 (196.14632200000003)


   

(+/-)-(5Z)-dodecen-11-olid|Dodec-5-en-11-olid|Phoracantholide M

(+/-)-(5Z)-dodecen-11-olid|Dodec-5-en-11-olid|Phoracantholide M

C12H20O2 (196.14632200000003)


   
   
   

3,4,4a,5,6,7,8,9,10,10a-Decahydro-4a-hydroxybenzocyclooctene-1(2H)-one

3,4,4a,5,6,7,8,9,10,10a-Decahydro-4a-hydroxybenzocyclooctene-1(2H)-one

C12H20O2 (196.14632200000003)


   

Myrcenyl acetate

pseudo linalyl acetate

C12H20O2 (196.14632200000003)


   
   
   

Lavandulyl_acetate

(R)-Lavandulyl acetate; (-)-Lavandulyl acetate; (-)-(R)-Lavandulyl acetate;

C12H20O2 (196.14632200000003)


Lavandulyl acetate is a natural product found in Alpinia galanga with data available. See also: Lavender Oil (part of).

   

Bornyl_acetate

BICYCLO[2.2.1]HEPTAN-2-OL,1,7,7-TRIMETHYL-, 2-ACETATE, (1S,2R,4S)-

C12H20O2 (196.14632200000003)


Bornyl acetate is a natural product found in Xylopia aromatica, Xylopia sericea, and other organisms with data available. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

Linalyl acetate

Linalyl acetate

C12H20O2 (196.14632200000003)


Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1]. Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1].

   

alpha-Terpineol acetate

(+/-)-alpha-Terpinyl acetate, predominantly alpha-isomer, technical, >=90\\% (GC)

C12H20O2 (196.14632200000003)


alpha-Terpineol acetate, also known as a-terpineol acetic acid or p-menth-1-en-8-yl acetate, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. alpha-Terpineol acetate is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Alpha-Terpinyl acetate is a p-menthane monoterpenoid. alpha-Terpinyl acetate is a natural product found in Xylopia sericea, Elettaria cardamomum, and other organisms with data available. Terpinyl acetate is a metabolite found in or produced by Saccharomyces cerevisiae. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2]. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2].

   

Neryl_acetate

2,6-Octadien-1-ol, 3,7-dimethyl-, 1-acetate, (2Z)-

C12H20O2 (196.14632200000003)


Neryl acetate is an acetate ester resulting from the formal condensation of the hydroxy group of nerol with the carboxy group of acetic acid. It has a role as a volatile oil component, a fragrance and a plant metabolite. It is an acetate ester, a monoterpenoid and an olefinic compound. It is functionally related to a nerol. Neryl acetate is a natural product found in Xylopia sericea, Eupatorium cannabinum, and other organisms with data available. Neryl acetate is found in cardamom. Neryl acetate is found in citrus, kumquat and pummelo peel oils, ginger, cardamon, clary sage, myrtle leaf and myrtle berries. Neryl acetate is a flavouring agent. Geranyl acetate belongs to the family of Fatty Alcohol Esters. These are ester derivatives of a fatty alcohol. See also: Lemon oil, cold pressed (part of). An acetate ester resulting from the formal condensation of the hydroxy group of nerol with the carboxy group of acetic acid. Neryl acetate is a chemical compound isolated from citrus oils[1]. Neryl acetate is a chemical compound isolated from citrus oils[1].

   
   

Chrysanthemic Acid, Ethyl Ester

Chrysanthemic Acid, Ethyl Ester

C12H20O2 (196.14632200000003)


   

Chrysanthemic Acid, Ethyl Ester_major

Chrysanthemic Acid, Ethyl Ester_major

C12H20O2 (196.14632200000003)


   
   
   
   
   
   
   
   
   
   
   

dodeca-3Z,6Z-dienoic acid

cis,cis-dodeca-3,6-dienoic acid

C12H20O2 (196.14632200000003)


   

3,7-Dimethyl-2Z,6-octadienyl acetate

3,7-Dimethyl-2Z,6-octadienyl acetate

C12H20O2 (196.14632200000003)


   
   
   
   

8E-Hydroxy-4,8-dimethyl-4,9-decadienal

8E-Hydroxy-4,8-dimethyl-4,9-decadienal

C12H20O2 (196.14632200000003)


   

C12:2n-8,10

2E,4E-dodecadienoic acid

C12H20O2 (196.14632200000003)


   

C12:2n-6,10

2E,6Z-dodecadienoic acid

C12H20O2 (196.14632200000003)


   

C12:2n-4,10

(2Z,8Z)-dodeca-2,8-dienoic acid

C12H20O2 (196.14632200000003)


   

C12:2n-5,7

5E,7E-dodecadienoic acid

C12H20O2 (196.14632200000003)


   

C12:2n-3,5

7Z,9E-dodecadienoic acid

C12H20O2 (196.14632200000003)


   

C12:2n-2,4

(8Z,10E)-dodeca-8,10-dienoic acid

C12H20O2 (196.14632200000003)


   
   
   
   
   
   
   
   
   
   

-lactone

Dihydro-5-(2-octenyl)-2(3H)-furanone

C12H20O2 (196.14632200000003)


   

FEMA 2751

2-Undecynoic acid, methyl ester

C12H20O2 (196.14632200000003)


   

FEMA 3802

6-Heptyl-5,6-dihydro-2H-pyran-2-one

C12H20O2 (196.14632200000003)


   

cis-3-Hexenyl trans-4-hexenoate

(3Z)-hex-3-en-1-yl (4E)-hex-4-enoate

C12H20O2 (196.14632200000003)


   

Campholene acetate

3-Cyclopentene-1-ethanol, 2,2,3-trimethyl-, acetate

C12H20O2 (196.14632200000003)


   

«

Dihydro-5-(2-octenyl)-(Z)-2(3H)-furanone

C12H20O2 (196.14632200000003)


   

Yuzu lactone

(10E)-1-oxacyclotridec-10-en-2-one

C12H20O2 (196.14632200000003)


   

3-butyl-octahydro-2-benzofuran-1-one

(3R,3aR,7aS)-3-Butylhexahydro-1(3H)-isobenzofuranone

C12H20O2 (196.14632200000003)


   

Artemisyl acetate

3,3,6-trimethylhepta-1,5-dien-4-yl acetate

C12H20O2 (196.14632200000003)


   

9-Acetoxy-1-P-menthene

3-Cyclohexene-1-ethanol, beta,4-dimethyl-, acetate

C12H20O2 (196.14632200000003)


   

FEMA 3689

(3Z)-3-Hexen-1-yl ester(3Z)-3-hexenoic acid

C12H20O2 (196.14632200000003)


   

FEMA 3928

(3Z)-hex-3-en-1-yl (2E)-hex-2-enoate

C12H20O2 (196.14632200000003)


   

Isopulegolacetate

Cyclohexanol,5-methyl-2-(1-methylethenyl)-, 1-acetate, (1R,2S,5R)-

C12H20O2 (196.14632200000003)


   

FEMA 2159

endo-(1S)-1,7,7-trimethylbicyclo[2.2.1]Hept-2-yl acetate

C12H20O2 (196.14632200000003)


(-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].

   

(−

Cyclohexanol, 2-methyl-5-(1-methylethenyl)-, 1-acetate

C12H20O2 (196.14632200000003)


   

(S)-Santolina acetate

3-ethenyl-2,5-dimethylhex-4-en-2-yl acetate

C12H20O2 (196.14632200000003)


   
   

WE(6:1(2E)/6:1(2E))

(E)-2-Hexenyl (E)-2-hexenoate

C12H20O2 (196.14632200000003)


   

WE(6:1(2E)/6:1(3Z))

(E)-2-Hexenyl (Z)-3-hexenoate

C12H20O2 (196.14632200000003)


   

trunc-call(heptadienoate)

Isopropyl 2,4-dimethyl-2E,4E-heptadienoate

C12H20O2 (196.14632200000003)


   

Buibuilactone

5R-(oct-1Z-enyl)dihydrofuran-2(3H)-one

C12H20O2 (196.14632200000003)


   

Cucujolide II

3Z-Dodecen-11R-olide

C12H20O2 (196.14632200000003)


   
   
   
   

FA 12:2

(2E,4E,6S)-4,6-dimethyldeca-2,4-dienoic acid

C12H20O2 (196.14632200000003)


   

FAL 12:2;O

8E-Hydroxy-4,8-dimethyl-4,9-decadienal

C12H20O2 (196.14632200000003)


   

WE 12:2

prop-2-en-1-yl 3-cyclohexylpropanoate

C12H20O2 (196.14632200000003)


   

SFE 12:2

Isopropyl 2,4-dimethyl-2E,4E-heptadienoate

C12H20O2 (196.14632200000003)


   

pear ester

ethyl 2E,4Z-decadienoate

C12H20O2 (196.14632200000003)


   

sodium,5-chloro-3-[[3-methyl-5-oxido-1-(3-sulfonatophenyl)pyrazol-4-yl]diazenyl]-2-oxidobenzenesulfonate,chromium(3+)

sodium,5-chloro-3-[[3-methyl-5-oxido-1-(3-sulfonatophenyl)pyrazol-4-yl]diazenyl]-2-oxidobenzenesulfonate,chromium(3+)

C12H20O2 (196.14632200000003)


   

cis,trans-5,9-Cyclododecadiene-cis-1,2-diol

cis,trans-5,9-Cyclododecadiene-cis-1,2-diol

C12H20O2 (196.14632200000003)


   

(2,2,4-trimethyl-5-bicyclo[2.2.1]heptanyl) acetate

(2,2,4-trimethyl-5-bicyclo[2.2.1]heptanyl) acetate

C12H20O2 (196.14632200000003)


   
   
   
   

2-Naphthalenol,decahydro-, 2-acetate

2-Naphthalenol,decahydro-, 2-acetate

C12H20O2 (196.14632200000003)


   

1,4-CYCLOHEXANEDIMETHANOL DIVINYL ETHER

1,4-CYCLOHEXANEDIMETHANOL DIVINYL ETHER

C12H20O2 (196.14632200000003)


   

(R)-Butaprost

Dihydrocarvyl acetate, (-)-

C12H20O2 (196.14632200000003)


   
   
   

3,5-Diisopropylbenzene hydroperoxide

3,5-Diisopropylbenzene hydroperoxide

C12H20O2 (196.14632200000003)


   

1-Cyclopentene-1-methanol,-alpha--(1-ethoxyethenyl)-4,4-dimethyl-(9CI)

1-Cyclopentene-1-methanol,-alpha--(1-ethoxyethenyl)-4,4-dimethyl-(9CI)

C12H20O2 (196.14632200000003)


   
   

1,3-dihydroxy-5,7-dimethyladamantane

1,3-dihydroxy-5,7-dimethyladamantane

C12H20O2 (196.14632200000003)


   

octahydro-4,7-methano-1H-indenedimethanol

octahydro-4,7-methano-1H-indenedimethanol

C12H20O2 (196.14632200000003)


   

1-Naphthaleneaceticacid, decahydro-

1-Naphthaleneaceticacid, decahydro-

C12H20O2 (196.14632200000003)


   

4,8-BIS(HYDROXYMETHYL)TRICYCLO[5.2.1.0(2,6)]DECANE

4,8-BIS(HYDROXYMETHYL)TRICYCLO[5.2.1.0(2,6)]DECANE

C12H20O2 (196.14632200000003)


   

Cyclohexanedimethanol divinyl ether

Cyclohexanedimethanol divinyl ether

C12H20O2 (196.14632200000003)


   

(4ξ,5E)-4-Isopropyl-7-methyl-5,7-octadienoic acid

(4ξ,5E)-4-Isopropyl-7-methyl-5,7-octadienoic acid

C12H20O2 (196.14632200000003)


   

(3E,5S)-5-Isopropyl-3-nonene-2,8-dione

(3E,5S)-5-Isopropyl-3-nonene-2,8-dione

C12H20O2 (196.14632200000003)


   

4-Isopropyl-7-methyl-5,7-octadienoic acid

4-Isopropyl-7-methyl-5,7-octadienoic acid

C12H20O2 (196.14632200000003)


   
   
   

ETHYL 1-METHYLBICYCLO[2.2.2]OCTANE-2-CARBOXYLATE

ETHYL 1-METHYLBICYCLO[2.2.2]OCTANE-2-CARBOXYLATE

C12H20O2 (196.14632200000003)


   
   

1,3-Dioxolane,2-(2,6-dimethyl-1,5-heptadien-1-yl)-

1,3-Dioxolane,2-(2,6-dimethyl-1,5-heptadien-1-yl)-

C12H20O2 (196.14632200000003)


   
   

(1S,2S,4R)-2-Acetyloxy-1,3,3-trimethylbicyclo[2.2.1]heptane

(1S,2S,4R)-2-Acetyloxy-1,3,3-trimethylbicyclo[2.2.1]heptane

C12H20O2 (196.14632200000003)


   

(±)-p-Menth-1-en-4-yl acetate

3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-, acetate

C12H20O2 (196.14632200000003)


(±)-p-menth-1-en-4-yl acetate is a member of the class of compounds known as menthane monoterpenoids. Menthane monoterpenoids are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes (±)-p-menth-1-en-4-yl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (±)-p-menth-1-en-4-yl acetate can be found in nutmeg, rosemary, sweet marjoram, and winter savory, which makes (±)-p-menth-1-en-4-yl acetate a potential biomarker for the consumption of these food products.

   
   

Oxacyclododec-4-en-2-one, 12-methyl-, (4Z,12S)-

Oxacyclododec-4-en-2-one, 12-methyl-, (4Z,12S)-

C12H20O2 (196.14632200000003)


   

(2E,6Z)-Dodeca-2,6-dienoic acid

(2E,6Z)-Dodeca-2,6-dienoic acid

C12H20O2 (196.14632200000003)


   

3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-acetate, (1R)-

3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-acetate, (1R)-

C12H20O2 (196.14632200000003)


   

6-(Isopropyl)-3-methylcyclohex-2-en-1-yl acetate

6-(Isopropyl)-3-methylcyclohex-2-en-1-yl acetate

C12H20O2 (196.14632200000003)


   

(E)-(E)-Hex-3-en-1-yl hex-3-enoate

(E)-(E)-Hex-3-en-1-yl hex-3-enoate

C12H20O2 (196.14632200000003)


   

2-Isopropyl-5-methyl-2-cyclohexen-1-yl acetate

2-Isopropyl-5-methyl-2-cyclohexen-1-yl acetate

C12H20O2 (196.14632200000003)


   

(+)-Bornyl acetate

Bornyl acetate, (-)-

C12H20O2 (196.14632200000003)


(-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

Bornyl acetate

(1R,2S,4R)-(+)-Bornyl acetate

C12H20O2 (196.14632200000003)


Same as: D09740 (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

AI3-00207

Geranyl acetate, food grade (71\\% geranyl acetate, 29\\% citronellyl acetate)

C12H20O2 (196.14632200000003)


Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent[1]. Geranyl acetate can induces cell apoptosis[2]. Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent[1]. Geranyl acetate can induces cell apoptosis[2].

   

nerol acetate

acetic acid [(2Z)-3,7-dimethylocta-2,6-dienyl] ester

C12H20O2 (196.14632200000003)


Neryl acetate is a chemical compound isolated from citrus oils[1]. Neryl acetate is a chemical compound isolated from citrus oils[1].

   

AI3-25079

2,6-Octadienoic acid, 3,7-dimethyl-, ethyl ester, (2E)-

C12H20O2 (196.14632200000003)


   

10235-63-9

acetic acid (4-isopropylidene-1-methyl-cyclohexyl) ester

C12H20O2 (196.14632200000003)


   

Terpineol, acetate

alpha-Terpinyl acetate

C12H20O2 (196.14632200000003)


(±)-alpha-terpinyl acetate, also known as P-menth-1-en-8-yl acetate or (±)-α-terpinyl acetic acid, is a member of the class of compounds known as menthane monoterpenoids. Menthane monoterpenoids are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Thus, (±)-alpha-terpinyl acetate is considered to be an isoprenoid lipid molecule (±)-alpha-terpinyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (±)-alpha-terpinyl acetate is a bergamot, citrus, and herbal tasting compound and can be found in a number of food items such as hyssop, rosemary, sweet bay, and roselle, which makes (±)-alpha-terpinyl acetate a potential biomarker for the consumption of these food products (±)-alpha-terpinyl acetate can be found primarily in saliva.

   

(2E,4E)-dodeca-2,4-dienoic acid

(2E,4E)-dodeca-2,4-dienoic acid

C12H20O2 (196.14632200000003)


   
   

2-(4-Methylenecyclohexyl)propan-2-yl acetate

2-(4-Methylenecyclohexyl)propan-2-yl acetate

C12H20O2 (196.14632200000003)


   
   
   

(-)-dihydrocarvyl acetate

5-Methyl-2-(1-methylethenyl)-4-hexen-1-ol acetate

C12H20O2 (196.14632200000003)


   

2,6-Octadienoic acid, 3,7-dimethyl-, ethyl ester

2,6-Octadienoic acid, 3,7-dimethyl-, ethyl ester

C12H20O2 (196.14632200000003)


   
   
   

3-(3-Methyl-3-butenyl)hepta-2,6-dione

3-(3-Methyl-3-butenyl)hepta-2,6-dione

C12H20O2 (196.14632200000003)


   

Acetic acid (1S)-2-methyl-5-(1-methylethenyl)cyclohexyl ester

Acetic acid (1S)-2-methyl-5-(1-methylethenyl)cyclohexyl ester

C12H20O2 (196.14632200000003)


   

Acetic acid (1R)-2-methyl-5-(1-methylethenyl)cyclohexyl ester

Acetic acid (1R)-2-methyl-5-(1-methylethenyl)cyclohexyl ester

C12H20O2 (196.14632200000003)


   

fema 3148

ethyl (2E,4Z)-deca-2,4-dienoate

C12H20O2 (196.14632200000003)


A fatty acid ethyl ester resulting from the formal condensation of the carboxy group of (2E,4E)-deca-2,4-dienoic acid with the hydroxy group of ethanol.

   

Linalyl acetate, (-)-

Linalyl acetate, (-)-

C12H20O2 (196.14632200000003)


Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1]. Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity[1].

   

isopulegyl acetate

Cyclohexanol,5-methyl-2-(1-methylethenyl)-, 1-acetate, (1R,2S,5R)-

C12H20O2 (196.14632200000003)


   

Dihydrocarvyl acetate

p-Menth-8-en-2-ol acetate

C12H20O2 (196.14632200000003)


   

Fenchyl acetate

2-Norbornanol, 1,3,3-trimethyl-, acetate

C12H20O2 (196.14632200000003)


   
   

(Z)-4-Hydroxy-6-dodecenoic acid lactone

(Z)-dihydro-5-(2-octenyl)furan-2(3H)-one

C12H20O2 (196.14632200000003)


   
   

cis-3-Hexenyl cis-3-hexenoate

(Z)-3-hexen-1-yl (Z)-3-hexenoate

C12H20O2 (196.14632200000003)


   

6-Heptyl-5,6-dihydro-2H-pyran-2-one

6-Heptyl-5,6-dihydro-2H-pyran-2-one

C12H20O2 (196.14632200000003)


   

cis-3-Hexenyl trans-2-hexenoate

cis-3-Hexenyl trans-2-hexenoate

C12H20O2 (196.14632200000003)


   
   

Dihydro-5-(2-octenyl)-2(3H)-furanone

Dihydro-5-(2-octenyl)-2(3H)-furanone

C12H20O2 (196.14632200000003)


   

(3R,3aR,7aS)-3-Butylhexahydro-1(3H)-isobenzofuranone

(3R,3aR,7aS)-3-Butylhexahydro-1(3H)-isobenzofuranone

C12H20O2 (196.14632200000003)


   

(10E)-1-oxacyclotridec-10-en-2-one

(10E)-1-oxacyclotridec-10-en-2-one

C12H20O2 (196.14632200000003)


   

3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-, acetate

3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-, acetate

C12H20O2 (196.14632200000003)


   
   
   

5R-(Oct-1Z-enyl)-oxacyclopentan-2-one

5R-(Oct-1Z-enyl)-oxacyclopentan-2-one

C12H20O2 (196.14632200000003)


   

delta-terpineol acetate

delta-terpineol acetate

C12H20O2 (196.14632200000003)


A p-menthane monoterpenoid that is delta-terpineol in which the hydroxy hydrogen has been replaced by an acetyl group.

   
   

cis,cis-dodeca-3,6-dienoic acid

cis,cis-dodeca-3,6-dienoic acid

C12H20O2 (196.14632200000003)


   

(R)-Linalyl acetate

(R)-Linalyl acetate

C12H20O2 (196.14632200000003)


The (R)-enantiomer of linalyl acetate.

   

(S)-linalyl acetate

(S)-linalyl acetate

C12H20O2 (196.14632200000003)


The (S)-enantiomer of linalyl acetate.

   

(2-trans,6-cis)-dodeca-2,6-dienoic acid

(2-trans,6-cis)-dodeca-2,6-dienoic acid

C12H20O2 (196.14632200000003)