Chemical Formula: C8H8O

Chemical Formula C8H8O

Found 41 metabolite its formula value is C8H8O

Acetophenone

Acetophenone, TraceCERT(R), certified reference material

C8H8O (120.0575118)


Acetophenone appears as a colorless liquid with a sweet pungent taste and odor resembling the odor of oranges. Freezes under cool conditions. Slightly soluble in water and denser than water. Hence sinks in water. Vapor heavier than air. A mild irritant to skin and eyes. Vapors can be narcotic in high concentrations. Used as a flavoring, solvent, and polymerization catalyst. Acetophenone is a methyl ketone that is acetone in which one of the methyl groups has been replaced by a phenyl group. It has a role as a photosensitizing agent, an animal metabolite and a xenobiotic. Acetophenone is used for fragrance in soaps and perfumes, as a flavoring agent in foods, and as a solvent for plastics and resins. Acute (short-term) exposure to acetophenone vapor may produce skin irritation and transient corneal injury in humans. No information is available on the chronic (long-term), reproductive, developmental, or carcinogenic effects of acetophenone in humans. EPA has classified acetophenone as a Group D, not classifiable as to human carcinogenicity. Acetophenone is a natural product found in Nepeta nepetella, Hypericum hyssopifolium, and other organisms with data available. Acetophenone is a metabolite found in or produced by Saccharomyces cerevisiae. Acetophenone is the organic compound with the formula C6H5C(O)CH3. It is the simplest aromatic ketone. This colourless, viscous liquid is a precursor to useful resins and fragrances. Acetophenone is found in chicory. Acetophenone is a flavouring ingredient used in fruit flavours. Acetophenone is a raw material for the synthesis of some pharmaceuticals and is also listed as an approved excipient by the U.S. FDA. In a 1994 report released by five top cigarette companies in the U.S., acetophenone was listed as one of the 599 additives to cigarettes. A methyl ketone that is acetone in which one of the methyl groups has been replaced by a phenyl group. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents Flavouring ingredient used in fruit flavours; leavening agent D003879 - Dermatologic Agents Acetophenone is an organic compound with simple structure[1]. Acetophenone is an organic compound with simple structure[1].

   

3-Methylbenzaldehyde

3-methylbenzaldehyde;3-Methylbenzaldehyde, stab. with 0.1\\% hydroquinone

C8H8O (120.0575118)


3-Methylbenzaldehyde, also known as 3-tolylaldehyde, belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-). 3-Methylbenzaldehyde exists in all living organisms, ranging from bacteria to humans. 3-Methylbenzaldehyde is a sweet, benzaldehyde, and cherry tasting compound. 3-Methylbenzaldehyde has been detected, but not quantified, in several different foods, such as sweet cherries, alcoholic beverages, garden tomato, coffee and coffee products, and tea. This could make 3-methylbenzaldehyde a potential biomarker for the consumption of these foods. A tolualdehyde compound with the methyl substituent at the 3-position. M-tolualdehyde is a tolualdehyde compound with the methyl substituent at the 3-position. It has a role as a plant metabolite. 3-Methylbenzaldehyde is a natural product found in Aloe africana, Cichorium endivia, and other organisms with data available. Flavouring ingredient. Component of FEMA 3068; see further under 4-Methylbenzaldehyde BHW21-S. 3-Methylbenzaldehyde is found in many foods, some of which are coffee and coffee products, nuts, tea, and garden tomato. A tolualdehyde compound with the methyl substituent at the 3-position. m-Tolualdehyde (3-Methylbenzaldehyde) is a tolualdehyde compound with the methyl substituent at the 3-position. m-Tolualdehyde can be used as a food additive. m-Tolualdehyde (3-Methylbenzaldehyde) is a tolualdehyde compound with the methyl substituent at the 3-position. m-Tolualdehyde can be used as a food additive.

   

4-Vinylphenol sulfate

4-06-00-03775 (Beilstein Handbook Reference)

C8H8O (120.0575118)


4-hydroxystyrene is a member of the class of phenols that is styrene carrying a hydroxy substituent at position 4. It has a role as a human urinary metabolite and a human xenobiotic metabolite. It derives from a hydride of a styrene. 4-Vinylphenol is a natural product found in Streptomyces, Cedronella canariensis, and other organisms with data available. 4-Vinylphenol is a metabolite found in or produced by Saccharomyces cerevisiae. 4-hydroxystyrene occurs frequently in different ciders, wines, foods and berries, e.g. cloudberry. Styrene is a prohapten metabolized in the skin by aryl hydrocarbon hydroxylase (AHH, EC 1.14.14.1) to styrene epoxide acting as the true hapten. Styrene occurs in nature and as a synthetic product.(PMID: 6713846). Flavour component of tea; flavouring ingredient

   

Phenylacetaldehyde

alpha-Phenylacetaldehyde

C8H8O (120.0575118)


Phenylacetaldehyde is one important oxidation-related aldehyde. Exposure to styrene gives phenylacetaldehyde as a secondary metabolite. Styrene has been implicated as reproductive toxicant, neurotoxicant, or carcinogen in vivo or in vitro. Phenylacetaldehyde could be formed by diverse thermal reactions during the cooking process together with C8 compounds is identified as a major aroma- active compound in cooked pine mushroom. Phenylacetaldehyde is readily oxidized to phenylacetic acid. Therefore will eventually be hydrolyzed and oxidized to yield phenylacetic acid that will be excreted primarily in the urine in conjugated form. (PMID: 16910727, 7818768, 15606130). Found in some essential oils, e.g. Citrus subspecies, Tagetes minuta (Mexican marigold) and in the mushroom Phallus impudicus (common stinkhorn). Flavouring ingredient COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Styrene Oxide

Styrene oxide, (+-)-isomer

C8H8O (120.0575118)


Styrene Oxide, also known as Epoxystyrene or Phenyloxirane, is classified as a benzene or a Benzene derivative. Benzenes are aromatic compounds containing one monocyclic ring system consisting of benzene. Styrene Oxide is considered to be slightly soluble (in water) and basic D009676 - Noxae > D002273 - Carcinogens D009676 - Noxae > D009153 - Mutagens

   

4-Methylbenzaldehyde

Para-methylbenzaldehyde

C8H8O (120.0575118)


4-Methylbenzaldehyde, also known as p-toluylaldehyde or p-formyltoluene, belongs to the class of organic compounds known as benzoyl derivatives. A tolualdehyde compound with the methyl substituent at the 4-position. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-). 4-Methylbenzaldehyde is a cherry and fruity tasting compound. 4-Methylbenzaldehyde has been detected, but not quantified, in several different foods, such as caraway, sweet cherries, tea, nuts, and coffee and coffee products. Component of *FEMA 3068* together with the o- and m-isomers. Flavouring ingredient. Methylbenzaldehydes are present in roasted nuts, cooked beef, cider, tomato, coffee, tea and elderberry juice. 4-Methylbenzaldehyde is found in many foods, some of which are tea, caraway, nuts, and garden tomato. p-Tolualdehyde is an endogenous metabolite. p-Tolualdehyde is an endogenous metabolite.

   

2-Methylbenzaldehyde

2-Methyl-benzaldehyde

C8H8O (120.0575118)


Component of FEMA 3068. Flavouring ingredient (see further under 4-Methylbenzaldehyde BHW21-S). 2-Methylbenzaldehyde is found in many foods, some of which are alcoholic beverages, soft-necked garlic, animal foods, and caraway. 2-Methylbenzaldehyde is found in alcoholic beverages. 2-Methylbenzaldehyde is a component of FEMA 3068. 2-Methylbenzaldehyde is a flavouring ingredient (see further under 4-Methylbenzaldehyde BHW21-S

   

(S)-Styrene oxide

(S)-Styrene oxide

C8H8O (120.0575118)


The (S)-enantiomer of styrene oxide.

   

2,3-Dihydrobenzofuran

InChI=1/C8H8O/c1-2-4-8-7(3-1)5-6-9-8/h1-4H,5-6H

C8H8O (120.0575118)


2,3-dihydrobenzofuran is a member of the class of 1-benzofurans that is the 2,3-dihydroderivative of benzofuran. It has a role as a metabolite. 2,3-Dihydrobenzofuran is a natural product found in Phyla nodiflora, Vitis vinifera, and other organisms with data available. 2,3-dihydrobenzofuran, also known as coumaran, is a clear very slight yellow oily liquid. It is slightly soluble in water, and is formed by reducing coumarone of which it is the dihydride. A member of the class of 1-benzofurans that is the 2,3-dihydroderivative of benzofuran. Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1]. Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1].

   

Lentialexin

oct-7-en-3,5-diyn-1-ol

C8H8O (120.0575118)


Lentialexin is found in mushrooms. Lentialexin is produced by a mixed culture of Lentinus edodes (shiitake) and Trichoderma polysporum. Production by a mixed culture of Lentinus edodes (shiitake) and Trichoderma polysporum. Lentialexin is found in mushrooms.

   

2-Ethenylphenol

2-Ethenylphenol

C8H8O (120.0575118)


   

phenylacetaldehyde

phenylacetaldehyde

C8H8O (120.0575118)


An aldehyde that consists of acetaldehyde bearing a methyl substituent; the parent member of the phenylacetaldehyde class of compounds. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

4-Vinylphenol

4-Vinylphenol

C8H8O (120.0575118)


   

4-vinyl phenol

4-vinyl phenol

C8H8O (120.0575118)


   

Kumaran

Coumaran (2,3-dihydrobenzofuran)

C8H8O (120.0575118)


Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1]. Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1].

   

Lentialexin

oct-7-en-3,5-diyn-1-ol

C8H8O (120.0575118)


   

FOH 8:5

oct-7-en-3,5-diyn-1-ol

C8H8O (120.0575118)


   

1-(13C)-1-phenyl-1-ethanone

1-(13C)-1-phenyl-1-ethanone

C8H8O (120.0575118)


   

3-Vinylphenol

3-Vinylphenol

C8H8O (120.0575118)


   

Acetophenone-1,2-13C2

Acetophenone-1,2-13C2

C8H8O (120.0575118)


   

1-phenylethanone-2-13C

1-phenylethanone-2-13C

C8H8O (120.0575118)


   
   

(R)-Styrene oxide

(R)-Styrene oxide

C8H8O (120.0575118)


The (R)-enantiomer of styrene oxide.

   

BICYCLO[4.2.0]OCTA-1,3,5,7-TETRAEN-7-OL

BICYCLO[4.2.0]OCTA-1,3,5,7-TETRAEN-7-OL

C8H8O (120.0575118)


   

1-Phenylethenol

1-Phenylethenol

C8H8O (120.0575118)


   

Phenyl vinyl ether

Phenyl vinyl ether

C8H8O (120.0575118)


   

Hyacinthin

InChI=1\C8H8O\c9-7-6-8-4-2-1-3-5-8\h1-5,7H,6H

C8H8O (120.0575118)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Hypnon

InChI=1\C8H8O\c1-7(9)8-5-3-2-4-6-8\h2-6H,1H

C8H8O (120.0575118)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents D003879 - Dermatologic Agents Acetophenone is an organic compound with simple structure[1]. Acetophenone is an organic compound with simple structure[1].

   

c0201

InChI=1\C8H8O\c1-7-2-4-8(6-9)5-3-7\h2-6H,1H

C8H8O (120.0575118)


p-Tolualdehyde is an endogenous metabolite. p-Tolualdehyde is an endogenous metabolite.

   

Coumaran

InChI=1\C8H8O\c1-2-4-8-7(3-1)5-6-9-8\h1-4H,5-6H

C8H8O (120.0575118)


Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1]. Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1].

   

c0242

InChI=1\C8H8O\c1-7-3-2-4-8(5-7)6-9\h2-6H,1H

C8H8O (120.0575118)


m-Tolualdehyde (3-Methylbenzaldehyde) is a tolualdehyde compound with the methyl substituent at the 3-position. m-Tolualdehyde can be used as a food additive. m-Tolualdehyde (3-Methylbenzaldehyde) is a tolualdehyde compound with the methyl substituent at the 3-position. m-Tolualdehyde can be used as a food additive.

   

LS-2404

InChI=1\C8H8O\c1-7-4-2-3-5-8(7)6-9\h2-6H,1H

C8H8O (120.0575118)


   

Acetophenone-alpha,alpha,alpha-d3

Acetophenone-alpha,alpha,alpha-d3

C8H8O (120.0575118)


   

p-Tolualdehyde

4-Methylbenzaldehyde

C8H8O (120.0575118)


A tolualdehyde compound with the methyl substituent at the 4-position. p-Tolualdehyde is an endogenous metabolite. p-Tolualdehyde is an endogenous metabolite.

   

Styrene oxide

Styrene oxide

C8H8O (120.0575118)


An epoxide that is oxirane in which one of the hydrogens has been replaced by a phenyl group. D009676 - Noxae > D002273 - Carcinogens D009676 - Noxae > D009153 - Mutagens

   

2-Methylbenzaldehyde

2-Methylbenzaldehyde

C8H8O (120.0575118)


   

oct-7-en-3,5-diyn-1-ol

oct-7-en-3,5-diyn-1-ol

C8H8O (120.0575118)


   

4-hydroxystyrene

4-hydroxystyrene

C8H8O (120.0575118)


A member of the class of phenols that is styrene carrying a hydroxy substituent at position 4.

   

O-Tolualdehyde

O-Tolualdehyde

C8H8O (120.0575118)


A tolualdehyde compound with the methyl substituent at the 2-position.

   

Methylbenzaldehyde

Methylbenzaldehyde

C8H8O (120.0575118)


   

Hydroxystyrene

Hydroxystyrene

C8H8O (120.0575118)