Exact Mass: 84.13593278

Exact Mass Matches: 84.13593278

Found 42 metabolites which its exact mass value is equals to given mass value 84.13593278, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Cyclohexan

hexahydro-Benzene

C6H12 (84.09389519999999)


Diluent in colour additive mixtures for food use. Cyclohexane is found in kohlrabi. Cyclohexane is found in kohlrabi. Diluent in colour additive mixtures for food us Cyclohexane appears as a clear colorless liquid with a petroleum-like odor. Used to make nylon, as a solvent, paint remover, and to make other chemicals. Flash point -4 °F. Density 6.5 lb / gal (less than water) and insoluble in water. Vapors heavier than air. Cyclohexane is an alicyclic hydrocarbon comprising a ring of six carbon atoms; the cyclic form of hexane, used as a raw material in the manufacture of nylon. It has a role as a non-polar solvent. It is a cycloalkane and a volatile organic compound. Cyclohexane is an organic compound with the molecular formula C6H12. It is a colorless, flammable liquid with a distinctive sweet odor. Cyclohexane is a saturated hydrocarbon, consisting of a six-membered ring of carbon atoms, with each carbon atom bonded to two hydrogen atoms. The carbon-carbon bonds in the ring are of equal length and angle, giving cyclohexane a regular, symmetrical structure. Due to its ring structure, cyclohexane is more stable than the open-chain aliphatic hydrocarbons with the same number of carbon atoms. It is widely used in industry as a solvent for oils, waxes, and alkaloids, and as a starting material in the production of various chemicals, including adipic acid, cyclohexanol, and cyclohexene. Cyclohexane is also used in the manufacturing of nylon and other synthetic fibers. Cyclohexane exhibits a unique conformational behavior, where it can exist in several different forms, known as conformers. The two most stable conformers are the chair form and the boat form. The chair conformation is the most stable and is characterized by alternating axial and equatorial hydrogen atoms, while the boat conformation has two pairs of hydrogen atoms that are close together, creating strain in the molecule. In terms of its physical properties, cyclohexane has a boiling point of around 80.7°C and a melting point of approximately 6.47°C. It is relatively insoluble in water but miscible with many organic solvents. Cyclohexane is non-polar and therefore does not dissolve ionic compounds or highly polar molecules. Cyclohexane. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=110-82-7 (retrieved 2024-07-12) (CAS RN: 110-82-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

Methylcyclopentane

Methylpentamethylene

C6H12 (84.09389519999999)


Methylcyclopentane, also known as methylpentamethylene, belongs to the class of organic compounds known as cycloalkanes. These are saturated monocyclic hydrocarbons (with or without side chains). Methylcyclopentane has been detected, but not quantified, in celeriacs and celery stalks. This could make methylcyclopentane a potential biomarker for the consumption of these foods. At high amounts methylcyclopentane is a potentially toxic compound and central nervous system depression may occur, with symptoms such as weakness, dizziness, slow and shallow respiration, unconsciousness, and convulsions. Methylcyclopentane is a volatile component of petroleum distillates. Petroleum distillates are aspiration hazards and may cause pulmonary damage, central nervous system depression, and cardiac effects such as cardiac arrhythmias. They may also affect the blood, immune system, liver, and kidney. Volatile hydrocarbons are absorbed mainly through the lungs, and may also enter the body after ingestion via aspiration. Treatment is mainly symptomatic and supportive. Petroleum distillates are also irritating to the skin. Petroleum distillate poisoning may cause nausea, vomiting, cough, pulmonary irritation progressing to pulmonary edema, bloody sputum, and bronchial pneumonia. Gastric lavage, emesis, and the administration of activated charcoal should be avoided, as vomiting increases the risk of aspiration. Isolated from Helianthus annuus (sunflower).

   

4-Methyl-1-pentene

Poly(4-methyl-1-pentene)

C6H12 (84.09389519999999)


   
   
   
   

2-METHYLPENTENE

2-METHYL-1-PENTENE

C6H12 (84.09389519999999)


An alkene that is pent-1-ene carrying a methyl group at position 2.

   

2-HEXENE

InChI=1\C6H12\c1-3-5-6-4-2\h3,5H,4,6H2,1-2H3\b5-3

C6H12 (84.09389519999999)


   

4-METHYL-1-PENTENE

1-Pentene, 4-methyl-

C6H12 (84.09389519999999)


   
   

Methyl cyclopentane

Methylcyclopentane [UN2298] [Flammable liquid]

C6H12 (84.09389519999999)


   
   

2-Pentene, 3-methyl-,(2Z)-

2-Pentene, 3-methyl-,(2Z)-

C6H12 (84.09389519999999)


   

2-Pentene, 4-methyl-,(2Z)-

2-Pentene, 4-methyl-,(2Z)-

C6H12 (84.09389519999999)


   
   
   

1,3-propanediol-d8

1,3-propanediol-d8

C3D8O2 (84.102644224)


   

trans-4-METHYL-2-PENTENE

trans-4-METHYL-2-PENTENE

C6H12 (84.09389519999999)


   

1-(2H9)Butan(2H)ol

1-(2H9)Butan(2H)ol

C4D10O (84.13593278)


   
   
   
   

2-(2H3)Methyl(2H6)propan-2-(2H)ol

2-(2H3)Methyl(2H6)propan-2-(2H)ol

C4D10O (84.13593278)


   

1-Butene - ethylene (1:1)

1-Butene - ethylene (1:1)

C6H12 (84.09389519999999)


   

Ammonium acetate-d7

Ammonium acetate-d7

C2D7NO2 (84.091616446)


   
   

trans-3-methyl-2-pentene

trans-3-methyl-2-pentene

C6H12 (84.09389519999999)


   
   

2-Pentene, 4-methyl-,(2E)-

2-Pentene, 4-methyl-,(2E)-

C6H12 (84.09389519999999)


   

2-Pentene, 3-methyl-,(2E)-

2-Pentene, 3-methyl-,(2E)-

C6H12 (84.09389519999999)


   

Diethylamine-d11

Diethylamine-d11

C4D11N (84.158193558)


   

Diethyl ether-D10

Diethyl ether-D10

C4D10O (84.13593278)


   
   

1,1,1,2,3,3-hexadeuterio-2,3-dideuteriooxypropane

1,1,1,2,3,3-hexadeuterio-2,3-dideuteriooxypropane

C3D8O2 (84.102644224)


   
   

Cyclopropane,1,1,2-trimethyl-

Cyclopropane,1,1,2-trimethyl-

C6H12 (84.09389519999999)


   
   

Hexene

InChI=1\C6H12\c1-3-5-6-4-2\h3H,1,4-6H2,2H

C6H12 (84.09389519999999)


   

LS-516

Cyclohexane, reaction product with oxygen, nonvolatile residue

C6H12 (84.09389519999999)


   

96-37-7

Methylcyclopentane [UN2298] [Flammable liquid]

C6H12 (84.09389519999999)


   

Cyclohexane

cyclohexane

C6H12 (84.09389519999999)


Cyclohexane appears as a clear colorless liquid with a petroleum-like odor. Used to make nylon, as a solvent, paint remover, and to make other chemicals. Flash point -4 °F. Density 6.5 lb / gal (less than water) and insoluble in water. Vapors heavier than air. Cyclohexane is an alicyclic hydrocarbon comprising a ring of six carbon atoms; the cyclic form of hexane, used as a raw material in the manufacture of nylon. It has a role as a non-polar solvent. It is a cycloalkane and a volatile organic compound. Cyclohexane is an organic compound with the molecular formula C6H12. It is a colorless, flammable liquid with a distinctive sweet odor. Cyclohexane is a saturated hydrocarbon, consisting of a six-membered ring of carbon atoms, with each carbon atom bonded to two hydrogen atoms. The carbon-carbon bonds in the ring are of equal length and angle, giving cyclohexane a regular, symmetrical structure. Due to its ring structure, cyclohexane is more stable than the open-chain aliphatic hydrocarbons with the same number of carbon atoms. It is widely used in industry as a solvent for oils, waxes, and alkaloids, and as a starting material in the production of various chemicals, including adipic acid, cyclohexanol, and cyclohexene. Cyclohexane is also used in the manufacturing of nylon and other synthetic fibers. Cyclohexane exhibits a unique conformational behavior, where it can exist in several different forms, known as conformers. The two most stable conformers are the chair form and the boat form. The chair conformation is the most stable and is characterized by alternating axial and equatorial hydrogen atoms, while the boat conformation has two pairs of hydrogen atoms that are close together, creating strain in the molecule. In terms of its physical properties, cyclohexane has a boiling point of around 80.7°C and a melting point of approximately 6.47°C. It is relatively insoluble in water but miscible with many organic solvents. Cyclohexane is non-polar and therefore does not dissolve ionic compounds or highly polar molecules. Cyclohexane. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=110-82-7 (retrieved 2024-07-12) (CAS RN: 110-82-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

METHYLCYCLOPENTANE

METHYLCYCLOPENTANE

C6H12 (84.09389519999999)


A cycloalkane that is cyclopentane substituted by a single methyl group.