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Table of Contents

1. 44 relations: Alkene, Alkyl group, Alkylbenzene sulfonate, Aromatic sulfonation, Benzene, Chemical ionization, Corrosion inhibitor, Cumene, Demulsifier, Dispersant, Durene, Emulsion, Ethylbenzene, Formylation, Friedel–Crafts reaction, Gas chromatography–mass spectrometry, Gattermann reaction, Haloalkane, Hydrocarbon, Hydrochloric acid, Isodurene, Julius Arnold Koch, Linear alkylbenzene, List of isomers of dodecane, Ludwig Gattermann, M-Xylene, Mesitylene, Methyl group, Molecular mass, O-Xylene, P-Cymene, P-Xylene, Prehnitene, Refining, Sodium dodecyl sulfate, Substituent, Surfactant, Tar, Tetramethylbenzene, Toluene, Trimethylbenzene, Xylene, 1,2,3-Trimethylbenzene, 1,2,4-Trimethylbenzene.

2. Alkylbenzenes

Alkene

In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond.

See Alkylbenzene and Alkene

Alkyl group

In organic chemistry, an alkyl group is an alkane missing one hydrogen.

See Alkylbenzene and Alkyl group

Alkylbenzene sulfonate

Alkylbenzene sulfonates are a class of anionic surfactants, consisting of a hydrophilic sulfonate head-group and a hydrophobic alkylbenzene tail-group.

See Alkylbenzene and Alkylbenzene sulfonate

Aromatic sulfonation

In organic chemistry, aromatic sulfonation is an organic reaction in which a hydrogen atom on an arene is replaced by a sulfonic acid functional group in an electrophilic aromatic substitution.

See Alkylbenzene and Aromatic sulfonation

Benzene

Benzene is an organic chemical compound with the molecular formula C6H6. The benzene molecule is composed of six carbon atoms joined in a planar hexagonal ring with one hydrogen atom attached to each. Because it contains only carbon and hydrogen atoms, benzene is classed as a hydrocarbon. Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals.

See Alkylbenzene and Benzene

Chemical ionization

Chemical ionization (CI) is a soft ionization technique used in mass spectrometry.

See Alkylbenzene and Chemical ionization

Corrosion inhibitor

A corrosion inhibitor or anti-corrosive is a chemical compound added to a liquid or gas to decrease the corrosion rate of a metal that comes into contact with the fluid.

See Alkylbenzene and Corrosion inhibitor

Cumene

Cumene (isopropylbenzene) is an organic compound that contains a benzene ring with an isopropyl substituent. Alkylbenzene and Cumene are alkylbenzenes.

See Alkylbenzene and Cumene

Demulsifier

Demulsifiers, or emulsion breakers, are a class of specialty chemicals used to separate emulsions, for example, water in oil.

See Alkylbenzene and Demulsifier

Dispersant

A dispersant or a dispersing agent is a substance, typically a surfactant, that is added to a suspension of solid or liquid particles in a liquid (such as a colloid or emulsion) to improve the separation of the particles and to prevent their settling or clumping.

See Alkylbenzene and Dispersant

Durene

Durene, or 1,2,4,5-tetramethylbenzene, is an organic compound with the formula C6H2(CH3)4. Alkylbenzene and Durene are alkylbenzenes.

See Alkylbenzene and Durene

Emulsion

An emulsion is a mixture of two or more liquids that are normally immiscible (unmixable or unblendable) owing to liquid-liquid phase separation.

See Alkylbenzene and Emulsion

Ethylbenzene

Ethylbenzene is an organic compound with the formula. Alkylbenzene and Ethylbenzene are alkylbenzenes.

See Alkylbenzene and Ethylbenzene

Formylation

Formylation refers to any chemical processes in which a compound is functionalized with a formyl group (-CH.

See Alkylbenzene and Formylation

Friedel–Crafts reaction

The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring.

See Alkylbenzene and Friedel–Crafts reaction

Gas chromatography–mass spectrometry

Gas chromatography–mass spectrometry (GC–MS) is an analytical method that combines the features of gas-chromatography and mass spectrometry to identify different substances within a test sample.

See Alkylbenzene and Gas chromatography–mass spectrometry

Gattermann reaction

The Gattermann reaction (also known as the Gattermann formylation and the Gattermann salicylaldehyde synthesis) is a chemical reaction in which aromatic compounds are formylated by a mixture of hydrogen cyanide (HCN) and hydrogen chloride (HCl) in the presence of a Lewis acid catalyst such as aluminium chloride (AlCl3).

See Alkylbenzene and Gattermann reaction

Haloalkane

The haloalkanes (also known as halogenoalkanes or alkyl halides) are alkanes containing one or more halogen substituents.

See Alkylbenzene and Haloalkane

Hydrocarbon

In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon.

See Alkylbenzene and Hydrocarbon

Hydrochloric acid

Hydrochloric acid, also known as muriatic acid or spirits of salt, is an aqueous solution of hydrogen chloride (HCl).

See Alkylbenzene and Hydrochloric acid

Isodurene

Isodurene or 1,2,3,5-tetramethylbenzene is an organic compound with the formula C6H2(CH3)4, classified as an aromatic hydrocarbon. Alkylbenzene and Isodurene are alkylbenzenes and hydrocarbon stubs.

See Alkylbenzene and Isodurene

Julius Arnold Koch

Julius Arnold Koch (August 15, 1864 – February 2, 1956) was an American chemist who was born in the Free Hanseatic City of Bremen.

See Alkylbenzene and Julius Arnold Koch

Linear alkylbenzene

Linear alkylbenzenes (sometimes also known as LABs) are a family of organic compounds with the formula C6H5CnH2n+1. Alkylbenzene and Linear alkylbenzene are alkylbenzenes.

See Alkylbenzene and Linear alkylbenzene

List of isomers of dodecane

This is the list of 355 isomers of dodecane.

See Alkylbenzene and List of isomers of dodecane

Ludwig Gattermann

Ludwig Gattermann (20 April 1860 – 20 June 1920) was a German chemist who contributed significantly to both organic and inorganic chemistry.

See Alkylbenzene and Ludwig Gattermann

M-Xylene

m-Xylene (''meta''-xylene) is an aromatic hydrocarbon. Alkylbenzene and m-Xylene are alkylbenzenes.

See Alkylbenzene and M-Xylene

Mesitylene

Mesitylene or 1,3,5-trimethylbenzene is a derivative of benzene with three methyl substituents positioned symmetrically around the ring. Alkylbenzene and Mesitylene are alkylbenzenes.

See Alkylbenzene and Mesitylene

Methyl group

In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula (whereas normal methane has the formula). In formulas, the group is often abbreviated as Me.

See Alkylbenzene and Methyl group

Molecular mass

The molecular mass (m) is the mass of a given molecule.

See Alkylbenzene and Molecular mass

O-Xylene

o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C6H4(CH3)2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration). Alkylbenzene and o-Xylene are alkylbenzenes.

See Alkylbenzene and O-Xylene

P-Cymene

p-Cymene is a naturally occurring aromatic organic compound. Alkylbenzene and p-Cymene are alkylbenzenes.

See Alkylbenzene and P-Cymene

P-Xylene

p-Xylene (''para''-xylene) is an aromatic hydrocarbon. Alkylbenzene and p-Xylene are alkylbenzenes.

See Alkylbenzene and P-Xylene

Prehnitene

Prehnitene or 1,2,3,4-tetramethylbenzene is an organic compound with the formula C6H2(CH3)4, classified as an aromatic hydrocarbon. Alkylbenzene and Prehnitene are alkylbenzenes and hydrocarbon stubs.

See Alkylbenzene and Prehnitene

Refining

Refining (also perhaps called by the mathematical term affining) is the process of purification of a (1) substance or a (2) form.

See Alkylbenzene and Refining

Sodium dodecyl sulfate

Sodium dodecyl sulfate (SDS) or sodium lauryl sulfate (SLS), sometimes written sodium laurilsulfate, is an organic compound with the formula and structure.

See Alkylbenzene and Sodium dodecyl sulfate

Substituent

In organic chemistry, a substituent is one or a group of atoms that replaces (one or more) atoms, thereby becoming a moiety in the resultant (new) molecule.

See Alkylbenzene and Substituent

Surfactant

Surfactants are chemical compounds that decrease the surface tension or interfacial tension between two liquids, a liquid and a gas, or a liquid and a solid.

See Alkylbenzene and Surfactant

Tar

Tar is a dark brown or black viscous liquid of hydrocarbons and free carbon, obtained from a wide variety of organic materials through destructive distillation.

See Alkylbenzene and Tar

Tetramethylbenzene

The tetramethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with four methyl groups (–CH3) as a substituent. Alkylbenzene and tetramethylbenzene are alkylbenzenes and hydrocarbon stubs.

See Alkylbenzene and Tetramethylbenzene

Toluene

Toluene, also known as toluol, is a substituted aromatic hydrocarbon with the chemical formula, often abbreviated as, where Ph stands for phenyl group. Alkylbenzene and Toluene are alkylbenzenes.

See Alkylbenzene and Toluene

Trimethylbenzene

The trimethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with three methyl groups (–CH3) as a substituent. Alkylbenzene and trimethylbenzene are alkylbenzenes.

See Alkylbenzene and Trimethylbenzene

Xylene

In organic chemistry, xylene or xylol (IUPAC name: dimethylbenzene) are any of three organic compounds with the formula. Alkylbenzene and xylene are alkylbenzenes.

See Alkylbenzene and Xylene

1,2,3-Trimethylbenzene

1,2,3-Trimethylbenzene is an organic compound with the chemical formula CH(CH). Alkylbenzene and 1,2,3-Trimethylbenzene are alkylbenzenes and hydrocarbon stubs.

See Alkylbenzene and 1,2,3-Trimethylbenzene

1,2,4-Trimethylbenzene

1,2,4-Trimethylbenzene, also known as pseudocumene, is an organic compound with the chemical formula CH(CH). Alkylbenzene and 1,2,4-Trimethylbenzene are alkylbenzenes.

See Alkylbenzene and 1,2,4-Trimethylbenzene

See also

Alkylbenzenes

• 1,2,3-Trimethylbenzene
• 1,2,4-Trimethylbenzene
• 1,3,5-Triethylbenzene
• 1,3,5-Triheptylbenzene
• 1,3-Diisopropylbenzene
• 2-Phenylhexane
• 4-Ethyltoluene
• Alkylbenzene
• BTX (chemistry)
• C2-Benzenes
• C3-Benzenes
• C4-Benzenes
• Cumene
• Cymene
• Diethylbenzenes
• Diisopropylbenzene
• Dodecylbenzene
• Durene
• Ethylbenzene
• Ethyltoluene
• Flavipin
• Hexamethylbenzene
• Isobutylbenzene
• Isodurene
• Linear alkylbenzene
• M-Cymene
• M-Xylene
• Mesitylene
• N-Butylbenzene
• N-Propylbenzene
• O-Cymene
• O-Xylene
• P-Cymene
• P-Xylene
• Pentamethylbenzene
• Prehnitene
• Sec-Butylbenzene
• Tert-Butylbenzene
• Tetramethylbenzene
• Toluene
• Trimethylbenzene
• Xylene

References

[1] https://en.wikipedia.org/wiki/Alkylbenzene

Also known as Alkylaromatic, Alkylbenzenes.

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