M-Xylene, the Glossary
m-Xylene (''meta''-xylene) is an aromatic hydrocarbon.[1]
Table of Contents
24 relations: Ammoxidation, Arene substitution pattern, Aromatic compound, Benzene, Catalysis, Copolymer, Debye, Isomer, Isophthalic acid, Isophthalonitrile, Monomer, O-Xylene, P-Xylene, Petroleum, Poise (unit), Polyethylene terephthalate, Redox, Royal Society of Chemistry, Steam distillation, Tetrachloro-m-xylene, Toluene, United States Environmental Protection Agency, Xylene, Xylidine.
- Alkylbenzenes
- C2-Benzenes
Ammoxidation
In organic chemistry, ammoxidation is a process for the production of nitriles using ammonia and oxygen.
Arene substitution pattern
Arene substitution patterns are part of organic chemistry IUPAC nomenclature and pinpoint the position of substituents other than hydrogen in relation to each other on an aromatic hydrocarbon.
See M-Xylene and Arene substitution pattern
Aromatic compound
Aromatic compounds or arenes usually refers to organic compounds "with a chemistry typified by benzene" and "cyclically conjugated." The word "aromatic" originates from the past grouping of molecules based on odor, before their general chemical properties were understood.
See M-Xylene and Aromatic compound
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.
Catalysis
Catalysis is the increase in rate of a chemical reaction due to an added substance known as a catalyst.
Copolymer
In polymer chemistry, a copolymer is a polymer derived from more than one species of monomer.
Debye
The debye (symbol: D) is a CGS unit (a non-SI metric unit) of electric dipole momentTwo equal and opposite charges separated by some distance constitute an electric dipole.
Isomer
In chemistry, isomers are molecules or polyatomic ions with identical molecular formula – that is, the same number of atoms of each element – but distinct arrangements of atoms in space.
Isophthalic acid
Isophthalic acid is an organic compound with the formula C6H4(CO2H)2.
See M-Xylene and Isophthalic acid
Isophthalonitrile
Isophthalonitrile is an organic compound with the formula C6H4(CN)2.
See M-Xylene and Isophthalonitrile
Monomer
A monomer (mono-, "one" + -mer, "part") is a molecule that can react together with other monomer molecules to form a larger polymer chain or three-dimensional network in a process called polymerization.
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). M-Xylene and o-Xylene are Alkylbenzenes and c2-Benzenes.
P-Xylene
p-Xylene (''para''-xylene) is an aromatic hydrocarbon. M-Xylene and p-Xylene are Alkylbenzenes and c2-Benzenes.
Petroleum
Petroleum or crude oil, also referred to as simply oil, is a naturally occurring yellowish-black liquid mixture of mainly hydrocarbons, and is found in geological formations.
Poise (unit)
The poise (symbol P) is the unit of dynamic viscosity (absolute viscosity) in the centimetre–gram–second system of units (CGS).
Polyethylene terephthalate
Polyethylene terephthalate (or poly(ethylene terephthalate), PET, PETE, or the obsolete PETP or PET-P), is the most common thermoplastic polymer resin of the polyester family and is used in fibres for clothing, containers for liquids and foods, and thermoforming for manufacturing, and in combination with glass fibre for engineering resins.
See M-Xylene and Polyethylene terephthalate
Redox
Redox (reduction–oxidation or oxidation–reduction) is a type of chemical reaction in which the oxidation states of the reactants change.
Royal Society of Chemistry
The Royal Society of Chemistry (RSC) is a learned society and professional association in the United Kingdom with the goal of "advancing the chemical sciences".
See M-Xylene and Royal Society of Chemistry
Steam distillation
Steam distillation is a separation process that consists of distilling water together with other volatile and non-volatile components.
See M-Xylene and Steam distillation
Tetrachloro-m-xylene
Tetrachloro-m-xylene (tetrachlorometaxylene, or TCMX) is the organochlorine compound with the formula C6Cl4(CH3)2.
See M-Xylene and Tetrachloro-m-xylene
Toluene
Toluene, also known as toluol, is a substituted aromatic hydrocarbon with the chemical formula, often abbreviated as, where Ph stands for phenyl group. M-Xylene and Toluene are Alkylbenzenes.
United States Environmental Protection Agency
The Environmental Protection Agency (EPA) is an independent agency of the United States government tasked with environmental protection matters.
See M-Xylene and United States Environmental Protection Agency
Xylene
In organic chemistry, xylene or xylol (IUPAC name: dimethylbenzene) are any of three organic compounds with the formula. M-Xylene and xylene are Alkylbenzenes and c2-Benzenes.
Xylidine
Xylidine can refer to any of the six isomers of xylene amine, or any mixture of them.
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
C2-Benzenes
References
[1] https://en.wikipedia.org/wiki/M-Xylene
Also known as 1,3-Dimethylbenzene, M-xylol, Meta-Xylene, Metaxylene.