m-Xylene
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Names | |||
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Other names
m-Xylol
1,3-Dimethylbenzene |
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Identifiers | |||
108-38-3 | |||
ChEBI | CHEBI:28488 | ||
ChEMBL | ChEMBL286727 | ||
ChemSpider | 7641 | ||
Jmol 3D model | Interactive image Interactive image |
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KEGG | C07208 | ||
PubChem | 7929 | ||
RTECS number | ZE2275000 | ||
UNII | O9XS864HTE | ||
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Properties | |||
C8H10 | |||
Molar mass | 106.16 g/mol | ||
Appearance | Colorless liquid | ||
Density | 0.86 g/mL | ||
Melting point | −48 °C (−54 °F; 225 K) | ||
Boiling point | 139 °C (282 °F; 412 K) | ||
insoluble | |||
Solubility in ethanol | very soluble | ||
Solubility in diethyl ether | very soluble | ||
Vapor pressure | 9 mmHg (20°C)[1] | ||
Refractive index (nD)
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1.49722 | ||
Viscosity | 0.8059 cP at 0 °C 0.6200 cP at 20 °C |
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0.33-0.37 D[2] | |||
Vapor pressure | {{{value}}} | ||
Related compounds | |||
Related aromatic
hydrocarbons |
benzene toluene o-xylene p-xylene |
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Supplementary data page | |||
Refractive index (n), Dielectric constant (εr), etc. |
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Thermodynamic
data |
Phase behaviour solid–liquid–gas |
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UV, IR, NMR, MS | |||
verify (what is ?) | |||
Infobox references | |||
m-Xylene (or meta-xylene) is an aromatic hydrocarbon, based on benzene with two methyl substituents. It is an isomer of o-xylene and p-xylene. The m stands for meta, meaning the two methyl substituents are at locants 1 and 3 on the aromatic ring. m-Xylene is commonly produced in BTX processes, and separated as needed from the other aromatic hydrocarbons.
The major chemical use of meta-xylene is in the manufacture of isophthalic acid, which is used as a copolymerizing monomer to alter the properties of polyethylene terephthalate (PET), making PET more suitable for the manufacture of soft drinks bottles. To convert m-xylene on an industrial scale to isophthalic acid, the two methyl groups are both catalytically oxidized to carboxyl groups. It is also used as a raw material in the manufacture of 2,4- and 2,6-xylidine as well as a range of smaller-volume chemicals.[3]