m-Xylene

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m-Xylene
Skeletal formula
Space-filling model
Names
Other names
m-Xylol
1,3-Dimethylbenzene
Identifiers
108-38-3 YesY
ChEBI CHEBI:28488 N
ChEMBL ChEMBL286727 N
ChemSpider 7641 YesY
Jmol 3D model Interactive image
Interactive image
KEGG C07208 N
PubChem 7929
RTECS number ZE2275000
UNII O9XS864HTE N
  • InChI=1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3 YesY
    Key: IVSZLXZYQVIEFR-UHFFFAOYSA-N YesY
  • Cc1cccc(c1)C
  • CC1=CC(C)=CC=C1
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]
1.49722
Viscosity 0.8059 cP at 0 °C
0.6200 cP at 20 °C
0.33-0.37 D[2]
Vapor pressure {{{value}}}
Related compounds
benzene
toluene
o-xylene
p-xylene
Supplementary data page
Refractive index (n),
Dielectric constantr), etc.
Thermodynamic
data
Phase behaviour
solid–liquid–gas
UV, IR, NMR, MS
N verify (what is YesYN ?)
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]

References

  1. Cite error: Invalid <ref> tag; no text was provided for refs named PGCH
  2. DeanHandb, Lange´s Handbook of chemistry, 15th edition,1999.
  3. Ashford's Dictionary of Industrial Chemicals, third edition, page 9692.