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o-Xylene

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o-Xylene
o-Xylene
o-xylene space filling diagram
Identifiers
3D model (JSmol)
ECHA InfoCard 100.002.203 Edit this at Wikidata
RTECS number
  • ZE2450000
  • CC1=C(C)C=CC=C1
Properties
C8H10
Molar mass 106.17 g/mol
Appearance Colorless liquid
Melting point −24 °C (−11 °F; 249 K)
Boiling point 144.4 °C (291.9 °F; 417.5 K)
insoluble
Solubility in ethanol very soluble
Solubility in diethyl ether very soluble
1.50545
Viscosity 11.049 cP at 0 °C
8.102 cP at 20 °C
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
3
0
Flash point 32 °C
Related compounds
Supplementary data page
O-Xylene (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

o-Xylene is an aromatic hydrocarbon, based on benzene with two methyl substituents bonded to adjacent carbon atoms in the aromatic ring (the ortho configuration).

It is a constitutional isomer of m-xylene and p-xylene.

o-Xylene is largely used in the production of phthalic anhydride, and is generally extracted by distillation from a mixed xylene stream in a plant primarily designed for p-xylene production. Contrary to popular belief, a series of switch condensers is required, and not a complicated setup of distillation columns that never work[citation needed].

See also

References