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Xylene is used in the laboratory to make baths with dry ice to cool reaction vessels, [17] and as a solvent to remove synthetic immersion oil from the microscope objective in light microscopy. [18] In histology, xylene is the most widely used clearing agent. [19] Xylene is used to remove paraffin from dried microscope slides prior to staining.
p-Xylene (para-xylene) is an aromatic hydrocarbon. It is one of the three isomers of dimethylbenzene known collectively as xylenes . The p- stands for para- , indicating that the two methyl groups in p -xylene occupy the diametrically opposite substituent positions 1 and 4.
m-Xylene is isomerized to o-xylene. Net production was approximately 500,000 tons in the year 2000. o-Xylene is largely used in the production of phthalic anhydride, which is a precursor to many materials, drugs, and other chemicals. [7] Related to their easy oxidation, the methyl groups are susceptible to halogenation.
Xylene is often used in paints, glues, pesticides and cleaning agents. Xylene also is used in the plastics, chemical and synthetic fiber industries. As a vapor, xylene is heavier than air, so it ...
Likewise, the para-xylene consumption showed unprecedented growth in 2010, growing by 2,800,000 tons, a full ten percent growth from 2009. [1] Toluene is also a valuable petrochemical for use as a solvent and intermediate in chemical manufacturing processes and as a high octane gasoline component. [2] [3] [4] [5]
Synthetic sulfonates are the most widely used detergents, as industrial oil, emulsifiers, demulsifiers, rust inhibitors, dispersants, surfactants for enhanced oil recovery, ore-floatation agents, and wetting agents, among others. LABs such as alkylbenzene, dialkylbenzene, and alkyltoluene are most commonly used to prepare sulfonate detergents.
m-Xylene (meta-xylene) is an aromatic hydrocarbon. It is one of the three isomers of dimethylbenzene known collectively as xylenes . The m- stands for meta- , indicating that the two methyl groups in m -xylene occupy positions 1 and 3 on a benzene ring.
For example, reaction of α,α'-dibromo-o-xylene with iron carbonyls affords low yields of the xylylene complex Fe(CO) 3 [η 4-C 6 H 4 (CH 2) 2]. This product is structurally analogous to Fe(CO) 3 [η 4-1,3-butadiene]. [11] At high temperatures, benzocyclobutenes undergo electrocyclic ring-opening to form o-xylylenes.