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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.
o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C 6 H 4 (CH 3) 2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration). It is a constitutional isomer of m-xylene and p-xylene, the mixture being called xylene or xylenes. o-Xylene is a colourless slightly oily flammable ...
log 10 of p-Xylene vapor pressure. Uses formula: log e P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ( 760 101.325 ) − 9.527348 log e ( T + 273.15 ) − 7637.951 T + 273.15 + 79.55720 + 5.748969 × 10 − 6 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-9.527348\log _{e}(T+273.15 ...
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.
Aromatics like benzene, toluene or xylene may also be used. [6] The hydrocarbons used are sometimes made by hydrogenation from naphtha. The lipophilic liquids dissolve fat-soluble lubricants or oils. Some products also contain polar solvents such as ethanol, [7] methanol, [8] isopropanol, and acetone in order to dissolve non-lipophilic ...
α,α'-dimethoxy-p-xylene. A similar synthesis for parylene N uses the precursor α,α'-dimethoxy-p-xylene. [28] The methoxy group H 3 CO − is the leaving group; while it condenses in the deposition chamber, it does not interfere with the deposition of the polymer. [23] This precursor is much less expensive than [2.2]para-cyclophane.
The structure of xylylene dichloride is characterized by an benzene ring with two chloromethyl groups and four hydrogen atoms bound to it. [4] The chloromethyl groups can be located on different sites on the ring, leading to a few different possible forms.
Water-based release agents will be less expensive to ship because of their inherently non-flammable nature and satisfy most plant-safety goals. Solvent-based release coatings dry almost instantly but present serious health and safety concerns. Fumes from solvent-based release agents may be hazardous without proper ventilation of the work area.
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