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  2. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    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.

  3. Surfactants in paint - Wikipedia

    en.wikipedia.org/wiki/Surfactants_in_paint

    The solvent also modifies the curing rate and viscosity of the paint in its liquid state. There are two types of paint: solvent-borne and water-borne paints. Solvent-borne paints use organic solvents as the primary vehicle carrying the solid components in a paint formulation, whereas water-borne paints use water as the continuous medium.

  4. Paint thinner - Wikipedia

    en.wikipedia.org/wiki/Paint_thinner

    A paint thinner is a diluent solvent used to dilute oil-based paints or varnish. [ 1 ] [ 2 ] In this context, to dilute is also known as to 'thin'. Organic solvents labelled "paint thinner" are usually white spirits / mineral spirits for use to dilute oil-based paints only.

  5. Varnish - Wikipedia

    en.wikipedia.org/wiki/Varnish

    Exterior use of polyurethane varnish may be problematic due to its heightened susceptibility to deterioration through ultra-violet light exposure. All clear or translucent varnishes, and indeed all film-polymer coatings (e.g. paint, stain, epoxy, synthetic plastic, etc.) are susceptible to this damage in varying degrees.

  6. Paint stripper - Wikipedia

    en.wikipedia.org/wiki/Paint_stripper

    Solvent-base paint strippers can be complex mixtures of various organic solvents, emulsifiers, thickening agents, alkaline or acid active ingredients as well as evaporation and corrosion inhibitors. Dichloromethane , also called methylene chloride, is a popular solvent, but its use has been declining because of health concerns. [ 1 ]

  7. Xylylene - Wikipedia

    en.wikipedia.org/wiki/Xylylene

    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.