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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. m-Xylene - Wikipedia

    en.wikipedia.org/wiki/M-Xylene

    The m-stands for meta-, indicating that the two methyl groups in m-xylene occupy positions 1 and 3 on a benzene ring. It is in the positions of the two methyl groups, their arene substitution pattern, that it differs from the other isomers, o-xylene and p-xylene. All have the same chemical formula C 6 H 4 (CH 3) 2. All xylene isomers are ...

  4. p-Xylene - Wikipedia

    en.wikipedia.org/wiki/P-Xylene

    p-Xylene is an important chemical feedstock. Among other industrial applications, it is a raw material in the large scale synthesis of various polymers . In particular it is a component in the production of terephthalic acid for polyesters such as polyethylene terephthalate (generally known as PET).

  5. o-Xylene - Wikipedia

    en.wikipedia.org/wiki/O-Xylene

    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 ...

  6. Xylidine - Wikipedia

    en.wikipedia.org/wiki/Xylidine

    Xylidine can refer to any of the six isomers of xylene amine, or any mixture of them. The chemical formula of xylidines is C 8 H 11 N or, more descriptively, (CH 3) 2 C 6 H 3 NH 2. The CAS number for the isomer mixture is . They are colorless solids or liquids, although commercial samples can appear yellow or darker.

  7. Recommended exposure limit - Wikipedia

    en.wikipedia.org/wiki/Recommended_exposure_limit

    All RELs are located in the NIOSH Pocket Guide to Chemical Hazards, along with other key data for 677 chemical or substance groupings. The Pocket Guide is a source of general industrial hygiene information for workers, employers, and occupational health professionals. [1] NIOSH recommendations are also published in a variety of documents ...

  8. m-Xylylenediamine - Wikipedia

    en.wikipedia.org/wiki/M-Xylylenediamine

    It can cause chemical burns, tissue damage, delayed pulmonary edema, shock, and skin sensitization. Symptoms of inhalation include a burning sensation in the respiratory tract, cough, sore throat, labored breathing, and dyspnea (shortness of breath). It is also flammable and produces toxic fumes when burned.

  9. Hexamethylene diisocyanate - Wikipedia

    en.wikipedia.org/wiki/Hexamethylene_diisocyanate

    Chemical formula. C 8 H 12 N 2 O 2 Molar mass: ... from the website of the National Institute for Occupational Safety and Health (NIOSH) NIOSH Pocket Guide to ...