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  2. Toluene (data page) - Wikipedia

    en.wikipedia.org/wiki/Toluene_(data_page)

    This page provides supplementary chemical data on toluene. MSDS sheets. Structure and properties. Structure and properties Index of refraction, n D: 1.4969 at 20 °C ...

  3. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Toluene is also found in cigarette smoke and car exhaust. If not in contact with air, toluene can remain unchanged in soil or water for a long time. [39] Toluene is a common solvent, e.g. for paints, paint thinners, silicone sealants, [40] many chemical reactants, rubber, printing ink, adhesives (glues), lacquers, leather tanners, and ...

  4. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  5. p-Toluenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/P-Toluenesulfonic_acid

    p-Toluenesulfonic acid (PTSA, pTSA, or pTsOH) or tosylic acid (TsOH) is an organic compound with the formula CH 3 C 6 H 4 SO 3 H.It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. [6]

  6. Toluene diisocyanate - Wikipedia

    en.wikipedia.org/wiki/Toluene_diisocyanate

    Toluene diisocyanate (TDI) is an organic compound with the formula CH 3 C 6 H 3 (NCO) 2.Two of the six possible isomers are commercially important: 2,4-TDI (CAS: 584-84-9) and 2,6-TDI (CAS: 91-08-7). 2,4-TDI is produced in the pure state, but TDI is often marketed as 80/20 and 65/35 mixtures of the 2,4 and 2,6 isomers respectively.

  7. p-Toluic acid - Wikipedia

    en.wikipedia.org/wiki/P-Toluic_acid

    p-Toluic acid is an intermediate in the conversion of p-xylene to terephthalic acid, a commodity chemical used in the manufacture of polyethylene terephthalate.It is generated both by the oxidation of p-xylene as well as the hydrogenolysis of 4-carboxybenzaldehyde.

  8. 4-Methylbenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Methylbenzaldehyde

    4-Methylbenzaldehyde is the aromatic aldehyde with the formula CH 3 C 6 H 4 CHO. It is a colorless liquid. Commercially available, it may be prepared from the Friedel-Crafts formylation of toluene with carbon monoxide and hydrogen chloride under Gattermann-Koch conditions.

  9. Parachlorobenzotrifluoride - Wikipedia

    en.wikipedia.org/wiki/Parachlorobenzotrifluoride

    Safety data sheet (SDS) ... An added benefit is that parachlorobenzotrifluoride dissolves most inks faster than toluene. Health and Environmental effects

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