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  2. 1,4-Dichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichlorobenzene

    1,4-Dichlorobenzene (1,4-DCB, p-DCB, or para-dichlorobenzene, sometimes abbreviated as PDCB or para) is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2. This colorless solid has a strong odor. The molecule consists of a benzene ring with two chlorine atoms (replacing hydrogen atoms) on opposing sites of the ring.

  3. Chlorobenzene (data page) - Wikipedia

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

    The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source and follow its directions. An external MSDS is available here.

  4. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    It is also used as a high-boiling solvent in industrial and laboratory applications, for materials such as oils, waxes, resins, and rubber. [ 7 ] [ 8 ] Chlorobenzene is nitrated on a large scale to give a mixture of 2-nitrochlorobenzene and 4-nitrochlorobenzene , which are separated and used as intermediates in production of other chemicals.

  5. Dichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Dichlorobenzene

    1,2-Dichlorobenzene or ortho-dichlorobenzene; 1,3-Dichlorobenzene or meta-dichlorobenzene; 1,4-Dichlorobenzene or para-dichlorobenzene. All three isomers are colorless chlorobenzenes with the formula C 6 H 4 Cl 2. They differ structurally based on where the two chlorine atoms are attached to the ring.

  6. 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.

  7. Polyphenylene sulfide - Wikipedia

    en.wikipedia.org/wiki/Polyphenylene_sulfide

    The PPS (polyphenylene sulfide) polymer is formed by reaction of sodium sulfide with 1,4-dichlorobenzene: n ClC 6 H 4 Cl + n Na 2 S → [C 6 H 4 S] n + 2n NaCl Hill and Edmonds, developers of PPS. The process for commercially producing this material was initially developed by Dr. H. Wayne Hill Jr. and James T. Edmonds at Phillips Petroleum. [7]

  8. 1,2,4-Trichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,4-Trichlorobenzene

    The LD50 (oral, rats) is 756 mg/kg. Animal studies have shown that 1,2,4-trichlorobenzene affects the liver and kidney, and is possibly a teratogen. [4] There is no regulated occupational exposure limit for chemical exposure, but the National Institute for Occupational Safety and Health recommends no greater exposure than 5 ppm, over an 8-hour workday.

  9. Mothball - Wikipedia

    en.wikipedia.org/wiki/Mothball

    Both naphthalene and 1,4-dichlorobenzene undergo sublimation, meaning that they transition from a solid state directly into a gas; this gas is toxic to moths and moth larvae. [ 1 ] Due to the health risks of 1,4-dichlorobenzene, and flammability of naphthalene, other substances like camphor are sometimes used.