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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. 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]

  4. 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.

  5. File:1,4 dichlorobenzene crystallised.jpg - Wikipedia

    en.wikipedia.org/wiki/File:1,4_dichlorobenzene...

    Download QR code; In other projects ... 1,4-dichlorobenzene crystallised from DCM on paper. ... One-chip color area sensor: DateTimeDigitized subseconds:

  6. 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.

  7. Hazardous Materials Identification System - Wikipedia

    en.wikipedia.org/wiki/Hazardous_Materials...

    Materials may react violently with water or form peroxides upon exposure to air (e.g., potassium, sodium). 1. Materials that are normally stable but can become unstable (self-react) at high temperatures and pressures. Materials may react non-violently with water or undergo hazardous polymerization in the absence of inhibitors (e.g., propene). 0.

  8. 1,4-Dichloro-2-nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichloro-2-nitrobenzene

    Disperse Yellow 42, a popular dye for polyesters, is derived from 1,4-dichloro-2-nitrobenzene. [1] 1,4-Dichloro-2-nitrobenzene is an organic compound with the formula C 6 H 3 Cl 2 NO 2. One of several isomers of dichloronitrobenzene, it is a yellow solid that is insoluble in water. It is produced by nitration of 1,4-dichlorobenzene. It is a ...

  9. Chlorobenzenes - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzenes

    They have the formula C 6 H 6–n Cl n, where n = 1–6 is the number of chlorine atoms. Depending on the number of chlorine substituents, there may be several constitutional isomers possible. Monochlorobenzene; Dichlorobenzene. 1,2-Dichlorobenzene; 1,3-Dichlorobenzene; 1,4-Dichlorobenzene; Trichlorobenzene. 1,2,3-Trichlorobenzene; 1,2,4 ...