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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. 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.

  4. Chlorobenzene (data page) - Wikipedia

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

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. ... 633.4 K (360.25°C), 4.52 MPa Std enthalpy change

  5. 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.

  6. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    1,4-dichlorobenzene: Supplementary data page Chlorobenzene (data page) Except where otherwise noted, data are given for materials in their standard state (at 25 °C ...

  7. 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 ...

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

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

    1,4-Dichlorobenzene; Metadata. This file contains additional information, probably added from the digital camera or scanner used to create or digitize it.

  9. 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]

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