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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. 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.

  5. Chlorobenzene (data page) - Wikipedia

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

    An external MSDS is available here. Structure and properties. Structure and properties Index of refraction, n D: 1.5241 ... 633.4 K (360.25°C), 4.52 MPa

  6. Mothball - Wikipedia

    en.wikipedia.org/wiki/Mothball

    Older mothballs consisted primarily of naphthalene, but due to naphthalene's flammability, many modern mothball formulations instead use 1,4-dichlorobenzene. The latter formulation may be somewhat less flammable, although both chemicals have the same NFPA 704 rating for flammability. The latter chemical is also variously labeled as para ...

  7. 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 ...

  8. 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]

  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 ...

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