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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. 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 ...

  5. 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 ...

  6. 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]

  7. C6H4Cl2 - Wikipedia

    en.wikipedia.org/wiki/C6H4Cl2

    1,4-Dichlorobenzene; Dichlorofulvenes; 1,6-Dichloro-2,4-hexadiyne This page was last edited on 28 August 2022, at 12:56 ...

  8. 2-chloro-4-carboxymethylenebut-2-en-1,4-olide isomerase

    en.wikipedia.org/wiki/2-chloro-4-carboxym...

    This enzyme participates in 1,4-dichlorobenzene degradation. References. Schwien U, Schmidt E, Knackmuss H-J and Reinecke W (1988). "Degradation of chlorosubstituted ...

  9. 1,2-Dichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichlorobenzene

    The 1,3- isomer is uncommon because it is a meta- compound, while chlorine, like all halogens, is an ortho/para-director in terms of electrophilic aromatic substitution. It is mainly used as a precursor to 1,2-dichloro-4-nitrobenzene, an intermediate in the synthesis of agrochemicals. [5] In terms of niche applications, 1,2-dichlorobenzene is a ...

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