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  2. Naphthalene - Wikipedia

    en.wikipedia.org/wiki/Naphthalene

    Naphthalene and its alkyl homologs are the major constituents of creosote. Trace amounts of naphthalene are produced by magnolias and some species of deer, as well as the Formosan subterranean termite, possibly produced by the termite as a repellant against "ants, poisonous fungi and nematode worms". [28]

  3. Naphthalene poisoning - Wikipedia

    en.wikipedia.org/wiki/Naphthalene_poisoning

    Naphthalene is a major component of some mothballs.It repels moths as well as some animals. [citation needed]Since mothballs that contain naphthalene are considered hazards, safer alternatives have been developed, such as the use of 1,4-dichlorobenzene, however, 1,4-dichlorobenzene has been declared as a potential neurotoxin. 1,4-dichlorobenzene has been linked to potentially causing ...

  4. Sodium naphthalene - Wikipedia

    en.wikipedia.org/wiki/Sodium_naphthalene

    Sodium naphthalene is an organic salt with the chemical formula Na + [C 10 H 8] −. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic , and inorganic chemistry.

  5. Alkylated naphthalene - Wikipedia

    en.wikipedia.org/wiki/Alkylated_naphthalene

    Alkylated naphthalenes are chemical compounds made by the alkylation of naphthalene or its derivatives with an olefin. These compounds are used as synthetic base oils, and are claimed to have improved oxidative stability over some conventional base oils.

  6. Naphthalenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Naphthalenesulfonate

    Naphthalenesulfonates are derivatives of sulfonic acid which contain a naphthalene functional unit. A related family of compounds are the aminonaphthalenesulfonic acids.Of commercial importance are the alkylnaphthalene sulfonates, which are used as superplasticizers in concrete.

  7. 1-Naphthylamine - Wikipedia

    en.wikipedia.org/wiki/1-Naphthylamine

    1-Naphthylamine is an aromatic amine derived from naphthalene. It can cause bladder cancer (transitional cell carcinoma). It crystallizes in colorless needles which melt at 50 °C. It possesses a disagreeable odor, sublimes readily, and turns brown on exposure to air. It is the precursor to a variety of dyes. [2]

  8. Diaminonaphthalene - Wikipedia

    en.wikipedia.org/wiki/Diaminonaphthalene

    Diaminonaphthalene describes several isomers containing naphthalene substituted with two amine groups (NH 2), also called naphthalenediamines. All isomers are white solids that tend to air-oxidize. The 2,3-, 1,5-, and 1,8- derivatives have attracted most attention. 1,2-Diaminonaphthalene 938-25-0 [1]

  9. Acenaphthene - Wikipedia

    en.wikipedia.org/wiki/Acenaphthene

    Acenaphthene is a polycyclic aromatic hydrocarbon (PAH) consisting of naphthalene with an ethylene bridge connecting positions 1 and 8. It is a colourless solid. Coal tar consists of about 0.3% of this compound. [3]