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  2. Naphthalene - Wikipedia

    en.wikipedia.org/wiki/Naphthalene

    With alkali metals, naphthalene forms the dark blue-green radical anion salts such as sodium naphthalene, Na + C 10 H − 8. The naphthalene anions are strong reducing agents. Naphthalene can be hydrogenated under high pressure in the presence of metal catalysts to give 1,2,3,4-tetrahydronaphthalene(C 10 H 12), also known as tetralin.

  3. 2-Methoxynaphthalene - Wikipedia

    en.wikipedia.org/wiki/2-Methoxynaphthalene

    2-Methoxynaphthalene, also called β-naphthol methyl ether or yara yara, [2] is a stabilizer found in gunpowder, particularly smokeless gunpowders.It is soluble in alcohol, and insoluble in water and dipropylene glycol.

  4. 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.

  5. Where to Buy Crystals Online (Whether You're Well ... - AOL

    www.aol.com/entertainment/where-buy-crystals...

    Healing crystals are all the rage in the wellness world right now (though, like a lot of... Skip to main content. Sign in. Mail. 24/7 Help. For premium support please call: 800-290-4726 more ways ...

  6. Lithium naphthalene - Wikipedia

    en.wikipedia.org/wiki/Lithium_naphthalene

    Lithium naphthalene is an organic salt with the chemical formula Li + [C 10 H 8] −. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. Lithium naphthalene crystallizes with ligands bound to Li +. [1] The anion is a well-known example of ...

  7. 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. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na +. [1]

  8. Urinal deodorizer block - Wikipedia

    en.wikipedia.org/wiki/Urinal_deodorizer_block

    The chemicals composing the block vary. The original formulations were based upon naphthalene and then later para-dichlorobenzene, both now known to be hazardous to health by inhalation. In some areas, the use of para-dichlorobenzene-based blocks has been banned; in other areas para-dichlorobenzene blocks or "para blocks" are still used.

  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. It is a colourless solid. Coal tar consists of about 0.3% of this compound.