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  2. Malononitrile - Wikipedia

    en.wikipedia.org/wiki/Malononitrile

    It can be prepared by dehydration of cyanoacetamide. [3] This method is mainly practiced in China where environmental rules are lax. [citation needed] Most commonly malononitrile is produced by the gas-phase reaction of acetonitrile and cyanogen chloride: [4] NCCl + CH 3 CN → NCCH 2 CN + HCl. About 20,000,000 kg are produced annually (2007).

  3. Solvent Yellow 7 - Wikipedia

    en.wikipedia.org/wiki/Solvent_Yellow_7

    Like most azobenzenes, Solvent Yellow 7 can be synthesized by the reaction of the phenyldiazonium salt with phenol.The optimal pH value for this azo coupling is 8.5-10. The reaction is carried out in water, since sodium chloride (or potassium chloride) formed in the reaction is soluble in water, while the product precipitates.

  4. Diaminomaleonitrile - Wikipedia

    en.wikipedia.org/wiki/Diaminomaleonitrile

    The cis-configuration of the amino groups was shown in 1928 through reaction with glyoxal to give 2,3-diaminopyrazine, and the full structure was shown in 1955 to be diaminomaleonitrile, as opposed to the isomeric aminoiminosuccinonitrile (AISN). [5] It can be prepared by cyanation of aminomalonitrile. [6] [7]

  5. Sodium maleonitriledithiolate - Wikipedia

    en.wikipedia.org/wiki/Sodium_maleonitriledithiolate

    Sodium maleonitriledithiolate is the chemical compound described by the formula Na 2 S 2 C 2 (CN) 2. The name refers to the cis compound, structurally related to maleonitrile ((CH(CN)) 2). Maleonitriledithiolate is often abbreviated mnt. It is a "dithiolene", i.e. a chelating alkene-1,2-dithiolate.

  6. m-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/M-Phenylenediamine

    m-Phenylenediamine, also called 1,3-diaminobenzene, is an organic compound with the formula C 6 H 4 (NH 2) 2.It is an isomer of o-phenylenediamine and p-phenylenediamine.This aromatic diamine is a colourless solid that appears as needles, but turns red or purple on exposure to air due to formation of oxidation products. [3]

  7. CS gas - Wikipedia

    en.wikipedia.org/wiki/CS_gas

    The compound 2-chlorobenzalmalononitrile (also called o-chlorobenzylidene malononitrile; chemical formula: C 10 H 5 ClN 2), a cyanocarbon, is the defining component of the lachrymatory agent commonly referred to as CS gas, a tear gas which is used as a riot control agent, and is banned for use in warfare due to the 1925 Geneva Protocol.

  8. Methyl yellow - Wikipedia

    en.wikipedia.org/wiki/Methyl_yellow

    Methyl yellow, or C.I. 11020, is an organic compound with the formula C 6 H 5 N 2 C 6 H 4 N(CH 3) 2. It is an azo dye derived from dimethylaniline. It is a yellow solid. According to X-ray crystallography, the C 14 N 3 core of the molecule is planar. [3] It is used as a dye for plastics and may be used as a pH indicator.

  9. 2-Phenylphenol - Wikipedia

    en.wikipedia.org/wiki/2-Phenylphenol

    2-Phenylphenol, or o-phenylphenol, is an organic compound. In terms of structure, it is one of the monohydroxylated isomers of biphenyl. [2] [3] It is a white solid. It is a biocide used as a preservative with E number E231 and under the trade names Dowicide, Torsite, Fungal, Preventol, Nipacide and many others.