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  2. N-Phenylnaphthalen-1-amine - Wikipedia

    en.wikipedia.org/wiki/N-Phenylnaphthalen-1-amine

    N-Phenylnaphthalen-1-amine (NPN) is an aromatic amine with the chemical formula C 16 H 12 NH.. This molecule is notable for its binding affinity in mouse major urinary protein (MUP).

  3. C16H13N - Wikipedia

    en.wikipedia.org/wiki/C16H13N

    The molecular formula C 16 H 13 N (molar mass: 219.28 g/mol, exact mass: 219.1048 u) may refer to: Benzylisoquinoline; N-Phenylnaphthalen-1-amine (NPN)

  4. Category:1-Naphthyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:1-Naphthyl_compounds

    This page was last edited on 8 November 2022, at 18:36 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. File:N-Phenylnaphthalen-1-amine.svg - Wikipedia

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  6. 1-Naphthylamine - Wikipedia

    en.wikipedia.org/wiki/1-Naphthylamine

    The sulfonic acid derivatives of 1-naphthylamine are used for the preparation of azo dye.These compounds possess the important property of dyeing unmordanted cotton.. An important derivative is naphthionic acid (1-aminonaphthalene-4-sulfonic acid), which is produced by heating 1-naphthylamine and sulfuric acid to 170–180 °C in the presence of crystallized oxalic acid.

  7. Aminonaphthalenesulfonic acids - Wikipedia

    en.wikipedia.org/wiki/Aminonaphthalenesulfonic_acids

    reduction of 1-nitroonaphthalene-8-sulfonic acid, precursor to C.I. Acid Blue 113 Notes: Peri-acid dehydrates to the sultam . Via the Bucherer reaction , heating periacid with anilinium salts gives the N-phenyl derivative, precursor to Acid Blue 113.

  8. N,N-Dimethyl-1-naphthylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-dimethyl-1-naphthylamine

    N,N-Dimethyl-1-naphthylamine is an aromatic amine. It is formally derived from 1-naphthylamine by replacing the hydrogen atoms on the amino group with methyl groups. N,N-Dimethyl-1-naphthylamine is used in the nitrate reductase test to form a precipitate of a red azo dye by reacting with a nitrite-sulfanilic acid complex. [3]

  9. Category:Amine stubs - Wikipedia

    en.wikipedia.org/wiki/Category:Amine_stubs

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