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  2. 1-Naphthol - Wikipedia

    en.wikipedia.org/wiki/1-naphthol

    1-Naphthol, or α-naphthol, is an organic compound with the formula C 10 H 7 OH. It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol. Both isomers are soluble in simple organic solvents. They are ...

  3. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  4. Carbaryl - Wikipedia

    en.wikipedia.org/wiki/Carbaryl

    Carbaryl is often inexpensively produced by direct reaction of methyl isocyanate with 1-naphthol. [5]C 10 H 7 OH + CH 3 NCO → C 10 H 7 OC(O)NHCH 3. Alternatively, 1-naphthol can be treated with excess phosgene to produce 1-naphthyl chloroformate, which is then converted to carbaryl by reaction with methylamine. [5]

  5. Category:Naphthalenes - Wikipedia

    en.wikipedia.org/wiki/Category:Naphthalenes

    1-Naphthyl compounds (46 P) 2-Naphthyl compounds (33 P) N. Naphthoic acids (8 P) Naphthol esters (3 P) Naphthol ethers (20 P) Naphthols (3 C, 4 P) Naphthoquinones (3 ...

  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. N-(1-Naphthyl)ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/N-(1-Naphthyl)ethylenediamine

    N-(1-Naphthyl)ethylenediamine dihydrochloride is widely used in the quantitative analysis of nitrate and nitrite in water samples by colorimetry. It readily undergoes a diazonium coupling reaction in the presence of nitrite to give a strongly colored azo compound .

  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.

  9. 1-Naphthaleneacetic acid - Wikipedia

    en.wikipedia.org/wiki/1-Naphthaleneacetic_acid

    1-Naphthaleneacetic acid (NAA) is an organic compound with the formula C 10 H 7 CH 2 CO 2 H. This colorless solid is soluble in organic solvents. This colorless solid is soluble in organic solvents. It features a carboxylmethyl group (CH 2 CO 2 H) linked to the "1-position" of naphthalene .

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