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naphthol
(redirected from 1-naphthol)

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naphthol (năf`thôl), C10H7OH, either of two crystalline monohydric alcohols. The naphthols are position isomers isomer , in chemistry, one of two or more compounds having the same molecular formula but different structures (arrangements of atoms in the molecule). Isomerism is the occurrence of such compounds. Isomerism was first recognized by J. J. Berzelius in 1827.
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, differing in the location of the hydroxyl group hydroxyl group , in chemistry, functional group that consists of an oxygen atom joined by a single bond to a hydrogen atom. An alcohol is formed when a hydroxyl group is joined by a single bond to an alkyl group or aryl group.
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, -OH, on the carbon skeleton of naphthalene naphthalene , colorless, crystalline, solid aromatic hydrocarbon with a pungent odor. It melts at 80°C;, boils at 218°C;, and sublimes upon heating. It is insoluble in water, somewhat soluble in ethanol, soluble in benzene, and very soluble in ether,
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; α-naphthol is 1-hydroxynaphthalene and β-naphthol is 2-hydroxynaphthalene: The naphthols have a number of similar properties. They melt at 95°C; and 122°C; and boil at 279°C; and 285°C;, respectively; both are soluble in alcohol and ether and slightly soluble in hot water. One way in which they differ is the form of their crystals—α-naphthol crystallizes in prisms and β-naphthol in plates. The naphthols are prepared by reacting naphthalene with sulfuric acid and hydrolyzing the resultant sulfate ester by heating it with sodium hydroxide solution. Both naphthols exhibit antiseptic properties. They are used in the synthesis of certain azo dyes and antioxidants antioxidant, substance that prevents or slows the breakdown of another substance by oxygen. Synthetic and natural antioxidants are used to slow the deterioration of gasoline and rubber, and such antioxidants as vitamin C (ascorbic acid), butylated hydroxytoluene
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 for rubbers. Naphthol solutions are used in chemical analysis to detect the ferric ion; dissolved ferric ion turns an α-naphthol solution violet and turns a β-naphthol solution green.


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Re-reviews were not reopened due to insufficient data for 1-naphthol isopropyl isostearate.
] Equation 1 Electrochemical oxidation of 1-naphthol formed the basis for determination of the activity of the AP enzyme and quantification of the enzyme label.
Our results show that both inhalation exposure and smoking significantly contributed to urinary 1-naphthol levels.
 
 
 
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