Methylaminophenols

Triclofos Sodium Dissolve 25 mg in 10 ml of DW, add 4 ml of 1 M H2S04, 1 ml of a 10% w/v soln. of ammonium molybdate and 2 ml of a methylaminophenol-sulphite soln. and allow to stand for 15 minutes. Add sufficient DW to produce 25 ml, allow to stand for a further 15 minutes and measure the absorbance of a 4 cm layer of the resulting soln. at 730 nm. Calculate the content of Phosphate from a calibration curve prepared by treating suitable vols. of a 0.00143% w/v soln. of KH2P04 in the same manner. NMT 1.0% calculated as po43-. 

Methylaminophenol-sulphite Solution Dissolve 0.1 g of 4-methylaminophenol sulphate, 20 g sodium metabisulphite and 0.5 g anhydrous sodium sulphite in sufficient DW to produce 100 ml. 

The tetrahydro-derivatives of the oxazole and isoxazole system are unstable. As a consequence, only acyclic products have been reported from the reductions with complex metal hydrides. 2,5-Diphenyl-oxazole (119) gave 2-benzylamino-l-phenylethanol (120),141 and 3,5-diphenyl-2-isoxazoline (121) was converted to 3-amino-l,3-diphenylpropanol (122)142 on reduction with lithium aluminum hydride. 3-Phenylbenzisoxazole was resistant to reduction with lithium aluminum hydride and sodium borohydride,143 but benz-oxazole (123), benzoxazol-2-one (124), and benzoxazol-2-thione (125) have been reported 141 to yield 2-methylaminophenol (126) on reduction with lithium aluminum hydride. 

Phosphate Evaporate 400 mg of sample to dryness on a steam bath. Dissolve the residue in 25 mL of approximately 0.5 N sulfuric acid, add 1 mL of ammonium molybdate solution [500 mg of (NH4)5Mo7024 4H20 in each 10 mL of water] and 1 mL of p-methylaminophenol sulfate TS, and allow it to stand for 2 h. Any blue color does not exceed that produced by 2.0 mL of Phosphate Standard Solution (20 pig PO4) (see Solutions and Indictors) in an equal volume of solution containing the quantities of the reagents used in the test. Residue on Evaporation Evaporate 25 g of sample to dryness in a tared porcelain or silica dish on a steam bath, and... 

Reducing agent—Dissolve 75 g of NaHS03 and 25 g of p-methylaminophenol in 2.5 liters of distilled water. Store in a brown bottle. Stable for 10 days. 

Aniline is converted into hydroquinone, a photographic developer in black and white photography used with metol (p-methylaminophenol). Production of hydroquinone commences with oxidation of aniline by manganese dioxide in aqueous sulfuric acid at 0-5 °C,... 

Permanent hair dyes are often derivatives of an aromatic amine, discovered as a hair dye in 1883, called /Mra-phenylenediamine (H2N-C6H4-NH2), including primary intermediates such as pcirci-aminophenol, dihydroxybenzene, 4-methylaminophenol, tetraaminopyrimidine, 2-aminomethyl-4-aminophenol, and / ara-aminodiphenylamine. The / zrra-phenylenedi-amine compound produces a black color, with its derivative parci- mmo-diphenylaminesulfonic acid used in blond formulations. Couplers are generally aromatic phenols or amines that have an available site that is subject to electrophilic interaction. Typical couplers include chemicals such as resorcinol, wrte-phenylenediamine, 2,4-diaminoanisole, mrm-aminophenol,... 

Equol. [Mackenzie Chem W< ks] n-Methylaminophenol sulfate photo-grtqjhic developer. 

The dihydric phenols are speciality products widely used industrially and commercially. Hydroquinone and its relative, 4-methylaminophenol (metol) are the main chemicals used for development in black and white photography. Butylated hydroxyanisole, (BHA) mainly 2,6-di-tert-butyl-4-methoxyphenol (5), an important food antioxidant is synthesised from 2,4,6-tri-t-butylphenol by reaction in methanolic solution with chlorine to give 2,4,6-tri-t-butyl-4-methoxy-... 

A novel neighbouring group has been introduced in which N-methyl-N -phenoxyurea in dichtoromethane after treatment at OX with trifluoroacetic acid was reacted to give N-(2-hydroxyphenyl)-N-methylurea in 85% yield, from which 2-N-methylaminophenol was obtain (ref.81). 

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