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Millon reagent

Millon reagent Variety of colors after heating 1... [Pg.207]

Millon reagent A solution of mercury (5 g) in fuming nitric acid (10 ml) diluted with water (10 ml) is sprayed on the plate to yield yellow/orange spots that are intensified by heat (100°C). [Pg.215]

Tile Berlin blue reaction shows arbutin as a blue (--413), the Millons reagent as a yellow zone (- C) in sample 1. In sample 3, in the II, range of arbutin two minor blue (->13) and yellow ( C) zones are detectable. [Pg.252]

If phenols react with nitrites in the presence of mercuric salts (Millon reagent), orange to red colors are formed. Positive reactions are also observed with p-substituted phenols, but not with o,o -disubstituted phenols (21). [Pg.196]

Quantitative estimation by the Millon reagent yielded 95.6 per cent and by the phenol reagent, 97.6 per cent of the respective values given by commercial tyrosine. Confirmatory evidence that fraction A was tyrosine was... [Pg.447]

Millon s reagent Dissolve one part of mercury in two parts of nitric acid (d. 142) first in the cold and then by warming. Dilute the solution with two volumes of water. [Pg.393]

TLC Color reactions with Millon s and Pauly s reagents ... [Pg.166]

Millon s reagent is prepared by dissolving 1 part of mercury in 1 part of nitric acid (D 1 -41) first in the cold and afterwards at a gentle heat the solution obtained is diluted with twice its volume of water and allowed to settle, the clear liquid being decanted off. [Pg.170]

A number of preparative methods are available for the synthesis of WVI nitrides. The reaction of Millon s base [Hg2N]Br with WBr6 provides nitride 86 (Eq. (32)) [37]. The same reagent has been utilized in the synthesis of an interesting Wv complex 87 (Eq. (33)). This W2(p-N) complex can, in turn, be utilized to prepare a W nitride 88. Thus, treatment of 87 with Ph4PBr leads to a disproportionation reaction affording 88 and 89. [Pg.150]

B. Add a few drops of Millon s Reagent to a 1 100 aqueous solution. A white, curdy precipitate forms. [Pg.237]

Millon s Reagent To 2 mL of mercury in an Erlenmeyer flask add 20 mL of nitric acid. Shake the flask in a hood to break the mercury into small globules. After about 10 min add 35 mL of water, and if a precipitate or crystals appear, add sufficient 1 5 nitric acid (prepared from nitric acid from which the oxides have been removed by blowing air through it until it is colorless) to dissolve the separated solid. Add a 1 10 solution of sodium hydroxide, drop wise, with thorough... [Pg.967]

Strong Acid Fraction Aromaticity Ferric Chloride Folin-Ciocalteu Reagent Liebermann s Test Millon s Reagent Nessler s Reagent... [Pg.129]

Colour Tests. Ferric Chloride—brown Folin-Ciocalteu Reagent—blue Liebermann s Test—black Millon s Reagent— pink— red. [Pg.328]

Colour Tests. Ammoniacal Silver Nitrate—black p-Dimethyl-aminobenzaldehyde—red/- Ferric Chloride—green-brown Folin-Ciocalteu Reagent—blue Methanolic Potassium Hydroxide—red Millon s Reagent—red-orange Nessler s Reagent—black Palladium Chloride—orange - brown Potassium Dichromate—brown. [Pg.378]

Colour Tests. Liebermann s Test—orange Marquis Test— yellow Millon s Reagent—red Sulphuric Acid—yellow. [Pg.404]

Colour Tests. Folin-Ciocalteu Reagent—blue Mandelin s Test—green- blue rim Millon s Reagent—red. [Pg.406]

Colour Tests. Aromaticity (Method 2 —yellow/brown Folin-Ciocalteu Reagent—blue Liebermann s Test—violet-brown Millon s Reagent—red. [Pg.531]


See other pages where Millon reagent is mentioned: [Pg.248]    [Pg.252]    [Pg.362]    [Pg.1778]    [Pg.751]    [Pg.909]    [Pg.184]    [Pg.248]    [Pg.252]    [Pg.362]    [Pg.1778]    [Pg.751]    [Pg.909]    [Pg.184]    [Pg.1193]    [Pg.751]    [Pg.133]    [Pg.1218]    [Pg.1462]    [Pg.73]    [Pg.392]    [Pg.40]    [Pg.246]    [Pg.15]    [Pg.216]    [Pg.284]    [Pg.277]    [Pg.55]    [Pg.336]    [Pg.131]    [Pg.84]    [Pg.141]    [Pg.432]    [Pg.603]   
See also in sourсe #XX -- [ Pg.196 ]




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