Colouration primary colours

The colour test is not specific for a-amino acids other primary amino compounds and also ammonia give a blue colouration with ninhydrin. 

Primary nitro compound intense red colour, disappearing upon acidification. The colouration is that of the alkali salt of the nitrolic acid (nitro oxime) -... 

DinitrophenyI derivatives. The halogen atom in 2 4-di-nitrochlorobenzene is reactive and coloured crystalline compounds (usually yellow or red) are formed with primary and with secondary amines ... 

Some reference to the use of nitrous acid merits mention here. Primary aromatic amines yield diazonium compounds, which may be coupled with phenols to yield highly-coloured azo dyes (see Section IV,100,(iii)). Secondary aromatic amines afford nitroso compounds, which give Liebermann a nitroso reaction Section IV,100,(v). Tertiary aromatic amines, of the type of dimethylaniline, yield p-nitroso derivatives see Section IV,100,(vii). ... 

The common impurities found in amines are nitro compounds (if prepared by reduction), the corresponding halides (if prepared from them) and the corresponding carbamate salts. Amines are dissolved in aqueous acid, the pH of the solution being at least three units below the pKg value of the base to ensure almost complete formation of the cation. They are extracted with diethyl ether to remove neutral impurities and to decompose the carbamate salts. The solution is then made strongly alkaline and the amines that separate are extracted into a suitable solvent (ether or toluene) or steam distilled. The latter process removes coloured impurities. Note that chloroform cannot be used as a solvent for primary amines because, in the presence of alkali, poisonous carbylamines (isocyanides) are formed. However, chloroform is a useful solvent for the extraction of heterocyclic bases. In this case it has the added advantage that while the extract is being freed from the chloroform most of the moisture is removed with the solvent. 

Aromatic amines are the most effective primary antioxidants (Fig. 34) but they are discolouring and can only be used where the darker colours are acceptable (for instance in rubber adhesive formulations containing carbon blacks as fillers). The... 

The other class of primary antioxidants are the phenols (hindered phenols, hindered bisphenols, hindered thiobisphenols, polyhydroxy phenols) (Fig. 34). Phenolic antioxidants are generally used when the discolouration of the amine antioxidants cannot be tolerated. Phenols may produce coloured reaction products (yellow, tan or pink) but the discolouration is significantly less than produced with amines. 

B. Naphthaquinone method Discussion. Many primary amines develop a blue colour when treated with ortho-quinones the preferred reagent is the sodium salt of l,2-naphthaquinone-4-sulphonic acid. 

Discussion. The formation of coloured compounds by coupling phenols with diazotised primary aromatic amines has long been recognised as a method of determining phenols, and procedures have been evolved whereby the phenol solution is titrated with a diazonium solution which has been calibrated against known concentrations of the phenol. The resultant reaction products are coloured, but many are only sparingly soluble in water and organic solvents and do not therefore lend themselves to colorimetric determination. 

Primary identification is by means of labelling with the name and chemical formula on the shoulder of the cylinder. Secondary identification is by use of ground colours on the cylinder body and colour bands on the cylinder shoulder to denote the nature of the gas, as exemplified by Table 8.2 for selected common gases. (The full scheme is given in BS 349 1973.)... 

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