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Nitrosamines amines

Used in basic solution for alcohols, amines, nitrosamines, amino acids, and steroids heptafluorobutylimidazole is used in a similar fashion in the analysis of phenols... [Pg.97]

Amines, nitrosamines Silica gel Derivitivisation of amines and nitrosamines with 1-dimethy lamino-5-napthalene sulphonyl chloride and 7-chloro-4-nitrobenzo-oxy 1,3 diazole Fluorescence after UV irradiation at 365nm [45]... [Pg.234]

Polycyclic aromatic hydrocarbons Arylamines, certain aminoazo dyes, heterocyclic amines Nitrosamines Urethan Ethionine Aflatoxin Safrole Mice Safrole Hamsters Nitrosamines... [Pg.77]

Selected analytes Selected analytes sometimes have to be analyzed at parts per million levels. Typical examples are aromatic amines, nitrosamines, reactive intermediates left from the synthesis, or certain solvent residues, i.e., all components that are known to be noxious and thus must be controlled separately. [Pg.3613]

A solution of 0.1 g of substance in 4 ml of 2 n HCl is cooled to 5 and mixed with a 10% NaN02 solution, until a drop of the mixture gives a blue color with Kl-starch paper. Nitrogen is set free by amides, aliphatic primary amines, and amino acids (amides are converted to acids, and amines to alcohols yields are often small, but the products can be isolated). A yellow oil or a solid substance (nitrosamine) is formed in the case of secondary aliphatic and aromatic amines. Nitrosamines can be extracted with ether. [Pg.112]


See other pages where Nitrosamines amines is mentioned: [Pg.188]    [Pg.798]    [Pg.117]    [Pg.163]    [Pg.221]    [Pg.163]    [Pg.45]    [Pg.804]    [Pg.199]    [Pg.293]    [Pg.1833]    [Pg.266]    [Pg.286]    [Pg.120]    [Pg.321]    [Pg.2177]    [Pg.236]    [Pg.69]    [Pg.210]   


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N-Nitrosamines amines

Nitrosamine

Nitrosamines

Nitrosamines formation from primary amines

Nitrosamines formation from secondary amines

Nitrosamines via secondary amines

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