2006
DOI: 10.1590/s1516-89132006000200012
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Determination of N-nitrosamines and N-nitrosables substances in rubber teats and sothers by GC-TEA

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Cited by 7 publications
(3 citation statements)
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“…[2][3][4] N-nitrosamine compounds, which are known as genotoxic and carcinogenic are formed by the reaction of a substance containing secondary amine groups and a nitrosating agent derived from the oxides of nitrogen (NOx). 2,[5][6][7] Nitrosamine formation in rubber articles is mainly due to the use of nitrogen-containing accelerators of vulcanization. 8 Most of the traditional accelerators such as thiurams, dithiocarbamates, some sulphenamides, and sulfur donors are capable of nitrosation during, and after, vulcanization in the presence of nitrosating agents.…”
Section: Introductionmentioning
confidence: 99%
“…[2][3][4] N-nitrosamine compounds, which are known as genotoxic and carcinogenic are formed by the reaction of a substance containing secondary amine groups and a nitrosating agent derived from the oxides of nitrogen (NOx). 2,[5][6][7] Nitrosamine formation in rubber articles is mainly due to the use of nitrogen-containing accelerators of vulcanization. 8 Most of the traditional accelerators such as thiurams, dithiocarbamates, some sulphenamides, and sulfur donors are capable of nitrosation during, and after, vulcanization in the presence of nitrosating agents.…”
Section: Introductionmentioning
confidence: 99%
“…Human exposure to nitrosamines in the rubber industry has been a matter of concern in recent years with the presence of N-nitrosamines in vulcanized rubber products (Blackley, 2012). N-nitroso compounds, which are known as genotoxic and carcinogenic (Fishbein, 2011;Vieira et al, 2006;Iavicoli and Carelli, 2006) are formed by the reaction of a substance containing secondary amine groups and a nitrosating agent derived from the oxides of nitrogen (NOx) or nitrite as shown in the Fig. 1 (Goss et al, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…Nitrosamines are found in rubber articles that are vulcanised with very common traditional accelerators such as tetra methyl thiuram disulphide (TMTD) [4]. These vulcanisates have been tested positive as mutagens and are carcinogenic [4,5]. Other accelerators and sulphur donors that form hazardous nitrosamines are tetra methyl thiuram monosulphide (TMTM), N-oxydiethylene dithiocarbamyl N l -oxydiethylene sulphenamide (OTOS) and N-oxydiethylene -2-benzothiazole sulphenamide (MBS) [6].…”
Section: Introductionmentioning
confidence: 99%