<<

12. CHEMICAL FACT SHEETS

Principal reference WHO (2003) Molybdenum in drinking-water. Background document for preparation of WHO Guidelines for drinking-water quality. Geneva, World Health Organization (WHO/SDE/WSH/03.04/11).

12.89 Monochloramine Mono-, di- and trichloramines are considered by-products of drinking-water chlori- nation, being formed when is added to chlorinated water. Monochloramine may also be added to maintain residual disinfection activity in potable water distri- bution systems. The use of chloramines for disinfection instead of reduces the formation of THMs in drinking-water supplies. However, formation of other by- products, such as haloketones, chloropicrin, cyanogen chloride, haloacetic acids, haloacetonitriles, aldehydes and chlorophenols, has been reported. Monochloramine is recognized as a less effective than chlorine. Only monochloramine, the most abundant chloramine, is considered here, as it has been the most extensively studied.

Guideline value 3 mg/litre Occurrence Typical chloramine of 0.5–2 mg/litre are found in drinking-water supplies where chloramine is used as a primary disinfectant or to provide a chlorine residual in the distribution system. TDI 94 mg/kg of body weight, based on a NOAEL of 9.4 mg/kg of body weight per day, the highest dose administered to male rats in a 2-year NTP drinking-water study (although mean body weights of rats given the highest dose were lower than those of their respective control groups, it is probable that the lower body weights were caused by the unpalatability of the drinking-water) Limit of detection 10 mg/litre by colorimetric methods Treatment achievability It is possible to reduce the of chloramine effectively to zero (<0.1 mg/litre) by reduction; however, it is normal practice to supply water with a chloramine residual of a few tenths of a milligram per litre to act as a preservative during distribution. Guideline derivation • allocation to water 100% of TDI • weight 60-kg adult • consumption 2 litres/day Additional comments • An additional uncertainty factor for possible carcinogenicity was not applied because equivocal effects reported in the NTP study in only one species and in only one sex were within the range observed in historical controls. • Most individuals are able to taste chloramines at concentrations below 5 mg/litre, and some at levels as low as 0.3 mg/litre.

411 GUIDELINES FOR DRINKING-WATER QUALITY

Toxicological review Although monochloramine has been shown to be mutagenic in some in vitro studies, it has not been found to be genotoxic in vivo. IARC has classified chloramine in Group 3, and the US EPA has classified monochloramine in group D (not classifiable as to human carcinogenicity, as there is inadequate human and animal evidence). In the NTP bioassay in two species, the incidence of mononuclear cell leukaemias in female F344/N rats was increased, but no other increases in tumour incidence were observed. IPCS (2000) did not consider that the increase in mononuclear cell leukaemia was treatment-related.

History of guideline development The 1958, 1963 and 1971 WHO International Standards for Drinking-water and the first edition of the Guidelines for Drinking-water Quality, published in 1984, did not refer to chloramines. The 1993 Guidelines established a health-based guideline value of 3mg/litre for monochloramine in drinking-water. Available data were insufficient for the establishment of guideline values for and trichloramine. It was noted that the odour thresholds for dichloramine and trichloramine are much lower than that for monochloramine.

Assessment date The risk assessment was conducted in 2003.

Principal references IPCS (2000) and disinfectant by-products. Geneva, World Health Orga- nization, International Programme on Chemical Safety (Environmental Health Criteria 216). WHO (2003) Monochloramine in drinking-water. Background document for prepara- tion of WHO Guidelines for drinking-water quality. Geneva, World Health Organi- zation (WHO/SDE/WSH/03.04/83).

12.90 Monochloroacetic acid Chlorinated acetic acids are formed from organic material during .

412