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POTASSIUM CHLORIDE CAS N°: 7447-40-7

POTASSIUM CHLORIDE CAS N°: 7447-40-7

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OECD SIDS <strong>POTASSIUM</strong> <strong>CHLORIDE</strong><br />

Date: 30-MAR-2003<br />

5. Toxicity Substance ID: <strong>7447</strong>-<strong>40</strong>-7<br />

activation: With Aroclor 1254 induced Fisher rat liver S9<br />

homogenate or with noninduced Fisher 344 rat liver<br />

S9, without activation<br />

Results:<br />

With metabolic activation (Aroclor 1254 induced):<br />

positive at 5000 µg/ml. With metabolic activation<br />

(noninduced): positive at <strong>40</strong>00 and 5000 µg/ml.<br />

Without metabolic activation: negative up to 5000<br />

µg/ml, however, higher, concentrations up to 8000<br />

µg/ml, appeared to be toxic and mutagenic.<br />

Method: OECD 476<br />

Year: 1988 GLP: no data<br />

Test substance:<br />

Remarks:<br />

as prescribed by 1.1-1.4, purity: commercial grade<br />

Media: Fischer's liquid medium for leucemic<br />

cells supplemented with 10 % horse serum. Positive<br />

control was Ethyl methanesulfonate or 3-<br />

methylcholantrene and was positive under all test<br />

conditions. Negative control was 10 % water and<br />

solvent for the test chemical, and was negative<br />

under all test conditions. Treatment up to 5000<br />

µg/ml was not toxic, and did not reduce the<br />

relative total growth below 50-65 %.<br />

Source:<br />

Norsk Hydro ASA<br />

Reliability: (1) reliable without restriction<br />

Flag:<br />

Key study for SIDS<br />

01-MAR-2001 (55)<br />

Type:<br />

mammalian cell gene mutation test<br />

System of<br />

testing: mouse lymphoma cell (L5178Y), TK +/- heterozygote<br />

Concentration: 0-5000 µg/ml<br />

Metabolic<br />

activation: With Aroclor 1254 induced male Fisher 344 rats S9<br />

liver homogenate. Without activation<br />

Results:<br />

With metabolic activation: In the first trial the<br />

relative total growth decreased with increased<br />

concentrations up to <strong>40</strong>00 µg/ml, and no<br />

mutagenicity was reported. The second trial yielded<br />

a positive mutagenic response with a twofold<br />

increase at <strong>40</strong>00 µg/ml and a 2.5 fold increase at<br />

5000 µg/ml. The third trial yielded a<br />

concentration-dependent increase in mutations of<br />

about twofold at 3645 µg/ml, and threefold at <strong>40</strong>50<br />

µg/ml. Overall the test with S9 activation was<br />

evaluated as positive.<br />

Without metabolic activation: negative up to 5000<br />

µg/ml in the first trial. In the second trial<br />

mutations was increased 2.5 fold from 1049 to 3200<br />

µg/ml, however, the increase was not dose-related.<br />

In the third trial cytotoxicity with no<br />

mutagenicity was reported. Overall the results<br />

without S9 activation were evaluated as negative.<br />

Method: OECD 476<br />

Year: 1988 GLP: no data<br />

Test substance: as prescribed by 1.1-1.4, purity: commercial grade<br />

Remarks:<br />

Media: Fischer's liquid medium for leucemic cells<br />

supplemented with 10 % horse serum. Positive<br />

control was Ethyl methanesulfonate or 3-<br />

methylcholantrene and was positive under all test<br />

conditions. Negative control was 10 % water and<br />

UNEP PUBLICATIONS 73

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