o-TOLUIDINE CAS N°: 95-53-4 - UNEP Chemicals
o-TOLUIDINE CAS N°: 95-53-4 - UNEP Chemicals
o-TOLUIDINE CAS N°: 95-53-4 - UNEP Chemicals
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OECD SIDS o-<strong>TOLUIDINE</strong><br />
5. TOXICITY ID: <strong>95</strong>-<strong>53</strong>-4<br />
DATE: 07.01.2005<br />
cells were treated for 6 hours with or without 5% S9-mix<br />
METABOLIC ACTIVATION:<br />
S9 mix liver homogenates from phenobarbital and 5,6-benzoflavone<br />
induced rats<br />
Controls:<br />
negative controls:<br />
untreated cultures; vehicle (DMSO) treated cultures;<br />
positive control:<br />
Dimethylnitrosamine (DMN)<br />
Reliability : (4) not assignable<br />
no data on cytoxicity<br />
15.07.2004 (215) (216)<br />
Type : Chromosomal aberration test<br />
System of testing : RL4 cells<br />
Test concentration : 0, 87.5, 175, 350, 700 µg/ml DMSO<br />
Cycotoxic concentr. : 500 - 750 µg/ml DMSO<br />
Metabolic activation : without<br />
Result : positive<br />
Method : other: chromosomal aberration test ( see freetext TC)<br />
Year : 1985<br />
GLP : no data<br />
Test substance : other TS: o-toluidine, no data on purity<br />
Result : Over the dose-range 87.5-700µg/ml o-toluidine induced a dose related<br />
increase in chromatid gaps that was significant at 700 µg/ml.<br />
In the absence of other chromatid or chromosome aberrations the increase<br />
in gaps alone is regarded as indicative of weak clastogenic activity.<br />
Test condition : ---Test system<br />
RL4 cells (epithelial-like cell isolated from liver of 10-day-old male Wistar<br />
rat, cycle time: 13 h)<br />
---Preliminary cytotoxicity test<br />
Cytotoxicity was measurement as plating efficiency<br />
Cytotoxicity reduced by 50% between 500 and 750 µg/ml and 700 µg/ml<br />
was used as the highest dose level.<br />
---Incubation time:<br />
22 hoursadditional 2 hrs after addition of colcemid solution<br />
---Controls<br />
positive controls: 7,12-dimethylbenzanthracene 1µg/ml<br />
negative controls: solvent (DMSO)<br />
Reliability : (4) not assignable<br />
Method evaluation, unsuitable cell system<br />
15.07.2004 (180) (281) (282)<br />
Type : Chromosomal aberration test<br />
System of testing : CH1-L (fibroblasts from the liver of Chinese hamster)<br />
Test concentration : 0, 12, 30, 60, 120 µg/ml DMSO<br />
Cycotoxic concentr. : preliminary test, tests carried out with dose up to 50% growth inhibition<br />
Metabolic activation : without<br />
Result : positive<br />
Method : other: chromosome aberrations and aneuploidy<br />
Year : 1985<br />
GLP : no data<br />
Test substance : other TS: o-toluidine, no data on purity<br />
Result : All concentrations tested, both excluding and including gaps, caused<br />
significant increase in the level of chromosome aberrations. Although doseresponse<br />
was observed, this was not statistically significant.<br />
A similar situation was found with regard to aneuploidy levels. The higher 2<br />
doses had significant greater levels of hyperdiploidy, but dose-response<br />
was non-significant.<br />
<strong>UNEP</strong> PUBLICATIONS 211