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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 />

212<br />

Thus o-toluidin was positive for both endpoints.<br />

Reliability : (4) not assignable<br />

IPCS Collaborative Study to evaluate an unusual test system<br />

15.07.2004 (283) (284) (180)<br />

Type : Chromosomal aberration test<br />

System of testing : Chinese Hamster Lung (CHL) cells<br />

Test concentration : 0, 1.0, 1.25, 1.5 mg/ml DMSO<br />

Cycotoxic concentr. : in preliminary screening the conc at which cell growth was inhibited was<br />

determined: data not given<br />

Metabolic activation : with and without<br />

Result : positive<br />

Method : other: see freetext ME<br />

Year : 1988<br />

GLP : no data<br />

Test substance : other TS: o-toluidine, no data on purity<br />

Method : Metabolic activation system (S9-mix)<br />

was prepared from Wistar or Fisher rats or BALB/c mice injected with 500<br />

mg/kg bw PCB<br />

Incubation and recovery time: 6-18 hours<br />

No of metaphases: 200<br />

Result : positive results only in the presence of the metabolic activation system<br />

no positive controls for the trials with and without S9-mix<br />

Reliability : (4) not assignable<br />

documentation insufficient for assessment<br />

15.07.2004 (285)<br />

Type : Chromosomal aberration test<br />

System of testing : Chinese hamster ovary (CHO) cells<br />

Test concentration : 0, 100, 300, 900 µg/ml<br />

Cycotoxic concentr. : top dose selected as 50% inhibition of the mitotic index, compaired with<br />

controls<br />

Metabolic activation : with and without<br />

Result : negative<br />

Method : other: see freetext TC<br />

Year : 1985<br />

GLP : no data<br />

Test substance : other TS: o-toluidine, no data on purity<br />

Result : An increased chromosomal aberration frequency was observed only at the<br />

intermediate dose (300 µg/ml) in the presence of metaboic activation and a<br />

treatment time of 3 hours.<br />

Summary results = negative<br />

Positive controls were functional.<br />

Test condition : Treatment time:<br />

with S9-mix. 3 hours<br />

without S9-mix: 12 hours<br />

Controls:<br />

negative controls:<br />

untreated cultures; solvent treated cultures<br />

positive controls:<br />

cyclophosphamide; aflatoxin B1<br />

METABOLIC ACTIVATION:<br />

S9 mix was prepared from rat liver homogenates from Phenobarbital<br />

induced male Sprague-Dawley rats<br />

Analysis of results<br />

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