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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Direct observations: clinical cases, poisoning incidents and other

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Administrative data

Endpoint:
direct observations: clinical cases, poisoning incidents and other
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: although secondary citation there is reliable information

Data source

Reference
Reference Type:
publication
Title:
No information
Author:
Stark M (cited by Greim 1992)
Year:
1982
Bibliographic source:
Ther Mh. 6: 376; cited in Greim 1992, Deutsche Forschungsgemeinschaft (DFG) (1992) Occupational Toxicants, critical data evaluation for MAK values and classification of Carcinogens: o-toluidine and o-toluidine hydrochloride, Vol 3: 307-322

Materials and methods

Study type:
poisoning incident
Endpoint addressed:
acute toxicity: inhalation
Principles of method if other than guideline:
Migrated dataset
GLP compliance:
no
Remarks:
GLP was not mandatory at the time of then study

Test material

Constituent 1
Chemical structure
Reference substance name:
o-toluidine
EC Number:
202-429-0
EC Name:
o-toluidine
Cas Number:
95-53-4
Molecular formula:
C7H9N
IUPAC Name:
2-methylaniline

Method

Reason of exposure:
accidental

Results and discussion

Outcome of incidence:
A worker transferred toluidine from one open vessel to another and , in the process inhaled enough vapour to cause mild poisoning, lost consiousness and remained unconscious in toluidine-contaminated clothes until evening. The patient was cyanotic and exhaled high levels of toluidine. the next day he urinated only very painfully and the urine contained blood. The strangury reached its peak on day 5. On day 8 the urinary complains regressed but blood was detectable in the urine until day 10. Full recovery required 5 weeks.

Applicant's summary and conclusion