[No public or meaningful name is available]

Endpoint summary

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records

Reference

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Qualifier:

according to guideline

Guideline:

other: Directive CEE - Méthode B1 ter et OCDE 423.

GLP compliance:

yes

Test type:

standard acute method

Limit test:

yes

Specific details on test material used for the study:

Lot DSC-9401

Species:

other: Rat, Sprague-Dawley

Vehicle:

other: Purified water

Sex:

male/female

Dose descriptor:

LD50

Effect level:

> 2 000 mg/kg bw

Mortality:

Female: 2000 mg/kg bw; Number of animals: 6; Number of deaths: 0

Clinical signs:

Signs of toxicity related to dose levels : no clinical sign and no mortality were observed during the study


L'évolution pondérale des animaux n'est pas influencée par
le traitement avec la substance.

Gross pathology:

Effects on organs: no apparent anomalies are observed during the macroscopic examination of the main organs of sacrificed animals at the end of the study

Interpretation of results:

not classified

Remarks:

Migrated information Criteria used for interpretation of results: EU

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Dose descriptor:

LD50

Value:

10 000 mg/kg bw