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Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)

Data source

Referenceopen allclose all

Reference Type:
review article or handbook
Title:
RTECS Number: BY4415000
Year:
2012
Bibliographic source:
RTECS (Registry of Toxic Effects of Chemical Substances):- 85JCAE "Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986 Volume(issue)/page/year: -,718,1986
Reference Type:
other: Authoritative data base
Title:
No information
Author:
IFA (GESTIS)
Year:
2011
Bibliographic source:
GESTIS - Substance Database (Information system on hazardous substances of the Berufsgenossenschaften)
Reference Type:
review article or handbook
Title:
DPIM: MFB000
Author:
Richard J. Lewis, Sr.
Year:
2007
Bibliographic source:
SAX (Sax's Handbook of Dangerous Industrial Materials):- 85JCAE    Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J., Prague, Czechoslovakia.:  , Avicenum, 1986, 718.
Reference Type:
review article or handbook
Title:
M143
Author:
RSC Publishing
Year:
2011
Bibliographic source:
Dictionary of Substances and their effects (DOSE):- Marhold, J. V. Sbornik Vysledku Toxixologickeho Vysetreni Latek A Pripravku 1972, Prague, Czechoslovakia.

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
other:
Principles of method if other than guideline:
standard acute method
GLP compliance:
not specified
Test type:
standard acute method

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
rat
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
unchanged (no vehicle)

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
14 100 mg/kg bw
Based on:
test mat.
Remarks on result:
other: Details of toxic effects not reported other than lethal dose value

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The LD50 value of the substance is found to be 14100 mg/kg in rats by oral route.