Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1999
Report date:
1999

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: OECD guideline No. 401
GLP compliance:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
5 females
5 males

Administration / exposure

Route of administration:
oral: gavage
Doses:
Undiluted dose of 2000/mg/kg, taking into consideration that its specific gravity was 0.99

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw

Applicant's summary and conclusion

Conclusions:
Under our experimental conditions, the oral LD50 of the test substance Pseudo Kharismal Step 1 is higher than 2000 mg/kg in rats. According to the classification criteria laid down in Commission Directive 93/21/EEC, concerning the potential toxicity by oral route, the test substance should not be classified.
Executive summary:

Under our experimental conditions, the oral LD50 of the test substance Pseudo Kharismal Step 1 is higher than 2000 mg/kg in rats. According to the classification criteria laid down in Commission Directive 93/21/EEC, concerning the potential toxicity by oral route, the test substance should not be classified.