Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute Toxicity: oral

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2001
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2001
Report date:
2001

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
EU Method B.1 tris (Acute Oral Toxicity - Acute Toxic Class Method)
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
GLP compliance:
yes
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
437-930-5
EC Name:
-
Cas Number:
51553-03-8
Molecular formula:
Hill formula: C22H23N7O5 CAS formula: C22H23N7O5
IUPAC Name:
N-{5-[bis(2-methoxyethyl)amino]-2-[2-(2,6-dicyano-4-nitrophenyl)diazen-1-yl]phenyl}acetamide
Test material form:
solid: particulate/powder

Test animals

Species:
other: Ratte rat (Wistar)

Administration / exposure

Vehicle:
other: Propylenglykol Das Vehikel wurde aufgrund eines Vorversuchs ausgewählt. Propylene glycol The vehicle was selected based on a pretest.

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Mortality:
Male: 2000 mg/kg bw; Number of animals: 3; Number of deaths: 0
Female: 2000 mg/kg bw; Number of animals: 3; Number of deaths: 0
Clinical signs:
other: Signs of toxicity related to dose levels: Zwischen Tag 1 und Tag 3 wurde Lethargie und/oder zusammengekauerte Haltung bei den Versuchtieren beobachtet. Die durchschnittliche Zunahme des Körpergewichts der Ratten während der Studie entspricht der zu er
Gross pathology:
Effects on organs:
Bei der Nekropsie sind keine makroskopischen Abnormalitäten
festgestellt worden.

No abnormalities were found at macroscopic post mortem
examination of the animals.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The oral LD50 value of BDF 054-1 in Wistar rats was established to exceed 2000 mg/kg body weight.