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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline study with acceptable restrictions (e.g. rel. low purity of test substance 86.3%)

Data source

Reference Type:
study report

Materials and methods

Test guideline
according to guideline
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
Test type:
standard acute method
Limit test:

Test material

Constituent 1
Chemical structure
Reference substance name:
EC Number:
EC Name:
Cas Number:
Molecular formula:
Hill formula: C36H40N2S6 CAS formula: C36H40N2S6
Details on test material:
purity: 86.3%, white, odorless solid

Test animals

other: Bor: WISW (SPF Cpb)
Details on test animals or test system and environmental conditions:
- Source:
- Age at study initiation: 6 to 8 week old
- Fasting period before study: 16 h
- Housing:separated by sex, max. 5 animals per Makrolon type III cage
- Diet: ad libitum
- Water: ad libitum
- Acclimation period:at least 5 d

- Temperature (°C): 20 +/- 3°C
- Humidity (%): 30-70%
- Photoperiod: 12hrs dark / 12hrs light


Administration / exposure

Route of administration:
oral: gavage
corn oil
Details on oral exposure:
- Concentration in vehicle: 30g/100cm3
- Amount of vehicle (if gavage):6.67 cm3/kg body weight
- Justification for choice of vehicle: corn oil was chosen because of low water solubility of test substance

2000 mg/kg bw
No. of animals per sex per dose:
Control animals:
Details on study design:
- Duration of observation period following administration: 1/2, 1, 2, 3, 4, 5, and 6 h post application, once daily during the following 14 days
- Frequency of observations and weighing: day 0, day 7, day 14
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight

Results and discussion

Preliminary study:
preliminary study: 2 males and 2 females were orally administered with 2000 mg/kg bw test substance
Effect levels
Dose descriptor:
Effect level:
> 2 000 mg/kg bw
Male: 2000 mg/kg bw; Number of animals: 5; Number of deaths: 0
Female: 2000 mg/kg bw; Number of animals: 5; Number of deaths: 0
Clinical signs:
other: Signs of toxicity related to dose levels: 5 - 6 h post applicationem bei drei von fünf männlichen Tieren kurzzeitig Diarrhoe. Ein weibliches Tier zeigte zu diesem Zeitpunkt Hockhaltung und ein gesträubtes Fell. 24 und 48 h post applicationem wurde led
Gross pathology:
Effects on organs:
Die Sektionen und makroskopischen Untersuchungen der Organe
am Versuchsende ergaben keine Hinweise auf substanzbedingte
Organveränderungen. Es wurden keine geschlechtsspezifischen
Toxizitätsunterschiede festgestellt.


The sections and macroscopic investigations of the organs at
the end of the test showed no indications of substance
related changes of the organs and no sex-specific
differences in toxicity.

Any other information on results incl. tables

Mortality: males: 0/5, females 0/5

Clinical signs:

Five and six hours after the application three of five males showed diarrhea. A female animal showed squatting position and rough coat 5 and 6 h after application, and rough coat after 48 h. After 72 hours the animal was free of all symptoms. Two males as well as four females showed no symptoms of toxicity during the whole observation period.

The body weight gain of the animals developed normally during the whole test period.

Necropsies and gross pathology: no evidence of substance-related organ changes was found

Applicant's summary and conclusion

Executive summary:

In a rat study, which was done under GLP and according to OECD guideline 401, the oral LD50 was >2000 mg/kg bw (Hüls AG 1992a). No effects were observed with regard to mortality, body weight gain and gross examinations. Three male rats showed diarrhoea five and six hours after application. One female showed squatting position and rough coat 5 and 6 hours after the application. After 48 hours only the rough coat was still present and no effects were seen after 72 hours. The other animals showed no symptoms of toxicity during the whole observation period.