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Diss Factsheets

Administrative data

Description of key information

According to the study results (acute toxic class method) the value of LD50 of the test substance, Reactive Blue 85, for female rats is higher than 2000 mg/kg of body weight.

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2.2.1997 - 4.2.1998
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
according to guideline
OECD Guideline 401 (Acute Oral Toxicity)
Version / remarks:
GLP compliance:
Test type:
standard acute method
Limit test:
Details on test animals or test system and environmental conditions:
TEST ANIMALS- Source: with veterinary health certificate (no parasites/patogen microorganisms/mold); clinical examination confirmed the good state of health- Age at study initiation: not specified- Weight at study initiation: males 161 - 167g, females 162 - 165g- Fasting period before study: yes (20 hours before aplikation)- Housing: 5 male or 5 female in plastic polypropylene cages T4 (TOP Velaz Praha), sterilized wooden shavings; regular cleaning and disinfection- Diet: 10g/animal/day (standard granulated diet for rats ST-1; Bergman)- Water: ad libitum (tap water acc. ČSN 757111)- Acclimation period: 1 week- Fasting: 20 hours before oral aplicationENVIRONMENTAL CONDITIONS- Temperature (°C): 22±2- Humidity (%): 30 – 70%- Air changes (per hr): not specified- Photoperiod (hrs dark / hrs light): 12 /12
Route of administration:
oral: gavage
Details on oral exposure:
VEHICLE - Concentration in vehicle: 20% suspension in water(based on weight of animal - volume 1 ml/100 g bw) MAXIMUM DOSE VOLUME APPLIED: 1 ml/100 g bw
2000 mg/kg
No. of animals per sex per dose:
5 males and 5 females/ dose in main studyThe difference in the weight of animals among a group not exceed 20%
Control animals:
Details on study design:
- Duration of observation period following administration: 14 days- Frequency of observation: after aplication, after 30 mins, after 3 hours, next day morning and afternoon, than dailyweighing: just before aplication and in the end of test- Necropsy of survivors performed: yes, macroscopic examination of muscles and organs (incl. their size, colour, shape, structure)- Other examinations performed: clinical signs, body weight,organ weights, histopathology, other:body weight and clinical signs (appearance of skin, fur, visible mucous membranes, nutritional status, psychic activity, somatomotoric activity, response to stimuli, lacrimation, examination of the function of the respiratory, digestive, urogenital and circulatory apparatus).
Preliminary study:
The selection of dose 2g/kg bw was based on orientative dose finding study.
Key result
Dose descriptor:
Effect level:
> 2 000 mg/kg bw
Based on:
test mat. (total fraction)
no mortality observed
Clinical signs:
no clinical signs of intoxication observed
Body weight:
weight gains in females were lower than their physiologic possibilities
Gross pathology:
no changes
Interpretation of results:
GHS criteria not met
After a single oral administration of the test substance to laboratory rats (2g/kg bw) no signs of intoxication were detected by clinical and pathological examination.
Executive summary:

In the sample Ostazinová žluť H8-G, the acute oral toxicity test was performed on the Wistar rats.

Examination of acute oral toxicity revealed that the rat LD50 was greater than 2000 mg/kg of body weight.

The acute oral toxicity testing was performed according to OECD methodology No. 401.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
2 000 mg/kg bw
Quality of whole database:
Reliability 1

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification