Trisodium [5-[[4-[(3-chloro-2-hydroxy-5-sulphophenyl)azo]-3-hydroxyphenyl]azoxy]-2-[2-(4-nitro-2-sulphophenyl)vinyl]benzenesulphonato(5-)]cuprate(3-)

Endpoint summary

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records

Reference

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Study period:

September - December 1976

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Meets generally accepted scientific standards and acceptable for assessment

Qualifier:

no guideline available

Principles of method if other than guideline:

- Principle of test: equivalent or similar to a standard acute method- Parameters analysed / observed: mortality and clinical signs of intoxication

GLP compliance:

no

Test type:

standard acute method

Limit test:

no

Species:

rat

Strain:

Wistar

Sex:

male

Details on test animals or test system and environmental conditions:

TEST ANIMALS- Source: not specified- Age at study initiation: not specified- Weight at study initiation: 115 - 150g- Fasting period before study: not specified- Housing: individually in cage - Diet (e.g. ad libitum): not specified- Water (e.g. ad libitum): not specified- Acclimation period: not specifiedENVIRONMENTAL CONDITIONSnot specified (laboratory conditions)

Route of administration:

other: unspecified, probably gavage

Vehicle:

water

Details on oral exposure:

VEHICLE - Concentration in vehicle: 20% suspension in waterMAXIMUM DOSE APPLIED: 10 g/kg

Doses:

5.02; 6.31; 7.943; 10.00 g/kg

No. of animals per sex per dose:

10

Control animals:

no

Key result

Sex:

male

Dose descriptor:

LD50

Effect level:

6 492 mg/kg bw

Based on:

test mat.

95% CL:

> 5 993 - < 7 031

Clinical signs:

strong diarrhea

Body weight:

not specified

Gross pathology:

not specified

Dose[g/kg]	Mortality
5.020	0/10
6.310	5/10
7.943	9/10
10.000	10/10

LD50 = 6.491 (5.993 – 7.031) g/kg b.w.

Interpretation of results:

GHS criteria not met

Conclusions:

very slightly toxic

Executive summary:

The test substance toxicity was evaluated on the basis of mortality and clinical signs of intoxication. According to the study results the value of LD50 of the test substance, Saturnová hněď LB, for male rats is 6.49 g/kg of body weight.

Endpoint conclusion

Endpoint conclusion:

adverse effect observed

Dose descriptor:

discriminating dose

Value:

6 491 mg/kg bw

Quality of whole database:

Reliability 2

Acute toxicity: via inhalation route

Endpoint conclusion

Endpoint conclusion:

no study available

Acute toxicity: via dermal route

Link to relevant study records

Reference

Endpoint:

acute toxicity: dermal

Type of information:

experimental study

Adequacy of study:

key study

Study period:

September - October 1988

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

study well documented, meets generally accepted scientific principles, acceptable for assessment

Qualifier:

no guideline available

Principles of method if other than guideline:

- Principle of test:The sample was applied at a dose of 5000 mg / kg A paste was prepared from sample by adding water and aplied on depilated rat skin of 4 × 6 cm area.- Short description of test conditions: 5 Wistar rats , males, individually caged After 24 h the plaster bandage was removed and followed by observation for 14 days.- Parameters analysed / observed: behaviour, macroscopic examination of organs (probably weight, but not specified)

GLP compliance:

no

Test type:

standard acute method

Limit test:

yes

Specific details on test material used for the study:

TREATMENT OF TEST MATERIAL PRIOR TO TESTING- Final dilution of a dissolved solid, stock liquid or gel: a paste with water was prepared from sample

Species:

rat

Strain:

Wistar

Sex:

male

Details on test animals or test system and environmental conditions:

TEST ANIMALS- Source: not specified- Age at study initiation: not specified- Weight at study initiation: 204 – 220 g - Fasting period before study: not specified- Housing: individually in cage - Diet (e.g. ad libitum): not specified- Water (e.g. ad libitum): not specified- Acclimation period: not specified ENVIRONMENTAL CONDITIONSnot specified (laboratory conditions)

Type of coverage:

occlusive

Vehicle:

water

Details on dermal exposure:

TEST SITE - Area of exposure: 4 × 6 cm REMOVAL OF TEST SUBSTANCE - Washing (if done): not specified - Time after start of exposure: 24 h TEST MATERIAL - Amount(s) applied (volume or weight with unit): 5000 mg/ kg - For solids, paste formed: yes, sample mixed with water

Duration of exposure:

24 h

Doses:

5000 mg/ kg

No. of animals per sex per dose:

5 males

Control animals:

no

Details on study design:

- Duration of observation period following administration: 14 days - Frequency of observations: before exposure and after observation period before autopsy - Necropsy of survivors performed: yes - Other examinations performed: clinical signs, body weight, macroscopic examination of organs

Key result

Sex:

male

Dose descriptor:

LD50

Effect level:

5 000 mg/kg bw

Based on:

test mat. (total fraction)

Mortality:

no

Clinical signs:

no clinical signs of intoxication

Gross pathology:

No pathomorphological changes in the macroscopic examination of organs.

Interpretation of results:

GHS criteria not met

Conclusions:

LD50> 5000 mg/kg

Executive summary:

The tested substance Saturnová hněď LB (Direct Brown 103 now) is not absorbed in toxic amount, therefore it is not classified as acute toxic by dermal route.

LD₅₀> 5000 mg/kg

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Dose descriptor:

LD50

Value:

5 000 mg/kg bw

Quality of whole database:

Reliability 2