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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: inhalation
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
1978-07-17 to 1978-08-01
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Only orientating information about the inhalation hazard but in light of the very low acute toxicity of the substance this stuy is taken into account following a weight of evidence approach.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1979
Report date:
1979

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: H.F. Smyth et al., Am. Ind. Hyg. Ass. J. 23, 95 - 107 (1962)
Deviations:
no
GLP compliance:
no
Test type:
other: inhalation hazard test

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium bis[2-[(4,5-dihydro-3-methyl-5-oxo-1-phenyl-1H-pyrazol-4-yl)azo]benzoato(2-)]chromate(1-)
EC Number:
255-527-0
EC Name:
Sodium bis[2-[(4,5-dihydro-3-methyl-5-oxo-1-phenyl-1H-pyrazol-4-yl)azo]benzoato(2-)]chromate(1-)
Cas Number:
41741-86-0
Molecular formula:
C34 H24 Cr N8 O6 .Na
IUPAC Name:
Sodium;chromium(3+);2-[(3-methyl-5-oxido-1-phenylpyrazol-4-yl)diazenyl]benzoate

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: dust
Vehicle:
air
Details on inhalation exposure:
Inhalation of atmosphere concentrated with test substance dust at room temperature. For enrichment of air 200 L air/h are led through a 5 cm high layer of test substance.
Duration of exposure:
7 h
Concentrations:
Mean concentration: 0.125 mg/L
No. of animals per sex per dose:
6
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 hours
- Frequency of observations and weighing:
* Observation after 3, 10, 30 min and 1, 3 and 7 hours of exposure
* Weight at beginning (1st trial): 558 g (male), 481 g (female)
* Weight at beginning (2nd trial): 633 g (male), 538 g (female)
- Necropsy of survivors performed: yes (14 days after trial start)

Results and discussion

Preliminary study:
none
Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 0.125 mg/L air
Mortality:
None
Clinical signs:
other: None
Gross pathology:
No abnormality of organs was detected.
Other findings:
After 7 hours of exposure in an atmosphere concentrated with the test substance (at room temperature) no animals died.

Applicant's summary and conclusion