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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
key study
Study period:
1980
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with national standard methods with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1980
Report date:
1980

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Test on the basis of H.F. Smyth et al.: Am. Ind. Hyg. Ass. J. .23, 95 - 107 (1962)
GLP compliance:
no
Test type:
other: BASF method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2'-[[3-acetamido-4-[(2-chloro-4-nitrophenyl)azo]phenyl]imino]diethyl diacetate
EC Number:
216-251-6
EC Name:
2,2'-[[3-acetamido-4-[(2-chloro-4-nitrophenyl)azo]phenyl]imino]diethyl diacetate
Cas Number:
1533-78-4
Molecular formula:
C22H24ClN5O7
IUPAC Name:
2,2'-[[3-acetamido-4-[(2-chloro-4-nitrophenyl)azo]phenyl]imino]diethyl diacetate
Test material form:
solid
Details on test material:
Disperse Red 167:1

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
not specified
Vehicle:
air
Details on inhalation exposure:
Inhalation by means of vapor saturated at 20°C for 7 hours. To achieve saturation, air (200 L/h) was fed through an approx. 5 cm deep layer of the product.
Analytical verification of test atmosphere concentrations:
not specified
Duration of exposure:
7 h
Concentrations:
saturation concentration
No. of animals per sex per dose:
12 rats
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Frequency of observations and weighing: daily observation, weekly weighing
- Necropsy of survivors performed: yes
Statistics:
NA

Results and discussion

Preliminary study:
NA
Effect levels
Key result
Sex:
not specified
Dose descriptor:
LC0
Based on:
test mat.
Exp. duration:
7 h
Remarks on result:
other: no effect on saturation concentration
Mortality:
no deaths
Clinical signs:
other: no effects
Body weight:
no data
Gross pathology:
no effects

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
In this acute inhalation study, 7 hours inhalation of the volatile constituents of the test material did not lead to any deaths in rats (0/12).
Executive summary:

In an acute inhalation toxicity study, 12 rats were exposed by inhalation route to the volatile constituents of the test material in a saturation concentration for 7 hours. Animals were then observed for 7 days.

No deaths occurred and no clinical signs as well as gross pathology signs were observed.