Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: inhalation

Currently viewing:

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: See 'Remark'
Remarks:
All information in this endpoint has been provided by the ECHA using the 12-year rule, this is data not owned by the registrant. The reliability is assumed to be at level 2. Therefore the following reliability statement can be used: Study conducted in accordance with generally accepted scientific principles, possibly with incorect reporting or methodological deficiencies, which do not affect the quality of the relevant results.

Data source

Reference
Reference Type:
other: All information in this endpoint has been provided by the ECHA using the 12-year rule, this is data not owned by the registrant.
Title:
Unnamed
Year:
1989

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: 92/69/EEC
Principles of method if other than guideline:
Information from migrated NONS file, as per inquiry number 06-0000021057-76-0000, permission to refer granted by ECHA.
GLP compliance:
yes
Limit test:
yes

Test material

1
Chemical structure
Reference substance name:
-
EC Number:
403-590-1
EC Name:
-
Cas Number:
104815-18-1
Molecular formula:
C46 H32 Cl2 Fe N7 O6
IUPAC Name:
iron(3+) ammonium bis(1-[2-(5-chloro-2-oxidophenyl)diazen-1-yl]-3-(phenylcarbamoyl)naphthalen-2-olate)

Test animals

Species:
rat
Strain:
Sprague-Dawley

Administration / exposure

Type of inhalation exposure:
whole body
Vehicle:
other: none
Duration of exposure:
4 h

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 3.37 mg/L air
Exp. duration:
4 h
Mortality:
Male: 0 mg/L; Number of animals: 5; Number of deaths: 0
Male: 3.37 mg/L; Number of animals: 5; Number of deaths: 0
Female: 0 mg/L; Number of animals: 5; Number of deaths: 0
Female: 3.37 mg/L; Number of animals: 5; Number of deaths: 0
Clinical signs:
other: Signs of toxicity related to dose levels: Signs of exposure were confined to staining of the skin, fur and tail by the substance. There was a small reduction in food and water consumption in male exposed rats on day 1.
Gross pathology:
Effects on organs:
The lungs of all treated animals were coloured greyish due to the substance. Lung to bodyweight ratios were unaffected. No treatment - related changes were found in tissues examined microscopically(lungs, liver, kidneys).

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met