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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: inhalation

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: unsuitable test system for a solid test substance

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1978
Report date:
1978
Reference Type:
secondary source
Title:
C.I. Pigment Brown 24
Author:
OECD
Year:
2002
Bibliographic source:
SIDS Initial Assessment Report for SIAM 15

Materials and methods

Principles of method if other than guideline:
The inhalation hazard test (IHT; synonymous to IRT, inhalation hazard test) was performed in principle as described in OECD Guideline 403 and in accordance to Smyth et al., Am.Ind.Hyg.Ass.J. 23,95-107 (1962). The aim of the test was to demonstrate the toxicity of an atmosphere saturated with vapors of the volatile components of the test substance at a temperature chosen for vapor generation (i.e. 20 °C for the present test substance).
The animals were exposed to the test substance for 7 hours (flow-through, 200 liters/hour).
GLP compliance:
no
Test type:
other: IHT

Test material

Constituent 1
Chemical structure
Reference substance name:
Chrome antimony titanium buff rutile
EC Number:
269-052-1
EC Name:
Chrome antimony titanium buff rutile
Cas Number:
68186-90-3
Molecular formula:
(Ti, Sb, Cr) O2
IUPAC Name:
manganese(4+) trititanium(4+) pentaantimony(3+) chromium(3+) nickel(2+) octadecaoxidandiide
Test material form:
solid

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: males 190 g/ females 170 g

Administration / exposure

Route of administration:
inhalation: vapour
Analytical verification of test atmosphere concentrations:
no
Remarks:
The nominal concentration was recalculated regarding the air flow and the test substance loss
Duration of exposure:
7 h
Concentrations:
0.1 mg/l
No. of animals per sex per dose:
6
Control animals:
no

Results and discussion

Effect levels
Key result
Dose descriptor:
other: IHT
Remarks on result:
other: No mortality within 7 hours in a saturated atmosphere.
Mortality:
none
Clinical signs:
other: nothing abnormal observed
Gross pathology:
nothing abnormal observed

Applicant's summary and conclusion