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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

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

Materials and methods

Principles of method if other than guideline:
BASF test (inhalation hazard test) according to Smyth et al. (1962). The test demonstrates the toxicity of an atmosphere saturated with vapours of the volatile components of the test item at 20 °C.

Reference:
Smyth HF et al. (1962). Am. Ind. Hyg. Ass. J. 23: 95-107.
GLP compliance:
no
Test type:
other: inhalation hazard test
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
2-(methylamino)ethanol, compound with sulphur dioxide
EC Number:
244-169-0
EC Name:
2-(methylamino)ethanol, compound with sulphur dioxide
Cas Number:
21049-70-7
Molecular formula:
C3H9NO.xO2S
IUPAC Name:
(oxo-λ⁴-sulfanylidene)oxidane; 2-(methylamino)ethan-1-ol
Details on test material:
- Name of test material: Kauramin-Härter CE 5162 flüssig; N-Methyläthanolammonium(-hydrogen) sulfit in Wasser (German)
- Physical state: liquid
- Composition of test material, percentage of components: N-Methylethanolamine: 49.4 %, Sulfur dioxide: 29.5 %, Water: 21.1 %

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: purchased from a breeder
- Age at study initiation: young adult

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
air
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Rate of air: 200 L/hour
- System of generating a saturated vapour atmosphere: air was bubbled through a substance column of about 5 cm above a fritted glass disk in a glass cylinder.
- Temperature in air chamber: 20 °C
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
7 h
Concentrations:
Saturated atmosphere, enriched with the volatile fraction of the test substance
No. of animals per sex per dose:
6 rats
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Frequency of observations and weighing: group-wise documentation of clinical signs was performed; body weight of groups was determined before the start of the study and at the end of the observation period in surviving animals.
- Necropsy of survivors performed: yes
Statistics:
No statistical analysis was performed.

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC0
Effect level:
other: saturated atmosphere
Based on:
test mat.
Exp. duration:
7 h
Remarks on result:
other: There were no effects.
Mortality:
There were no deaths.
Clinical signs:
other: There were no clinical signs.
Body weight:
No data
Gross pathology:
There were no test substance-related macroscopic findings.

Applicant's summary and conclusion