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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
Comparable to guideline study OECD 403 (adopted 1981, IHT). Methodological deficiencies: no analytical determination of test atmosphere concentration; test substance purity not specified; limited documentation. Only conclusion on saturated vapor athmosphere possible.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1978
Report date:
1978

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Version / remarks:
adopted 1981; Inhalation Hazard Test
Deviations:
yes
Remarks:
no analytical verification of test substance concentration.
Principles of method if other than guideline:
According to Smyth H.F. et al.: Am. Ind. Hyg. Ass. J., 23, 95-107; comparable to the inhalation hazard test in the Annex of the OECD test guideline 403It demonstrates the toxicity of an atmosphere saturated with vapors of the volatile components of a test substance at 20 °C. 12 rats were exposed to the vapors generated by bubbling 200 L/h air through a substance column of about 5 cm above a fritted glass disc in a glass cylinder for 7 h. No analytical determination of the atmosphere concentrations was performed. The nominal concentration was calculated as quotient of the amount of test substance weight loss during exposure, and the amount of air used during exposure. Group-wise documentation of clinical signs was performed over the 14 days study period. Body weight of groups was determined before the start of the study and at the end of the observation period. The exposure time not causing lethality was usually tested twice.
GLP compliance:
no
Test type:
other: Inhalation Hazard Test

Test material

Constituent 1
Chemical structure
Reference substance name:
Glycerol, ethoxylated
EC Number:
500-075-4
EC Name:
Glycerol, ethoxylated
Cas Number:
31694-55-0
Molecular formula:
(C2 H4 O)n (C2 H4 O)n (C2 H4 O)n C3 H8 O3 3n =>1-<6.5 mol EO
IUPAC Name:
Alkoxylation reaction product of glycerin as starter and ethylene oxyde (EO) as monomer
Details on test material:
- Name of test material (as cited in study report): Schmiermittel LK 2200
- pH: 6.5 - 7.5
- Purity: 'technical' purity

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: male mean 196 g; female mean: 178 g

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
other: unchanged (no vehicle)
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
7 h
Concentrations:
Experiment 1: 0.178 mg/L nominal (calculated as quotient of the amount of test substance weight loss during exposure)
Experiment 2: 0,143 mg/L nominal (calculated as quotient of the amount of test substance weight loss during exposure)
No. of animals per sex per dose:
6 animals (males and females) per experiment (total of 12 animals)
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of weighing: at the beginning and at the end of the study
- Frequency of observations: several times at the application day and thereafter once each working day
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight, gross pathology
Statistics:
none

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
other: IHT
Exp. duration:
7 h
Remarks on result:
other: no mortality occurred
Mortality:
No mortality occurred
Clinical signs:
other: Nothing abnormal detected
Body weight:
At the end of the study: females mean: 266 g; males mean: 200 g
Gross pathology:
Nothing abnormal detected
Other findings:
None

Applicant's summary and conclusion