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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1981
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study
Justification for type of information:
The study was conducted in the early days of GLP and prior to guidelines. So there is a general lack of detail in the reports, but the work was conducted in a superior facility, so the quality is not in question.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1981

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
GLP compliance:
yes
Test type:
fixed dose procedure
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
2-[(2-ethylhexyl)oxy]ethanol
EC Number:
216-323-7
EC Name:
2-[(2-ethylhexyl)oxy]ethanol
Cas Number:
1559-35-9
Molecular formula:
C10H22O2
IUPAC Name:
2-[(2-ethylhexyl)oxy]ethan-1-ol
Specific details on test material used for the study:
None

Test animals

Species:
guinea pig
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
not specified

Administration / exposure

Type of coverage:
occlusive
Vehicle:
not specified
Details on dermal exposure:
24 hour exposure to the depiliated abdomen under an occlusive wrap for 24 hours
Duration of exposure:
24 hours
Doses:
1
No. of animals per sex per dose:
not specified
Control animals:
no
Details on study design:
not specified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 20 mL/kg bw
Based on:
test mat.
Mortality:
not specified
Clinical signs:
other: not specified
Gross pathology:
not specified
Other findings:
not specified

Applicant's summary and conclusion

Interpretation of results:
Category 5 based on GHS criteria