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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
weight of evidence
Study period:
Not reported
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
Although this pre-dates international guidelines for acute inhalation toxicity studies and GLP, in accordance with REACH Annex XI, Section 1.1.2, the study was conducted under sound scientific principles of acute toxicity studies. The study is therefore considered adequate for contributing evidence towards this endpoint in a weight of evidence approach.

Data source

Reference
Reference Type:
publication
Title:
The toxicology of glycidol and some glycidyl ethers
Author:
C. H. Hine
Year:
1956
Bibliographic source:
Hine, C.H., Kodama, J.K., Wellington, J.S., Dunlap, M.K. and Anderson, H.H. (1956) The toxicology of glycidol and some glycidyl ethers. Archives of Industrial Health, 14: 250-264.

Materials and methods

Principles of method if other than guideline:
Male Long-Evans rats were exposed to a single dose phenylglycidyl ether vapours for 8 hours and the observation period was 10 days.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,3-epoxypropyl phenyl ether
EC Number:
204-557-2
EC Name:
2,3-epoxypropyl phenyl ether
Cas Number:
122-60-1
Molecular formula:
C9H10O2
IUPAC Name:
2-(phenoxymethyl)oxirane

Test animals

Species:
rat
Strain:
Long-Evans
Sex:
male

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure:
not specified
Vehicle:
air
Analytical verification of test atmosphere concentrations:
not specified
Duration of exposure:
8 h
No. of animals per sex per dose:
6 male rats per group.
Control animals:
not specified

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LC50
Effect level:
> 100 ppm
Based on:
test mat.
Exp. duration:
8 h
Sex:
male
Dose descriptor:
LC50
Effect level:
> 200 ppm
Based on:
test mat.
Exp. duration:
4 h
Remarks on result:
other: Experimental LC50 (100 ppm) for 8 hour exposure was modified to 4 h using Haber's Law (C1t1=C2t2)
Clinical signs:
other: Dyspnoea, watering eyes, salivation, rhinitis and aerophagy were observed in the animals. At post-mortem, marked irritation of the lung accompanied by acute interstitial pneumonia was seen. This was confirmed by histological examination.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The 4h acute inhalation LC50 of phenylglycidyl ether to rats was estimated as >200 ppm.