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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
short-term repeated dose toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP non-guideline, available as unpublished report, limitations in design and/or reporting (no information on duration of treatment) but otherwise adequate for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1961
Report date:
1961

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Rabbits were exposed to the test substance by oral gavage.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,5-dihydrofuran
EC Number:
216-957-4
EC Name:
2,5-dihydrofuran
Cas Number:
1708-29-8
Molecular formula:
C4H6O
IUPAC Name:
2,5-dihydrofuran
Details on test material:
- Name of test material (as cited in study report): 2,5-Dihydrofuran
- Purity: 94%
- Physical state: colorless clear liquid

Test animals

Species:
rabbit
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 2.5 - 2.9 and 2.7 - 2.9 kg, for females and males respectively

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Details on oral exposure:
- 2 animals dosed 0.4 mL/kg; 2 times per week
- 2 animals dosed 0.4 mL/kg; first week ones, thereafter 2 times per week
- 1 animal dosed 0.4 mL/kg; first week ones, thereafter 3 times per week treated with 0.2 mL/kg
- 1 animal dosed 0.4 mL/kg; first week ones, thereafter 4 times per week treated with 0.2 mL/kg
Analytical verification of doses or concentrations:
no
Duration of treatment / exposure:
- not specified
Control animals:
no

Examinations

Observations and examinations performed and frequency:
Clinical observations
Sacrifice and pathology:
GROSS PATHOLOGY: Yes
HISTOPATHOLOGY: Yes

Results and discussion

Results of examinations

Details on results:
CLINICAL SIGNS AND MORTALITY: Diarrhea was observed in all exposed animals. All exposed animals died.
PATHOLOGY: Autopsy revealed in 4 out of 6 animals a mild to moderate edema in the lungs. No effects on liver, kidneys and hematological parameters were observed. In one exposed animal kidney damage was histologically detectable.

Effect levels

Dose descriptor:
NOAEL
Basis for effect level:
other: No NOAEL derivation was possible
Remarks on result:
not determinable
Remarks:
no NOAEL identified

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion