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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study is comparable to OECD Guideline 401 with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1969
Report date:
1969

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-ethylhex-2-enal
EC Number:
211-448-3
EC Name:
2-ethylhex-2-enal
Cas Number:
645-62-5
Molecular formula:
C8H14O
IUPAC Name:
2-ethylhex-2-enal
Test material form:
liquid
Details on test material:
- Name of test material (as cited in study report): 2-Hexenal, 2-ethyl
- Impurities: Butyraldehyd

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: 140 - 216 g; female: 118 - 174 g


Administration / exposure

Route of administration:
oral: gavage
Doses:
5440, 4250, 3400, 2720, 1360, 170 mg/kg
No. of animals per sex per dose:
10 males and 10 females per dose
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Frequency of observations and weighing: 1h after application; daily observations
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs; body weight was determined before the start of the study only

Results and discussion

Effect levels
Dose descriptor:
LD50
Effect level:
4 675 mg/kg bw
Mortality:
see: remarks on results
Clinical signs:
other: Dyspnea, abdominal position, lateral position, stagger
Gross pathology:
Sacrified animals: no macroscopic pathologic abnormalities were noted
Animals that died: atonic gastro-intestinal tract

Any other information on results incl. tables

Mortality:

 Dose in mg/kg bw  concentration %  1 hour  24 hours  48 hours  7 days
 5440  30  0/20  9/20  9/20  9/20
 4250  30  0/20  12/20  12/20  12/20
 3400  30  0/20  4/20  4/20  4/20
 2720  30  0/20  0/20  0/20  0/20
 1360  20  0/20  0/20  0/20  0/20
 170  2  0/20  0/20  0/20 0/20

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met