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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
weight of evidence
Study period:
1977-08-09
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Meets generally accepted scientific standards, well documented and acceptable for assessment; pre-GLP study with restrictions (only one dose level tested, short observation period, limited examinations).

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1979
Report date:
1979

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: DOT guidelines
Deviations:
yes
Principles of method if other than guideline:
The test was carried out according to DOT guidelines. A definite LD50 was not calculated. No further data.
GLP compliance:
no
Remarks:
pre-GPL study
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
(E)-3-formylbut-2-enyl acetate
EC Number:
247-825-4
EC Name:
(E)-3-formylbut-2-enyl acetate
Cas Number:
26586-02-7
Molecular formula:
C7H10O3
IUPAC Name:
(2E)-3-methyl-4-oxobut-2-en-1-yl acetate
Details on test material:
- Name of test material (as cited in study report): beta-formylcrotylacetate (2-methyl-4-acetoxy-butenal)
- Physical state: liquid
- Analytical purity: no data
No further data

Test animals

Species:
rabbit
Strain:
other: albino
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
5 male and 5 female albino rabbits
- Weight at study initiation: ca. 2 - 3 kg
- Housing: individually in stainless steel cages; size: (57 cm x 44 cm) x 35 cm
- Diet (ad libitum): pelleted standard diet for rabbits
- Acclimation period: at least 3 days
no further data

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21 - 23°C
- Humidity (%): 50 - 70%
- Photoperiod (hrs dark / hrs light): 12/12

IN-LIFE DATES: no data

Administration / exposure

Type of coverage:
occlusive
Vehicle:
unchanged (no vehicle)
Details on dermal exposure:
TEST SITE
- Area of exposure: spinal region caudal to the ribs
- % coverage: application area; 7 cm x 7 cm (ca. 50 cm²)
- Type of wrap if used: The treated skin site was covered with a vellum-paper, the vellum-paper was fixed with a cohesive tape (Gazofix (TM))
The skin of the back and flanks of each rabbit was shaved at 2 to 16 hours prior to treatment.

REMOVAL OF TEST SUBSTANCE: no data

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 200 µl/kg bw (ca. 212 mg/kg bw; estimated with a density of 1.605 g/ml) of the unchanged test substance
Duration of exposure:
24 hours
Doses:
ca. 212 mg/kg bw (200 µl/kg bw)
No. of animals per sex per dose:
5 males and 5 females (only one dose level tested)
Control animals:
no
Details on study design:
- Duration of observation period following administration: 72 hours
- Frequency of observations and weighing: no data
- Necropsy of survivors performed: no

Mortality was determined at 1, 24, 48 , and 72 hour(s) after beginning of application; local signs of irritation and/or toxicity were monitored. Animals that died spontaneously were subjected to a gross post-mortem examination.
Statistics:
no data

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 212 mg/kg bw
Remarks on result:
other: Original value: LD50 > 200 µl/kg bw
Mortality:
No deaths occurred.
Clinical signs:
other: No clinical signs of toxicity were observed. Local signs: Slight, solid strengthening of the skin, partially cracked and fissured was seen at the application site at 5 days after beginning of the application.
Gross pathology:
Pathological examination was not performed since no animal died.

Any other information on results incl. tables

Table: cumulative mortality
Dose
Concentration
Animals
No. of dead animals / no. of exposed animals
1 h
24 h
48 h
72 h
200 µl /kg bw
(ca. 212 mg/kg bw)
Undiluted
Males
0/5
0/5
0/5
0/5
Females
0/5
0/5
0/5
0/5
Males + Females
0/10
0/10
0/10
0/10
 

Applicant's summary and conclusion