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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Meets generally accepted scientific standard methods

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1972
Report date:
1972

Materials and methods

Principles of method if other than guideline:
Internal BASF method was used
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-methylbut-3-en-2-ol
EC Number:
204-068-4
EC Name:
2-methylbut-3-en-2-ol
Cas Number:
115-18-4
Molecular formula:
C5H10O
IUPAC Name:
2-methylbut-3-en-2-ol
Details on test material:
- Name of test material (as cited in study report): 2-methylbut-3-en-2-ol
- Analytical purity: 98.5-99%
- Physical state: clear liquid

Test animals

Species:
mouse
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Kisslegg
- Weight at study initiation: mean 33.2 g (males), 26.4 g (females)

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
other: 20 % aqueous emulsion
Doses:
640, 800, 1000, 1250, 1600, 2000, 2500 and 3200 mg/kg bw
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: weighing prior to begin of study; observations were made daily
- Necropsy of survivors performed: yes

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 1 000 mg/kg bw
Mortality:
3200 mg/kg bw: 5/5 males and 5/5 females within 24 h
2500 mg/kg bw: 5/5 males and 5/5 females within 24 h
2000 mg/kg bw: 4/5 males and 5/5 females within 24 h
1600 mg/kg bw: 1/5 males within 24 h; 5/5 males and 5/5 females within 7 days
1250 mg/kg bw: 5/5 males and 3/5 females within 7 days
1000 mg/kg bw: 1/5 females within 24 h; 4/5 females within 7 days, 5/5 females within 14 days
800 mg/kg bw: 1/5 males within 7 days
640 mg/kg bw: 1/5 males within 24 h
Clinical signs:
- Immediately after injection and at the following observation days the animals showed disturbance of equilibrium, dyspnoea, cyanosis, abdominal and lateral position;
- after 90 min: apathy, shallow respiration, staggering, reddened eyes, squatting posture and poorly general condition.
- After 11 days the surviving animals showed no symptoms
Gross pathology:
- Most animals showed livers of yellow loam colour (degeneration); sporadic observations: general congestion, slightly agglutination from liver and stomach, distinctive appearance of liver lobules.

Applicant's summary and conclusion