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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: other routes

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Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
April 1967
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
documentation insufficient for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1967
Report date:
1967

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The test substance was i.p. injected into mice.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
But-3-yn-2-ol
EC Number:
217-978-1
EC Name:
But-3-yn-2-ol
Cas Number:
2028-63-9
Molecular formula:
C4H6O
IUPAC Name:
but-3-yn-2-ol
Details on test material:
purity 56.1%
other component: water
according to order sheet from Dec 2nd 1988

Test animals

Species:
mouse
Strain:
other: "Kisslegg" mice
Sex:
male/female
Details on test animals or test system and environmental conditions:
No data

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
water
Details on exposure:
Form of application: solution
Concentrations used: 0.5 and 1 % (w/v) (1 % was used for 100 mm3/kg bw)
Doses:
25, 50, 64, 80 and 100 mm3/kg
30, 59, 76, 95 and 119 mg/kg bw (calculated based on density at 20 °C = 1.189)
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs
Statistics:
No data

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 71 mg/kg bw
Based on:
test mat.
Remarks on result:
other: original value: LD50 ca. 60 mm3/kg bw, mg/kg bw calculated based on density at 20 °C = 1.189
Mortality:
Animals that died:
25 mm3/kg bw: 1 h: 0/10; 24 h: 0/10; 48 h: 0/10; 7 d: 0/10
50 mm3/kg bw: 1 h: 0/10; 24 h: 1/10; 48 h: 1/10; 7 d: 1/10
64 mm3/kg bw: 1 h: 0/10; 24 h: 2/10; 48 h: 4/10; 7 d: 5/10
80 mm3/kg bw: 1 h: 0/10; 24 h: 10/10; 48 h: 10/10; 7 d: 10/10
100 mm3/kg bw: 1 h: 0/10; 24 h: 10/10; 48 h: 10/10; 7 d: 10/10
Clinical signs:
In animals with high dose treatment dyspnea, apathy, seizures and hypothermia were detected. Animals treaten with 64 mm3/kg bw and lower showed only slight symptoms and some recovered.
Body weight:
Only recorded before application.
Gross pathology:
Partly fatty metamorphosis of the liver was detected in 7 of the animals that died after treatment and 2 sacrifised after 7 days.

Applicant's summary and conclusion