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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Skin irritation / corrosion

Currently viewing:

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
April 1967
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

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

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
yes
Remarks:
exposure for 1, 5, 15 min, 20 h, 24 h; shorter observaton period
Principles of method if other than guideline:
Before OECD Guideline 404 was established in 1982, skin irritation was tested using an internal method (BASF test).

GLP compliance:
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:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
No further details were provided

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
water
Controls:
no
Amount / concentration applied:
The test substance was applied in a 55 % solution in water. 0.2 mL/kg bw were used.
Duration of treatment / exposure:
2 animals were treated on different skin areas for 1, 5 and 15 min;
2 animals were treated for 20 h.
Observation period:
8 days
Number of animals:
4
Details on study design:
After the 1, 5 and 15 min or 20 h application the test substance was washed off. First it was washed with Lutol 9 (100 %) and afterwards with Lutrol 9 in water (50 %). Animals were fixated by binding of the animal to an exposure board during application.

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
animal #1
Time point:
other: 3.5 h
Max. score:
4
Reversibility:
not reversible
Remarks on result:
other: animal died
Irritation parameter:
edema score
Basis:
animal #1
Time point:
other: 3.5 h
Max. score:
4
Remarks on result:
other: animal died
Other effects:
Treatment for 20 h led to the death of the animals during exposure. Animals died 3.5 to 20 h after application.
Pathology revealed an increased fluid accumulation in the thoracic region, starting lungedema and diarrhea.

Any other information on results incl. tables

    24h   48 h   d7  
exposure animal #1 erythema edema erythema edema erythema edema
1 ´ #1 - - - - - -
  #2 2 - 1 - - -
#1 - - - - - -
  #2 1 - 1 - - -
15´ #1 - - - - - -
  #2 1 - 1 - - -
20 h #1 exitus over night        
  #2 exitus over night        

OECD / Draize Score (max: 4)

Applicant's summary and conclusion

Interpretation of results:
Category 2 (irritant) based on GHS criteria