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Toxicological information

Skin irritation / corrosion

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Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study meets generally accepted scientific standards, acceptable for assessment.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1959
Report date:
1959

Materials and methods

Principles of method if other than guideline:
Standardized test method (BASF-Test)
Before OECD Guideline 404 was established in 1982, skin irritation was tested using an internal method (BASF test). White Vienna rabbits were used. 2 animals were treated for 1, 5, 15 minutes using occlusive conditions. An application site of 2.5 x 2.5 cm was covered with the liquid test substance on a patch. After the application time of 1, 5, and 15 minutes, respectively, the skin was first washed with undiluted Lutrol 9, then with an aqueous Lutrol solution (50 %). The animals were observed for 7 weeks and skin reactions were recorded daily in the beginning and every 4 to 7 days after 10 days.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Pyrrolidine
EC Number:
204-648-7
EC Name:
Pyrrolidine
Cas Number:
123-75-1
Molecular formula:
C4H9N
IUPAC Name:
pyrrolidine
Details on test material:
- Name of test material (as cited in study report): Pyrrolidin
- Physical state: liquid
- Analytical purity: 95 - 97 %

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 3.25 and 3.14 kg

ENVIRONMENTAL CONDITIONS
no data

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
no
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): undiluted, no amount specified
Duration of treatment / exposure:
1 min, 5 min, 15 min
Observation period:
7 weeks
Number of animals:
2 animals
Details on study design:
TEST SITE
- Area of exposure: 2.5 x 2.5 cm
- Type of wrap if used: no data

REMOVAL OF TEST SUBSTANCE
- Washing: yes (exposure 1, 5, 15 min) first with undiluted Lutrol 9, then with an aqueous Lutrol solution (50 %)
- Time after start of exposure: 1, 5, and 15 min, respectively

Results and discussion

In vivo

Results
Irritation parameter:
erythema score
Remarks on result:
other: 1 min exposure duration led to full-thickness necrosis observed after 24 hours.
Irritant / corrosive response data:
1 min exposure:
after removal of the test substance: blood loss at the whole application side;
after 24 hours: hard, deep and black necrosis with reddened oedematous edge;
after 8 days: not relocatable, deep necrosis;
after 7 weeks: relocatable scar.
5 min exposure:
Except for a non-relocatable scar, grown together with the muscle, the same findings as after 1 min exposure were observed.
15 min exposure:
Same findings as observed after 5 min exposure.

Applicant's summary and conclusion

Interpretation of results:
Category 1A (corrosive)
Remarks:
Migrated information
Conclusions:
The test item is considered to be corrosive to the skin.
Executive summary:

In this non-GLP test (BASF IX/409, 1959) skin irritation was tested according to an internal method (BASF test). White Vienna rabbits were used. 2 animals were treated for 1, 5, 15 minutes using occlusive conditions. An application site of 2.5 x 2.5 cm was covered with the liquid test substance on a patch. After the application time of 1, 5, and 15 minutes, respectively, the skin was first washed with undiluted Lutrol 9, then with an aqueous Lutrol solution (50 %). The animals were observed for 7 weeks and skin reactions were recorded daily in the beginning and every 4 to 7 days after 10 days.

Already the one-minute exposure duration led to full-thickness necrosis on the skin observed after 24 hours. The test item is considered to be corrosive to the skin and is classified cat. 1.