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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
August 1979
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study performed according to a standard even if not EU, however the substance is poorly described, no observation is done at 48 h and after 72 h. The treatment duration is 24 h instead of 4.

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: CFR Title 16, section 1500.41
Principles of method if other than guideline:
The exposure duration in this guideline is 24 h instead of 4 according to the OECD guideline.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Quinoline
EC Number:
202-051-6
EC Name:
Quinoline
Cas Number:
91-22-5
Molecular formula:
C9H7N
IUPAC Name:
quinoline
Details on test material:
- Name of test material (as cited in study report): 110 831
- Substance type: no data
- Physical state: no data
- Analytical purity: no data
- Impurities (identity and concentrations): no data
- Composition of test material, percentage of components: no data
- Isomers composition: no data
- Purity test date: no data
- Lot/batch No.: no data
- Expiration date of the lot/batch: no data
- Stability under test conditions: no data
- Storage condition of test material: no data

Test animals

Species:
rabbit
Strain:
not specified
Details on test animals or test system and environmental conditions:
no data

Test system

Type of coverage:
occlusive
Preparation of test site:
other: both intact and abraded
Vehicle:
unchanged (no vehicle)
Controls:
no
Amount / concentration applied:
0.5 mL
Duration of treatment / exposure:
24 h
Observation period:
72 h
Number of animals:
6
Details on study design:
TEST SITE
- Area of exposure: 1 inch x 1 inch (around 2.5 cm x 2.5 cm)
- % coverage: no data
- Type of wrap if used: the patch is secured in place by adhesive tape. The entire trunk of the animal is then wrapped with an impervious material such as rubberized cloth.


REMOVAL OF TEST SUBSTANCE
- Washing (if done): no data
- Time after start of exposure: 24 h


SCORING SYSTEM: Draize score

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Remarks:
intact skin
Basis:
mean
Time point:
other: 24-72 h
Score:
0.9
Max. score:
3
Reversibility:
not reversible
Remarks:
over 72 h
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 24-72 h
Score:
1.5
Max. score:
3
Reversibility:
not reversible
Remarks:
over 72 h
Other effects:
1 animal died during the study

Any other information on results incl. tables

Animal

Effect

24 h

72 h

Left side (intact)

Right side (abraded)

Left side (intact)

Right side (abraded)

1

Erythema

1

1

1

1

Oedema

2

2

1

1

2

Erythema

0

0

0

0

Oedema

2

2

0

0

3

Erythema

0

0

1

1

Oedema

1

1

1

1

4

Erythema

1

1

2

2

Oedema

3

3

1

1

5*

Erythema

-

-

-

-

Oedema

-

-

-

-

6

Erythema

0

0

3

3

Oedema

2

2

2

2

*Animal 5 died during the study

Applicant's summary and conclusion

Interpretation of results:
irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
After exposure for 24 h, the mean scores are below 2 but the effects are not reversible over 72h, so the substance is considered as irritating R38 according to 67/548/EEC directive, and according to CLP (cat 2).
Executive summary:

The skin irritation properties of quinoline have been assessed in a test on 6 rabbits according to a US guideline (CFR Title 16, section 1500.41). The exposure duration was 24 h. The effects were observed at 24 and 72 h only. 1 rabbit died during the test.

The mean erythema score over 24 -72 h is 0.9 on intact skin and the mean oedema score is 1.5. However, the effects are not reversible at the end of the 72 h period, so the product is considered as irritating for the skin.