Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
Date of Study Report: August 9, 1976
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:
1976

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
other: 16 CFR 1500.41
Deviations:
not specified
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
yes
Remarks:
: Exposure duration, testing included abraded skin, Scoring following other criterias
Principles of method if other than guideline:
The exposure period was 24 h instead of 4 h. Post-dose observations were made up to 7 d instead of 14 d. Part of the shaven skin was abraded, which is not according to OECD guideline 404, which says:"Care should be taken to avoid abrading the skin."
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Diallyl phthalate
EC Number:
205-016-3
EC Name:
Diallyl phthalate
Cas Number:
131-17-9
Molecular formula:
C14H14O4
IUPAC Name:
1,2-bis(prop-2-en-1-yl) benzene-1,2-dicarboxylate
Test material form:
other: liquid
Details on test material:
- Name of test material (as cited in study report): Diallyl Phthalate (DAP)
- Analytical purity:
- Other:
- Identified as No. C-8013-3)
- Specific gravity: 1.117-1.123 at 20°C/20°C
- Solubility in methanol: 1 cm³ in 5 cm³, clear-only slightly turbid
- Acidity as acetic acid, % by weight: 0.1 max
- Moisture (Karl Fischer), %: 0.1 max
- Color APHA Pt-Co: 90 max
- Odor: mild

Test animals

Species:
rabbit
Strain:
not specified
Details on test animals or test system and environmental conditions:
Test was conducted on 6 adult albino rabbits selected from healthy, acclimated animals.

Test system

Type of coverage:
semiocclusive
Preparation of test site:
other: Each rabbit: shaven skin, partly abraded
Vehicle:
unchanged (no vehicle)
Controls:
not specified
Amount / concentration applied:
0.5 mL or 0.5 g
Duration of treatment / exposure:
24 hour(s)
Observation period:
24, 72 h and 7 d
Number of animals:
6
Details on study design:
TEST SITE
- Area of exposure: 1 inch x 1 inch
- Each rabbit treated with a patch on shaven skin and on abraded skin

REMOVAL OF TEST SUBSTANCE
- Washing (if done): not indicated
- Time after start of exposure: Patches were removed after 24 hrs

OBSERVATIONS:
- 24 h, 72 h and 7 d after start of the exposure.

SCORING SYSTEM: Draize Scoring Criteria

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
24/48/72 h
Score:
1
Max. score:
1
Reversibility:
fully reversible
Remarks on result:
probability of weak irritation
Irritation parameter:
edema score
Basis:
mean
Time point:
24/48/72 h
Score:
< 1
Max. score:
1
Reversibility:
fully reversible within: 7 days
Remarks on result:
probability of weak irritation

Any other information on results incl. tables

Table: Primary Skin Irritation Scores of Rabbits dosed with Diallyl phthalate (According to Draize Scoring Criteria)

Findings

Exposure Time

Exposure Unit (Value)

Rabbit No.

1

2

3

4

5

6

Erythema and eschar formation:

Intact Skin

24 hrs

2

2

2

2

2

2

Intact Skin

72 hrs

1

1

1

1

1

1

Intact Skin

7 days

1

1

0

1

1

1

Abraded skin

24 hrs

2

2

2

2

2

2

Abraded skin

72 hrs

1

1

2

1

1

1

Abraded skin

7 days

1

1

1

1

1

1

Subtotal

 

 

 

 

 

 

 

Edema formation:

Intact Skin

24 hrs

1

1

1

1

1

1

Intact Skin

72 hrs

1

1

0

0

1

0

Intact Skin

7 days

1

0

0

0

0

0

Abraded skin

24 hrs

1

1

1

1

1

1

Abraded skin

72 hrs

1

1

0

0

0

1

Abraded skin

7 days

0

0

0

0

0

0

Subtotal

 

4

4

2

2

3

3

Total

 

10

10

9

8

9

9

Score

 

2.50

2.50

2.25

2.00

2.25

2.25

Average

 

2.29

- 7 -Day values not included in calculating the score.

Erythema and edema were observed in the intact and abraded skin of all six animals. Erythema cleared in the intact skin of one animal. Edema cleared in the intact skin of five animals, and abraded skin of all six animals during the 7-day observation period.

Draize Scoring Criteria:

- Primary Skin Irritation Indexes of less than 2.0 are mild irritants.

- Primary Skin Irritation Indexes of 2.0 to 5.0 are moderate irritants.

- Primary Skin Irritation indexes of greater than 5.0 are severe irritants.

Applicant's summary and conclusion

Interpretation of results:
slightly irritating
Remarks:
Migrated information Criteria used for interpretation of results: OECD GHS
Conclusions:
Primary skin irritation testing of DAP at a dose of 0.5g by FDRL during 24 h, showed the sample to be moderately irritant up to 72 h after the start of exposure (within the range of 2.0 to 5.0) and decreased to mildly irritant after 7 days post-exposure. Hence, based on the fact that exposure duration was 6 times longer than that prescribed by OECD Guideline 404, and the scoring decreased to mildly irritant within 7 days of exposure, the final conclusion is that DAP can be expected to be only slightly irritant, when evaluated according to OECD guideline 404.
Executive summary:

On the basis of the data presented herein, the test material, FMC Corporation D.A.P. (1 Qt. Net Wt.) C-8013-3; is a moderate irritant to the rabbit skin.