Fatty acids, tall-oil, manganese salts

Skin irritation / corrosion

Administrative data

Endpoint:

skin irritation: in vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

2018-07-30 to 2018-09-04

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2018

Report date:

2019

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 404 (Acute Dermal Irritation / Corrosion)

Version / remarks:

2015-07-28

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Remarks:

signed 2018-04-26

Test material

Test material information

Constituent 1

Reference substance name:

Fatty acids, tall-oil, manganese salts

EC Number:

232-445-3

EC Name:

Fatty acids, tall-oil, manganese salts

Cas Number:

8030-70-4

IUPAC Name:

Fatty acids, tall-oil, manganese salts

Test material form:

other: highly viscous, sticky

Details on test material:

- State of aggregation: highly viscous, sticky, brown

Test animals

Species:

rabbit

Strain:

New Zealand White

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Charles River Deutschland, 97633 Sulzfeld, Germany
- Age at study initiation:
animal #1: approximately 50 weeks old
animal #2: approximately 51 weeks old
animal #3: approximately 14-15 weeks old
- Weight at study initiation: 2.7 – 4.0 kg
- Housing: individually housed in ABS-plastic or Noryl rabbit cages, floor 4200 cm2
- Diet (ad libitum): autoclaved hay and Altromin 2123 maintenance diet for rabbits, rich in crude fibre
- Water (ad libitum): tap water
- Acclimation period: at least 5 days

ENVIRONMENTAL CONDITIONS
- Temperature: 18 ± 3 °C
- Relative humidity: 55 ± 10 %
- Air changes: at least 10 x / hour
- Photoperiod (hrs dark / hrs light): 12/12

Test system

Type of coverage:

semiocclusive

Preparation of test site:

clipped

Vehicle:

unchanged (no vehicle)

Amount / concentration applied:

TEST MATERIAL
500 mg of the test item was first applied to a gauze patch, which was then carefully applied to the skin with good contact and uniform distribution of the test item on the skin. In order to ensure good contact with the skin, it was moistened with the smallest amount of aqua ad injectionem.
The vehicle was chosen due to its non-irritating characteristics.

Duration of treatment / exposure:

initial animal #1: 3 minutes, 1 hour and 4 hours
confirmatory animals #2 and #3: 4 hours

Observation period:

animal #1: 6 days
animal #2: 14 days
animal #3: 7 days

Number of animals:

3 male rabbits

Details on study design:

TEST SITE
500 mg of the moistened test item was applied at a single dose to a small area (approximately 6 cm²) of skin on one side of the dorsal area and covered with a gauze patch, which was held in place with a non-irritating tape. The untreated other side served as control. The test item was applied to the patch first, moistened with the smallest amount of aqua ad injectionem and then applied to the skin. The patch was fixed with a semi-occlusive dressing. The untreated other side served as control. The limits of the application site were marked with an ink marker. Access by the animal to the patch and ingestion or inhalation of the test chemical were prevented.

INITIAL AND CONFIRMATORY TESTING
As there was no information about the skin irritation/ corrosion potential of the test item, a single animal test was employed. Up to three test patches were applied sequentially to the animal. The first patch was removed after three minutes. No serious skin reaction was observed, so a second patch was applied at a different site and removed after one hour. The observations at this stage indicated that exposure can humanely be allowed to extend to four hours, so a third patch was applied and removed after four hours, and the response was graded. No corrosive effect was observed after the last patch was removed, so the animal was further observed.
The results of the initial test indicated that the test item is not corrosive to the skin using the procedure described. In order to confirm the response, two additional animals were treated in the same manner.

REMOVAL OF TEST SUBSTANCE
At the end of the exposure period, sterile water was used to remove residual test item from animal #1. Thereafter, as the test item showed a water-repellent effect, an appropriate solvent, cottonseed oil was used for rinsing the application site in animal #1. For animal #2 and #3 solely cottonseed oil was used to remove test item residues immediately after patch removal. The solvent was chosen in order not to alter the existing response or the integrity of the epidermis.

OBSERVATION TIME POINTS
- animal #1: immediately and 1 hour, 24, 48,72 and 96 hours after patch removal
- animal #2 and #3: 1 hour, 24, 48 and 72 hours after patch removal

SCORING SYSTEM
according to the Draize scale

FURTHER OBSERVATIONS
- body weights: prior to the administration and at the end of the observation period
- local effects such as hyperplasia, scaling, discolouration, fissures and scabs
- systemic effects

Results and discussion

In vivo

Results

Results 1

Irritation parameter:

erythema score

Basis:

animal #1

Time point:

24/48/72 h

Score:

1

Max. score:

4

Reversibility:

fully reversible within: 6 days

Results 2

Irritation parameter:

edema score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

4

Results 3

Irritation parameter:

erythema score

Basis:

animal #2

Time point:

24/48/72 h

Score:

1

Max. score:

4

Reversibility:

not reversible

Results 4

Irritation parameter:

edema score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

4

Results 5

Irritation parameter:

erythema score

Basis:

animal #3

Time point:

24/48/72 h

Score:

2

Max. score:

4

Reversibility:

fully reversible within: 6 days

Results 6

Irritation parameter:

edema score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritant / corrosive response data:

ANIMAL #1:
After patch removal during and immediately after sequential application (3 min, 1 hour, 4 hours) signs of irritation were noted in animal #1 (erythema grade 1 immediately after the 1-hour and the 4-hour exposure periods). 1 hour later no signs of irritation were observed. Slight irritation was noted from 24 hours until 5 days after exposure and was fully reversible within 6 days after patch removal. The mean erythema score of animal #1, following grading at 24, 48 and 72 hours post-application, was calculated to be 1.00.

ANIMAL #2:
Animal #2 started showing erythema grade 1 at 24 hours after patch removal. This slight sign of irritation persisted until study end, 14 days after application. The mean erythema score of animal #2, following grading at 24, 48 and 72 hours after installation of the test material, was calculated to be 1.00.

ANIMAL #3:
Animal #3 showed erythema grade 1 at 1 hour after patch removal. Irritation score increased to erythema grade 2 24 hours after exposure and decreased again to grade 1 2 days later. By 7 days after application signs of irritation were fully reversible. The mean erythema score of animal #3, following grading at 24, 48 and 72 hours after installation of the test material, was calculated to be 2.00.

Other effects:

- No adverse changes apart from irritant/corrosive response data were observed at the skin sites. However,
- Test item residues were detected at the application sites in all animals almost throughout the whole observation period.
- Neither mortalities nor significant clinical signs of toxicity were observed.
- The body weight development was within the expected range.

Applicant's summary and conclusion

Interpretation of results:

GHS criteria not met

Conclusions:

The test item is not irritating to the skin.
According to Regulation (EC) No 1272/2008 and subsequent adaptations, the substance does not require classification as skin irritant.