1,2,3-tris(2,3-epoxypropoxy)propane

Endpoint summary

Key value for chemical safety assessment

Skin irritation / corrosion

Link to relevant study records

Reference

Endpoint:

skin irritation: in vivo

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Qualifier:

according to guideline

Guideline:

OECD Guideline 404 (Acute Dermal Irritation / Corrosion)

GLP compliance:

yes (incl. QA statement)

Species:

rabbit

Strain:

New Zealand White

Details on test animals or test system and environmental conditions:

During the test period, the temperature and humidity of the animal room were recorded with measured data every 1 hours by an automatic temperature and humidity meter in every 5 min intervals.

Type of coverage:

open

Preparation of test site:

not specified

Vehicle:

unchanged (no vehicle)

Controls:

yes, concurrent no treatment

Duration of treatment / exposure:

up to 72 hr

Observation period:

3 min, 1, 4, 24, 48 and 72 hr

Number of animals:

3

Details on study design:

1. Room No.: Rabbit room 1
2. Cage type and size: Stainless steel cages (W 420 x L 270 x H 180 mm)
3. Animals per cage: 1 animal
4. Temperature: 18.1 ~ 20.6ºC
5. Relative humidity: 49.1 ~ 60.2%
6. Air exchange: 10 ~ 15 / hr
7. Light cycle: 12 hr light / 12 hr dark
8. Illumination: 150 ~ 300 lux

Irritation parameter:

erythema score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

erythema score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

erythema score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

edema score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

edema score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

edema score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

0

Remarks on result:

no indication of irritation

Irritant / corrosive response data:

1. As a result of observing the test substance administration site, skin irritation and corrosiveness were not observed in all the test substance the administration and control sites.
2. Evaluation of skin irritation scores at 24, 48 and 72 hours after administration of test substance resulted in a skin irritation score of "0.0" for erythema & edema and edema in all animals.

Other effects:

1. No mortality was observed in this study.
2. No treatment-related clinical signs were observed in any treated animals.
3. All tested animals observed normal gains in body weights.

Interpretation of results:

GHS criteria not met

Conclusions:

It was judged that it was not classified as according to CLP.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed (not irritating)

Eye irritation

Link to relevant study records

Reference

Endpoint:

eye irritation: in vivo

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Qualifier:

according to guideline

Guideline:

OECD Guideline 405 (Acute Eye Irritation / Corrosion)

GLP compliance:

yes (incl. QA statement)

Species:

rabbit

Strain:

New Zealand White

Details on test animals or tissues and environmental conditions:

1. Select reason test system
NZW rabbit is commonly used for this type of acute eye irritation and corrosion study for several decades and accumulated enough raw data to be compared and easy to be interpreted of experimental results.
2. Quarantine and Acclimation
The animals were examined for quarantine on the receipt and acclimatized to the Centralbio Animal Breeding Room for 5 days. Four healthy animals were selected and used for the study based on general health conditions.
3. Animal and cage identification
The animals was marked in the ear pinna using a permanent marker and identification cards was attached to each cage for an individual discrimination.

Vehicle:

unchanged (no vehicle)

Controls:

yes

Irritation parameter:

cornea opacity score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Reversibility:

not fully reversible within: 21 days

Remarks on result:

positive indication of irritation

Remarks:

it indicated after 72 hours.

Irritation parameter:

cornea opacity score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

cornea opacity score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

cornea opacity score

Basis:

animal #4

Time point:

24/48/72 h

Score:

0

Remarks on result:

no indication of irritation

Irritation parameter:

iris score

Basis:

animal #1

Time point:

24/48/72 h

Score:

1

Reversibility:

not fully reversible within: 72 h

Irritation parameter:

iris score

Basis:

animal #2

Time point:

24/48/72 h

Score:

1

Reversibility:

not fully reversible within: 72 h

Irritation parameter:

iris score

Basis:

animal #3

Time point:

24/48/72 h

Score:

1

Reversibility:

not fully reversible within: 72 h

Irritation parameter:

iris score

Basis:

animal #4

Time point:

24/48/72 h

Score:

0.7

Reversibility:

fully reversible within: 72 h

Irritation parameter:

conjunctivae score

Basis:

animal #1

Time point:

24/48/72 h

Score:

2.3

Reversibility:

not fully reversible within: 20 d

Irritation parameter:

conjunctivae score

Basis:

animal #2

Time point:

24/48/72 h

Score:

2.3

Reversibility:

not fully reversible within: 8 d

Irritation parameter:

conjunctivae score

Basis:

animal #3

Time point:

24/48/72 h

Score:

2.3

Reversibility:

not fully reversible within: 8 d

Irritation parameter:

conjunctivae score

Basis:

animal #4

Time point:

24/48/72 h

Score:

2.3

Reversibility:

not fully reversible within: 8 d

Irritation parameter:

chemosis score

Basis:

animal #1

Time point:

24/48/72 h

Score:

2

Reversibility:

not fully reversible within: 15 d

Irritation parameter:

chemosis score

Basis:

animal #2

Time point:

24/48/72 h

Score:

2

Reversibility:

not fully reversible within: 6 d

Irritation parameter:

chemosis score

Basis:

animal #3

Time point:

24/48/72 h

Score:

2

Reversibility:

not fully reversible within: 6 d

Irritation parameter:

chemosis score

Basis:

animal #4

Time point:

24/48/72 h

Score:

2

Reversibility:

not fully reversible within: 6 d

Irritant / corrosive response data:

After 3 minutes of the initial test administration, no significant eye injury was observed as a result of observing the test substance administration site. Therefore, three additional animals were used for the confirmation test. As a result of observing the test substance administration sites at 1, 24, 48 and 72 hours after the test substance administration in the initial test and confirmation test, iris hyperemia was observed as 1 point in all cases at form 24 hours to 48 hours, 1 case was recovered at 72 hours and observed as 1 point in 3 cases. Observed iris hyperemia was recovered in 2 cases on the day 4 and 1 case on the day 16. Conjunctival redness was observed as 2 points in 2 cases at 1 hour and as 3 point in all cases at 24 hours, as 2 points in all cases at from 48 hours to 72 hours. Observed conjunctival redness was recovered as 3 cases on the day 9 and as 1 case on the day 21. Conjunctival swelling was observed as 2 points in all cases at from 1 hour to 72 hours. Observed conjunctival swelling was recovered as 3 cases on the day 7 and as 1 case on the day 16. Lacrima was observed as 2 points in all cases at from 1 hour to 24 hours and as 1 point in all cases at from 48 hours to 72 hours. Observed Lacrima was recovered as all cases on the day 6. In addition, corneal opacity was observed in 1 cases on day 4 and was not recovered until 21 days. No specific symptoms were observed in the cornea, iris, and conjunctiva in the left eye.

Other effects:

1. Mortality and Clinical Signs
No clinical sign and mortality was observed relating to test substance treatment.
2. Body Weights
All the animals showed normal gains in body weights during the study period.

Interpretation of results:

Category 1 (irreversible effects on the eye) based on GHS criteria

Conclusions:

As a result, eye irritation and corrosion test of eye of female NewZealand White rabbits of 1,2,3-tris(2,3-epoxypropoxy)propane under the test conditions showed that the turbidity of the cornea was not recovered until 21 days after administration of the test substance. It is solted to "Category 1" in the classification according to CLP.

Endpoint conclusion

Endpoint conclusion:

adverse effect observed (irritating)