Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Description of key information

Skin irritation / corrosion:


In vivo: Read across from Sarolaner API


A primary dermal irritation study was conducted on three albino rabbits using test item in accordance with OECD 404. The erythema and edema scores for each animal are all 0 for 24, 48, and 72 h observations. The test item is rated non-irritating.


 


Eye irritation, Read across from Sarolaner API:


An acute eye irritation study was conducted on three albino rabbits using test item, according to OECD 405.


There were no positive effects exhibited in any eyes after treatment. The test item is rated minimally irritating to rabbit eyes.

Key value for chemical safety assessment

Skin irritation / corrosion

Link to relevant study records
Reference
Endpoint:
skin irritation: in vivo
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Read across based on structural similarity
Justification for type of information:
Read across from Sarolaner API
Reason / purpose for cross-reference:
read-across source
Irritation parameter:
erythema score
Basis:
animal #1
Time point:
24/48/72 h
Score:
0
Irritation parameter:
erythema score
Basis:
animal #2
Time point:
24/48/72 h
Score:
0
Irritation parameter:
erythema score
Basis:
animal #3
Time point:
24/48/72 h
Score:
0
Irritation parameter:
edema score
Basis:
animal #1
Time point:
24/48/72 h
Score:
0
Irritation parameter:
edema score
Basis:
animal #2
Time point:
24/48/72 h
Score:
0
Irritation parameter:
edema score
Basis:
animal #3
Time point:
24/48/72 h
Score:
0
Interpretation of results:
GHS criteria not met
Conclusions:
The test item is rated non-irritating.
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:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Read across based on structural similarity
Justification for type of information:
Read across from Sarolaner step 2
Reason / purpose for cross-reference:
read-across source
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
0
Irritation parameter:
iris score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
0
Irritation parameter:
conjunctivae score
Basis:
mean
Time point:
24/48/72 h
Score:
0.11
Max. score:
1
Reversibility:
fully reversible within: 48 hours
Irritation parameter:
chemosis score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
0
Interpretation of results:
GHS criteria not met
Conclusions:
The test item is rated minimally irritating to rabbit eyes.
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not irritating)

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification

Skin irritation / corrosion:


In vivo skin irritation, Read across from Sarolaner API, OECD 404:


Mean score for erythema at 24, 48, 72 h for 3 tested animals: 0, 0, 0


Mean score for edema at 24, 48, 72 h for 3 tested animals: 0, 0, 0


According to Regulation (EC) No 1272/2008, table 3.2.2, this substance should not be classified for this endpoint.


 


Eye irritation:


In vivo eye irritation, Read across from Sarolaner API, OECD 405:


Mean score for Cornea Opacity, Iris, Conjunctivae Redness and Chemosis at 24, 48, 72 h for 3 tested animals: 0, 0, 0.11, 0.


According to Regulation (EC) No 1272/2008, table 3.3.2, this substance should not be classified for this endpoint.