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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.

Eye Irritation:

Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be not irritating to eyes.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomentholcan be classified under the category “Not Classified”.

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:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Weight of evidence approach based on structurally similar substances
Justification for type of information:
Weight of evidence approach based on structurally similar substances
Reason / purpose for cross-reference:
read-across: supporting information
Reason / purpose for cross-reference:
read-across: supporting information
Qualifier:
according to guideline
Guideline:
other: Weight of evidence approach based on structurally similar substances
Principles of method if other than guideline:
Weight of evidence approach based on structurally similar substances
GLP compliance:
not specified
Specific details on test material used for the study:
Name of the test chemical: (1S,2S,5R)-5-methyl-2-propan-2-ylcyclohexan-1-olCommon Name: (+)-NeomentholMolecular Formula: C10H20OMolecular Weight: 156.269 g/molSubstance Type: OrganicPhysical State: Solid
Species:
rabbit
Strain:
not specified
Type of coverage:
other: 1. open, 2. occlusive
Preparation of test site:
other: 1. hairless, 2. intact and abraded skin
Vehicle:
unchanged (no vehicle)
Controls:
not specified
Amount / concentration applied:
1. 0.05 ml2. 5 ml/kg
Duration of treatment / exposure:
1.The dosing was repeated between 5 and 10 times2. 24 hours
Observation period:
1. 2 weeks2. 24 hours
Number of animals:
1. 52. 4
Details on study design:
The study is based on the weight of evidence approach based on structurally similar chemicals
Irritation parameter:
overall irritation score
Basis:
mean
Reversibility:
not specified
Remarks on result:
positive indication of irritation
Irritant / corrosive response data:
Signs of irritation observed
Interpretation of results:
Category 2 (irritant) based on GHS criteria
Conclusions:
Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.
Executive summary:

Based on the available studies for the structurally similar read across chemicals, weight of evidence approach was applied to assess the dermal irritation potential of (+)-Neomenthol

The dermal irritation potential of the structurally similar chemical was assessed in rabbits. Hairless sites on the skin of 5 White rabbits were intradermally injected with 0.05ml of the test chemical. The dosing was repeated between 5 and 10 times. Gross examinations were made at 24 and 48 hours, at 1 and 2 weeks and in some cases 1 month following dosing. Microscopic examination of the skin was performed after the gross examination.

Moderate reactions characterized by polymorphonucelar leukocytes, and plasma cells(without necrosis) were noted in 3 rabbits. Severe reactions as well as necrosis were noted in the other 2 rabbits.

Hence, the test chemical can be considered to be a skin irritant.

This is supported by the results of another dermal irritation study performed in rabbits to assess the irritation potential of structurally similar chemical. 5 ml/kg undiluted test chemical was applied to the intact and abraded skin of 4 rabbits under occlusive conditions for 24 hours. The readings for dermal reactions were taken after patch removal. Mild erythema was observed at 24 hours, but no edema. Hence, the test chemical can be considered to be irritating to rabbit skin.

Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (irritating)

Eye irritation

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not irritating)

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Skin Irritation:

Based on the available studies for the structurally similar read across chemicals, weight of evidence approach was applied to assess the dermal irritation potential of (+)-Neomenthol

The dermal irritation potential of the structurally similar chemical was assessed in rabbits.

Hairless sites on the skin of 5 White rabbits were intradermally injected with 0.05ml of the test chemical. The dosing was repeated between 5 and 10 times. Gross examinations were made at 24 and 48 hours, at 1 and 2 weeks and in some cases 1 month following dosing. Microscopic examination of the skin was performed after the gross examination.

Moderate reactions characterized by polymorphonucelar leukocytes, and plasma cells(without necrosis) were noted in 3 rabbits. Severe reactions as well as necrosis were noted in the other 2 rabbits.

Hence, the test chemical can be considered to be a skin irritant.

This is supported by the results of another dermal irritation study performed in rabbits to assess the irritation potential of structurally similar chemical. 5 ml/kg undiluted test chemical was applied to the intact and abraded skin of 4 rabbits under occlusive conditions for 24 hours. The readings for dermal reactions were taken after patch removal. Mild erythema was observed at 24 hours, but no edema. Hence, the test chemical can be considered to be irritating to rabbit skin.

Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.

Eye Irritation:

Based on the available studies for the structurally similar read across chemicals, weight of evidence approach was applied to assess the ocular irritation potential of (+)-Neomenthol

An eye irritation study was conducted on rabbits to assess the degree of eye irritancy caused by the structurally similar according to Draize method.

The test substance was initially applied in 10, 20 and 30 % solution. The eyes of 4 animals were rinsed 1 minute after application with physiological saline, substance remained in the eyes of 4 animals. In a second step animals were treated with concentration of 40, 50 and 60 %.

No signs of eye irritation were observed. Hence, the chemical was considered to be not irritating to the eyes of rabbits.

This is supported by the results of another ocular irritation study performed on rabbits to determine the degree of irritation caused by the structurally similar chemical.

Undiluted 0.1 ml of the test chemical was instilled in the right eye of 6 New Zealand White rabbits. The untreated left eye served as control. Reactions were scored as per the Draize method against the control, on days 1–8.

The mean irritation scores of the test group were 6.0 (24-h), 2.0 (48-h), 0.3 (96-h), and 0.0 respectively. The effects were fully reversible within 8 days.

Hence, the test chemical can be considered to be not irritating to eyes.

Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be not irritating to eyes.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomentholcan be classified under the category “Not Classified”.

Justification for classification or non-classification

The results of the experimental studies from the structurally similar read across substances indicate a possibility that (+)-Neomenthol can be irritating to skin but not irritating to eyes.

Hence by applying the weight of evidence approach, (+)-Neomenthol can be considered to be irritating to skin and not irritating to eyes. It can be classified under the category “Not Classified” for eye irritation and “Category 2” for skin irritation as per CLP regulation.