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EC number: 204-260-8 | CAS number: 118-56-9
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Published article fulfilled basic scientific principles.
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 989
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- yes
- Remarks:
- Using UV generater to find the photoallergy of the test substance
- Principles of method if other than guideline:
- The literature does not give information for whether it was conducted with any standard or guideline, but comparing the method used in the report with OECD 406, it can be concluded the test procedure is similar to OECD test guideline 406.
- GLP compliance:
- no
- Remarks:
- Old publication
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Sensitization endpoint information was published in 1989, when GMPT test was still state of the art. To avoid additional animal testing LLNA was not performed.
Test material
- Reference substance name:
- Homosalate
- EC Number:
- 204-260-8
- EC Name:
- Homosalate
- Cas Number:
- 118-56-9
- Molecular formula:
- C16H22O3
- IUPAC Name:
- 3,3,5-trimethylcyclohexyl salicylate
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- male/female
- Details on test animals and environmental conditions:
- Hartley outbred guinea pigs, weighing 350 to 450 gm were used for the study. Groups were composed of equal numbers of males and females.
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: Ethanol
- Concentration / amount:
- Induction conditions; 1 % w/v in methanol or methanol alone; Challenge conditions 1 % w/v in acetone or acetone alone;
Challengeopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: Ethanol
- Concentration / amount:
- Induction conditions; 1 % w/v in methanol or methanol alone; Challenge conditions 1 % w/v in acetone or acetone alone;
- No. of animals per dose:
- 20 animals per test group for induction with homosalate and UVA, 5 animal per test group for induction with sham and 10 animals per test group for induction with methanol and UVA
- Details on study design:
- RANGE FINDING TESTS:
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 6
- Exposure period: 2 hours everytime
- Control group: yes
- Site: nuchal area
- Frequency of applications: 3 times per week
- Duration: 2 weeks
- Concentrations: HMS was applied as a 1 % (w/v) concentration in methanol for induction.
B. CHALLENGE EXPOSURE
- No. of exposures: one
- Day(s) of challenge: 10 to 14 day
- Exposure period: 2 hours
- Control group: yes
- Site: dorsal area
- Concentrations: 1 % (w/v) concentration in acetone for challenge; The animals were then exposed to 10 J/cm2 UVA radiation.
- Evaluation (hr after challenge): 24 and 48 hours - Challenge controls:
- vehicle control of acetone was used.
- Positive control substance(s):
- yes
- Remarks:
- musk ambrette (MA) and tetrachlorosalicylanilide (TCSA)
Results and discussion
- Positive control results:
- The results show that guinea pigs treated with MA + 10 J/cm2 UVA for both induction and challenge demonstrated incidence and severity indexes of 12/20 and 1.1, respectively. The data clearly indicate a classic photo-allergic response.
Guinea pigs treated with TCSA plus UVA at induction and challenge demonstrated approximately a 2-fold increase in both the incidence and severity response
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Induction with HMS+UVA; Test group challenge with UVA and 1% HMS in acetone
- Dose level:
- 1% in acetone
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Induction with HMS+UVA; Test group challenge with UVA and 1% HMS in acetone. Dose level: 1% in acetone. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Induction with HMS+UVA; Test group challenge with UVA and 1% HMS in acetone
- Dose level:
- 1% in acetone
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Induction with HMS+UVA; Test group challenge with UVA and 1% HMS in acetone. Dose level: 1% in acetone. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Sham induction; challenged by HMS + UVA
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Sham induction; challenged by HMS + UVA. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Sham induction; challenged by HMS + UVA
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Sham induction; challenged by HMS + UVA. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Sham induction; challenged by HMS only
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Sham induction; challenged by HMS only. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Sham induction; challenged by HMS only
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Sham induction; challenged by HMS only. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Sham induction; challenged by Acetone + UVA
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Sham induction; challenged by Acetone + UVA. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Sham induction; challenged by acetone + UVA
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Sham induction; challenged by acetone + UVA. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Sham induction; challenged by Acetone only
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Sham induction; challenged by Acetone only. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Sham induction; challenged by acetone only
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Sham induction; challenged by acetone only. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: induced by methanol + UVA; challenged by Acetone + UVA
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: induced by methanol + UVA; challenged by Acetone + UVA. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: induced by methanol + UVA; challenged by Acetone + UVA
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: induced by methanol + UVA; challenged by Acetone + UVA. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: induced by methanol + UVA; challenged by Acetone only
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: induced by methanol + UVA; challenged by Acetone only. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- other: induced by methanol + UVA; challenged by Acetone only
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: other: induced by methanol + UVA; challenged by Acetone only. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Induced by HMS+UVA; challenged byHMS only
- Dose level:
- 1% in acetone
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Induced by HMS+UVA; challenged byHMS only. Dose level: 1% in acetone. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Induced by HMS+UVA; challenged byHMS only
- Dose level:
- 1% in acetone
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Induced by HMS+UVA; challenged byHMS only. Dose level: 1% in acetone. No with. + reactions: 0.0. Total no. in groups: 20.0.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- It can be concluded the homosalate can not cause skin sensitisation both under and without UV radiation.
- Executive summary:
The potential of homosalate and 2 known human photoallergens (musk ambrette and tetrachiorosalicylanilide) to cause photoallergy, and/or contact sensitization was determined using Guinea Pig Maximisation Test (GPMT), which was similar to OECD test guideline 406. The model was slightly modified by employing 6 exposures over 2 weeks and using Hill Top Chambers®for application of the test material. Musk ambrette and tetrachlorosalicylanilide (TCSA) was used as positive control in guinea pigs, although with TCSA. The results of studies conducted with homosalate showed that homosalate was neither allergen nor photoallergen.
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