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EC number: 287-636-4 | CAS number: 85566-26-3
- 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
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- 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

Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1988-03-11 to 1988-03-31
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 988
- Report date:
- 1988
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- : lack of details on test substance; lack of individual tabulated data on cornea and iris; reading at 72 in only 1 animal
- GLP compliance:
- yes
Test material
- Reference substance name:
- Fatty acids, C8-10, Me esters
- EC Number:
- 287-636-4
- EC Name:
- Fatty acids, C8-10, Me esters
- Cas Number:
- 85566-26-3
- Molecular formula:
- C9-11H18-22O2
- IUPAC Name:
- Fatty acids, C8-10 (even numbered), Me esters
- Details on test material:
- - Substance type: Fatty acid methyl ester, C8-10
- Physical state: clear yellowish liquid
no further details
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- other: Kleinrussen , Chbb:HM
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Thomae GmbH, Biberach, Germany
- Weight at study initiation: mean 2467.5 g
- Housing: individually
- Diet: ad libitum (Altromin Haltungsdiät 2023)
- Water: ad libitum
- Acclimation period: 1 week
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 21
- Humidity (%): 45 - 55
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 mL - Duration of treatment / exposure:
- single instillation
- Observation period (in vivo):
- 72 h
- Number of animals or in vitro replicates:
- 4
- Details on study design:
- SCORING SYSTEM: according to 79/831/EWG, Annex, Part B
TOOL USED TO ASSESS SCORE: fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- of 4 tested animals and mean of readings at
- Time point:
- other: 24 h and 48 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- of 4 tested animals and mean of readings at
- Time point:
- other: 24 h and 48 h
- Score:
- 0
- Max. score:
- 3
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- of 4 tested animals and mean of readings at
- Time point:
- other: 24 h and 48 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- of 4 tested animals and mean of readings at
- Time point:
- other: 24 h and 48 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- No reactions were observed on the cornea and the iris.
The conjunctival reactions were slight to moderate and disappeared totally within 24 hours after application.
Any other information on results incl. tables
Evaluation of the eye lesions
Animal |
Hours after application |
||||||||
24 |
48 |
72 |
|||||||
A |
B |
C |
A |
B |
C |
A |
B |
C |
|
718 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
0 |
0 |
917 |
0 |
0 |
0 |
0 |
0 |
0 |
- |
- |
- |
918 |
0 |
0 |
0 |
0 |
0 |
0 |
- |
- |
- |
920 |
0 |
0 |
0 |
0 |
0 |
0 |
- |
- |
- |
A = Redness
B = Chemosis
C = Exsudation
- = Not evaluated
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
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