Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 205-525-0 | CAS number: 142-17-6
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP-compliant, guideline study, available as an unpublished proprietary study report.
- Justification for type of information:
- For read across justification, see Section 13 of IUCLID
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 013
- Report date:
- 2013
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Calcium myristate
- EC Number:
- 239-328-6
- EC Name:
- Calcium myristate
- Cas Number:
- 15284-51-2
- Molecular formula:
- C14H27O2.1/2Ca
- IUPAC Name:
- calcium ditetradecanoate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Physical state: White powder
- Purity: ≥95%
- Substance identity: Calcium myristate synthetic sample
- Batch number: Not reported
- Analysis code: A047/99
- Expiration date: 2013-07-09
- Storage of test material: Room temperature in the dark
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- - Selection of animals: Immediately prior to test initiation, both eyes of the provisionally selected test rabbits were examined and any animals showing evidence of ocular irritation or defect were rejected
- Age at test initiation: 12 to 20 weeks
- Acclimatisation period: At least 5 days
- Housing: Individually in suspended cages
- Feeding: Free access to mains drinking water and commercial food
- Temperature: 17 to 23°C
- Relative humidity: 30 to 70 %
- Air flow: At least fifteen changes per hour
- Photoperiod: Twelve hours continuous light (06:00 to 18:00) and twelve hours darkness
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- - Volume: 0.1 mL of calcium myristate, equivalent to approximately 34 mg, was applied to the conjunctival sac of the right eye and the upper and lower eyelids were held together for about one second immediately after treatment
- Duration of treatment / exposure:
- - Duration of exposure: The rabbits' eyes were not washed
- Observation period (in vivo):
- - Observations of eyes: Assessment of ocular damage/irritation was made approximately 1 hour and 24, 48 and 72 hours following treatment
- Observations of reversibility: An observation was made in one treated eye on Day 7 to assess the reversibility of the ocular effects - Number of animals or in vitro replicates:
- - Number of animals: Initially, a single rabbit was treated and after consideration of the ocular response, a second animal was treated
- Details on study design:
- - Control: The left eye remained untreated and was used for control purposes
- Observations of rabbits: Any other ocular effects and any clinical signs of toxicity were also noted and individual bodyweights were recorded on the day of dosing and at the end of the observation period
- Assessment method: Occular irritation potential results were interpreted according to the Globally Harmonized System of Classification and Labelling of Chemicals
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.3
- Max. score:
- 1
- Reversibility:
- fully reversible
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- fully reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.7
- Max. score:
- 2
- Reversibility:
- fully reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.7
- Max. score:
- 2
- Reversibility:
- fully reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- fully reversible
- Irritant / corrosive response data:
- - Corneal effects: None were noted during the study
- Iridial effects: Inflammation was noted in both treated eyes one hour after treatment and in one treated eye at the 24 Hour observation
- Conjunctival effects: Moderate irritation in both treated eyes at 1 and 24 hours after treatment, with minimal irritation in both treated eyes at 48 hours and in 1 treated eye at 72 hours
- Reversibility: One treated eye appeared normal after 72 hours and the other treated eye appeared normal at 7 days
- Conclusion: Calcium myristate produced a maximum group mean score of 16.0 and was classified as a moderate irritant (Class 5 on a 1 to 8 scale) to the rabbit eye according to a modified Kay and Calandra classification system. Calcium myristate does not meet the criteria for classification according to the Globally Harmonised System of Classification and Labelling of Chemicals or Regulation (EC) No 1272/2008, relating to the Classification, Labelling and Packaging of Dangerous Substances. - Other effects:
- - Body weight: Both animals showed expected gain in bodyweight during the study
Any other information on results incl. tables
Individual scores and individual total scores for occular irritation
Rabbit Number and Sex |
72630Male |
72652Male |
|||||||
IPR = 0 |
IPR = 0 |
||||||||
Time After Treatment |
1 |
24 |
48 |
72 |
1 |
24 |
48 |
72 |
7 |
CORNEA |
|
|
|
|
|
|
|
|
|
E = Degree of Opacity |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
F = Area of Cornea Involved |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
Score (E x F) x 5 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
IRIS |
|
|
|
|
|
|
|
|
|
D |
1 |
1 |
0 |
0 |
1 |
0 |
0 |
0 |
0 |
Score (D x 5) |
5 |
5 |
0 |
0 |
5 |
0 |
0 |
0 |
0 |
CONJUNCTIVAE |
|
|
|
|
|
|
|
|
|
A = Redness |
2 |
2 |
1 |
0 |
2 |
2 |
2 |
1 |
0 |
B = Chemosis |
2 |
1 |
1 |
0 |
2 |
1 |
1 |
1 |
0 |
C = Discharge |
1 |
1 |
0 |
0 |
2 |
1 |
0 |
0 |
0 |
Score (A + B + C) x 2 |
10 |
8 |
4 |
0 |
12 |
8 |
6 |
4 |
0 |
Total Score |
15 |
13 |
4 |
0 |
17 |
8 |
6 |
4 |
0 |
IPR = Initial pain reaction
Individual total scores and group mean scores for occular irritation
Rabbit Number and Sex |
Individual Total Scores At: |
||||
1 Hour |
24 Hours |
48 Hours |
72 Hours |
7 Days |
|
72630Male |
15 |
13 |
4 |
0 |
- |
72652Male |
17 |
8 |
6 |
4 |
0 |
Group Total |
32 |
21 |
10 |
4 |
0 |
Group Mean Score |
16.0 |
10.5 |
5.0 |
2.0 |
0.0 |
- = Observation not required - considered to be zero for calculation of Group Mean Score
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Calcium myristate does not meet the criteria for classification according to the Globally Harmonised System of Classification and Labelling of Chemicals or Regulation (EC) No 1272/2008, relating to the Classification, Labelling and Packaging of Dangerous Substances.
- Executive summary:
The eye irritation of calcium myristate was assessed in a GLP-compliant, in vivo eye irritation study following OECD guideline 405 (Harlan 2013). A single treatment of calcium myristate was applied to the non-irrigated eye of two rabbits and observations made at 1, 24, 48 and 72 hours and 7 days for effects on conjunctivae, iris and cornea and for reversibility of effects. The study is considered relevant and reliable for use for this endpoint.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.