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EC number: 203-990-4 | CAS number: 112-61-8
- 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- GLP - Guideline study, tested with the source substance methyl myristate (CAS 124-10-7). In accordance to the ECHA guidance document “Practical guide 6: How to report read-across and categories (March 2010)”, the reliability was changed from RL1 to RL2 to reflect the fact that this study was conducted on a read-across substance.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method C.3 (Algal Inhibition test)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- ISO 8692 (Water Quality - Fresh Water Algal Growth Inhibition Test with Scenedesmus subspicatus and Selenastrum capricornutum)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: OECD Guideline 23 (Guidance document on aquatic toxicity testing of difficult substances and mixtures)
- GLP compliance:
- yes
Test material
- Reference substance name:
- Methyl myristate
- EC Number:
- 204-680-1
- EC Name:
- Methyl myristate
- Cas Number:
- 124-10-7
- Molecular formula:
- C15H30O2
- IUPAC Name:
- methyl myristate
- Details on test material:
- - Name of test material (as cited in study report): Fettsäuremethylester-C14
- Physical state: Clear colourless liquid
- Analytical purity: > 99%
- Lot/batch No.: S5327813912
- Expiration date of the lot/batch: 23 February 2011
- Storage condition of test material: At room temperature in the dark
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- - Sampling method: Singular samples (3 mL) for analysis were taken from the WSF prepared at 100 mg/L and all other test solutions at 0, 24 and 72h.
- Sample storage conditions before analysis: Samples were stored in a freezer until analysis, if not already used.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: Water Soluble Fraction (WSF): The preparation of test solution started with an aqueous mixture at a loading rate of 100 mg/L. The mixture was magnetically stirred for 25 hours resulting in a clear and colourless solution with a floating layer. The mixture was left to settle for 2 hours and the WSF was collected by siphoning. The lower test concnetrations were prepared by subsequent dilutions of the WSF in test medium.
Test organisms
- Test organisms (species):
- Pseudokirchneriella subcapitata (previous names: Raphidocelis subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Strain: NIVA CHL 1
- Source: In-house laboratory culture
- Method of cultivation: Algae stock cultures were started by inoculating growth medium (M1 according to NPR 6505, "Nederlandse Praktijk Richtlijn no. 6505") with algal cells from a pure culture on agar. The suspensions were continuously aerated and exposed to light in a climate room at a temperature of 21-24°C.
ACCLIMATION
- Acclimation period: 3 days before the start of the test, cells from the algal stock culture were inoculated in culture medium at a cell density of 1x10E4 cells/mL.
- Culturing media and conditions: Same conditions and medium (M2) as used in the test
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
Test conditions
- Nominal and measured concentrations:
- nominal: 100 mg/L and dilutions containing 0.1, 1.0 and 10% of the WSF
measured for 100 mg/L WSF: 0 h 0.42 mg/L, 24 h < 0.014 mg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Material, size, headspace, fill volume: 100 mL (all-glass) containing 50 mL of test solution
- Initial cells density: 10000 cells/mL
- No. of vessels per concentration (replicates): 6 of the WSF for 100 mg/L, 3 of each WSF dilution
- No. of vessels per control (replicates): 6
- Other: Singular reserve samples of 3 mL were taken from all test solutions for possible analysis.
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: M2 according to OECD 201
- Culture medium different from test medium: Yes, M1 according to the NPR 6505 ("Nederlandse Praktijk Richtlijn no. 6505")
- Intervals of water quality measurement: PH at the beginning and at the end of the test, temperature continously in a temperature control vessel.
OTHER TEST CONDITIONS
- Photoperiod: Continously
- Light intensity and quality: 62 to 69 µE/mE2/s, TLD-lamps of cool-white of 30 Watt
EFFECT PARAMETERS MEASURED:
- Determination of cell concentrations: At the beginning: microscope and a counting chamber; after 24, 48 and 72 h: spectrophotometric measurement of samples at 720 nm
- Other: At the end microscopic observations were performed on the limit concentration. - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 72 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOELR
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.023 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 0.023 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- NOELR
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Details on results:
- - Exponential growth in the control (for algal test): Yes
- Observation of abnormalities (for algal test): No - Results with reference substance (positive control):
- - Results with reference substance valid? Yes
- EC50: 1.2 mg/L for growth rate (95% confidence interval 0.77 to 2.0 mg/L)
Any other information on results incl. tables
No reduction of growth rate or inhibition of yield was recorded at any of the tested concentrations (100 mg/L WSF and dilutions of 0.1, 1.0 and 10% of the WSF). Therefore the NOELR was ≥ 100 mg/L and the ErL50 (72h) > 100 mg/L. The loading rate of 100 mg/L corresponds to a TWA concentration of 0.023 mg/L.
Table 1: Mean cell densities (x 10000 cells/ML) at 0, 24, 48 and 72 h of exposure to the test material.
% WSF prep. at 100 mg/L |
Exposure time (hours) |
|||
0 |
24 |
48 |
72 |
|
Control |
1.0 |
8.0 |
30.8 |
109.9 |
0.10 |
1.0 |
8.1 |
29.2 |
105.1 |
1.0 |
1.0 |
7.9 |
31.5 |
110.6 |
10 |
1.0 |
8.0 |
32.3 |
115.0 |
100 |
1.0 |
7.5 |
31.9 |
129.6 |
Table 2: Percentage reduction of growth rate and percentage inhibition of yield
% WSF prep. at 100 mg/L |
Mean growth rate r (0-72 h) |
Yield (0-72 h) |
||
r |
Reduction (%) |
x10000 cells/mL |
Inhibition (%) |
|
Control |
0.06524 |
|
108.91 |
|
0.10 |
0.06464 |
0.9 |
104.13 |
4.4 |
1.0 |
0.06531 |
-0,1 |
109.61 |
-0.6 |
10 |
0.06587 |
-1.0 |
113.96 |
-4.6 |
100 |
0.06755 |
-3.5 |
128.57 |
-18.0 |
Applicant's summary and conclusion
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.
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