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EC number: 266-928-5 | CAS number: 67701-03-5 This substance is identified by SDA Substance Name: C16-C18 alkyl carboxylic acid and SDA Reporting Number: 19-005-00.
- 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 microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to microorganisms
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- not reported
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: National guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- other: Bewertung wassergefährdender Stoffe, III Bestimmung der akuten Bakterientoxizität
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: ISO 10712
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Sampling method: 50 mL of the test substance stock solutions were taken after filtration of the saturated stock solution
- Sample storage conditions before analysis: frozen at -20 °C - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: A saturated test substance solution with a nominal concentration of 10 mg/L was prepared by sonication for 30 minutes and a subsequent 24 h lasting mixing with a magnetic stirrer. Afterwards the solution was filtered and neutralised to a pH of 7.1 with NaOH
- Controls: 10 with inoculum without test substance to determine turbidity and for each test concentration 1 control without inoculum to determine possibly occuring colouration - Test organisms (species):
- Pseudomonas putida
- Details on inoculum:
- - Preparation of inoculum for exposure: Bacteria from 7 days old stock culture were inoculated in a fluid nutrient medium in Erlenmeyer flasks and incubated for 16-20 h at 25 °C. Afterwards the extinction of the monochromatic radiation at 436 nm was determined for a 10 mm layer of the bacterial suspension by photoelectric measurement.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 16 h
- Remarks on exposure duration:
- 16 - 20 h
- Test temperature:
- 23 - 27 °C
- pH:
- pH was neutralised to 7.1 with NaOH
- Nominal and measured concentrations:
- nominal: 3.9, 7.8, 15.6, 31.3, 62.5, 125.0, 250.0, 500.0, 1000.0, 2000.0, 4000.0, 8000.0 mg/L (mean measured)
actual: (0.11 % of the nominal concentrations) - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): closed with aluminum foil caps
- Material, size, headspace, fill volume: 300 mL Erlenmeyer flasks
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 10
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Milli-Q water: water was first purified by reverse osmosis and thereafter passed over activated carbon and ion exchange cartridges
OTHER TEST CONDITIONS
- Adjustment of pH: with NaOH to 7.1
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : extinction of monochromatic radiation at 436 nm in a 10 mm layer after 16 - 20 h - Reference substance (positive control):
- yes
- Remarks:
- Methanol
- Duration:
- 18 h
- Dose descriptor:
- EC10
- Effect conc.:
- 883 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: given as TT (toxicity threshold)
- Results with reference substance (positive control):
- - Other: The toxicity threshold value of the reference substance was in the usual range known at RCC Notox
Reference
Table 1: Extinction of the test substances solutions after 16 - 20 h
Concentration [mg/L] |
Extinction at 436 nm |
||||||
Replicate I |
Replicate II |
Replicate III |
Arithm. mean of replicates |
Replicate without inoculum |
Corrected arithmetic mean* |
|
|
3.9 |
0.822 |
0.910 |
0.927 |
0.886 |
0.001 |
0.885 |
|
7.8 |
0.760 |
0.745 |
0.827 |
0.777 |
0.000 |
0.777 |
|
15.6 |
0.801 |
0.836 |
0.842 |
0.826 |
0.000 |
0.826 |
|
31.3 |
0.823 |
0.829 |
0.843 |
0.832 |
0.000 |
0.832 |
|
62.5 |
0.849 |
0.815 |
0.827 |
0.830 |
0.000 |
0.830 |
|
125.0 |
0.845 |
0.816 |
0.832 |
0.831 |
0.000 |
0.831 |
|
250.0 |
0.843 |
0.834 |
0.833 |
0.837 |
0.000 |
0.837 |
|
500.0 |
0.796 |
0.807 |
0.852 |
0.818 |
0.000 |
0.818 |
|
1000.0 |
0.775 |
0.740 |
0.699 |
0.738 |
0.001 |
0.737 |
|
2000.0 |
0.672 |
0.658 |
0.654 |
0.661 |
0.009 |
0.652 |
|
4000.0 |
0.680 |
0.694 |
0.703 |
0.692 |
0.024 |
0.668 |
|
8000.0 |
0.746 |
0.731 |
0.781 |
0.753 |
0.057 |
0.696 |
|
* corrected with extinction values from replicate without inoculum
The resulting nominal toxicity threshold (TT), determined graphically at 883 mg prod./L. However, due to the DOC and TCC measurements only 0.11 % of the added test substance persist in the test medium. Thus, the actual TT (which is equivalent to the EC10) must be 0.97 mg prod./L.
Table 2: Extinction after 16 - 20 h in the reference substance and the blank control
Concentration [mg prod./L] |
Extinction at 436 nm |
|
Reference substance |
Blank controls |
|
3950.0 |
0.775 |
0.855 |
7900.0 |
0.695 |
0.901 |
15800.0 |
0.490 |
0.912 |
31600.0 |
0.220 |
0.903 |
63200.0 |
0.057 |
0.830 |
|
0.810 |
|
0.790 |
||
0.788 |
||
0.803 |
||
0.809 |
||
Arithmetic mean |
0.840 |
With respect to the historical test with the reference substance methanol, it can be concluded that the test conditions were optimal and the results are valid.
Description of key information
No toxic effects on microorganisms were observed up to the limit of water solubililty, no PNEC is derived.
Key value for chemical safety assessment
Additional information
Within the fatty acid category studies describing the toxicity of fatty acids to Pseudomonas putida are available. For the mixture under discussion read-across is performed to a study conducted with stearic acid C18 (CAS 57 -11 -4). The cell multiplication inhibition test was conducted following GLP-requirements. The used method in the test was similar to the ISO guideline 10712. In the study an EC10 (18 h) of 883 mg/L (nominal) (Coenen, 1989) was reported. Concluding from the results of this study the considered mixture is regarded to be not toxic to microorganisms. As no toxic effects on microorganisms were observed up to the limit of water solubililty, no PNEC is derived.
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