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EC number: 942-293-6 | CAS number: -
- 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
Short-term toxicity to fish
Administrative data
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 16 February - 23 March 1990
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study performed according to GLP adn OECD guidelines. No monitoring of concentration, but substance fully watersoluble.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 990
- Report date:
- 1990
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Deviations:
- yes
- Remarks:
- No measurements of concentrations.
- GLP compliance:
- yes
Test material
- Reference substance name:
- Ethanol, 2,2'-iminobis-, N-coco alkyl derivs., N-oxides
- EC Number:
- 263-180-1
- EC Name:
- Ethanol, 2,2'-iminobis-, N-coco alkyl derivs., N-oxides
- Cas Number:
- 61791-47-7
- Molecular formula:
- not applicable
- IUPAC Name:
- N,N-Bis(2-hydroxyethyl)-C12-18(even numbered) alkyl-1-amine oxides
- Details on test material:
- The test material was identified by name and specifications:
- chemical name: Cocobis(2-hydroxyethyl)amine oxide
- cas nr : 61791-47-7
- batch no: 900110 (CoA attached to the report):
Amine oxide: 30.5%
Free amine: 0.3%
Free peroxide: 0.13%
It was supplied by the study sponsor on 5 Feb 1990. Stored in the dark at room temperature.
Constituent 1
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
Liquid. Stable at test conditions (biodegradability information available).
Water soluble at test concentrations
Sampling and analysis
- Analytical monitoring:
- no
Test solutions
- Vehicle:
- no
- Details on test solutions:
- The test solutions were prepared from stock solutions of the test substance in deionized water. The stock solution was prepared by intensive mixing and was homogeneous. The test concentrations were prepared by addition of the respective amounts of the stock solution to the
DutchStandardWater (DSW).
Test organisms
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- Obtained from a local aquarium retailer and identified by batch 20-2-90. The fish were appromiximately 2.5-3.0 cm in size and the medium wet
weight per fish was approximately 0.3 g. Before being used in the test, the fish were kept for at least 12 days in the facilities to determine the
acceptability of the batch. The water they were kept in was Dutch Standard Water (DSW).
The fish were fed daily, the last feeding taking place 24 hours before the start of the test.
Study design
- Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
Test conditions
- Hardness:
- 13 dH
- Test temperature:
- 22 -23 C
- pH:
- 7.3 - 7.7
- Dissolved oxygen:
- 3.2 - 7.8 mg/l (36% - 87% oxygen of air saturation value). The low oxygen values would not have affected the study outcome,
namely also in control groups (no exposure and reference substance) low oxygen was measured, but did not affect mortality. - Nominal and measured concentrations:
- Nominal concentrations:
6.0 - 8.4 - 11.8 - 16.5 - 23.0 mg/L - Details on test conditions:
- 10 fish were used per test concentration and control: approximately 1.0 g biomass/L.
As test vessels 5 L glass aquaria containing 3L of test medium were used, which were covered with a plass plate. The diluting water used for
preparation of the test concentrations was a synthetic water: Dutch Standard Water (pH= 8.2, hardness: 13 dH).
The test was carried out in a temperature controlled incubator. The light regime was 12 hours of ambient light per day, provided by fluorescent
tubes. Oxygen and pH were measured daily. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 3.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CI 3.1-3.8 mg/L
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 11.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CI 10.1 - 12.5 mg/L
- Details on results:
- The LC50 (96h) was calculated to be 11.2 mg/L with 95% confidence limits of 10.1 and 12.5 mg/L. The highest concentration causing no mortality
(No Observed Effect Concentration, NOEC) after 96 hours amounted to 8.4 mg/L, whereas 100% mortality was produced within 23 hours at 16.5
mg/L. No other effects (deviations in behaviour or appearance) were obeserved at non lethal dose rates. - Results with reference substance (positive control):
- The LC50 for potassium dichromate was calculated to be:
mg/L (95% CL)
24h: 396 (197 -796)
48h: 210 (193 - 229)
72h: 198 (150 - 262)
96h: 198 (150 - 262)
which is in line with a reference EEC study stating a mean value for LC50(48h) of 205.5 mg/L. - Reported statistics and error estimates:
- The LC50 was determined with a LC50 programme of Griffioen (RIZA, NL) based on a model by Kooyman (1981).
Any other information on results incl. tables
- Sublethal observations / clinical signs:
Number of surviving animals
Conc (mg/L)
0h
5h
23h
29h
46h
48h
53h
70h
72h
90h
94h
96h
Control
10
10
10
10
10
10
10
10
10
10
10
10
6.0
10
10
10
10
10
10
10
10
10
10
10
10
8.4
10
10
10
10
10
10
10
10
10
10
10
10
11.8
10
10
9
9
9
9
7
5
5
4
2
2
16.5
10
7
0
0
23.0
10
0*
0*
* Unclear for timepoint
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The LC50(96h) was calculated to be 11.2 mg/L with 95% confidence limits of 10.1 and 12.5 mg/L. the NOEC was 8.4 mg/L. If it is assumed that the product has a 100% pure active ingredient and that the toxicity is related to the active ingredient only, the LC50 and NOEC (96h) amounts to 3.4 and
2.6 mg/L amine oxide respectively. - Executive summary:
A study was performed according to OECD203 and GLP to investigate the acute toxicity of the test item to fish. The study was semi-static and was performed also using a reference substance (potassium dichromate). Based on nominal concentrations only, the LC50 was calculated to be 11.2 mg/L and the NOEC was 8.4 mg/L. The reference substance showed the acceptability of both the test system and batch of fish. No other effects such as deviations in behaviour or appearance of the fish were observed in non-lethal concentrations.
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