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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 229-194-7 | CAS number: 6425-39-4
- 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 aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2011-08-22 to 2011-09-25
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- Study performed according to internationally accepted test guidelines for toxicity to algae (OECD 201) and conform CLP requirements
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: PFW100113
- Expiration date of the lot/batch: 2012-12-01
- Analytical purity: 99.3 %
- Impurities (identity and concentrations): not reported
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: room temperature in the dark
- Stability under test conditions: not reported
OTHER SPECIFICS:
- Name of test material (as cited in study report): DMDEE (Morpholine, 4,4'-(oxydi-2,1-ethanediyl)bis-)
- Substance type: pale yellow liquid
- Physical state: liquid - Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: control and 100 mg/l
- Sample storage conditions before analysis: all 0-hour and 48-hour samples stored at approximately -20 °C prior to analysis
- Four replicates were sampled and pooled for analysis in both treatments - Vehicle:
- no
- Details on test solutions:
- - 200 mg of test substance was dissolved in reconstituted water and the volume adjusted to 2 litres to give the required test concentration of 100 mg/l
- the solutions were inverted several times to ensure adequate mixing and homogeneity
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Strain: not reported
- Source: not reported
- Age at study initiation (mean and range, SD): the main part of daphnids was 24 hours old, although some of the young may have been up to 25 hours old
- Method of breeding: adult Daphnia were maintained in 150 ml glass beakers containing Elendt M7 medium in a temperature controlled room at approximately 20 °C
- Feeding during test
- Food type: mixture of algal suspension (Desmodesmus subspicatus) and Tetram® flake food suspension
- Amount: not reported
- Frequency: daily
ACCLIMATION
- Acclimation period: one day prior to initiation of test gravid adults were isolated to produce young
- Acclimation conditions (same as test or not): yes - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Hardness:
- 250 mg/l CaCO3
- Test temperature:
- 21-22 °C
- pH:
- at initiation of test: 7.7 in control and 8.4 in 100 mg/l
after 48 hours exposure: 8.0 in control and 8.1 in 100 mg - Dissolved oxygen:
- at initiation of test: 9.1 mg/l O2 in control and 9.05 mg/l O2 in 100 mg/l
after 48 hours exposure: 8.65 mg/l O2 in control and 8.6 mg/l O2 in 100 mg - Salinity:
- Not applicable.
- Nominal and measured concentrations:
- nominal concentrations: 0 and 100 mg/l
measured concentrations: < LOQ in control, both at initiation and after 48 hours, and 114 and 118 mg/l at initiation, and 119 and 110 mg/l (after 48 hours) (samples of 100 mg/l were pooled 2 by 2) - Details on test conditions:
- TEST SYSTEM
- Test vessel: jars
- Type (delete if not applicable): covered, to reduce evaporation
- Material, size, headspace, fill volume: glass, 250 ml, headspace not defined, 200 ml
- Aeration: not during test, only prior to test until dissolved oxygen concentration was approximately air-saturation value
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
- no feeding during test
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: reconstituted water
- Culture medium different from test medium: yes:
* culture medium Elendt M7 medium, pH 8.0 ± 0.2 and not adjusted
* test medium: reconstituted water, pH 7.8 ± 0.2 and adjusted if necessary, conductivity < 5 µS/cm^-1
- Intervals of water quality measurement:
* temperature was recorded daily (Hanna Instruments HI 93510 digital thermometer)
* dissolved oxygen and pH were recorded at start and termination of the test (Hach HQ30d Flexi Handheld meter)
OTHER TEST CONDITIONS
- Adjustment of pH: the pH of the test medium was adjusted with NaOH or HCl
- Photoperiod: 16h:8h light:dark, with 20 minutes dawn and dusk transition periods
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- immobilisation (defined as unable to swim for approximately 15 seconds after gentle agitation) or adverse reactions
- at 24 and 48 hours after the start of exposure
TEST CONCENTRATIONS
- Spacing factor for test concentrations: limit test
- Range finding study
- Test concentrations: 0.10, 1.0, 10 and 100 mg/l
- Results used to determine the conditions for the definitive study: no immobilisation or adverse reactions were observed at the test concentrations of 0.10, 1.0, 10 and 100 mg/l - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: zero immobilisation
- Details on results:
- - Color differences: all control and 100 mg/l test preparations were observed to be clear colourless solutions throughout the duration of the test.
- Results with reference substance (positive control):
- - analysis of immobilisation by means of maximum-likelihood probit method (Finney, 1971)
- EC50 (24h) = 1.5 mg/l, 95 % C.I. 1.3-1.8 mg/l
- EC50 (48h) = 0.99 mg/l, 95 % C.I. 0.85-1.1 mg/l
- NOEC (24 and 48h) = 0.56 mg/l (based upon zero immobilisation at this concentration)
- the results were within the normal ranges for this reference item - Validity criteria fulfilled:
- yes
- Conclusions:
- In this study, Daphnia magna were exposed to a single concentration of 100 mg/l of test substance for 48 hours. Based on immobilisation, the EC50 was found to be > 100 mg/l after 48 hours of exposure.
Reference
Description of key information
The key value for acute toxicity to invertebrates was obtained from a study exposing Daphnia magna to a single test concentrations during 48 hours under GLP conditions and according to OECD 202 (limit test).
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 100 mg/L
Additional information
A study investigating the acute toxicity of the test substance to aquatic invertebrates was available. The study of Vryenhoef and Mullee (2011) performed by Harlan Laboratories exposed Daphnia magna to 100 mg/l of test substance during 48 hours and observed mobility. The results showed an EC50(48h) of > 100 mg/l.
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.