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EC number: 619-422-7 | CAS number: 99305-42-7
- 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
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2003-12-09- to 2003-12-11
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 004
- Report date:
- 2004
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 4,4'-Methylenebis(N-butoxycarbonylcyclohexanamine)
- EC Number:
- 619-422-7
- Cas Number:
- 99305-42-7
- Molecular formula:
- C23 H42 N2 O4
- IUPAC Name:
- 4,4'-Methylenebis(N-butoxycarbonylcyclohexanamine)
- Details on test material:
- - Test substance:: 4,4'-Methylenebis(N-butoxycarbonylcyclohexanamine) of Degussa AG
- Batch 4/032, purity approximately 95 % determined 04-Nov-2003
- White solid
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- MONITORING OF TEST SUBSTANCE CONCENTRATION: Analysis of samples at start and end of study
Test solutions
- Vehicle:
- no
- Details on test solutions:
- STOCK AND TEST SOLUTION AND THEIR PREPARATION
- Dispersion: Weighing of test substance, mixing with water, homogenization with Ultra-Turax, stirring for approx. 24 hours (magnetic), filtration
(0.45 µm pore size)
- Vehicle, solvent: None
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISMS
- Strain: Daphnia magna, clone 5
- Source/supplier: Aventis Pharma Deutschland GmbH, ProTox (inhouse)
- Breeding method: 100 ml beakers with 70 ml test water (Elendt, M4), one daphnid per culture vessel, maximum age used for breeding 42 days,
monitoring of repdoduction rate and state of health daily except weekends
- Age: < 24 hours
- Feeding: Three times a week with Desmodesmus subspicatus at a level of 0.2 mg carbon / day for each animal
- Feeding during test: No
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Test temperature:
- - 21.0 - 21.3 °C
- pH:
- 7.8-8.1
- Dissolved oxygen:
- 8.7-9.1 mg/L
- Nominal and measured concentrations:
- 0 mg/l, 100 mg/l (nominal)
- Details on test conditions:
- DILUTION WATER
- Source: Prepared from demineralized water according to Elendt (M4) at least 24 hours before use and aerated until saturation
- Hardness: 2.5 mmol Ca2+ + Mg2+ / l
- Ca/Mg ratio: 80.1 / 12.2 [mg/l]
- Na/K ratio: 19.8 / 3.2 [mg/l]
TEST SYSTEM
- Renewal of test solution: No
- Exposure vessel type: 250 ml beakers filled with 200 ml test solution
- Number of replicates, individuals per replicate: 2 replicates with 10 individuals each l
- Adjustment of pH: No
- Photoperiod: 16 hours/day (fluorescent tubes)
TEST PARAMETER: Immobility
SAMPLING: Inspections after 24 and 48 hours with stimulation of passive daphnids and removal of immobile animals - Reference substance (positive control):
- not specified
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- >= 0.024 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.024 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Effect data (Immobilisation): No immobility was observed in both test and
control groups.
- EC50 (Daphnia magna, 48 h) > 100 mg/l (nominal) and 0.024 mg/l (analytical) - Results with reference substance (positive control):
- - no data available
Any other information on results incl. tables
Analytical results:
- Nominal/measured concentrations: Measured concentrations were always in
a range 20-27 µg/L (mean 24 µg/l), corresponding to 0.020-0.027% (mean 0.024%)
of nominal, i.e. the solubility was far below the nominal concentration.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- No toxic effects on Daphnia magna could be observed up to the solubility limit of the test substance. Thus the EC50 is >0.024 mg/L
- Executive summary:
The acute effects of H12MDU on Daphnia magna were evaluated in a static 48h-limit test according to EU method C.2 and OECD TGD 202. H12MDU was tested at a nominal concentration of 100 mg/L. The analytical monitoring demonstrated that the test substance was soluble up to a concentration of 0.024 mg/L (mean value). Thus the EC50 was determined as >0.024 mg/L.
The study was assessed as "reliable without restrictions".
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