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EC number: 616-105-5 | CAS number: 74504-65-7
- 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

Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 7 May 2008 - 4 June 2008
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Version / remarks:
- 1994
- Qualifier:
- according to guideline
- Guideline:
- other: SS-EN ISO 9408:2000
- GLP compliance:
- no
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- Activated sludge from Klagshamn wastewater plant in Malmö, Sweden.
The concentration of suspended solid: 4.5 g/L.
The final conentration of suspended solids in the mediums was 30 mg/L. - Duration of test (contact time):
- 28 d
- Initial conc.:
- 0.045 other: mL/L
- Based on:
- test mat.
- Initial conc.:
- 101 mg/L
- Based on:
- COD
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- A closed manometric respirometer (Hach) was used. The equipment contained six bottles and each of them was connected to a manometer. The contents in the bottles were stirred with a magnetic stirrer. During the degradation, organic material was reduced, oxygen was consumed and carbon dioxide was produced. Since the produced carbon dioxide was trapped in potassium hydroxide, the oxygen consumption led to a decrease in the pressure, which was monitored by the manometer. Pressure changes within the closed manometric system were displayed directly in milligrams per liter (mg/L), Biochemical Oxygen Demand (BOD) on a precalibrated scale. Four direct-reading scales were provided with the apparatus. The required volume of medium and the required scale depended on the test substance's expected BOD value.
- Reference substance:
- other: sodium acetate
- Key result
- Parameter:
- % degradation (CO2 evolution)
- Value:
- >= 62 - <= 64
- Sampling time:
- 28 d
- Remarks on result:
- other: Percentage biodegradation of COD
- Details on results:
- The pass value of 60% for readily biodegradability has been been reached in a 10-day window within the 28-day period of test. This means that the substance can be regarded as readily biodegradable.
- Results with reference substance:
- The % degradation of the reference substance was 65 % within the 28-day period of testing.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The pass value of 60% for readily biodegradability in the OECD 301F test has been been reached in the 10-day window within the 28-day period of the test on Dermosoft DGMC. This means that the test substance can be regarded as readily biodegradable.
- Executive summary:
The aerobic biodegradability of Dermosoft DGMC was tested in a study performed according to OECD 301F Manometric Respirometry Test. The validation criteria of the test were fulfilled.
According to OECD guidelines for testing of chemicals, a test substance is regarded as readily biodegradable if the removal of ThOD within 28 days is greater than 60%. The pass value has to be reached in a 10-day window within the 28-day period of the test. The 10-day window begins when the degree of biodegradation has reached 10% ThOD and must end before 28 day of the test. This criterion was reached for the test substance (biodegradation of ≥62 - ≤64%), which means that it can be regarded as readily biodegradable.
Reference
Description of key information
The pass value of 60% for readily biodegradability in the OECD 301F test has been reached in the 10-day window within the 28-day period of the test on Dermosoft DGMC. This means that the test substance can be regarded as readily biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
- Type of water:
- freshwater
Additional information
The pass value of 60% for readily biodegradability in the OECD 301F test has been reached in the 10-day window within the 28-day period of the test on Dermosoft DGMC. This means that the test substance can be regarded as readily biodegradable.
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.

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