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EC number: 640-964-5 | CAS number: 218451-68-4
- 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
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1996-08-30
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- other: EG-Richtlinie L 133/118 vom 30.5.1988
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: The test substance was directly given into the test vessels in five different concentrations, the test vessels were 3 h incubated and stirred under permanent ventilation with clean, oil-free air in a water-filled pan
Controls: two replicates blank control, reference control (3,5-Dichlorophenol) in three different concentrations
- Evidence of undissolved material (e.g. precipitate, surface film, etc): no data - Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Method of cultivation: not applicable
- Preparation of inoculum for exposure: approximately 5 l activated sludge of the sewage "Marl-Ost" was one-time sedimentated, three-times centrifuged each for 5 minutes 2000 min-1 and washed with 500 - 600 mL drinking water. The activated sludge was taken into 3.5 L drinking water and had a concentration of 3.603 g TS/L, that means for 500 mL test and 200 mL inoculum 1.44 g TS/L.. - Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Post exposure observation period:
- none
- Hardness:
- no data
- Test temperature:
- 18 - 22 °C
- pH:
- 7.6-7.8
- Dissolved oxygen:
- >= 2,5 mg/L
- Nominal and measured concentrations:
- 57.4; 92.8; 189.4; 290.8; 380 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: flasks
- Material, fill volume: glass, 500 ml fill volume
- Aeration: continuous
- Renewal rate of test solution (frequency/flow rate): not applicable
- No. of organisms per vessel: not applicable
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 2
- No. of vessels per vehicle control (replicates): not applicable
- Biomass loading rate: 200 mL inoculum; 1.44 g dry weight/L
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Oxygen consumption, pH
- Reference substance (positive control):
- yes
- Remarks:
- 3,5-Dichlorophenol
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 370 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Results with reference substance (positive control):
- - Results with reference substance valid: yes
- Relevant effect levels: EC50 = 5.1 mg/L - Validity criteria fulfilled:
- yes
- Executive summary:
Marlowet 4753 (Coconut oil, reaction products with polyethylene glycol and trimethylolpropane) was tested in Activated Sludge Respiration Inhibition Test according to EC guideline 88/302/EC. Within the tested concentration of 57.4; 92.8; 189.4; 290.8 and 380 mg/L there was no significant toxic effect. The determined positive effects were not proportional to increasing concentration. The EC50 was > 370 mg/L rounded up to two significant places. The test substance contents 98.4 % active substance.
Reference
Description of key information
Marlowet 4753 (Coconut oil, reaction products with polyethylene glycol and trimethylolpropane) was tested in Activated Sludge Respiration Inhibition Test according to EC guideline 88/302/EC. Within the tested concentration of 57.4; 92.8; 189.4; 290.8 and 380 mg/L there was no significant toxic effect. The determined positive effects were not proportional to increasing concentration. The EC50 was > 370 mg/L rounded up to two significant places. The test substance contents 98.4 % active substance.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 370 mg/L
Additional information
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.