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EC number: 500-058-1 | CAS number: 27252-75-1 1 - 2.5 moles ethoxylated
- 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:
- toxicity to microorganisms, other
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- Data based on the inhibition control of a ready biodegradability study
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- other: OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- 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 item was dissolved directly in mineral medium with the aid of ultrasonication for appr. 20 minutes. - Test organisms (species):
- activated sludge, domestic
- Details on inoculum:
- - Source of inoculum/activated sludge: Sewage treatment micro-organisms from the final effluent stage of the Severn Trent Water Plc sewage treatment plant at Loughborough, Leicestershire, UK (obtianed on 28 Jan 2019). The STP treats predominantly domestic sewage.
- Pretreatment: The sample of effluent was filtered through coarse filter paper (first approximate 200 mL discarded) and maintained on aeration in a temperature controlled room at temperatures of between 20 and 21 °C prior to use. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 14 d
- Test temperature:
- 21 - 22 °C
- pH:
- 7.4 - 7.5
- Nominal and measured concentrations:
- Toxicity control: 100 mg test item/L and 100 mg aniline/L
- Details on test conditions:
- TEST SYSTEM
- Culturing apparatus: CES Multi-Channel Aerobic Respirometer
- Number of culture flasks/concentration: 3
- Method used to create aerobic conditions: the pressure reduction caused by the adsorption of carbon dioxide triggers an electrolytic process, generating oxygen and restoring the pressure in the sample flask.
- Details of trap for CO2 and volatile organics if used: ethanolamine solution (50% v/v)
- No. of vessels per concentration (replicates): 2
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: according to OECD guideline 301F
- Particulate matter:
OTHER TEST CONDITIONS
- Adjustment of pH: no
- Light intensity: diffuse light - Reference substance (positive control):
- yes
- Remarks:
- Aniline
- Duration:
- 14 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: O2 consumption
- Remarks:
- Result of toxicity control from ready biodegradability test
- Results with reference substance (positive control):
- Reference contol (Anilin): 76% degradation after 14 days (ten-day window criterion met)
Reference
The toxicity control attained 76% degradation after 14 days of incubation.
“If in a toxicity test, containing both the test and reference substance, less than 35% degradation (based on total DOC) or less than 25% (based on total ThOD or ThCO2) occurred within 14 days, the test substance can be assumed to be inhibitory.” (OECD guideline 301)
Since more than 35% degradation occurred in the toxicity control, the substance is with high probability not toxic to aquatic microorganisms. The test item concentration in the toxicity control of 100 mg/L can be used as NOEC value for the toxicity to aquatic microorganisms.
Description of key information
The assessment of the toxicity of the target substance to microorganisms is based on the results of the toxicity control of the available biodegradation study. A NOEC(14 d): 100 mg/L (based on toxicity control of OECD 301 F) is used as key value for the CSA of the target substance.
Key value for chemical safety assessment
Additional information
The toxicity of the Ethoxylates (AE) category substances to microorganisms was assessed by read-across based on the grouping of substances (category approach). The available data were used for a general assessment of the toxicity of the Alcohol Ethoxylates (AE) category substances to microorganisms. Based on the available data adverse effects on microbial activity are not expected. The substances of the Alcohol Ethoxylates (AE) category are readily biodegradable. In all studies conducted with a toxicity control, no inhibition of the degradation process by the test substance was observed. The available studies investigating the respiration inhibition of activated sludge organisms and Pseudomonas putida determined no detrimental effects of the tested Alcohol Ethoxylates.
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.