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EC number: 939-412-9 | CAS number: 85586-38-5
- 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:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Deviations:
- no
- Principles of method if other than guideline:
- The respiration inhibition of the test substance to a sludge concentration of 1.5 g/L suspended solids is recorded after 3 hours.
- GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- activated sludge
- Details on inoculum:
- - Initial biomass concentration: 1.5 g/L suspended solids
- Source: Rungsted municipal treatment plant, Denmark, treating almost exclusively domestic sewage - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Reference substance (positive control):
- not specified
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- 135 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 30 min
- Dose descriptor:
- EC50
- Effect conc.:
- 188 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 04. Jul 1997
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
- Version / remarks:
- reported as EG-guideline 88/302/EG (30.05.1988)
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Stock solution (5000,3 mg test substance in VE water) ad 200 mL (VE-Water) plus 200 µL Baysilone (foam killer) - Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Source: Municipal sewage treatment plant "Marl-West"
- Preparation of inoculum for exposure: sludge was sampled, allowed to settle, washed with 2 L tap water, aerated for 30 min and stirred; 200 mL synthetic effluenct were added to the cleaned sludge and tap water added ad 4 L
- Pretreatment: On test day, the sludge was allowed to settle and was washed twice with 2 L tap water
- Initial biomass concentration: 3.82 g dry substance/L - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Post exposure observation period:
- not relevant
- Hardness:
- no data
- Test temperature:
- 20 ± 2 °C
- pH:
- 8.0-8.4
- Dissolved oxygen:
- >2.5 mg/L
- Salinity:
- not relevant
- Nominal and measured concentrations:
- Nominal: 0, 260, 390, 578.5, 864.5 and 1300 mg a-WAS/L (= active substance)
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 500 mL beaker
- Renewal rate of test solution (frequency/flow rate): none
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 2
- No. of vessels per reference control (replicates): 3
- Culture medium different from test medium: no
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : oxygen consumption rate (manometric)
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.5 - Reference substance (positive control):
- yes
- Remarks:
- Dichlorophenol
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- 680 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Remarks:
- a-WAS
- 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 between 5 and 30 mg/L (test result: 8.1 mg/L) - Reported statistics and error estimates:
- Excel, program auswert.msk, probit and logarithm of concentration calculated, results from linear section of regression curve
- Endpoint:
- toxicity to microorganisms
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Comparable to national guideline study with acceptable restrictions.
- Qualifier:
- according to guideline
- Guideline:
- other: cell multiplication inhibition test acc. to Bringmann and Kühn (1977)
- GLP compliance:
- not specified
- Analytical monitoring:
- not specified
- Vehicle:
- not specified
- Test organisms (species):
- Pseudomonas putida
- Test type:
- not specified
- Water media type:
- freshwater
- Total exposure duration:
- 18 h
- Duration:
- 18 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 550 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth inhibition
- Endpoint:
- toxicity to microorganisms
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 12 Nov - 15 Nov 1991
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP study performed according to national guideline.
- Qualifier:
- according to guideline
- Guideline:
- DIN 38412-8 (Pseudomonas Zellvermehrungshemmtest)
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- Pseudomonas putida
- Details on inoculum:
- - Laboratory culture: Stamm Berlin 33/2 (DSM 50026)
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 16 h
- Post exposure observation period:
- not relevant
- Test temperature:
- 21 °C
- pH:
- 6.6 - 6.8
- Nominal and measured concentrations:
- nominal: 0, 1000, 3000 and 10000 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Clim-o-shake at 100 rpm
EFFECT PARAMETERS MEASURED: growth inhibition, measured photometrically at 436 nm (Zeiss filterphotometer PL4) - Reference substance (positive control):
- no
- Duration:
- 16 h
- Dose descriptor:
- EC0
- Effect conc.:
- 409 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth inhibition
- Duration:
- 16 h
- Dose descriptor:
- EC10
- Effect conc.:
- 1 083.85 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth inhibition
Referenceopen allclose all
0.58% inhibition at 1000 mg prod./L
15.3% inhibition at 3000 mg prod./L
60.63% inhibition at 10000 mg prod./L
Description of key information
EC50(3h) = 135 mg/L (nominal) for respiration inhibition of activated sludge (EU Method C.11, read across CAS 151-21-3)
Key value for chemical safety assessment
- EC50 for microorganisms:
- 135 mg/L
Additional information
Since no reliable studies on toxic effects of C8-18AS Mg & TEA (CAS 85586-38-5) to microorganisms are available, in accordance to Regulation (EC) No. 1907/2006 Annex XI, 1.5, a read-across to other structurally related alkyl sulfates was conducted. A key study was performed with C12AS Na (CAS 151-21-3) using activated sludge from a municipal sewage treatment plant (Dutka 1983). The test was performed according to a guideline similar to OECD 209. The EC50 values of 188 and 135 mg/L (nominal concentrations) were obtained for the endpoint respiration inhibition after 30 minutes and 3 hours of exposure, respectively. Since the toxicity of alkyl sulfates is dependent on the carbon chain length reaching its maximum at the C14/C15 carbon chain, it is expected that the toxic effects of the C12AS Na are similiar to a worst case scenario for C8-18AS Mg & TEA. The 3-hour EC50 value of 135 mg/L was used for the PNEC STP derivation for C8-18AS Mg & TEA (CAS 85586-38-5).
Moreover, a study on microorganisms was performed with C12-18AS Na (CAS 68955-19-1). The respiration inhibition test with activated sludge was conducted according to the EU Method C.11 and is GLP compliant. An EC50 of 680 mg a.i./L was reported for the respiration rate after 3 h of exposure. Due to structural and property similarities with the tested category members it can be concluded that the above results apply also to C8-18AS Mg & TEA (CAS 85586-38-5). Additionally, a GLP test according to DIN 38412 part 8 with Pseudomonas putida using C12-14AS TEA (CAS 90583-18-9) is available (Guhl 1992). In this study, the growth inhibition of Pseudomonas putida was recorded after approximately 16 hours of exposure. The 16-h EC10 value was determined to be 1084 mg a.i./L (nominal concentration). Finally, a reliable study with Pseudomonas putida is available for C16-18AS Na (CAS 68955-20-4; Steber 1988). The study followed the procedure of cell multiplication inhibition test according to Bringmann and Kühn (1977). The growth inhibition of Pseudomonas putida was recorded after 18 hours of exposure to the test substance. The 18-hour NOEC value was determined to be 550 mg a.i./L (nominal concentration).
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