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Diss Factsheets
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EC number: 239-806-4 | CAS number: 15717-25-6
- 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
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 17 Aug - 14 Sep 2001
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP - Guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 001
- Report date:
- 2001
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- The Department of health of the Government of the United Kingdom
Test material
- Reference substance name:
- Potassium 3-sulphonatopropyl acrylate
- EC Number:
- 250-465-0
- EC Name:
- Potassium 3-sulphonatopropyl acrylate
- Cas Number:
- 31098-20-1
- Molecular formula:
- C6H10O5S.K
- IUPAC Name:
- potassium 3-(acryloyloxy)propane-1-sulfonate
- Details on test material:
- - Name of test material (as cited in study report): SPA (sulfopropyl acrylate)
- Physical state: powder
- Analytical purity: no data
- Lot/batch No.: 0200014/001
- Storage condition of test material: at room temperature in the dark
Constituent 1
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- sewage, domestic, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge: Final effluent of Severn Trent Water Plc sewage treatment plant at Loughborough, Leicestershire, United Kingdom, obtained on 17 Aug 2001
- Pretreatment: The effluent was filtered through coarse filter paper, while approx. the first 200 mL were discarded. The filtrate was maintained on continuous aeration in a temperature controlled room at 21 °C. - Duration of test (contact time):
- 28 d
Initial test substance concentration
- Initial conc.:
- 5 mg/L
- Based on:
- test mat.
Parameter followed for biodegradation estimation
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- TEST CONDITIONS
- Composition of medium: 100 mg test substance were directly added to the culture medium (according to OECD 301D) and dissolved with the aid of ultrasonication (5 min). The volume was adjusted to 100 mL to give a 1000 mg/L stock solution which was inverted several times to ensure adequate mixing and homogeneity. An aliquot of 30 mL was dispersed into the final volume of 6 L to give a concentration of 5 mg/L. 1 drop inoculum per litre was added to each test flask.
- Test temperature: 20 °C
- pH adjusted: no
TEST SYSTEM
- Culturing apparatus: 250 - 300 mL darkened glass bottles (BOD bottles), stoppered
- Number of culture flasks/concentration: 2
- Measuring equipment: Yellow Springs oxygen meter and BOD Probe
SAMPLING
- Sampling frequency: after 0. 3, 6, 9, 12, 15, 18, 21, 24 and 28 d
CONTROL AND BLANK SYSTEM
- Inoculum blank: yes
- Abiotic sterile control: -
- Toxicity control: yes, containing 5 mg/L test substance and 1.5 mg/L reference substance
Reference substance
- Reference substance:
- benzoic acid, sodium salt
- Remarks:
- 3 mg/L
Results and discussion
% Degradation
- Parameter:
- % degradation (O2 consumption)
- Value:
- 28
- Sampling time:
- 28 d
- Details on results:
- The test substance was degraded by 28% within 28 d and thus, can not be considered to be readily biodegradable.
The toxicity control was degraded by 27% within 15 d. Since the biodegradation was > 25 % the test substance is not considered to be inhibitory to the inoculum.
BOD5 / COD results
- Results with reference substance:
- The reference substance is degraded by 74% within the 14-day window, confirming the inoculum and the test set-up to be appropriate.
Any other information on results incl. tables
Table 1: Biodegradation of the test substance, control, reference und toxic control after 28 d
days | mean biodegradation [%] | |||
test substance | inoculum blank | reference substance | toxicity control | |
3 | 5 | 0.450 | 41 | 10 |
6 | 7 | 0.575 | 56 | 10 |
9 | 10 | 0.625 | 57 | 11 |
12 | 29 | 0.675 | 65 | 29 |
15 | 28 | 0.825 | 65 | 27 |
18 | 27 | 0.850 | 73 | 28 |
21 | 27 | 0.850 | 74 | 29 |
24 | 27 | 0.950 | 75 | 29 |
28 | 28 | 1.050 | 74 | 29 |
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- other: not 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.
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