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EC number: 500-287-7 | CAS number: 103170-26-9
- 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:
- 2001-04-19 to 2001-07-31
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-D (Determination of the "Ready" Biodegradability - Manometric Respirometry Test)
- Deviations:
- no
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- INOCULUM/TEST ORGANISM
- Source: STP Gross-Zimmern (Germany)
- Preparation of inoculum: Centrifugation, decantation and resuspension in tap water (repeated twice); preparation of 1.5 g dry weight/l in test wate aeration until use - Duration of test (contact time):
- 28 d
- Initial conc.:
- 103.5 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- METHOD OF PREPARATION OF TEST SOLUTION
- Direct weighing of substances into test flasks, continuous stirring during the exposure period
TEST SYSTEM
- Culturing apparatus: 500 mL flasks filled with 244 mL test solution
- Number of culture flasks per concentration: 2 with test substance and inoculum; 2 with inoculum only (inoculum control); 1 with reference substance (25.7 mg/244 mL = 105.3 mg/L) and inoculum (procedure control); 1 with test substance (102.9 mg/L) and sterile filtered test water (abiotic control); 1 with test (104.1 mg/L) and reference (102.9 mg/L) substances and inoculum (toxicity control)
- Measuring equipment: manometer (BSB/BOD-Sensor-System, Aqualytic)
- Closed vessels used: yes
TEST CONDITIONS
- Composition of medium: (A) Dissolved deionized water, total volume 1000 mL: 8.50 g KH2PO4; 21.75 g K2HPO4; 33.40 g Na2HPO4 * 2 H2O; 0.50 g NH4Cl; (B) Dissolved deionized water, total volume 1000 mL: 22.50 g MgSO4 * 7 H2O; (C) Dissolved deionized water, total volume 1000 mL: 36.40 g CaCl2 * 2 H2O; (D) Dissolved deionized water, total volume 1000 mL: 0.25 g FeCl3 * 6 H2O; 1 drop of concentrated HCl; 10 mL (A) + 1 mL each (B), (C), (D) in deionized water, total volume 1000 mL
- Test temperature: 21-22 °C
- pH value: 7.6 (start); 7.6 (end)
- Concentration of suspended solids: 30 mg dry solids/L
- Other relevant factors: darkness; absorption of evolved CO2 in 45 % KOH solution - Reference substance:
- aniline
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 28 d
- Details on results:
- - Toxicity control
41 % degradation (14 days)
49 % degradation (28 days)
Conclusion: The test substance does not inhibit the microorganisms.
- Abiotic control
No oxygen demand was determined. - Results with reference substance:
- Kinetic of control substance (in %):
= 10 after 4 day(s)
= 87 after 14 day(s) - Validity criteria fulfilled:
- yes
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- The substance can therefore be considered to be not readly biodegradable.
- Executive summary:
The substance can therefore be considered to be not readly biodegradable.
Reference
Description of key information
In a biodegredation study according to OECD Guideline 301 F 0 % degredation were observed (Hertl, 2001). The substance can therefore be considered to be not readily biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- not biodegradable
Additional information
Study rel.2, Müller, 1992:
Ready biodegradability of the substance was assessed according to EC method C.4.D fulfilling all validity criteria. Bacterial respiration was measured as theoretical oxygen demand and gave 21 % biodegradation within 28 days (positive control aniline: 80 % within 28 days). Test sample included 35 % solvent naphtha and observed biodegradation is expected to be that of the solvent. As a conclusion these results are considered to support the results of the respective key study.
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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