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EC number: 500-230-6 | CAS number: 68698-70-4
- 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 aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- Samples were collected of the Stock Solution (WAF) and of each treatment at the beginning and end of exposure for analysis.
- Vehicle:
- no
- Details on test solutions:
- Algal medium was prepared in accordance with OECD 201. Specifically, the AAP medium specified in Annex 3 from that method was used. Algae medium was prepared using deionized water (DI). Each of the stock solutions was prepared in DI . One ml of each stock was added to a flask and diluted to one liter with DI. This water was mixed on a magnetic stir plate and filtered through a 0.2 micron filter for sanitization. This medium was used for all culturing and testing of algae for this study.
Component Concentration in Prepared Medium mg/L
NaHCO3 15.0
NaNO3 25.5
MgCl2-6(H2O) 12.16
CaCl-2(H2O) 4.41
MgSO4-7H2O 14.6
K2HPO4 1.044
FeCl3-6(H2O) 0.160
Na2EDTA-2(H2O) 0.300
H3BO3 0.186
MnCl2-4(H2O) 0.415
ZnCl2 0.00327
CoCl2-6(H2O) 0.00143
Na2MoO4-(H2O) 0.00726
CuCl2-2(H2O) 0.000012 - Test organisms (species):
- other: Raphidocelis subcapitata
- Details on test organisms:
- An algal starter culture was purchased from Aquatic Biosystems, Inc. (Fort Collins,
Colorado) prior to testing. BMI cultures were inoculated at 104 cells/ml and allowed to
incubate for 72 hours. Cell counts were performed to ensure logarithmic growth. Testing
was performed using these cultures. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Nominal and measured concentrations:
- Summary of Measured Concentrations
Nominal Concentration mg/L 0h mg/L 72h mg/L Concentration used for Calculations mg/L
0 BDL BDL 0
0.3125 BDL BDL 0.012
0.625 BDL BDL 0.023
1.25 BDL BDL 0.046
2.5 BDL BDL 0.092
5 BDL BDL 0.185
10 BDL BDL 0.369
Stock Solution 1 g/L (WAF) 36.9 - Details on test conditions:
- Test Requirement : Condition
1. Test type: Static
2. Renewal of test solutions: Not Renewed
3. Temperature (°C): 22 + 2°C
4. Light quality: Full Spectrum
5. Light intensity: 60 - 100 μE/(m-2 s-1)
6. Photoperiod: Continuous
7. Size of test vessel: 250 ml
8. Volume of test solution: 100 ml
9. Cell Density at test initiation: 104 cells/ml
11. Number of replicates per concentration: 3
14. Aeration: None
15. Medium: See section 3.2
16. Test duration: 72 hours
17. Test concentrations: Five product concentrations and a control
18. Dilution series: 0.1 dilution series for range-finding test
0.5 dilution series for definitive test
19. Endpoint: Growth Inhibition
20. Sampling and sample: WAF stock solution
21. Test acceptability criterion: Biomass of control cultures increase by a factor of at
least 16. Section – by – section specific growth rate
coefficient of variation not more than 35%.
Coefficient of variation during the whole test period
not greater than 7% in the controls. - Reference substance (positive control):
- yes
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 0.062 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.13 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Details on results:
- The results of the range-finding study suggested that the endpoint would fall between 1 and 10 mg/L (Nominal WAF). Therefore, nominal treatments for the definitive test were 0, 0.3125,
0.625, 1.25, 2.5, 5.0 and 10 mg/L WAF.
The EC10 for specific growth rate was 0.062 mg/L based on measured concentrations. The EC50 for specific growth rate was 0.130 mg/L. - Validity criteria fulfilled:
- yes
- Conclusions:
- Aquatic toxicity study following OECD 201 was performed with 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane, reaction products with 3-aminopropyldiethylamine and 2-piperazin-1-ylethylamine. The EC10 for specific growth rate was determined to be 0.062 mg/L based on measured concentrations. The
EC50 for specific growth rate was determined to be 0.130 mg/L. - Executive summary:
Aquatic toxicity study following OECD 201 was performed with 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane, reaction products with 3-aminopropyldiethylamine and 2-piperazin-1-ylethylamine. The EC10 for specific growth rate was determined to be 0.062 mg/L based on measured concentrations. The
EC50 for specific growth rate was determined to be 0.130 mg/L.
Reference
Description of key information
Aquatic toxicity study following OECD 201 was performed with 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane, reaction products with 3-aminopropyldiethylamine and 2-piperazin-1-ylethylamine. The EC10 for specific growth rate was determined to be 0.062 mg/L based on measured concentrations. The EC50 for specific growth rate was determined to be 0.130 mg/L.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 0.13 mg/L
- EC10 or NOEC for freshwater algae:
- 0.062 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.
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