Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 213-510-5 | CAS number: 961-69-3
- 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:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- end on 05-MAY-2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: study performed according to OECD guideline and GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Potassium (R)-(4-hydroxyphenyl)[(3-methoxy-1-methyl-3-oxoprop-1-enyl)amino]acetate
- EC Number:
- 273-992-8
- EC Name:
- Potassium (R)-(4-hydroxyphenyl)[(3-methoxy-1-methyl-3-oxoprop-1-enyl)amino]acetate
- Cas Number:
- 69416-61-1
- IUPAC Name:
- potassium (4-hydroxyphenyl)[(3-methoxy-1-methyl-3-oxoprop-1-en-1-yl)amino]acetate
- Details on test material:
- - Name of test material (as cited in study report): D(-)-p-Hydroxyphenylglycine Dane Salt(K, Methyl)
- Substance type: monoconstituent substance
- Physical state: powder
- Stability under test conditions: this is the subject of the study
- Storage condition of test material: at room temperature, protected from light
Constituent 1
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
PHYSICO-CHEMICAL PROPERTIES
- Melting point: 421 - 432 °C
- Boiling point: 439°C (the sample decomposes)
- Vapour pressure: 8.64E-12 mmHg at 25°C
- Water solubility: not determined (form micelles in aqueous phases due to properties of surface tension)
- log Pow: LogKow < -2.3
- UV absorption: 224 nm, 276 nm
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- Prior to use a sample of activated sludge from the sewage plant at Taunusstein-Bleidenstadt was washed twice with mineral nutrient solution of the CO2-Evolution-Test to eliminate organic components and carbonates from the sludge. After resolution with mineral nutrient medium the sludge was aerated by means of compressed humidified air for about four hours. Before use as inoculum for the CO2-Evolution-Test the sludge was homogenised in a "Waring Blender" at low speed for 2 minutes and then filtered through a cotton filter previously carefully rinsed with deionised water. The filtrate was used as inoculum (1% of the final volume of the test solution) on the same day of preparation.
- Duration of test (contact time):
- 28 d
Initial test substance concentration
- Initial conc.:
- 19.5 - 19.7 mg/L
- Based on:
- test mat.
Parameter followed for biodegradation estimation
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- TEST CONDITIONS
- Composition of medium: according to OECD guideline
- Additional substrate: no
- Solubilising agent: no
- Test temperature: 19.4 to 22.8 °C (mean 20.0°C)
- pH: not measured
- pH adjusted: no
- Aeration of dilution water: the aeration rate of the test system was controlled at 4 L/h being assured by precise flowmeters
- Continuous darkness: data not available
TEST SYSTEM
- 5-litre amber carboys served as test vessels
- Number of culture flasks/concentration: 2 (test item), 1 (sodium benzoate and toxicity control)
- Method used to create aerobic conditions: the aeration rate of the test system was controlled at 4 L/h being assured by precise flowmeters
- Test performed in closed vessels due to significant volatility of test substance: the vessels were closed with stoppers with tubing for gas inlet and outlet (gas exit line)
- Details of trap for CO2 and volatile organics if used: CO2 generated by the test item was trapped by 0.025 N Ba(OH)2 in a trap system described in the Guideline. Resting Ba(OH)2 (0.025 N) in the CO2 trap removed from the trap system was titrated with HCl (0.05 N) using phenolphthalein as an indicator.
SAMPLING
- Sampling frequency: Titrations were performed at t4d, t6d, t8d, t12d, t19d, t26d, t28d, and t29d
- Sample storage before analysis: data not available
CONTROL AND BLANK SYSTEM
- Inoculum blank: yes
- Abiotic sterile control: no
- Toxicity control: yes
- Positive control: yes (sodium benzoate)
STATISTICAL METHODS: not applicable
Reference substance
- Reference substance:
- benzoic acid, sodium salt
Results and discussion
% Degradation
- Parameter:
- % degradation (CO2 evolution)
- Value:
- ca. 88
- Sampling time:
- 28 d
- Remarks on result:
- other: the “10-days-window” was met
- Details on results:
- Calculated from the organic carbon content of the test item and the measured CO2 generation, 92% of the theoretical CO2 (ThCO2) has been generated by the test item within 28 d of test period in the first culture with 69.1 mg of test item. 85% of the theoretical CO2 (ThCO2) has been generated by the test item within 28 d in the second culture with 68.3 mg of test item. The calculated mean degradation value of the test item was 88%. The “10-days-window” was met, too.
BOD5 / COD results
- Results with reference substance:
- The control item sodium benzoate was degraded 83% the threshold of 60% degradation being met within 8 days.
Any other information on results incl. tables
Table 1: Degradation / elimination kinetics
Type of suspension |
Vessel no. |
% degradation at sampling time (days) |
||||||||
4 |
6 |
8 |
12 |
19 |
26 |
28 |
29 |
|
||
Test item |
1 |
2 |
11 |
27 |
69 |
86 |
88 |
89 |
92 |
|
|
2 |
2 |
11 |
19 |
28 |
61 |
83 |
83 |
84 |
|
Reference substance |
3 |
34 |
56 |
69 |
73 |
77 |
80 |
81 |
83 |
|
Toxicity control |
4 |
7 |
32 |
38 |
49 |
56 |
57 |
58 |
60 |
|
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The test item D(-)-p-Hydroxyphenylglycine Dane Salt(K, Methyl) should be regarded “readily biodegradable”.
- Executive summary:
D(-)-p-Hydroxyphenylglycine Dane Salt(K, Methyl) was tested for biodegradability according to 'CO2-Evolution-Test' (OECD Guideline 301B, GLP). Calculated from the organic carbon content of the test item and the measured CO2generation, 92% of the theoretical CO2(ThCO2) has been generated by the test item within 28 d of test period in the first culture with 69.1 mg of test item. 85% of the theoretical CO2(ThCO2) has been generated by the test item within 28 d in the second culture with 68.3 mg of test item. The calculated mean degradation value of the test item was 88%. The “10-days-window” was met, too. Thus, the test item D(-)-p-Hydroxyphenylglycine Dane Salt(K, Methyl) should be regarded “readily biodegradable”. The total CO2-evolution of the Blank was 79 mg CO2being in the requested range of the OECD test guideline 301B. The control item sodium benzoate was degraded 83% the threshold of 60% degradation being met within 8 days. Thus, all conditions of validity were met and the test is regarded to be valid. The results obtained with the toxicity control indicate that there was no toxicity of the test item towards microorganisms at the concentration used within the test.
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.