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EC number: 696-577-7 | CAS number: 34335-10-9
- 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

Short-term toxicity to aquatic invertebrates
Administrative data
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 20 to 22 January 2009
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Study undertaken to GLP using internationally accepted guidelines.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2009
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Qualifier:
- according to guideline
- Guideline:
- other:
stated in Method oj Testing New Chemical Substances (November 21,2003, Yakushoku hatsu No. 1121002, Nov. 13, 2003, Seikyoku No.2, Kanpoki hatsu No. 031121002)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- zinc(2+) phenylphosphonate
- EC Number:
- 696-577-7
- Cas Number:
- 34335-10-9
- Molecular formula:
- C6 H7 O3 P. Zn C6H5-P(=O)O2,2+Zn2-
- IUPAC Name:
- zinc(2+) phenylphosphonate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Name of test material (as cited in study report): Phenylphosphonic acid zinc salt
- Substance type: Inorganic
- Physical state:Powder
- Analytical purity: > 99%
- Impurities (identity and concentrations):
- Purity test date:
- Lot/batch No.: 6381
- Expiration date of the lot/batch:
- Stability under test conditions: Stable under nonnal handling
- Storage condition of test material: Stored in desiccators in a dark place at room temperature
- Other:
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 100, 56, 31,17, and 9.5 mg/l
- Sampling method:
- Sample storage conditions before analysis:
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: The test sample and test water were mixed to make a 100 mg/L solution (nominal value), stirred for about 48 hours, and filtrated. The solution was diluted with the test water to prepare stock solution.
- Eluate: Dechlorinated tap water
- Differential loading:
- Controls: One
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Water flea (Daphnia magna)
- Strain: Clone A
- Source: The test organisms were descendants of Daphnia magna (Clone A) purchased from the University of Sheffield in the United Kingdom
- Method of breeding: parthenogenesis
- Feeding during test: no
- Food type: the test organisms were fed 0.1 - 0.2 mgC (amount of organic carbon content) of Chiarella vulgaris per flea per day.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- Immobilization and conditions were observed at 24 and 48 hours after the start of exposure.
Test conditions
- Hardness:
- 28 mg/l (CaCO3)
- Test temperature:
- 20.1°C
- pH:
- 7.6 (22°C)
- Dissolved oxygen:
- 8.8 mg/l
- Salinity:
- 9.8 mg/l (Na)
- Nominal and measured concentrations:
- nominal; content ratio ofthe stock solution: 100,56,31,17, and 9.5%
measured; 0.95, 1.6, 3.0, 5.4 and 9.5 mg/l - Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 ml glass beaker
- Type: closed
- Fill volume: 100 ml
- Aeration: no
- Type of flow-through (e.g. peristaltic or proportional diluter): n/a
- Renewal rate of test solution (frequency/flow rate): none
- No. of organisms per vessel: 4
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Dechlorinated tap water
- Total organic carbon: 0.9 mg/l
- Pesticides: < 0.0001 mg/l
- Chlorine: < 0.02 mg/l
- Alkalinity: 20 mg/l
- Ca/mg ratio: 8.2/1.9 mg/l
- Conductivity: 11.6 mSM
- Culture medium different from test medium: no
- Intervals of water quality measurement: 24h
OTHER TEST CONDITIONS
- Adjustment of pH: pH of the test solution was not adjusted.
- Photoperiod: Photocycle of l6-hour light and 8-hour darkness using room lights.
- Light intensity: no data
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.8 - Reference substance (positive control):
- no
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 5.8 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: 95% confidence limits: 4.7 -7.5 mg/L
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 3.3 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: 95% confidence limits: 2.8 - 3.8 mgIL
- Details on results:
- 24-hour EC,a of the test substance to the water fleas was 5.8 mg/L (95% confidence limits:
4.7 -7.5 mg/L), 48-hour EC,a was 3.3 mg/L (95% confidence limits: 2.8 - 3.8 mgIL).
Immobilization rate
The lowest concentration of 100% immobilization at 48 hour was 9.5 mgIL, and the highest concentration of0% immobilization was 1.6 mgIL. No water flea exhibited abnormal symptoms or behavior (such as discoloration or floating on the surface of the water) in the control group during exposure
period; therefore the immobilization ratio was 0%, and the validity criteria (less than 10%) ofthis test were also fulfilled.
symptom observation
No symptom was observed in the control group. The following observations are all based on comparison with the control group. Symptoms observed
during exposure period were lethargy, immobilization, and reduced activity.
Any other information on results incl. tables
Immoblization rate
Measured concentration * (mg/L) |
Immobilisation rate (%) |
||||
24 hours |
48 Hours |
||||
Individual test vessel |
Individual test group |
Individual test vessel |
Individual test group |
||
Control group |
A |
0 |
0 |
0 |
0 |
B |
0 |
0 |
|||
C |
0 |
0 |
|||
D |
0 |
0 |
|||
0.95
|
A |
0 |
0 |
0 |
0 |
B |
0 |
0 |
|||
C |
0 |
0 |
|||
D |
0 |
0 |
|||
1.6
|
A |
0 |
0 |
0 |
0 |
B |
0 |
0 |
|||
C |
0 |
0 |
|||
D |
0 |
0 |
|||
3.0
|
A |
60 |
20 |
80 |
40 |
B |
0 |
20 |
|||
C |
0 |
40 |
|||
D |
20 |
20 |
|||
5.4
|
A |
40 |
40 |
80 |
95 |
B |
20 |
100 |
|||
C |
60 |
100 |
|||
D |
40 |
100 |
|||
9.5
|
A |
100 |
80 |
100 |
100 |
B |
60 |
100 |
|||
C |
80 |
100 |
|||
D |
80 |
100 |
*: Geometric average of measured concentrations (hereinafter described as "measured concentration")
Observed symptoms
Content ratio of stock solution (%) |
24 hour |
48 hour |
||
Immobilisation rate (%) |
Other symptoms |
Immobilisation rate (%) |
Other symptoms |
|
Control group |
- |
- |
- |
- |
0.95 |
- |
- |
0 |
- |
1.6 |
- |
- |
0 |
RA (1) |
3.0 |
IM (4) |
RA (2) |
IM (8) LETH (8) |
RA (4) |
5.4 |
IM (8) LETH (8) |
- |
IM (19) LETH (16) |
RA (1) |
9.5 |
IM (16) LETH (15) |
- |
IM (20) LETH (20) |
- |
"-" indicates that there was no symptom.
Abbreviations of symptoms
IM (Immobilization)
LETI-! (Lethargic)
RA (Reduced activity)
EC50on the water fleas
Duration of exposure |
EC50(mg/L) |
95% confidence limits (mg/L) (Angle of regression line) |
EC50calculation method |
24 hours |
5.8 |
4.7 – 7.5 (3.8) |
Probit method |
48 hours |
3.3 |
2.8 – 3.8 (7.9) |
Probit method |
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- 24-hour EC50, was 5.8 mg/L (95% confidence limits: 4.7 -7.5 mg/L),
48-hour EC50 was 3.3 mg/L (95% confidence limits: 2.8 - 3.8 mgIL).
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