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EC number: 946-138-3 | CAS number: -
- 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 microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 15-31 March 1989
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP and according to guideline. Limited info on identity.
- Justification for type of information:
- Data from structural analogue sodium heptogluconate (CAS no.: 31138-65-5) is used for read across to (Gluconate)3 -FeNa3 (CAS no.: 2101772-89-6)
REPORTING FORMAT FOR THE ANALOGUE APPROACH
See Chapter 13 for read across document - Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- according to guideline
- Guideline:
- other: ISO/TC 147/SC 5/WG
- Deviations:
- yes
- Remarks:
- described in test conditions
- Principles of method if other than guideline:
- The study design is very similar to current ISO 10712 (1995) guideline apart from the absence of a reference substance
- GLP compliance:
- yes
- Remarks:
- in house QA
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- The media for bacterial growth (culture and preculture) contained per dm3 demiwater; K2HPO4 1.55 g; NaH2P04, 0.85 g; NH4CL, 0.5 g; MgSO4(H20)7 0.1 g; 0.2 cm3 trace element solution; glucose, 2 g; yeast extract, 0.1 g.
The test substance was dissolved in the growth medium.
All media were sterilized for at least 20 minutes at 120°C.
After inoculation of the cultures, the extinction did not exceed 0.1.
Bacterial suspensions with extinction values >= 0.8 were diluted with demiwater - Test organisms (species):
- Pseudomonas putida
- Details on inoculum:
- The P. putida strain was obtained from the Agricultural University Wageningen, Dept. of microbiology, Wageningen, The Netherlands.
The strain was maintained on yeast/glucose slants which contain per dm3 demiwater 15 g agar; 5 g glucose and 1 g yeast extract. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 16 h
- Post exposure observation period:
- None
- Hardness:
- No specific data
- Test temperature:
- Not given
- pH:
- No data given
- Dissolved oxygen:
- No data
- Nominal and measured concentrations:
- Nominal concentrations: 0.25-0.50-1.00-2.00-4.00 g/L
- Details on test conditions:
- See test solutions. Incubation for 16 hours. The extinction values of the diluted suspensions were used for the calculation of inhibition percentages. Triplicate measurements per concentration were performed at 435 nm with monochromatic light.
- Reference substance (positive control):
- no
- Duration:
- 16 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 4 g/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
- Details on results:
- No dose dependent inhibition could be observed. Inhibition compared to the controls were 5-16% based on triplicate measurements.
- Reported statistics and error estimates:
- No data given
- Validity criteria fulfilled:
- no
- Remarks:
- partly due to lack of positive control, but growth validity fulfilled
- Conclusions:
- Study lacks some data (e.g. temperature). Principle of test according to current ISO guideline. The absence of reference substance and the lack of result wrt toxicity it can not be concluded the test was properly performed. Results are considered supportive when additional data/other studies would be available.
- Executive summary:
In this study the toxicity of Dissolvine CSA to Pseudomonas putida was investigated. Triplicate measurements of the extinction as indication of growth were performed and compared to controls. Although some minor inhibition was observed (5 -16%) no dose dependency was apparent. It is therefore concluded that the test substance is not toxic for P. putida at nominal concentrations ranging 0.25-4.0 g/L. The EC50 would therefore be concluded at > 4.0 g/L.
Reference
Concentration (g/L) |
Mean Extinction after 16 hours (n=3) |
% inhibition |
control |
0.255 |
- |
0.25 |
0.214 |
16 |
0.5 |
0.219 |
14 |
1.0 |
0.233 |
12 |
2.0 |
0.242 |
5 |
4.0 |
0.237 |
7 |
Description of key information
No activated sludge respiration inhibition tests have been performed with the Reaction mass of (Gluconate)3Fe-Na3 and NaCl. No inhibition of the oxidation was observed in the preliminary ready biodegradability screening study at 9.3 mg/L the Reaction mass of (Gluconate)3Fe-Na3 and NaCl or 7.1 mg a.i./L (Ginkel, 2018). Based on the absence of any effect on daphnia in the acute daphnia test upto 1000 mg/L it is expected that Reaction mass of (Gluconate)3Fe-Na3 and NaCl will have like Sodium glucoheptonate no effect the respiration of activated sludge upto 1000 mg/L.
For this reason the available study from the structurally similar substance Sodium glucoheptonate (CAS no 31138 -65 -5) has been read across to the Reaction mass of (Gluconate)3Fe-Na3 and NaCl.
One toxicity test with micro-organisms have been performed for which a NOEC of 1000 mg a.i./L was found. In the study from van Ginkel (1989) which was performed according to ISO/TC 147/SC 5/WG after 16 h exposure of P. putida bacteria was evaluated.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 1 000 mg/L
- EC10 or NOEC for microorganisms:
- 1 000 mg/L
Additional information
Introduction:
A study was performed to assess the effect of the test item on the respiration of activated sewage sludge. The method followed was designed to be compatible with the OECD Guidelines for Testing of Chemicals (2010) No. 209 "Activated Sludge, Respiration Inhibition Test (Carbon and Ammonium Oxidation) ".
Methods:
Activated sewage sludge was exposed to an aqueous dispersion of the test item at concentrations of 10, 100 and 1000 mg active ingredient (a.i.)/L (3 replicates of the 1000 mg a.i./L test concentration) for a period of 3 hours at a temperature of 20 ± 2°C with the addition of a synthetic sewage as a respiratory substrate.
The rate of respiration was determined after 3 hours contact time and compared to data for the control and a reference item, 3,5-dichlorophenol.
Results:
The effect of the test item on the respiration of activated sewage sludge gave a 3‑Hour EC50value of greater than 1000 mg a.i./L. The No Observed Effect Concentration (NOEC) after 3 hours exposure was 1000 mg a.i./L.
It was considered unnecessary and unrealistic to test at concentrations in excess of 1000 mg a.i./L.
The reference item gave a 3-Hour EC50value of 12 mg/L, 95% confidence limits 9.6 - 15 mg/L.
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