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EC number: 305-230-8 | CAS number: 94350-12-6
- 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

Water solubility
Administrative data
Link to relevant study record(s)
- Endpoint:
- water solubility
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 17 March 2018 to 24 March 2018
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- Due to the UVCB nature of the substance and the presence of one fraction totally insoluble (cell walls) and one fraction with a very high water solubility, the water solubility of this soluble fraction was determined. Since after 2 and 3 days of agitation the carbon content decreases, only the result after 1 day of agitation was taken into account to determine the water solubility.
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.6 (Water Solubility)
- Version / remarks:
- version 2008
- Deviations:
- yes
- Remarks:
- Since after 2 and 3 days of agitation the carbon content decreases, only the result after 1 day of agitation was taken into account to determine the water solubility
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 105 (Water Solubility)
- Deviations:
- yes
- Remarks:
- Since after 2 and 3 days of agitation the carbon content decreases, only the result after 1 day of agitation was taken into account to determine the water solubility
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- flask method
- Key result
- Water solubility:
- 104.9 mg/L
- Conc. based on:
- other: carbon content of the dissolved fraction
- Loading of aqueous phase:
- 1 g/L
- Incubation duration:
- 1 d
- Temp.:
- 30 °C
- pH:
- >= 6.84 - <= 7
- Details on results:
- After 1 and 2 days agitation time at 30°C, the relative standard deviations of obtained data are very low, but after 3 days agitation time, the measured carbon contents in the parallel vessels show a very high RSD%. Since the conditions are not sterile, after 3 days some biological degradation activity in some flasks at 30°C may occur, so this data was not taken into consideration for the evaluation. The decreasing carbon content between day 1 and day 2 can be explained by the same phenomenon. The carbon content of the soluble fraction from Saccharomyces cerevisiae, lysate was 104.9 mg/L Carbon with 0.59 RSD% in case of preparation 1 g/L nominal loading rate, after 1 day agitation time at 30°C and 1 day re-equilibration time at 20°C.
- Conclusions:
- The carbon content of the water soluble fraction from Saccharomyces cerevisiae, lysate was 104.9 mg carbon/L with 0.59 RSD% in case of preparation 1 g/L nominal loading rate, after 1 day agitation time at 30°C and 1 day re-equilibration time at 20°C.
- Executive summary:
The water solubility of Saccharomyces cerevisiae, lysate was determined following the EU method A.6 and OECD 105, and in compliance with GLP.
Since the test item is an UVCB with no single chemical marker that can be readily analysed, the NPOC (Non Purgeable Organic Carbon) method was used. The results of preliminary tests have demonstrated that 1 g/L nominal loading rate ensures the highest measurable carbon content. So three parallel samples at the loading rate of 1 g/L were prepared and agitated at 30°C for 1, 2 and 3 days. Then the flasks were removed and re-equilibrated preferably at 20 ± 0.5°C for 1 day. The content of the vessels was centrifuged at 8500 rpm for 10 minutes, then the supernatant was filtered by 0.2 µm filter, and the organic carbon content in the clear phase was determined by TOC.
Since the carbon content decreases on day 2 and 3 with a very high variability of the carbon content analysis on Day 3, the obtained results on Day 1 are considered as the most reliable and representative of the water solubility of the soluble fraction of Saccharomyces cerevisiae, lysate.
The carbon content of the soluble fraction of Saccharomyces cerevisiae, lysate was 104.9 mg/L Carbon with 0.59 RSD% in case of preparation 1 g/L nominal loading rate, after 1 day agitation time at 30°C and 1 day re-equilibration time at 20°C.
This water solubility study is classified as acceptable, and satisfies the guideline requirements of the EU method A.6 and OECD 105.
Reference
Results of the determination of the test item concentrations (carbon content) from a saturated solution of 1 g/L loading rate
Parallel sample preparation |
Measured carbon content |
pH |
Measured carbon content |
pH |
Measured carbon content |
pH |
1 |
104.3 |
7.00 |
85.6 |
6.84 |
51.3 |
6.88 |
2 |
105.5 |
6.97 |
83.6 |
6.93 |
87.4 |
6.90 |
3 |
104.8 |
6.98 |
87.6 |
6.90 |
134.6 |
6.85 |
Mean |
104.9 |
- |
85.7 |
- |
91.1 |
- |
RSD% |
0.59 |
- |
2.5 |
- |
45.85 |
- |
Mean |
93.9 ± 17.4 (with 95% confidence interval) |
|||||
RSD% |
24.1 |
Results of the Method Validation
Repeatability |
CV% ≤ 2.5% |
Linear range |
10 – 100 mg carbon/ L |
Limit of Quantification (LOQ) |
10 mg carbon/ L |
Test item nominal loading rate for the water solubility study |
1 g/L |
Description of key information
The carbon content of the water soluble fraction from Saccharomyces cerevisiae, lysate was 104.9 mg Carbon /L with 0.59 RSD% in case of preparation 1 g/L nominal loading rate, after 1 day agitation time at 30°C and 1 day re-equilibration time at 20°C.
Key value for chemical safety assessment
Additional information
The water solubility of Saccharomyces cerevisiae, lysate was determined following the EU method A.6 and OECD 105, and in compliance with GLP.
Since the test item is an UVCB with no single chemical marker that can be readily analysed, the NPOC (Non Purgeable Organic Carbon) method was used. The results of preliminary tests have demonstrated that 1 g/L nominal loading rate ensures the highest measurable carbon content. So three parallel samples at the loading rate of 1 g/L were prepared and agitated at 30°C for 1, 2 and 3 days. Then the flasks were removed and re-equilibrated preferably at 20 ± 0.5°C for 1 day. The content of the vessels was centrifuged at 8500 rpm for 10 minutes, then the supernatant was filtered by 0.2 µm filter, and the organic carbon content in the clear phase was determined by TOC.
Since the carbon content decreases on day 2 and 3 with a very high variability of the carbon content analysis on Day 3, the obtained results on Day 1 are considered as the most reliable and representative of the water solubility of the soluble fraction of Saccharomyces cerevisiae, lysate.
The carbon content of the soluble fraction of Saccharomyces cerevisiae, lysate was 104.9 mg/L Carbon with 0.59 RSD% in case of preparation 1 g/L nominal loading rate, after 1 day agitation time at 30°C and 1 day re-equilibration time at 20°C.
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