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EC number: 231-669-9 | CAS number: 7681-53-0
- 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
Additional physico-chemical information
Administrative data
- Endpoint:
- other: crystallisation point
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study meets generally accepted scientific principles
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 998
- Report date:
- 1998
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- In a cryostatic bath, a reactor is stirred and the temperature is measured with a probe. The temperatures are recorded continously on a tracing table.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Sodium phosphinate
- EC Number:
- 231-669-9
- EC Name:
- Sodium phosphinate
- Cas Number:
- 7681-53-0
- Molecular formula:
- H3O2P.Na
- IUPAC Name:
- sodium phosphinate
- Details on test material:
- - Name of test material: liquid sample, hyposphosphite de sodium 810 g/L
- Lot/batch No.: 4 samples have been tested at different concentrations in the same conditions
- concentrations tested between 810 g/L and 850 g/L
commercial concentration is at 810 g/L and correspond to an oversaturated solution. But this solution seems to be stable at 20°C
For details see table 1 in Results freetext.
Constituent 1
Results and discussion
- Results:
- Without spiking, at a concentration of 810 g/L a mass crystallisation is observed, followed by a rapid increase in temperature. Redissolution is low.
At higher concentrations crystallisation start slowly without mass crystallisation nor increase in temperature.
Spiking does not accelerate significantively the crystallisation.
Any other information on results incl. tables
Table 1: summary of the measured crystallisation points for the the 4 samples tested
Name |
Sample designation |
Number of lot |
Concentration (g/L) |
Crystallisation point (°C) |
Sodium hypophosphite |
L1 |
97-51 |
810 |
-25 |
H3PO2 |
L11 |
nd |
50% |
-27 *; |
Sodium hypophosphite |
L12 |
nd |
855 |
17 *; 19 ** |
Sodium hypophosphite |
L13 |
nd |
820 |
-5 *; -1 ** |
* without spiking
** with spiking
nd: no data
Applicant's summary and conclusion
- Conclusions:
- In the test conditions, the crystallisation of saturated solutions of sodium hypophosphite is very low and occur at: -25°C at 810 g/L (commercial concentration). Only one particularity is observed at this concentration: the phenomenon occurs in mass and is followed with a rapid increase in temperature. However at the same concentration the solution is stable at 20°C.
Spiking does not accelerate crystallisation. - Executive summary:
The crystallisation point of saturated solutions of sodium hypophosphite was measured under stirring in a cryostatic bath at 4 concentrations.
Without spiking, at a concentration of 810 g/L a mass crystallisation is observed at -25°C, followed by a rapid increase in temperature. Redissolution is low. At higher concentrations (820 g/L and 850 g/L) crystallisation start slowly and occurs at -5°C and 17°C respectively. No mass crystallisation nor increase in temperature was observed in those cases.
Spiking does not accelerate significatively the crystallisation.
As the study meets generally scientific principles the study is considered as reliable with restrictions
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