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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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- no precise data, 72 hours minimum
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study with acceptable restrictions performed using a method equivalent to the OECD guideline 404. No data on the purity of the tested substance, no observation period for the reversibility and no scoring at 60 minutes after patch removal.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 977
- Report date:
- 1977
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: DOT, Hazardous Materials Regulations, 49 CFR Part 173.240
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- . Reliability scoring based on 1981 OECD guideline for test n° 404.
- Deviations:
- yes
- Remarks:
- : no observation period for reversibility, no scoring at 60 minutes after patch removal.
- GLP compliance:
- no
- Remarks:
- study predates GLP requirements.
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
- Reference substance name:
- Sodium hypophosphite
- IUPAC Name:
- Sodium hypophosphite
- Details on test material:
- - Name of test material: Sodium hypophosphite, Filter Press Cake
- Batch number: T-6103
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 2530 - 3167 grams
No more data available
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: each animal served as its own control
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 500 milligrams by rabbit on shaved backs (intact or abraded sites) - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72 hours
- Number of animals:
- 3 males and 3 females
- Details on study design:
- TEST SITE
- Type of wrap if used: occlusive
- Testing area: intact (shaved) and abraded skins
REMOVAL OF TEST SUBSTANCE
- Washing: tepid tap water
- Time after start of exposure: 4 hours
SCORING SYSTEM: according to OECD guideline 404
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24, 72 hours
- Score:
- <= 0.6
- Irritation parameter:
- erythema score
- Remarks:
- Test item applied onto intact skin
- Basis:
- animal #1
- Time point:
- other: mean of the 24, 48 and 72-hour readings
- Score:
- 0.66
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- erythema score
- Remarks:
- Test item apllied onto the intact skin
- Basis:
- animal #2
- Time point:
- other: mean of the 24, 48 and 72-hour readings
- Score:
- 0.66
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- erythema score
- Remarks:
- Test item applied onto the intact skin
- Basis:
- animal #3
- Time point:
- other: mean of the 24, 48 and 72-hour readings
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- edema score
- Remarks:
- Test item applied onto the intact skin
- Basis:
- animal #1
- Time point:
- other: mean of the 24, 48 and 72-hour readings
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Remarks:
- test item applied onto the intact skin
- Basis:
- animal #2
- Time point:
- other: mean of the 24, 48 and 72-hour readings
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Remarks:
- Test item applied onto the intact skin
- Basis:
- animal #3
- Time point:
- other: mean of the 24, 48 and 72-hour readings
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- no data
- Irritant / corrosive response data:
- For raw data see tables in the "remarks on results" freetext.
Any other information on results incl. tables
Raw data for irritant/corrosive response:
Each animal was evaluated according to the grading scale of theOECD 404 guideline.
Table 1: Primary skin irritation scoring values
Intact skin |
Abraded skin |
||||||||
Hours |
Hours |
||||||||
Observations | Grade | 4 | 24 | 48 | 72 | 4 | 24 | 48 | 72 |
Erythema, Eschar formation |
0 |
2/3 |
2/3 |
1/3 |
|||||
1 |
3/3 | 3/3 | 3/3 | 1/3 | 1/3 |
3/3 | 3/3 | 2/3 | |
2 |
|||||||||
3 |
|||||||||
4 |
|||||||||
Edema Formation |
0 |
3/3 | 3/3 | 3/3 | 2/3 | 3/3 | 3/3 | 3/3 | 3/3 |
1 |
1/3 |
||||||||
2 |
|||||||||
3 |
|||||||||
4 |
Table 2: Corrosion results
Intact skin | Abraded skin | |||||||
Hours |
Hours |
|||||||
Observations | 4 | 24 | 48 | 72 | 4 |
24 |
48 |
72 |
Necrosis (corrosion) |
0/3 | 0/3 | 0/3 | 0/3 | 0/3 | 0/3 | 0/3 | 0/3 |
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: other: CLP (Reg. 1272/2008/EC)
- Conclusions:
- Under the experimental conditions of this study and according to the criterai laid down in CLP (Reg 1272/2008/EC), the test item Sodium hypophosphite is considered as non-irritant to the skin.
- Executive summary:
The potential of sodium hypophosphite to induce skin irritation or corrosion was assessed in adult New Zealand white rabbits (3 males and 3 females) using the 49 CFR Part 173.240 method from the US Hazardous Materials Regulations. This method was comparable to the OECD 404 guideline issued in 1981. The study predates GLP requirements.
The rabbits were dermally exposed to 500 mg of sodium hypophosphite for 4 hours on prepared shaved backs. 3 animals received the test item onto an intact skin while the remaining received the test item onto an abraded area.The test substance was held in contact with the skin by means of an occlusive dressing. Cutaneous reactions were observed 24, 48 and 72 hours after removal of the dressing.
A slight erythema (scoring value 1) was observed in all animals at the 24 -hour reading and was still persistent in 1out 3 animals treated onto an intact skin and 2 out 3 animals treated on an abraded area at the 72 -hour reading. Only one animal with intact skin showed a slight oedema (soring value 1) at the 72 -hour reading.
According to the criteria laid down in EC regulation 1272/2008/EC, Sodium hypophosphite is considered as non-irritant to the skin and is not classified.
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