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EC number: - | 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Comparable to guideline study reliable with restrictions. Minor deviations with no effect on the results: - Purity and stability was missing - According to guideline, observations should be made at 30-60 minutes and at 24, 48, and 72 hours after patch removal and not 24 hours, 48 hours and 8 days after start of exposure. -The narrative desciption of the degree and nature of irritation observed is missing
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 981
- Report date:
- 1981
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- , see "rationale for reliability"
- GLP compliance:
- no
Test material
- Reference substance name:
- Sodium sulphite
- EC Number:
- 231-821-4
- EC Name:
- Sodium sulphite
- Cas Number:
- 7757-83-7
- Molecular formula:
- H2O3S.2Na
- IUPAC Name:
- disodium sulfite
- Test material form:
- other: solution in water
- Details on test material:
- - Name of test material (as cited in study report): Natriumsulfit wasserfrei Z
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Firma Gaukler; 6050 Offenbach/Main
- Weight at study initiation: Mean weight males: 3.03 kg; mean weight females: 2.80 kg (Individual weights of the test animals: 3.26 kg (male); 2.98 kg (female); 2.79 kg (male); 2.62 kg (female))
- Housing: The animals were housed individually; Cage made of stainless steel with wire mesh walk floor, floor area: 40 cm x 51 cm; No bedding in the cages; sawdust in the waste trays
- Diet: Ovator Solikanin 4 mm; Muskator-Werke, 4000 Düsseldorf, FRG (about 130 g per animal per day)
- Drinking water: About 250 ml per animal per day: fully demineralized water (Monday - Friday), tap water (Saturday/Sunday)
- Acclimatization period: About 8 days before the beginning of the study in the skin laboratory; same housing conditions as during the study.
ENVIRONMENTAL CONDITIONS
- Temperature: 20 - 26°C
- Relative humidity: approx. 30 - 70%
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- water
- Controls:
- no
- Amount / concentration applied:
- - Amount(s) applied (volume or weight with unit): Applying an approx. 0.5 mm thick layer of the 50 % solution of the test substance (comparable to 0.5 g of the test substance).
- Duration of treatment / exposure:
- 4 h
- Observation period:
- 8 d
- Number of animals:
- 2 males / 2 females
- Details on study design:
- TEST SITE
The fur of the rabbits was clipped at least 15 hours before the beginning of the study. The application area was 2.5 cm X 2.5 cm on the upper third of the back or flanks. The test patch was covered with the test substance. In order to prepare the solution distilled water was used. The untreated skin sites of the same animals was used as negative control.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): The test substance was removed with lutrol and lutrol/water (1:1).
- Time after start of exposure: At the end of the exposure period.
OBSERVATION PERIOD
8 days; Readings at 30-60 minutes after application as well as at 24 hours, 48 hours and 8 days after start of application.
SCORING SYSTEM: Draize scoring system
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (erythema = 0).
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (oedema = 0).
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (erythema = 0).
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (oedema = 0).
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (erythema = 0).
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (oedema = 0).
- Irritation parameter:
- erythema score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (erythema = 0).
- Irritation parameter:
- edema score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: Assumed no skin irritation present at 72 h reading (oedema = 0).
- Irritant / corrosive response data:
- In the raw data no observation for 72 hours was included. Since at the 48 hours reading no skin irritation was observed, it was concluded that it could be safely assumed that no skin irritation was present at the 72 hour reading (erythema or oedema = 0).
At the 8 day reading no erythema or oedema were observed. - Other effects:
- No data
Any other information on results incl. tables
Results:
Readings | Animal | Erythema | Edema | Additional findings |
24 h | 1 | 1 | 0 | |
2 | 1 | 0 | ||
3 | 1 | 0 | overlapping erythema | |
4 | 1 | 0 | ||
48 h | 1 | 0 | 0 | |
2 | 0 | 0 | ||
3 | 0 | 0 | ||
4 | 0 | 0 | ||
8 d | 1 | 0 | 0 | |
2 | 0 | 0 | ||
3 | 0 | 0 | ||
4 | 0 | 0 | ||
mean 24 - 48 h | 1 | 0.5 | 0.0 | |
2 | 0.5 | 0.0 | ||
3 | 0.5 | 0.0 | ||
4 | 0.5 | 0.0 | ||
mean | 0.5 | 0.0 |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Sodium sulphite is not an skin irritant.
According to the criteria specified by Directive 67/548/EEC and subsequent regulations, the test item is not classified as skin irritant.
According to the EC Regulation No. 1272/2008 and subsequent regulations, the test item is not classified as skin irritant.
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