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EC number: 215-252-9 | CAS number: 1315-01-1
- 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:
- 2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to standard methods under GLP as a final step of skin irritation testing. The study is reliable, relevant, and adequate for classifcation.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 012
- Report date:
- 2012
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Tin disulphide
- EC Number:
- 215-252-9
- EC Name:
- Tin disulphide
- Cas Number:
- 1315-01-1
- Molecular formula:
- S2Sn
- IUPAC Name:
- tin disulphide
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Covance Research Products Inc., Denver, PA
- Age at study initiation: 5-6 months
- Weight at study initiation: 2.8 - 3.3 kg
- Fasting period before study: Not provided
- Housing: Individually in suspended cages. Absorbent paper bedding was placed beneath the cages and changed at least three times per week.
- Diet (e.g. ad libitum): Fresh PMI Rabbit Chow (Diet #5321) was provided daily
- Water (e.g. ad libitum): Ad libitum
- Acclimation period: At least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): Controlled
- Humidity (%): Not provided
- Air changes (per hr): Not provided
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- other: distilled water
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 g
VEHICLE
- Amount(s) applied (volume or weight with unit): 0.3 mL - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 7 days
- Number of animals:
- 3 males
- Details on study design:
- TEST SITE
- Area of exposure: dorsal area of the trunk
- % coverage: 6cm2 (2 x 3 cm gauze patch)
- Type of wrap if used: porous dressing (semi-occlusive) and porous, non-irritating tape
REMOVAL OF TEST SUBSTANCE
- Washing (if done): gently washing with distilled water at the end of the exposure period
- Time after start of exposure: 4 hours
SCORING SYSTEM: Erythema and edema were scored according to the numerical Draize technique below. The skin was also evaluated for ulceration and necrosis or any evidence of tissue destruction. Additional signs were described.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24-72 h
- Score:
- 0.55
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 24-72 h
- Score:
- 0.55
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24-72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: no edema
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: no oedema
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: no oedema
Any other information on results incl. tables
Table 2. Dermal and Systemic observations
Time after patch removal |
Rabbit H4909 male |
Rabbit H4933 male |
Rabbit H4936 male |
Mean Scores |
|
1 Hour |
Erythema |
1 |
1 |
0 |
|
|
Edema |
0 |
0 |
0 |
|
Systemic Observations |
A |
A |
A |
||
|
|
|
|
|
|
24 Hour |
Erythema |
1s |
1 |
1 |
1.00 |
|
Edema |
0 |
0 |
0 |
0.00 |
Systemic Observations |
A |
A |
A |
|
|
|
|
|
|
|
|
48 Hour |
Erythema |
1s |
0 |
0f |
0.33 |
|
Edema |
0 |
0 |
0 |
0.00 |
Systemic Observations |
A |
A |
A |
|
|
|
|
|
|
|
|
72 Hour |
Erythema |
1 |
0 |
0f |
0.33 |
|
Edema |
0 |
0 |
0 |
0.00 |
Systemic Observations |
A |
A |
A |
|
|
|
|
|
|
|
|
Day 7 |
Erythema |
0 |
0 |
0 |
|
|
Edema |
0 |
0 |
0 |
|
Systemic Observations |
A |
A |
A |
||
|
|||||
|
Sum of Mean Scores = |
1.66 |
|||
Modified Primary Irritation Index (PII) |
= Sum of Mean Scores/3 = |
0.55 |
|||
|
|
|
|||
A=appeared normal |
f= flaking skin |
s= shiny areas |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The Modified Primary irritation Index is 0.55. Tin disulfide is a dermal irritant.
- Executive summary:
Three healthy New Zealand White rabbits (males) were dosed dermally with Tin disulfide. The test article (0.56 g) was applied dermally to one intact site per rabbit and wrapped with a piece of porous dressing (semi-occlusive) large enough to cover all dose sites with at least 5 cm square to spare on all sides of the gauze patch. The test article was kept in contact with the skin for 4 hours at which time the wrappings were removed. Erythema and edema were scored at 1, 24, 48 and 72 hours and on Day 7 following patch removal. The skin was also evaluated for ulceration and necrosis or any evidence of tissue destruction at these time periods. Animals were observed for toxicological and pharmacological effects at each dermal observation period and observed for mortality daily. Body weights were recorded pretest, at 72 hours and at termination. At 1 hour post exposure, erythema was absent to very slight and edema was absent. At 24 hours erythema was very slight, edema was absent and shiny areas were observed on one animal. By 48 hours, erythema was absent to very slight and edema was absent with shiny areas and flaking skin observed. Erythema remained absent to very slight, edema was absent and flaking skin persisted at 72 hours. Both erythema and edema were absent by Day 7. No abnormal physical signs were observed. Two animals had net body weight gain by study termination, although one of the animals lost weight between 72 hours and Day 7. The remaining animal lost weight by study termination. The Modified Primary Irritation Index was 0.55. Tin disulfide (CAS 1315-01-1; EINECS: 215- 252-9), Tin disulphide; Trade name: Tribotecc® - SNS2 Grade A, Batch# E 10320 is not a Category 2 irritant according to Regulation (EC) No. 1272/2008, Section 3.2.2.7.
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