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EC number: 231-900-3 | CAS number: 7778-18-9
- 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:
- Not specified
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was performed according to internationally accepted testing guidelines.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 990
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Calcium sulfate
- EC Number:
- 231-900-3
- EC Name:
- Calcium sulfate
- Cas Number:
- 7778-18-9
- Molecular formula:
- CaSO4
- IUPAC Name:
- calcium sulfate
- Details on test material:
- - Name of test material (as cited in study report): Calcium sulfate anhydrite
- Analytical purity: 92.9%
- Lot no: 7439
- Storage condition of test material: Kept at room temperature in the dark.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Provided by Grabjas Jordi
- Age at study initiation: ~ 12 weeks
- Weight at study initiation: 2.5 - 2.7 kg
- Housing: The rabbits were accommodated individually in stainless steel cages. The cages were provided with a rack floor and placed on shelves
- Diet: Rabbit standard diet ad libitum
- Water: ad libitum
- Acclimation period:
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19 ± 2ºC
- Humidity (%): 40 - 70 %
- Photoperiod (hrs dark / hrs light): 12 h of light and 12 h of darkness every 24 h.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- water
- Controls:
- no
- Amount / concentration applied:
- 0.5 g, moistened with distilled water.
- Duration of treatment / exposure:
- 4 h
- Observation period:
- The response in the application area was evaluated after 30 - 60 min and 24, 48 and 72 h approximately once the exposure period had finished.
- Number of animals:
- 3 animals
- Details on study design:
- The animals were shaved 24 h before the application using an electric shaver. Fur was removed from the dorsal area and flanks from the pelvic waist to the scapular waist. Over the shaved and healthy skin of the right side, a square test area of approximately 6 cm2 was delimited.
The substance was applied using an only dose of 0.5 g moistened with distilled water. Each time the test substance was placed over the corresponding test area and covered with an hydrophillic gauze of 2.5 x 2.5 cm approximately. The semi-occlusive patches were attached to the animal body using surgical tape.
Finally a gauze band was wrapped around the trunk of the rabbit and it was stuck with hypoallergenic surgical tape to keep the bandage in place. The objective of this bandage was maximising the cutaneous absorption of the test substance.
After 4 h of exposure, the bandage and the patches were removed. The residual product was cleaned softly using cotton wet with distilled water.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible within: 24 hours
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 hours
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 hours
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- 30 min after the removal of the semi-occlusive patch, very light erythema (grade 1) was observed for the three animals. 24 h after the application, only 2 animals showed hardly visible erythema (grade 1). During the readings performed 48 and 72 h after the treatment, no dermal alterations were observed in rabbits, so that the study was considered finished after this reading.
The average of the erythema and edema assessments for the 3 animals after 24, 48 and 72 h was 0.2 and 0.0 respectively. - Other effects:
- The behaviour and physical condition of the rabbits were normal during the whole study. There were no mortalities.
Any other information on results incl. tables
Table 1: Primary dermal irritation following application of 0.5 g of the test substance:
Animal No. |
Reaction |
30 – 60 min |
24 h |
48 h |
72 h |
970 |
Erythema |
1 |
0 |
0 |
0 |
Edema |
0 |
0 |
0 |
0 |
|
966 |
Erythema |
1 |
1 |
0 |
0 |
Edema |
0 |
0 |
0 |
0 |
|
987 |
Erythema |
1 |
1 |
0 |
0 |
Edema |
0 |
0 |
0 |
0 |
Interpretation of results:
The substance was classified according to the following scale, in accordance with Guideline 83/467/CEE, Annex VI, part IIB.
A substance or preparation is considered irritant if the inflammation of the skin with duration of at least 24 h corresponds to one of the following values:
- average value for the whole group of animals:
Erythemose lesions - 2 or higher
Edematose lesions - 2 or higher
- or lesions equivalent to the average values mentioned above, calculated for each animal, to 2 animals at least.
It is necessary to use the measure performed in every reading (24, 48, 72 h) of each type of lesion to calculate the respective average values. A substance is considered corrosive if it produces tissue destruction in the whole skin thickness, to at least 1 animal. It is considered to produce burns if tissue lesions in the whole skin thickness appear in an exposure period no longer than 4 h. If tissue lesions in the whole skin thickness appear in an exposure period no longer than 3 min, the product is considered to produce serious burns.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Calcium sulfate is not irritating to skin.
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