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Diss Factsheets
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EC number: 448-020-2 | 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
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- from 2000-02-01 into 2000-02-15
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- other: Body responsible for the test
- Title:
- Unnamed
- Year:
- 2 000
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: EC 92/69/EEC, B.3 Acute toxicity cutaneously OECD 402
- GLP compliance:
- yes
- Test type:
- standard acute method
- Limit test:
- yes
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
- Details on test material:
- Test batch: No.: 7/99
Test animals
- Species:
- other: rat- Wistar
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Wistar
- Housing: cage per 5 animals by sex
- Diet (e.g. ad libitum): standard food ST-1, ad libidum
- Water (e.g. ad libitum): ad libidum
- Acclimation period: 1 week
ENVIRONMENTAL CONDITIONS
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: To:
Administration / exposure
- Type of coverage:
- occlusive
- Vehicle:
- other: The sample was applied in delivered form "as is" tempered at 20-C.
- Details on dermal exposure:
- TEST SITE
-Area: 6x6 cm
- Type of wrap if used: gauze, foil
REMOVAL OF TEST SUBSTANCE
- Washing (if done): by water
- Time after start of exposure: 24 hours
TEST MATERIAL
- Amount(s) applied (volume or weight with unit):2 ml/kg
- Concentration (if solution): direct sample - Duration of exposure:
- 24 h
- Doses:
- 2037 kg/kg
- No. of animals per sex per dose:
- Male dose: 2037 mg/kg bw Nr. of animals. 5 Nr. of deaths 0
Female 2037 mf/kg bw 5 0 - Control animals:
- no
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- >= 2 000 mg/kg bw
- 95% CL:
- 95
- Mortality:
- Male: 2037 mg/kg bw; Number of animals: 5; Number of deaths: 0
Female: 2037 mg/kg bw; Number of animals: 5; Number of deaths: 0 - Clinical signs:
- Signs of toxicity related to dose levels: During 14 days observantion period the percentage of the mortality was accounted. Futher the body weight was found out at the beginning and at the end of the experiment and from the difference the increase and the loss were calculated. The clinical symptoms of intoxication were observed next the application, in 30 minutes, in 3 hours, next morning and in the afternoon and further days once a day for 14 days. The clinical diagnistic was concentratedon the observation of skin appearance, fell, visible mucouses, nutrition state, mental and motor activity, reaction to the impulses and the examination of the function of aspirative,digestive, urogenital and circulatory apparatus. All the animals survived the testing period without any symptoms of intoxication.
- Body weight:
- The animals were weighted in 1., 8., and 15. day.
On the base of body weight of rats at the beginning and at the end of test, weight increase or decrease was calculated. - Gross pathology:
- Effects on organs:
After 14 days the surviving animals were killed and
disemboweled, their apparatuses and their muscles were
macroscopicly considered. Their size, colour, shape,
structure and consistency were considered.
No toxic effect on the organs were found after sacrifice on
day 15. - Other findings:
- Signs of toxicity (local):
The light local effects of the substance were fully lost at
the end of the test.
Any other information on results incl. tables
Table of body weight:
Dose 2 ml/kg | Nr. of animals | body weight in g 1 day (mean) |
body weight in g 8. day (mean) |
body weight in g 15. day (mean) |
weight difference (g) |
Male | 5 | 233 +/-11,6 | 285,6 +/-20 | 331,5 +/-27,8 | + 98,4 |
Female | 5 | 217,8 +/-10 | 239,4 +/-15 | 261,2 +/-17,2 | +43,4 |
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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