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EC number: 283-619-0 | CAS number: 84695-99-8 Extractives and their physically modified derivatives such as tinctures, concretes, absolutes, essential oils, oleoresins, terpenes, terpene-free fractions, distillates, residues, etc., obtained from Castanea sativa, Fagaceae.
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- April 2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Cross-reference
- Reason / purpose for cross-reference:
- read-across source
Reference
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- other information
- Justification for type of information:
- Cf. the attached Read across argumentation
- Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- yes
- Remarks:
- It concerns the number of replicates for the concentration 100 mg/L: 8 replicates instead of 4 replicates were done to have enough solution at the end of the test for the chemical analyses. This has no influence on the results of this study.
- GLP compliance:
- yes
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 g/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: highest tested concentration
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: highest tested concentration
- Details on results:
- - No immobilization was observed at 24 h and 48 h (including controls).
- No sign of stress was observed on the mobile daphnids after 48 h of exposure - Results with reference substance (positive control):
- The last toxic response obtained on the reference item K2Cr2O7 (March 24, 2016) gives an EC50-24h of 1.58 mg/L (1.44 – 1.76), indicating that the daphnids sensitivity is correct (within the accepted interval of 0.6–2.1 mg/L fixed by the International Standard ISO 6341 December 2012 as mentioned in the OECD 202 Guideline) and in accordance with historical data obtained by the laboratory.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The results obtained for the reference substance on the toxicological endpoint “immobilisation” give an EC50-24h and an EC50-48h higher than the highest tested concentration, i.e. 100 mg/L, based on nominal test item concentration.
- Executive summary:
Based on the consideration mentioned in the attached argumentation, it can be concluded that the results of the study made on Daphnia magna, acute immobilization test performed on the reference substance “Polysaccharides of glucose from Oat” is likely to predict the properties of the target substance “Oligosaccharides of Castanea sativa seed” and are considered as adequate to fulfil
the information requirement of the Annex VII 9.1.1: 1. Short term toxicity to aquatic invertebrates:
=> EC50-24h and EC50-48h > 100 mg/L (highest tested concentration)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 016
- Report date:
- 2016
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- yes
- Remarks:
- It concerns the number of replicates for the concentration 100 mg/L: 8 replicates instead of 4 r eplicates were done to have enough solution at the end of the test for the chemical analyses. This has no influence on the results of this study.
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Polysaccharids of kernel Avena sativa, Poaceae
- EC Number:
- 944-507-3
- IUPAC Name:
- Polysaccharids of kernel Avena sativa, Poaceae
- Reference substance name:
- Water
- EC Number:
- 231-791-2
- EC Name:
- Water
- Cas Number:
- 7732-18-5
- Molecular formula:
- H2O
- IUPAC Name:
- oxidane
- Test material form:
- solid
- Details on test material:
- Osilift AT is the atomized product of Osilift
Appearance: clear beige powder
Storage conditions: 20°C in a dark place and protected from humidity
Batch number : 131121-0027
Expiration date: November 2016
Constituent 1
additive 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- In order to verify the initial concentrations and maintenance of the exposure concentrations of the test item during the ecotoxicological testing, chemical analyses in daphnids test solutions were performed according to the Analytical Protocol FCBA Chimie No.315-e version 2: Method for the chemical analysis of Total Organic Carbon (TOC) in samples containing the test item OSILIFT AT from daphnids ecotoxicology solutions by Total Organic Carbon Analyzer, (described in the study 15/1268F/b) and the following protocol:
- at the beginning of the test (T = 0h)
- at the end of the test (T = 48h)
- for the control (i.e. daphnids test medium filtered) and concentration 100 mg/L
These solutions were analysed taken directly from the starting solutions without daphnids.
At the end of the test (48h), the solutions were analysed with daphnids (biotic solutions) and without daphnids (abiotic solutions).
The measured concentrations of the test item should not vary more than ± 20 % during the test (48h).
Test solutions
- Vehicle:
- no
- Details on test solutions:
- The test item was soluble in the test medium.
At the request of the sponsor, the test medium and the solution (100 mg test item/L) were filtered through a membrane filter (cellulose acetate) with a mesh size of 0.22 μm to sterilizing and all the manipulations were done under sterile conditions to prevent contamination
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna Straus, clone number 5, from at least the third generation (i.e. the third brood) obtained with a non-cyclic parthenogenesis reproduction.
The daphnids breeding was carried out in closed bottles placed in a climatic chamber free from any toxic vapour and in medium M4.
Daphnids used in this experimentation were previously filtered in order to obtain animals from a size between 560 μm and 800 μm (corresponding to daphnids less than 24 hours old).
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- none
Test conditions
- Hardness:
- 250 mg/L of CaCO3
- Test temperature:
- 18 - 22 °C
- pH:
- pH (Dilution water M4) = 8.2
- Dissolved oxygen:
- 9.0 mg/L
- Salinity:
- no data
- Nominal and measured concentrations:
- Nominal concentration: 100 mg/L
Measured concentration: 98.5 mg/L (at initial time) and 97.95 mg/L (after 48 hours of exposure) - Details on test conditions:
- TEST SYSTEM
Daphnia magna Straus, clone number 5, from at least the third generation (i.e. the third brood) obtained with a non-cyclic parthenogenesis reproduction.
The daphnids breeding was carried out in closed bottles placed in a climatic chamber free from any toxic vapour and in medium M4.
Daphnids used in this experimentation were previously filtered in order to obtain animals from a size between 560 μm and 800 μm (corresponding to daphnids less than 24 hours old).
The test will contain a minimum of 8 glass test tubes as follow:
• Control: 4 replicates
• Concentration 100.0 mg/l: 4 replicates
Each glass test tube (sterilized by autoclave) contained 10 mL of test solution and 5 daphnids; they were covered in order to avoid evaporation and dust deposition.
OTHER TEST CONDITIONS
- Light intensity: Darkness
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
Observations of the daphnid’s mobility were done after 24 and 48 hours of exposition to the test item.
Every sign of stress observed on the daphnids after 48 hours of exposition to the test item were reported if need be.
pH and dissolved oxygen were measured at the beginning and at the end of the test for each test solutions (including the controls). - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: highest tested concentration
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: highest tested concentration
- Details on results:
- - No immobilization was observed at 24 h and 48 h (including controls).
- No sign of stress was observed on the mobile daphnids after 48 h of exposure - Results with reference substance (positive control):
- The last toxic response obtained on the reference item K2Cr2O7 (March 24, 2016) gives an EC50-24h of 1.58 mg/L (1.44 – 1.76), indicating that the daphnids sensitivity is correct (within the accepted interval of 0.6–2.1 mg/L fixed by the International Standard ISO 6341 December 2012 as mentioned in the OECD 202 Guideline) and in accordance with historical data obtained by the laboratory
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The results obtained for the test item on the toxicological endpoint “immobilisation” give an EC50-24h and an EC50-48h higher than the highest tested concentration, i.e. 100 mg/L, based on nominal test item concentration.
- Executive summary:
The aim of this study was to assess the effects of the test item “OSILIFT AT”on the daphnids Daphnia magna, according to the OECD 202 guideline, at 100 mg/L, limit test, in static conditions.
The concentrations which immobilise 50% of the daphnids exposed to the test item after 24 and 48 hours, reported as EC50-24h and EC50-48h were evaluated, relative to the tested concentration : 100 mg/L.
At the nominal concentration of 100 mg/L, the test item « OSILIFT AT» is considered as stable in the testing conditions because the measured concentrations of the “OSILIFT AT” did not vary more than ± 20 % of initial measured concentration during the test.
The results obtained for the test item “OSILIFT AT” on the toxicological endpoint “immobilisation” give an EC50-24h and anEC50-48h superior to the highest tested concentration,i.e. 100mg/L, value expressed in nominal test item concentration.
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