Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 232-800-2 | CAS number: 9025-57-4
- 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
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992-08-17 to 1993-06-11
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- 2004
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0 and 100 mg TOS/L
- Sampling method: At the start of the test, three samples (10 mL) were taken from freshly prepared control and test meida. After 48h,the contents of the test vessels from each group were pooled and further samples taken for nalysis.
- Sample storage conditions before analysis: frozen - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: The test substance (957.4 mg) was dissolved in dilution medium (Elendt M4) to provide the test medium at a nominal concentration of 100 mg TOS/L. The contents of the flask were shaken vigorousley before being poured in the test vessels.
- Controls: dilution medium ( Elendt M4) - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia
- Strain: Daphnia magna Straus
- Source: Institute National de Recherche Chimique Appliqué (IRChA), France
- Age at study initiation (mean and range, SD): less than 24 hours
- Feeding during test: no - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Hardness:
- 260 mg CaCO3/L
- Test temperature:
- 20.8 - 21.2°C
- pH:
- 6.16 - 6.68
- Dissolved oxygen:
- 72 - 100% ASV
- Nominal and measured concentrations:
- nominal: 0 and 100 mg TOS/L
Measured: 92.5% of the nominal activity - Details on test conditions:
- TEST SYSTEM
- Test vessel: glass dishes
- Type (delete if not applicable): loosely covered
- Material, size, fill volume: : glass, 120 mL, 100 mL
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Elendt M4 medium. The medium was prepared in deionised, reversed osmosis water. The dilution medium was adjusted to pH 6.0 ± 0.2 to maintain the stability of the test substance.
- Culture medium different from test medium: no
OTHER TEST CONDITIONS
- Photoperiod: 16 hours light: 8 hours dark
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : The numbers of mobile, immobile and floating daphnia were counted approximately 24 and 48h after the start of the study.
TEST CONCENTRATIONS
- 0 and 100 mg TOS/L corresponding to 0 and 22.2 mg active enzyme protein/L - Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 22.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Remarks:
- active enzyme protein
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 22.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Remarks:
- active enzyme protein
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: TOS
- Basis for effect:
- mobility
- Remarks on result:
- other:
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: TOS
- Basis for effect:
- mobility
- Details on results:
- - Mortality of control: 0
- Other adverse effects control:no
- Abnormal responses: no
- Validity criteria fulfilled:
- yes
- Conclusions:
- Xylanase was not toxic towards Daphnia magna under the given conditions and hence no EC50 value could be determined. The NOEC is thus the highest exposure concentration i.e. 100 mg TOS/L corresponding to 22.2 mg aep/L.
- Executive summary:
The acute toxicity of Xylanase, PPQ 30189 to Daphnia magna was assessed under static exposure conditions. The active component of the test substance is an enzyme, which was known to be pH sensitive with reduced enzymatic activity under alkaline conditions. In order to maintain the stability of the enzyme the dilution medium used in the study was adjusted to pH 6 before use.
The study was conducted in accordance with EC Methods for Determination of Ecotoxicity, Annex to Commission Regulation (EC) No 440/2008 (O.J. No. L142/456, 2008) Part C, Method 2 “Daphnia sp. Acute Immobilisation Test” and the OECD Guideline for Testing of Chemicals No. 202, “Daphnia Acute Immobilisation Test” (2004).
A group of twenty Daphnia, less than 24 hours old, was exposed for 48 hours to Xylanase, PPQ 30189 at a nominal concentration of 100 mg TOS (Total Organic Solids)/L. The test medium was prepared in Elendt M4 medium by the direct addition of the test substance to the dilution medium.
At the request of the Sponsor, the test concentrations were verified by analysis of the enzyme concentrations, which was performed at the Sponsor’s laboratory.
Observations of the Daphnia in each control and test vessel were made after 24 and 48 hours.
No immobilisation or adverse effects on the Daphnia were noted at a nominal concentration of 100 mg TOS/L (22.2 mg aep/L).
Based on these findings the following values have been estimated:
- 48-hour EC50 value : >100 mg TOS/L corresponding to 22.2 mg aep/L
- “No observed effect concentration” : 100 mg TOS/L corresponding to 22.2. mg aep/L
Reference
Description of key information
Xylanase was not toxic towards daphnia magna and hence the 48 h EC50 value for xylanase could not be determined and is above > 100 mg TOS/L corresponding to 22.2 mg aep/L. The NOEC value was determined to be >=100 mg TOS/L or 22.2 mg aep/L. The NOEC is >= 100 mg TOS/L equivalent to 22.2 mg aep/L.
Key value for chemical safety assessment
Additional information
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.