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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 813-338-6 | CAS number: 106155-02-6
- 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 fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1996-11-11 to 1997-01-15
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Deviations:
- yes
- Remarks:
- pH, oxygen and hardness of the test water missing
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: nominal
- Sampling method:
- Sample storage conditions before analysis:
- Concentrations: The test substance was weighed, directly mixed into the test system and stirred for 24 hours using an ultraturrax. Afterwards, the test water was clear without oily drops on the water surface (main test 1) or with oily drops on the water surface (maintest 2). In main test 2, approximatly one liter of the test system including the oily drops were removed afterv 3.5 hours, treated by an ultraturrax and transferred back to the test system. Accordingl, the study duration was adapted, i.e. study start was postponed by 3.5 hours.
- Sampling method: from the test water
- Sample storage conditions before analysis: not reported - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: directly weighing ino the test systenms and stirring for 24 hours
- Eluate: not applicable
- Differential loading: not applicable
- Controls: water control
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): no vehicle used
- Evidence of undissolved material (e.g. precipitate, surface film, etc): no (see above) - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: zebra fish
- Strain: not applicable
- Source: Charles River Aquatics (delivery from 1996-08-06)
- Age at study initiation (mean and range, SD): not reported
- Length at study initiation (length definition, mean, range and SD): not reported
- Weight at study initiation (mean and range, SD): not reported
- Method of breeding: not applicable
- Feeding during test: no
ACCLIMATION
- Acclimation period: not reported
- Acclimation conditions (same as test or not): not reported
- Type and amount of food: SSNIFF M (Charge: 9556413)
- Feeding frequency: not reported
- Health during acclimation: mortality < 5 % during the last wekk before test start - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Hardness:
- not reported
- Test temperature:
- 20.4-21.8 °C
- pH:
- 8.2-8.6
- Dissolved oxygen:
- minimum: 75 %
- Salinity:
- not applicable
- Nominal and measured concentrations:
- nominal 2.0, 4.0, 8.0 and 13 mg/L
mean measured for nominal 2.0 mg/L (0-24 h): 64.0 %
mean measured for nominal 4.0 mg/L (0-24 h): 69.8 %
mean measured for nominal 8.0 mg/L (0-24 h): 62.3 %
mean of mean measured: 65.4 %
resulting mean measured test concentrations: 1.3, 2.6, 5.2 and 8.5 mg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel: 10 L
- Type: open
- Material, size, headspace, fill volume: not reported, 5 L, 5 L
- Aeration: not reported
- Renewal rate of test solution: semistatic (24 hours renewal):
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
- Biomass loading rate: not reported
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: drinking water
- Total organic carbon: not reported
- Particulate matter: not reported
- Metals: free of copper
- Pesticides: not reported
- Chlorine: free of chlorine
- Alkalinity: not reported
- Ca/mg ratio: not reported
- Conductivity: not reported
- Culture medium different from test medium: no
- Intervals of water quality measurement: not reported
OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16 h light, 8 h dark
- Light intensity: not reported
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): mortality, imbalance, apathy
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.625 to 2
- Range finding study: main test 1 cited but no results presented (with the exception of observations after application) - Reference substance (positive control):
- no
- Duration:
- 0 h
- Dose descriptor:
- LC0
- Effect conc.:
- 13 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 0 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 8 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 0 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 13 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 4 h
- Dose descriptor:
- LC0
- Effect conc.:
- 8 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 4 h
- Dose descriptor:
- LC100
- Effect conc.:
- 13 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 4 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 4 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 8 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 24 h
- Dose descriptor:
- LC0
- Effect conc.:
- 5.2 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 24 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 2.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 24 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 5.2 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 48 h
- Dose descriptor:
- LC0
- Effect conc.:
- 5.2 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 48 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 2.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 72 h
- Dose descriptor:
- LC0
- Effect conc.:
- 2.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 72 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 2.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- 2.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 6.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 96 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 2.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Sublethal observations / clinical signs:
Table 1 Analytics
Nominal test concnetration (mg/L) measured at 0 h (mg/L) measured at 24 h (mg/L % from nominal at 0 h % from nominal at 24 h mean % from nominal 0 -24 h --- 0.70 --- 35.0 2.0 1.96 0.92 98.0 46.0 64.0 1.58 0.75 79.0 370.5 --- 2.01 --- 50.3 4.0 4.16 2.43 104.0 60.8 69.8 2.96 1.63 74.0 40.8 --- 3.67 --- 45.9 8.0 7.33 4.57 91.6 57.1 62.3 5.05 3.10 63.1 38.8 Tabe 2 Mortality and symptoms of toxicity (main test 2)
Conc. Exposure time (h) (mg/L) 0 2 -4 24 48 72 96 0 0 0 0 0 0 0 2.0 0 0 0 0 0 0 4.0 0 0 0 0 A 0 A 0 A 8.0 0 0 GA 0 GA 0 GA 10 GA 20 GA 13 0 GA 100 100 100 100 100 G: imbalancies
A: apathy
- Validity criteria fulfilled:
- yes
- Conclusions:
- In a valid, reliable and conclusive study according to EU method C1 (1992), the test substance Sandalice resulted to the following values for acute fish toxicity after 96 hours of exposure: LC0 = 2.6 mg/L (mean measured), LC50 = 6.3 mg/L (mean measured), LC100 = 8.5 mg/L (mean measured).
- Executive summary:
The acute toxicity of the test substance Sandelice on zebra fish was determined according to EU method C1 (1992). The following nominal test concnetrations were used: 2.0, 4.0, 8.0 and 13 mg/L. The test organisms were exposed to the test substance for 96 hours in a semi-static test design with a daily renewal of the treated test water. The LC50 was calculated using semi-logarithmic interpolation including LC100. Since the analytical recovery of the test concentration after 24 hours decreased below 80 % of nominal, the mean measured test concentration was calculated by using all recovery values (%). The following LC-values were determined:
LC0 = 2.6 mg/L
LC50 = 6.3 mg/L
LC100 = 8.5 mg/L
Reference
Description of key information
The acute toxicity of the test substance Sandelice on zebra fish was determined according to EU method C1 (1992). The following nominal test concentrations were used: 2.0, 4.0, 8.0 and 13 mg/L. The test organisms were exposed to the test substance for 96 hours in a semi-static test design with a daily renewal of the treated test water. The LC50 was calculated using semi-logarithmic interpolation including LC100. Since the analytical recovery of the test concentration after 24 hours decreased below 80 % of nominal, the mean measured test concentration was calculated by using all recovery values (%).
The following LC-values were determined:
LC0 = 2.6 mg/L
LC50 = 6.3 mg/L
LC100 = 8.5 mg/L
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 6.3 mg/L
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.