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EC number: 248-326-4 | CAS number: 27213-90-7
- 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
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1994
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 994
- Report date:
- 1994
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- GLP compliance:
- yes
Test material
- Reference substance name:
- Sodium diisobutylnaphthalenesulphonate
- EC Number:
- 248-326-4
- EC Name:
- Sodium diisobutylnaphthalenesulphonate
- Cas Number:
- 27213-90-7
- Molecular formula:
- Not applicable (UVCB substance)
- IUPAC Name:
- sodium 2,3-bis(2-methylpropyl)naphthalene-1-sulfonate
- Test material form:
- solid: particulate/powder
Constituent 1
Test organisms
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
Study design
- Test type:
- static
- Water media type:
- freshwater
- Total exposure duration:
- 96 h
Results and discussion
Effect concentrations
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 100 - < 220 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
Any other information on results incl. tables
- Sublethal observations / clinical signs:
The purpose of this study was to determine the acute toxicity of test item on the Zebra fish (Brachydanio rerio HAM. and BUCH.) using a static procedure. Zebra fish were exposed aver a 96-hour period to a range of 5 concentrations spaced by a factor of about 2.2: 46.4, 100. 215, 464 and 1000 mg/l.
An untreated control was included. The study procedure was based an the OECD guideline.
Results (on the basis of the nominal concentrations):
LC 50 after 96 hours
GREATER 100 (MG/L)(1% SIGNIFICANCE LEVEL)
SMALLER 220 (MG/L)(1% SIGNIFICANCE LEVEL)
Symptoms:
apathy
No observed effect concentration (NOEC): 100 mg/l
Maximum concentration tested causing no mortality: 100 mg/l
Minimum concentration tested causing 100% mortality: 215 mg/l
Results (on the basis of the measured concentrations):
Values after 96 hours
LC 50:
GREATER 100 <MG/L) ( 1% SIGNIFICANCE LEVEL)
SMALLER 220 <MG/L) ( 1% SIGMIFICANCE LEVEL)
Na observed effect concentration (NOEC): 100 mg/l
Maximum concentration tested causing no mortality: 100 mg/l
Minimum concentration tested causing 100% mortality: 216 mg/l
The analytically detected concentrations were initially in the range of 99.5% - 105.6% and after about 96 hours between 100.0% - 103.4% of the nominal concentrations
Applicant's summary and conclusion
- Conclusions:
- Based on the nominal concentrations the median lethal concentration LC 50 <96 h) is > 100 < 220 mg/l.
Mortality (10/10) occurred from the concentration 215 mg/l upward.
Another substance-related effect was the symptom apathy.
The no observed effect concentration MOEC (96 h) Is 100 mg/l.
Based on the analytically determined concentrations the median lethal concentration LC 50 <96 h) is 100 < 220 mg/l.
The no observed effect concentration NOEC (96 h) is 100 mg/l.
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