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EC number: 947-329-4 | 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

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:
- 1975
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with national standard methods with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- other: Japanese Industrial Standard JIS K0102
- Deviations:
- not specified
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Test organisms (species):
- Cyprinus carpio
- Details on test organisms:
- TEST ORGANISM
- Common name: carp, prelarvae, 1 week old
- Source: Fish farm in Tokyo
- Length at study initiation: 9 mm
- Weight at study initiation: 4.4 mg
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- none
- Hardness:
- 25 mg/L as CaCO3
- Test temperature:
- 22 °C
- pH:
- 7.0
- Dissolved oxygen:
- 7.2 mg/L
- Nominal and measured concentrations:
- not reported
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 800 mL beaker
- Renewal rate of test solution: the water was not changed during the experiment
- No. of organisms per vessel: 20
- No. of vessels per concentration (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: softened water was used.
EFFECT PARAMETERS MEASURED: mortality - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 13 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Sublethal observations / clinical signs:
6h-LC50: 190 mg/L
12h-LC50: 180 mg/L
24h-LC50: 180 mg/L- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 02 Feb - 06 Feb 1998
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Freie und Hansestadt Hamburg, Behörde für Arbeit, Gesundheit und Soziales
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- Leuciscus idus
- Details on test organisms:
- TEST ORGANISM
- Common name: golden orfe
- Source: Fish farm eggers, Martensweg 18, 24594 Hohenwestedt, Germany
- Length at study initiation: 5.5-6.3 cm
- Feeding during test: not fed for 24 hours before the start of the test
ACCLIMATION
- Acclimation period: 12 day acclimation in 70 L tank with aeration
- Acclimation conditions: for 7 days conditions similar to test conditions; 19.8-20.8 °C, 75.8-98.4% oxygen saturation, semi-static, pH: 7.33-7.87, 16 hours photoperiod, aerated
- Type and amount of food: flocculent food Idus-Fit (Interquell, 86517 Wehringen, Germany)
- Health during acclimation: 0% mortality in 7-day acclimation period - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- none
- Hardness:
- 250 mg CaCO3/L
- Test temperature:
- 20.0 - 21.1 °C
- pH:
- control: 7.47-7.95
100 mg/L: 7.19-7.95 - Dissolved oxygen:
- control: 77.5 - 98.8% (air saturated value)
100 mg/L: 51.5 - 98.7 % (air saturated value) - Nominal and measured concentrations:
- nominal: 0 and 100 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 10 L tank
- Material, size, headspace, fill volume: 10 L
- Aeration: via pasteur pipettes (2 to 3 air bubbles per second)
- Renewal rate of test solution: daily
- No. of organisms per vessel: 10 per tank
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: reconstituted water
- Ca/Mg ratio: 4:1
- Na:K 10:1
OTHER TEST CONDITIONS
- Photoperiod: 16 hours light, 8 hours dark
EFFECT PARAMETERS MEASURED: mortality, behaviour and appearance after 2-4 h, 24, 28, 72 and 96 h
- Reference substance (positive control):
- no
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- - Mortality: Two out of ten fish died at the test concentration 100 mg/L (one after 72 and one after 96-hour exposure period).
- Behavioural abnormalities: None, one fish was found in angular position
- Observations on body length and weight: no difference in weight and length between control and 100 mg/L - Results with reference substance (positive control):
- not reported
- Reported statistics and error estimates:
- No LC50 was calculated since a limit test was performed.
- Endpoint:
- short-term toxicity to fish
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Remarks:
- Summary of available data used for the endpoint assessment of the target substance
- Adequacy of study:
- key study
- Justification for type of information:
- Refer to the Category Approach Justification document provided in IUCLID6 Section 13.
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 13 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other:
- Remarks:
- Source, key, 142-87-0, 1976
Referenceopen allclose all
Description of key information
48hr LC50 (Cyprinus carpio pre-larvae, mortality) = 13 mg/L (nominal concentration, Japanese Industrial Standard JIS K0102)
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 13 mg/L
Additional information
Since no reliable acute toxicity test with fish is available for Sulfuric acids, C9-11-iso-C10 rich, alkyl esters, sodium salt, in accordance to Regulation (EC) No. 1907/2006 Annex XI, 1.5 a read-across to other structurally related substances was conducted. As the toxicity of alkyl sulfates is dependent on the carbon chain length, it is expected that the toxic effects are comparable for the similar homologues.
In the key, non-GLP study performed with C10AS Na (CAS 142-87-0) according to Japanese Industrial Standard JIS K0102, 1-week old carp pre-larvae (Cyprinus carpio) were exposed to C10AS Na for 48 hours under static conditions (Kikuchi et al. 1976a). Based on pre-larvae mortality, the LC50 value was 13 mg/L (nominal concentrations in agreement with the measured ones). Since the obtained value was the most critical, it is considered as a reliable short-term LC50 value for fish.
One GLP compliant study investigating effects of C12-isoAS Na (CAS 94200-74-5) is available (Sasol, 1998). The test was performed with golden orfe fish (Leuciscus idus) according to OECD guideline 203. Mortality of fish caused by the test substance was determined after 24, 48, 72 and 96 hours of exposure to the nominal test concentration of 100 mg/L in a limit test. No analytical measurement of test concentration is available. The results showed that the 96-hour LC50 value was above 100 mg/L (nominal concentration).
Due to structural and property similarities with the tested substances, it can be concluded that the above results apply also to Sulfuric acids, C9-11-iso-C10 rich, alkyl esters, sodium salt.
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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