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EC number: 701-198-8 | 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 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:
- May 1994
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This robust summary has a reliability rating of 1 because the study followed a standard guideline, followed GLP guidelines, and was conducted without deviations that would invalidate the study.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- The water accommodated fraction (WAF) of the test material was prepared by stirring the test material in the exposure solution for approximately 24 hours. The stirring was as vigorous as possible without causing an emulsion to form. After stirring, the WAF was allowed to settle for 1 hour before removing the aqueous phase for testing.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Organisms used in the test were from a laboratory culture were less than 24 hour old. The source of the culture was from Zeneca Brixham Laboratory from I.R.Ch.A., France.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Hardness:
- 196 mg/L CaCO3
- Test temperature:
- 18 to 20 degrees C
- pH:
- Within Guideline requirement
- Dissolved oxygen:
- 8.9 to 9.2 mg/L
- Nominal and measured concentrations:
- The nominal loading rate was 1000 mg/L. A control was also tested.
- Details on test conditions:
- The study was conducted in closed test systems that were not renewed during the study. The test systems used were 150 ml glass Erlenmeyer flasks. The control and treatment level was evaluated in replicate test systems. Ten organisms, less than 24 hours old, were exposed in each of the control and treatment solution flasks and were not fed during the study.
- Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- LL0
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL0
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- There was no immobility reported in the treatment and control solutions at test termination.
- Reported statistics and error estimates:
- None
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- May 1994
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This robust summary has a reliability rating of 1 because the study followed a standard guideline, followed GLP guidelines, and was conducted without deviations that would invalidate the study.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- The water accommodated fraction of the test material was prepared by stirring the test material in the exposure solution for 22 hours after which the the aqueous phase was removed for testing.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Organisms used in the test were from a laboratory culture were less than 24 hour old. The source of the culture was from Zeneca Brixham Laboratory from I.R.Ch.A., France.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Hardness:
- 196 mg/L CaCO3
- Test temperature:
- 18 to 20 degrees C
- pH:
- Within Guideline requirement
- Dissolved oxygen:
- 9.0 mg/L
- Nominal and measured concentrations:
- The nominal loading rate was 1000 mg/L. A control was also tested.
- Details on test conditions:
- The study was conducted in closed test systems that were not renewed during the study. The test systems used were 150 ml glass Erlenmeyer flasks. The control and treatment level was evaluated in replicate test systems. Ten organisms, less than 24 hours old, were exposed in each of the control and treatment solution flasks and were not fed during the study.
- Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- LL0
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL0
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- There was no immobility reported in the treatment and control solutions at test termination.
- Reported statistics and error estimates:
- None
- Validity criteria fulfilled:
- yes
- Conclusions:
- The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
- Executive summary:
The water accommodated fraction (WAF) of the test substance did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- August 1983
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: This robust summary has a reliability rating of 2 because the study did not follow a GLP guideline and included limited water quality results, but did appear to use a standard procedure and generally acceptable testing procedures.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: U.S. Environmental Protection Agency (1978) Bioassay procedures for the ocean disposal permit program EPA-600/9-78-010
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- The treatment solutions were prepared as percent dilutions of a 100% water soluble fraction (WSF). The 100% WSF was prepared by adding 1 part of test material to 9 parts of artificial seawater (v:v). The mixture was stirred for 20 hours. After mixing, the aqueous phase was removed for further dilution to prepare the treatment levels, which were 10, 25, 40, 60, and 100% of the water soluble fraction.
- Test organisms (species):
- Americamysis bahia (previous name: Mysidopsis bahia)
- Details on test organisms:
- Test organisms were obtained from an in-house culture, cultivated under test conditions.
- Test type:
- static
- Water media type:
- saltwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Test temperature:
- 19 to 21 degrees C
- pH:
- 7.8
- Dissolved oxygen:
- 7.0 to 7.4 mg/L
- Nominal and measured concentrations:
- The nominal treatment levels were 10, 25, 40, 60, and 100% of the water soluble fraction.
- Details on test conditions:
- The test material was evaluated in three separate tests. Each test exposed 30 organisms to a range of water soluble fractions (WSFs) of the test substance including a 100% WSF.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 81 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Details on results:
- Although mortality was observed in some of the treatment levels, which were dilutions of the 100% water soluble fraction (WSF) of the test substance prepared at a loading of 81,000 mg/L, a clear dose dependent relationship was not observed and mortality did not exceed 20%. The dilutions are represented as percents of the 100% WSF. A control was also tested.
Immobility results from the second definitive test:
Exposure Total
Solution Mortality*
(% WSF) (Test 1, 2, 3 @ 96 hrs)
Control 0, 0, 0
10 0, 0, 0
25 1, 0, 1
40 0, 0, 0
60 0, 0, 1
100 0, 2, 1
* 30 organisms tested in each of the control and treatment levels - Reported statistics and error estimates:
- Statistical analyses were not conducted.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The 100% water soluble fraction (WSF) of the test substance at a loading of 81,000 mg/L did not produce a 50% mortality with Mysidopsis bahia after a 96-hour exposure. Therefore, the 496-hour LL50 value is reported as >81,000 mg/L. There was also no mortality in the control.
- Executive summary:
The 100% water soluble fraction (WSF) of the test substance at a loading of 81,000 mg/L did not produce a 50% mortality with Mysidopsis bahia after a 96-hour exposure. Therefore, the 496-hour LL50 value is reported as >81,000 mg/L. There was also no mortality in the control.
Referenceopen allclose all
Description of key information
Freshwater:
Water accommodated fractions of hydrocarbons, C10-C12, isoalkanes, <2% aromatics, did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the
48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
The water accommodated fraction (WAF) of hydrocarbons, C10-C13, n-alkanes, isoalkanes, cyclics, <2% aromatics, did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
The data from these two studies are used as read-across data to hydrocarbons, C10-C13, isoalkanes, cyclics, <2% aromatics.
Marine:
The 100% water soluble fraction (WSF) of hydrocarbons, C10-C14, isoalkanes, cyclics, <2% aromatics, at a loading of 81,000 mg/L did not produce a 50% mortality with Mysidopsis bahia after a 96-hour exposure. Therefore, the 96-hour LL50 value is reported as >81,000 mg/L. There was also no mortality in the control. These data are used as read-across data to hydrocarbons, C12-C13, isoalkanes, cyclics, <2% aromatics.
Key value for chemical safety assessment
Additional information
Freshwater:
Water accommodated fractions of hydrocarbons, C10-C12, isoalkanes, <2%
aromatics, did not produce a 50% effect (immobility) with Daphnia
magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore,
the
48-hour LL50 is reported as >1000
mg/L. There was no mortality at the 1000 mg/L loading level after 48
hours. Therefore, the 48-hour LL0 for mortality is reported
as 1000 mg/L. There was also no mortality in the control.
The water accommodated fraction (WAF) of hydrocarbons, C10-C13, n-alkanes, isoalkanes, cyclics, <2% aromatics, did not produce a 50% effect (immobility) with Daphnia magna at a loading of 1000 mg/L after a 48-hour exposure. Therefore, the 48-hour LL50 is reported as >1000 mg/L. There was no mortality at the 1000 mg/L loading level after 48 hours. Therefore, the 48-hour LL0 for mortality is reported as 1000 mg/L. There was also no mortality in the control.
The data from these two studies are used as
read-across data to hydrocarbons, C10-C13, isoalkanes, cyclics, <2%
aromatics.
Marine:
The 100% water soluble fraction (WSF) of hydrocarbons, C10-C14,
isoalkanes, cyclics, <2% aromatics, at a loading of 81,000 mg/L did not
produce a 50% mortality with Mysidopsis bahia after a 96-hour
exposure. Therefore, the 96-hour LL50 value is reported as
>81,000 mg/L. There was also no mortality in the control. These data are
used as read-across data to hydrocarbons, C12-C13, isoalkanes, cyclics,
<2% aromatics.
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.