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EC number: 929-018-5 | CAS number: 129813-66-7
- 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
Biodegradation in water and sediment: simulation tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: simulation testing on ultimate degradation in surface water
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- April to May 2004
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to a standard guideline without deviations from the protocol, but it was not conducted under GLP guidelines.
- 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 306 (Biodegradability in Seawater)
- Deviations:
- no
- GLP compliance:
- no
- Radiolabelling:
- no
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- other: Seawater
- Details on source and properties of surface water:
- The medium was prepared using seawater collected on April 5, 2004 from the Manasquan Inlet, New Jersey, USA, a designated New Jersey Department of Environmental Protection collection site, the salinity was 32 ppt and the DOC was 0.6 ppm C. The collected seawater was aerated and stored in an environmental chamber at 20 degrees C. On Day -1 of the test, mineral salts were added to the seawater and it was aerated.
- Details on inoculum:
- The inoculum included only the indigenous microorganisms present in the seawater sample.
- Duration of test (contact time):
- 28 d
- Details on study design:
- The amount of oxygen consumed by the microorganisms from oxidation of the test substance was monitored by an automated respirometer during a 28-day testing period. The control, sodium benzoate, and the test substance were evaluated in duplicate test systems. The amount of oxygen reported for each test system was corrected for oxygen consumption due to endogenous respiration in blank test systems. Temperature range for the 28 day testing period was 22 ± 1 degrees C.
Biodegradation results were calculated by the respirometer software using the theoretical oxygen demand (ThOD) and the mass of the test or positive control substance added. The ThOD was calculated using the empirical formula of each substance and the caclulations as defined in the OECD guideline. - % Degr.:
- 6.2
- St. dev.:
- 0.5
- Parameter:
- O2 consumption
- Sampling time:
- 4 d
- % Degr.:
- 11.6
- St. dev.:
- 1.2
- Parameter:
- O2 consumption
- Sampling time:
- 5 d
- % Degr.:
- 51.6
- St. dev.:
- 5.9
- Parameter:
- O2 consumption
- Sampling time:
- 11 d
- % Degr.:
- 61
- St. dev.:
- 5.1
- Parameter:
- O2 consumption
- Sampling time:
- 17 d
- Key result
- % Degr.:
- 68.8
- St. dev.:
- 3.3
- Parameter:
- O2 consumption
- Sampling time:
- 28 d
- Remarks on result:
- other: The test substance biodegradation was still increasing, albeit slowly, on day 28.
- Compartment:
- water
- DT50:
- ca. 10 d
- Type:
- not specified
- Remarks on result:
- other: Temperature not specified
- Transformation products:
- not measured
- Evaporation of parent compound:
- no
- Volatile metabolites:
- not measured
- Residues:
- not measured
- Validity criteria fulfilled:
- yes
- Conclusions:
- Hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, <2% aromatics, biodegraded to an extent of 69% after 28 days in seawater that used the indigenous microorganisms in the seawater sample as a sole source of the inoculum.
- Executive summary:
Hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, <2% aromatics, demonstrated a high extent of biodegradation in seawater following a standard OECD test guideline, which suggests that it has the potential to rapidly biodegrade in the marine environment. The test substance biodegraded to an extent of 69% after 28 days in seawater that used the indigenous microorganisms in the seawater sample as a sole source of the inoculum.
- Endpoint:
- biodegradation in water: simulation testing on ultimate degradation in surface water
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- March to April 2003
- 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 306 (Biodegradability in Seawater)
- Deviations:
- no
- GLP compliance:
- yes
- Radiolabelling:
- no
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- other: Natural seawater
- Details on source and properties of surface water:
- Seawater was collected from the Burnham-on-Crouch estuary at high tide. The estuary has no industrial input.
- Details on inoculum:
- Indigenous microorganisms contined in natural seawater.
- Duration of test (contact time):
- 28 d
- Initial conc.:
- 1.21 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- A surfactant (Nonidet P40) was used to emulsify the test substance. Background BOD for the surfactant was determined by evaluating the BOD of the surfactant alone in parallel test systems.
- Reference substance:
- acetic acid, sodium salt
- % Degr.:
- 0
- Parameter:
- O2 consumption
- Sampling time:
- 7 d
- % Degr.:
- 5
- Parameter:
- O2 consumption
- Sampling time:
- 14 d
- % Degr.:
- 4
- Parameter:
- O2 consumption
- Sampling time:
- 21 d
- Key result
- % Degr.:
- 11
- Parameter:
- O2 consumption
- Sampling time:
- 28 d
- Transformation products:
- not measured
- Evaporation of parent compound:
- not measured
- Volatile metabolites:
- not measured
- Residues:
- not measured
- Validity criteria fulfilled:
- yes
- Conclusions:
- The test substance biodegraded to an extent of 11% after 28 days.
- Executive summary:
The test substance biodegraded to an extent of 11% after 28 days.
- Endpoint:
- biodegradation in water: sediment simulation testing
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- the study does not need to be conducted because the substance is readily biodegradable
- Transformation products:
- not measured
Referenceopen allclose all
Description of key information
Biodegradation in seawater:
There is no data available for this substance. However, key data is available for structural analogues Hydrocarbons, C11-C14, n-alkanes, isoalkanes; cyclics, <2% aromatics and Hydrocarbons, C12-C14, isoalkanes, <2% aromatics The data is read across to this substance based on analogue read across and a discussion and report on the read across strategy is provided as an attachment in IUCLID Section 13.
Hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, <2% aromatics biodegraded to an extent of 69% after 28 days in seawater that used the indigenous microorganisms in the seawater sample as a sole source of the inoculum.
Hydrocarbons, C12-C14, isoalkanes, <2% aromatics biodegraded to an extent of 11% after 28 days.
Biodegradation in sediment:
This substance is considered readily biodegradable. Therefore, in accordance with REACH Annex IX column 2 exemption, the simulation testing in sediment does not need to be conducted.
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.