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EC number: 204-000-3 | CAS number: 112-72-1
- 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

Sediment toxicity
Administrative data
Link to relevant study record(s)
- Endpoint:
- sediment toxicity: short-term
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Remarks:
- Study conducted according to a modified OECD guideline, no mention of GLP, no analytical monitoring and lack of water quality measurements.
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EPA OPPTS 850.1735 (Whole Sediment Acute Toxicity of Invertebrates, freshwater)
- Deviations:
- yes
- Remarks:
- the media used was soil and water
- GLP compliance:
- not specified
- Analytical monitoring:
- no
- Vehicle:
- yes
- Details on sediment and application:
- PREPARATION OF SPIKED SEDIMENT
- Pooling or mixing of different substrates: soil and water
- Method of mixing: not reported
- Details of spiking: sand spike, using 10% of the total dry weight of soil. This involved adding an appropriate amount of compound to analar grade acetone to form a stock solution for the 1000 mg/kg dose. Aliquots of the stock solution were then diluted with acetone to prepare lower doses. Acetone solutions were added to silica sand in 500 ml amber glass jars. Mixtures were mixed thoroughly with a stainless steel spatula. The acetone was left to evaporate in a fume cupboard, leaving the test item coated onto the sand. Appropriate amount of moist soil was added to each of the glass jars. The dosed or undosed sand was incorporated into the bulk of the soil using a paletted knife. Jars were then sealed with screw top lids containing aluminium foil inserts and tumbled overnight (ca. 16 h) on a rotary soil tumbler 50 rpm.
- Equilibration time: not reported
- Controls: One aliquot of sand was dosed with acetone only to serve as solvent control. A jar with an aliquot of sand only served as untreated control - both with the appropriate amount of moist soil added thereafter.
- Chemical name of vehicle (organic solvent, emulsifier or dispersant):
- Concentration of vehicle in test medium (stock solution and final test solution): acetone solutions was added between 1-7 ml to 5-35g of silica sand. The sand was left to evaporate the acetone completely before initial exposure, so that the concentration of vehicle would be negligible.
- Evaporation of vehicle before use: yes
PREPARATION OF SPIKED WATER
- Details of spiking: not spiked - Test organisms (species):
- other: Heterocypris incongruens
- Details on test organisms:
- TEST ORGANISM
- Common name: ostracods
- Justification for species other than prescribed by test guideline: testing new method
- Source: obtained as dormant cysts in test kits (Ostracodtoxkit F. Chronic "direct contact" Toxicity Test for Freshwater Sediments, MicroBio Tests Inc. Deinze, Belgium).
- Breeding conditions: as test kit instructed. Organism were hatched in standard hard water in a covered petri dish for 52 h at 25 degC before introduction to the prepared soil.
- Age of animals at beginning of exposure: a few hours old
- Feeding during test
- Food type: algae powder (Spirulina sp, provided with the toxkit)
- Amount: one tube
- Frequency: once, four hours before the test began
ACCLIMATION
- Acclimation period: none - Study type:
- laboratory study
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Duration:
- 6 d
- Exposure phase:
- total exposure duration
- Test temperature:
- 25 +/- 2 degC
- pH:
- not reported
- Dissolved oxygen:
- not reported
- Nominal and measured concentrations:
- Nominal concentrations: 0, 300, 1000 mg/kg dw soil
- Details on test conditions:
- TEST SYSTEM
- Test container (material, size): polystyerene, multi well plates, supplied with the Ostracodtoxkit F.
- Amount of soil or substrate: 300ul og either reference sediment (supplied with the kit) or treated soil
- No. of organisms per container (treatment): 10
- No. of replicates per treatment group: 3
- No. of replicates per control: 3
- No. of replicates per vehicle control: 3
SOURCE AND PROPERTIES OF SUBSTRATE
- Geographic location: Heath Farm, Leicester Lane, LandLook (Midlands), Leamington Spa, from Dr Graham Beard. OS map reference 32896926.
- Pesticide use history at the collection site: assumed to be pesticide free, as the field the soil was taken from land that had been set aside for 3-4 years.
- Collection procedures: the soil was sieved to 2 mm.
- Sampling depth (cm): 5-20cm to avoid surface root mat
- Soil texture
- % sand: 63.8%-64.8%
- Soil classification: sandy loam soil. The soil is described as soil series, Bomsgrove, standard soil number 33, variant.
- Organic carbon (%): 1.3%
- Maximum water holding capacity: ca. 40%
- Pretreatment of soil: the soil was treated with gamma radiation (27 KGy) in order to kill the indigenous nematodes and potential predators. However observation from extracted fresh soil indicated that interference from the indigenous population was likely to be insignificant. Consequently, the definitive test were carried out using unsterilised soil.
- Storage: stored in closed black plastic bags at 4 degC until required.
OTHER TEST CONDITIONS
- Photoperiod: plates were incubated in the dark
-Other: animals were fed with 3x10^7 algal cells
EFFECT PARAMETERS MEASURED: Growth was determined by measuring the length of ostracods at the beginning (on a sub-sample) and end of the exposure period (surviving individuals). Measured once the ostracods were fixed in Lugols solution and via a calibrated graticule under a binocular microscope. Mortality (immobilisation) was measured at the end of the test.
VEHICLE CONTROL PERFORMED: yes
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 3
- Range finding study: no - Reference substance (positive control):
- yes
- Remarks:
- dimethoate
- Key result
- Duration:
- 6 d
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/kg sediment dw
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: reproduction and survival
- Details on results:
- - Mortality at end of exposure period: 0%
- Results with reference substance (positive control):
- - Results with reference substance valid? yes
- Relevant effect levels: 160 mg/kg dw soil - Reported statistics and error estimates:
- Probit analysis (Finney 1971) was used to determine EC50 values and their corresponding 95% intervals in definitive tests.
- Validity criteria fulfilled:
- yes
- Remarks:
- on the data provided, however not enough data on water quality
- Conclusions:
- A 6 d EC50 value of >1000 mg/kg dw soil has been determined for the effects of the test substance on population numbers of the ostracod H. incongruens.
- Endpoint:
- sediment toxicity: long-term
- Data waiving:
- other justification
- Justification for data waiving:
- other:
- Justification for type of information:
- JUSTIFICATION FOR DATA WAIVING
In respect of test design and feasibility:
- Standard sediment studies are designed to assess the effects of prolonged exposure to substances which persist in sediments over long time periods. The standard OECD guideline methods for long-term sediment ecotoxicity require spiking of substrate with the test substance initially, with an equilibration phase and in-life exposure phase of several weeks duration, and replenishment during the test is not realistic.
- It is expected that test organism exposure could not be consistently maintained for test substance in a bioavailable form, or primary degradation products, for the duration of a long-term test, due to very rapid biodegradation and mineralisation of bioavailable alcohol in a sediment-water system.
- Considerable technical difficulties would be expected in the conduct of either short or long-term sediment ecotoxicity tests, due to the expected very rapid biotic removal (primary degradation and mineralisation) of bioavailable substance from such a test system.
- Sediment simulation studies (Federle and Itrich, 2010; Itrich, 2010) have demonstrated the very short sediment half-life for the 'readily bioavailable' alcohol 'pool' (see Section 5.2.2); similarly rapid degradation rates are anticipated for other substances in the carbon chain length range C6-24, including this substance.
- for tetradecan-1-ol, in two different natural sediments: half-life 0.04 days and 0.08 days (primary degradation); 0.4 days and 0.15 days (mineralisation)
- for octadecan-1-ol, in two different natural sediments: half-life 1.1 days and 0.04 days (primary degradation); 1.7 days and 0.2 days (mineralisation).
It is considered that this would prevent maintenance of ‘readily bioavailable’ alcohol in pore-water for the duration of a standard long-term test (28 days duration for OECD 225), or even a shorter-term test. (While the sorbed alcohol ‘pool’ has a longer biodegradation half-life (for tetradecan-1-ol, in two different natural sediments: half-life 11.4 days and 11.4 days; for octadecan-1-ol, in two different natural sediments: half-life 17.3 days and 34.7 days (primary degradation)), alcohols are also ‘less bioavailable’ in the sorbed state).
- Please refer to discussion of the long-term aquatic invertebrate and fish studies which were complicated by the rapid degradation in the test system (Section 6.1.2 and 6.1.4).
- Please refer to discussion of the method development for the adsorption/desorption study (decan-1-ol) with natural soils, which was complicated by the rapid removal of test substance in non-sterilised soils (Section 5.4.1 and 5.2.3).
In the context of the chemical safety assessment:
- The substance is readily biodegradable and is very rapidly degradable in all compartments relevant to the environment (please refer to discussion in Section 5.2 of the IUCLID technical dossier for further information).
- In the wider environment, sediment biota are adapted to exposure to fatty alcohols from natural sources (please refer to Section 5.5 of the IUCLID technical dossier for further information).
- The exposure assessment indicates in the course of normal use some releases of alcohols to waste water is possible from both local and wide-dispersive uses. However, investigations have demonstrated that for both freshwater and marine sediments, LCAAs from anthropogenic sources are a minor proportion (1% or less in river environments) of the total present (see Section 5.5 on monitoring data).
- In general it is reasonable to conclude that natural freshwater and marine sediment biota would already be well-adapted to the presence of fatty alcohols from exposure to the many natural sources and the additional exposure to anthropogenic alcohols would not be expected to be a significant concern particularly given that biodegradation would be rapid following release. As such in accordance with column 2 in REACH Annex X, the chemical safety assessment does not indicate a need to investigate further the effects of the substance and/or relevant degradation products on sediment organisms. - Reason / purpose for cross-reference:
- data waiving: supporting information
Referenceopen allclose all
Table 1. Summary of findings.
Concentration (mg/kg dw soil | Mortality (%) |
Control | 0 |
10 | |
10 | |
Acetone control | 0 |
0 | |
0 | |
30 | 0 |
0 | |
0 | |
100 | 0 |
0 | |
10 | |
300 | 20 |
10 | |
10 | |
1000 | 40 |
0 | |
0 |
Description of key information
Key value for chemical safety assessment
Additional information
Short-term toxicity
A 6 d EC50 value of >1000 mg/kg dw soil (1.3% organic carbon) has been determined for the effects of the test substance on population numbers of the ostracod Heterocypris incongruens (Shell, 2004). This study was conducted using a mixture of water and soil as a substrate.
The study reflects the only value that is available for this endpoint.
Long-term toxicity
In accordance with Section 1.2 of REACH Annex XI (testing does not appear scientifically necessary (based on weight of evidence)), the toxicity to sediment organism study does not need to be conducted based on weight of evidence.
This is based on considerations relating to test design and feasibility and chemical safety assessment context.
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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