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EC number: 292-334-0 | CAS number: 90604-40-3
- 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
Endpoint summary
Administrative data
Description of key information
Additional information
Short-term toxicity
Reliable short-term toxicity tests results are available for freshwater fish (Oncorhynchus mykiss), invertebrates (Daphnia magna) and algae (Raphidocelis subcapitata) for alcohols C12-C15 branched and linear, as a whole substance.
The relevant short-term values are:
Fish: Key: LC50 (96 h): 100-300 mg/l (WAF) (Eadsforth et al, 2000).
Invertebrates: EC50 (24 h): <1 mg/l (WAF) (Palmer and Sherrin, 2001)
Algae: ErL50 72h: 0.085-0.097 mg/l; NOELR: 0.003 mg/L (WAF) (Palmer and Cann, 2000)
Long-term toxicity
There are no measured long-term toxicity data available for alcohols C12-C15 branched and linear as a whole substance. The needs associated with a sound understanding of long-term aquatic toxicity to fish and invertebrates are adequately met by the available data on constituents. For the purpose of risk assessment aquatic PNECs for individual constituents have been derived.
Long-term invertebrate data is available for each constituent. The relevant values are:
C12: Measured 21-d EC10 value of 0.013 mg/l based on reproduction of Daphnia magna (Schafers 2005).
C13: Predicted 21-d EC10 value has been calculated (QSAR) to lie in the range of 0.018 - 0.14 mg/l based on reproduction of Daphnia magna (Schafers 2009).
C14: Measured 21-d EC10 value of 0.0063 mg/l based on reproduction of Daphnia magna (Schafers 2005).
C15: Measured 21-d EC10 value of 0.012 mg/l based on reproduction of Daphnia magna (Schafers 2005).
The extremely rapid biodegradation of aliphatic alcohols means that it is very difficult to maintain exposure concentrations during long-term tests. Even when measures were undertaken to prevent loss of test substance during testing, significant losses still occurred.
Toxicity to microorganisms
There are no data available for toxicity of alcohols C12-C15 branched and linear to microorganisms. The study does not need to be conducted because the needs associated with a sound understanding of toxicity to microorganisms are adequately met by the available data on constituents. In view of the ready biodegradability, further information is not required in REACH. A data waiver is in place for the activated sludge respiration inhibition as the substance is readily biodegradable and the applied test concentrations are in the range that can be expected in the influent to a sewage treatment plant.
Discussion of trends in the Category of C6-24 linear and essentially-linear aliphatic alcohols:
Many short-term aquatic toxicity tests have been carried out on this family of long chain aliphatic (LCAAs), addressing toxicity to organisms from three trophic levels; fish, invertebrates and algae. For studies in which the test substance had a single carbon chain length, a key study has been identified for each taxonomic level. Where there were two or more reliable studies of the same quality but on different species within the same taxonomic group, the lower toxicity value (highest level of toxicity) was chosen. For studies in which the test substance was a multi-constituent LCAAs (commercial products) and where there was more than one type of the substance a key study was identified for each type.
The results of short-term tests performed on single carbon chain length LCAAs are generally reported in terms of the nominal or measured dissolved concentration of the alcohol in the test medium and are identified as EC50 or LC50 values. However there are also instances where the reported effect concentration exceeded the solubility of the LCAA. These instances are distinguished in the results tables either by the result being reported as an LL50 or EL50, implying that the test medium was a water accommodated fraction (WAF), or by a note indicating that the test substance loading exceeded the solubility of the LCAA. In the latter case it has had to be assumed (because it is not apparent from the test report) that undissolved LCAA may have been present in the test medium and that there was the potential for physical (rather than toxicity) effects to occur.
For studies using multi-constituent substances it is possible to interpret the results on the basis of measured dissolved concentrations of the LCAA constituents but they cannot be directly related to the concentration of the multi-constituent substance itself. This is because the test medium does not contain dissolved concentrations of the constituents in the same ratio as present in the substance itself. The toxicity data for mixed carbon chain length LCAAs are therefore also expressed using different conventions. Where the effect concentrations occurred at concentrations below the solubility limit of a multi-constituent substance they are reported as nominal or measured concentrations and are again identified as EC50 or LC50 values. In cases where the test media were WAFs, or where the loading of a multi-constituent substance exceeded the solubility of one or more of its constituents, the result is reported either as an LL50 or EL50, denoting that the test medium was a Water Accommodated Fraction (WAF), or by a note indicating that the test substance loading exceeded the solubility limit of the multi-constituent substance. Once again in the latter case it has had to be assumed (because it is not apparent from the test report) that undissolved LCAA may have been present in the test medium and that there was the potential for physical (rather than toxicity) effects to occur.
In the environmental fate and pathways section it was highlighted that biodegradation is likely to be a significant loss mechanism from aquatic media for the LCAAs under review. If loss of test substance from aquatic test media is significant it will undermine the results of tests where analysis of exposure was not performed. For example, exposure concentrations of 1-octanol (No. 111-87-5) in a 7-day test with the fathead minnow (Pimephales promelas) declined by >90% in the unspecified period between media renewals (Pickering et al., 1996). However the NOEC has been expressed relative to nominal concentrations and must represent a significant overestimate of the true value and therefore an underestimate of the true toxicity. Similarly, the exposure concentration of the same substance that corresponded to the NOEC determined in a 21-day semi-static long-term test with Daphnia magna, declined by >35% over the 3-4 day period between media renewals (Kuhn et al., 1989). This suggests that exposure concentrations, expressed as nominal values, would have significantly overestimated the actual concentrations. The above examples highlight that test results expressed only in terms of nominal concentrations must be treated with considerable caution and may underestimate the toxicity of the substance.
Trends in results, described in this section, are supported by reliable measured data for branched LCAAs which are members of the Oxo Alcohols Category. For full details please refer to the Oxo alcohols SIAR and SIDS dossiers.
Where there were no available data for a linear LCAA the data has been read-across (see CSR section 1.4) from reliable data for the closest linear alcohols with a smaller carbon chain length.
For multi-constituent substances lacking measured short-term toxicity data, the data has been read-across from the major constituent linear LCAAs in cases where these formed >90% of the multi-constituent substance. This approach is deemed valid because it is considered very unlikely that the minor constituents present at <10% will contribute significantly to short-term effects. This approach has not been adopted for long-term toxicity data because here the potential for the minor constituents to contribute to effects is much greater.
In the absence of suitable read-across data for linear and multi-constituent LCAAs, validated QSAR methods have also been developed to fill data gaps for short-term toxicity to fish and invertebrates. QSARs for linear alcohols have also been developed to fill data gaps for long-term toxicity to invertebrates.
References:
Kuhn, R., Pattard, M., Pernak, K., and Winter, A. (1989). Results of the harmful effects of water pollutants to Daphnia magna in the 21 day reproduction test. Wat. Res. 23(4): 501-510.
Pickering, Q.H., Lazorchak, J.M., and Winks, K.L. (1996). Subchronic sensitivity of one-, four-, and seven-day-old fathead minnow (Pimephales promelas) larvae to five toxicants. Environ. Toxicol. Chem. 15(3): 353-359.
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