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EC number: 500-018-3 | CAS number: 9005-64-5 1 - 6.5 moles ethoxylated
- 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
Justification for grouping of substances and read-across
There are no data available for the Terrestrial toxicity of Sorbitan monolaurate, ethoxylated (CAS 9005-64-5). In order to fulfil the standard information requirements set out in Annex X, X.X, in accordance with Annex XI, 1.5, of Regulation (EC) No 1907/2006, read-across from structurally related substances was conducted.
In accordance with Article 13 (1) of Regulation (EC) No 1907/2006, "information on intrinsic properties of substances may be generated by means other than tests, provided that the conditions set out in Annex XI are met.” In particular for human toxicity, information shall be generated whenever possible by means other than vertebrate animal tests, which includes the use of information from structurally related substances (grouping or read-across).
Having regard to the general rules for grouping of substances and read-across approach laid down in Annex XI, Item 1.5, of Regulation (EC) No 1907/2006 whereby substances may be predicted as similar provided that their physico-chemical, toxicological and ecotoxicological properties are likely to be similar or follow a regular pattern as a result of structural similarity.
The ecotoxicological parameters for terrestrial toxicity are presented in the table below.
Table 2. Ecotoxicological parameters for terrestrial toxicity
CAS No. |
Soil macroorganisms |
Terrestrial arthropods |
Terrestrial plants |
Soil microorganisms |
Target substance |
||||
9005-64-5 |
RA: CAS 91844-53-0 RA: CAS 26266-58-0 |
Waiving |
Waiving |
WoE |
Source substances |
||||
91844-53-0 |
LC50 (14d) > 1000 mg/L |
Waiving |
Waiving |
WoE |
26266-58-0 |
LC50 (14d) > 1000 mg/L |
Waiving |
Waiving |
WoE |
Terrestrial toxicity
In absence of a clear indication of selective toxicity towards a specific group of organisms, terrestrial toxicity of Sorbitan esters was tested on the earthworm Eisenia fetida, as recommended by the “Guidance on information requirements and chemical safety assessment Chapter R.7c: Endpoint specific guidance” (ECHA, 2012). No studies are available for terrestrial arthropods, terrestrial plants or soil microorganisms. However, since Sorbitan esters are mainly poorly soluble in water and have potential to adsorb to solid soil particles, a soil dwelling organisms, such as the earthworm, which is exposed to the complete soil system via both dermal and oral uptake, is the most relevant test organism to evaluate the terrestrial toxicity of these substances.
Studies according to the OECD Guideline 207 were conducted with the read-across substances Sorbitan, octanoate (2:3) (CAS No. 91844-53-0) and Anhydro-D-glucitol trioleate (CAS No. 26266-58-0), and no mortality occurred during the 14 day exposure period with none of the two substances. Sorbitan, octanoate (2:3) is smaller than the target substance and represents a worst case in terms of bioavailability from pore water. Anhydro-D-glucitol trioleate is larger and has a higher adsorption potential based on Koc and a higher log Kow. It thus represents a worst case for uptake via soil particle bound substance. Since no effects were observed for any of the two substances, there is no reason to expect effects for Sorbitan monolaurate, ethoxylated, and the data gap can be covered by interpolation.
The earthworm studies indicate that the toxicity of Sorbitan monolaurate, ethoxylated to terrestrial organisms is low. Moreover, the substance is expected to be metabolised by organisms after ingestion, which is probably the main uptake route. Esters are known to hydrolyse into carboxylic acids and alcohols by esterases (Fukami and Yokoi, 2012). Carboxylesterase activity has been noted in a wide variety of tissues in invertebrates as well as in fish (Leinweber, 1987; Suldano et al, 1992; Barron et al., 1999, Wheelock et al., 2008). Therefore, it is expected that under physiological conditions, Sorbitan monolaurate, ethoxylated will hydrolyse to D-glucitol and the respective fatty acids. The hydrolysis of Sorbitan fatty acid esters occurs within a maximum of 48h for mono-, di- and tri-ester (Croda 1951, Mattson and Nolen 1972, Treon 1967, Wick and Joseph 1953). The resulting fatty acids are either metabolised via the β-oxidation pathway in order to generate energy for the cell or reconstituted into glyceride esters and stored in the fat depots in the body (Berg, 2002). The first step of D-glucitol metabolism involves oxidation by L-iditol dehydrogenase to fructose, which is metabolised by the fructose metabolic pathway (Senti, 1986). D-glucitol is naturally found in several berries and fruits as well as in seaweed and algae (FDA, 1972), and is thus naturally present in the terrestrial environment. The ethoxylation is not expected to significantly increase the toxicity of D-glucitol. Using the OECD toolbox Vs. 2.3, the liver metabolism simulator provided 42 potential metabolites indicating that the ethoxylated part of the substance remains intact. Studies on genotoxicity (Ames test, chromosomal aberration and gene mutation in mammalian cells) were negative, indicating no reactivity of the test substance or its metabolites under the test conditions. Additionally, Sorbitan monolaurate, ethoxylated is readily biodegradable and is thus expected to be rapidly removed from the terrestrial environment by soil microorganisms.
Furthermore, the aquatic studies indicate no hazard. In the acute studies with Sorbitan monolaurate, ethoxylated, an EC50 values above 10 mg/L were obtained. Such aquatic data can be used as an indicator for potential effects on soil organisms (ECHA, 2012), and in the case of Sorbitan monolaurate, ethoxylated effects are not to be expected. Furthermore, the chronic study with Daphnia magna, available for Sorbitan monolaurate, ethoxylated, resulted in a NOEC > 1 mg/L.
Moreover, no effects were observed in the long-term study with Daphnia magna up to a loading rate of 10 mg/L. Acute aquatic EL50 values were > 10 mg/L or above the water solubility limit of the substance.
Based on the available information, i.e. very low toxicity to earthworm and to aquatic organisms, rapid metabolism and ready biodegradation, short- and long-term effects on terrestrial organisms are very unlikely. Consequently, no further testing is proposed.
References:
Barron, M.G., Mayes, M.A., Murphy, P.G., Nolan, R.J. (1990): Pharmacokinetics and metabolism of triclopyr butoxyethyl ester in coho salmon. Aquatic Tox., 16, 19-32.
Berg, J.M., Tymoczko, J.L. and Stryer, L. (2002) Biochemistry, 5th edition, W.H. Freeman and Company
Croda (Atlas Powder Company), 1951-12-20: Effect in vitro of pancreatic lipase on the following: Tween 60, 65, 80, Myrj 45, 52, Span 60 (WER-149-329, 1951-12-20)
ECHA (2012), Guidance on information requirements and chemical safety assessment. Chapter R.7c: Endpoint specific guidance, European Chemicals Agency, Helsinki.
FDA (1972): Study of the mutagenic effects of Sorbitol. Report No PB 221816, U.S. Food and Drug Administration, Washington, USA
Fukami and Yokoi (2012). The Emerging Role of Human Esterases. Drug Metabolism and Pharmacokinetics, Advance publication July 17th, 2012.
Leinweber, F.J. (1987): Possible physiological roles of carboxylic ester hydrolases. Drug. Metab. Rev. 18: 379-439.
Mattson, F.H. and Nolen, G.A., 1972: Absorbability by rats of compounds containing from one to eight ester groups. J Nutrition, 102: 1171-1176
Senti, F.R. 1986. Health aspects of sugar alcohols and lactose. Contract No. 223-83-2020, Center for food safety and applied nutrition, Food and Drug Administration, Dept. of Health and Human Services, Washington, DC 20204, USA
Soldano, S., Gramenzi, F., Cirianni, M., Vittozzi, L. (1992): Xenobiotic-metabolizing enzyme systems in test fish - IV. Comparative studies of liver microsomal and cytosolic hydrolases. Comparative Biochemistry and Physiology Part C: Comparative Pharmacology. 101(1), 117-123.
Tocher, D.R. (2003):Metabolism and function of lipids and fatty acids in teleost fish,Reviews of Fisheries Science, 11 (2), 197
Treon J.F. et al., 1967: Physiologic and metabolic patterns of non-ionic surfactants: Chem. Phys. Appl. Surface Active Subst., Proc. Int. Congr., 4th, 1964, 3, 381-395. Edited by Paquot, C., Gordon Breach Sci. Publ., London, England
Wheelock, C.E., Phillips, B.M., Anderson, B.S., Miller, J.L., Hammock, B.D. (2008): Applications of carboxylesterase activity in environmental monitoring and toxicity identification evaluations (TIEs). Reviews in Environmental Contamination and Toxicology 195:117-178.
Wick A.N. and Joseph L. (1953): The metabolism of Sorbitan monostearate. Food Research, 18, 79
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