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Diss Factsheets
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EC number: 942-252-2 | 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
Endpoint summary
Administrative data
Description of key information
Short-term toxicity to fish
The acute toxicity to the zebra fish Danio rerio of the REACH substance "Stearic acid, reaction product with 2-aminoethanol, maleic anhydride and sodium sulfite" (UVCB) was investigated in a GLP-compliant study performed according to OECD Guideline 203. Up to and including the limit test concentration (100% filtrate of a saturated solution at a loading rate of 398.4 mg test item/L equivalent to 100 mg active ingredients/L), no mortalities were observed during the 96-hour exposure period. Therefore, it can be concluded that the LC50 (96 h) to fish based on nominal concentrations is higher than 398.4 mg test item/L, equivalent to 100 mg active ingredients/L.
Short-term toxicity to aquatic invertebrates
The acute toxicity to the water flea Daphnia magna of the REACH substance "Stearic acid, reaction product with 2-aminoethanol, maleic anhydride and sodium sulfite" (UVCB) was investigated in a GLP-compliant study performed according to OECD Guideline 202. No clear concentration-response relationship was observed between the control and the saturated solutions at loading rates of 398.4, 199.2, 99.6, 49.8 and 24.9 mg test item/L, equivalent to 100, 50, 25, 12.5 and 6.3 mg active ingredients/L. No considerable effect was found up to and including the highest concentration tested. It is therefore concluded that the EC50 is higher than 398.4 mg test item/L ,equivalent to 100 mg active ingredients/L.
Toxicity to aquatic algae
The toxicity to the green algaRaphidocelis subcapitata(former name:Pseudokirchneriella subcapitata) of the REACH substance "Stearic acid, reaction product with 2-aminoethanol, maleic anhydride and sodium sulfite" (UVCB) was investigated in a GLP-compliant study performed according to OECD Guideline 201. A clear concentration-response relationship was observed for the biological parameters yield and growth rate during the exposure period.
The ErC50 ofRaphidocelis subcapitatawas stated to be >504 mg test item/L (statistically evaluated value: 708 mg test item/L, equivalent to 177.7 mg active ingredients/L) based on nominal concentrations. The ErC10 was evaluated to be 4.52 mg test item/L (equivalent to 1.13 mg active ingredients/L). The NOEC based on nominal concentration appeared to be lower than 0.960 mg test item/L (equivalent to 0.242 mg active ingredients/L).
The EyC50 ofRaphidocelis subcapitatawas stated to be 6.99 mg test item/L (equivalent to 1.75 mg active ingredients/L) based on nominal concentrations. The EyC10 was evaluated to be 0.20 mg test item/L (equivalent to 0.05 mg active ingredients/L). The NOEC based on nominal concentration appeared to be lower than 0.960 mg test item/L (equivalent to 0.242 mg active ingredients/L).
Toxicity to activated sludge bacteria
The effect of the REACH substance "Stearic acid, reaction product with 2-aminoethanol, maleic anhydride and sodium sulfite" (UVCB) on the respiration rate of activated sludge bacteria was investigated in a GLP-compliant study performed according to OECD Guideline 209. The respiration rate of the test system was measured after a 3-hour contact period with the test item. The effect of the test item on the respiration of nitrifying bacteria was investigated in a preliminary non-GLP range-finding test.
The preliminary non-GLP range-finding test including a nitrification inhibition control showed no inhibition of total respiration at up to 1000 mg test item/L (equivalent to 251 mg active ingredients/L); an inhibition of nitrification-related respiration was not observed in the range-finding test. The definitive test showed no concentration-response relationship with no inhibition of total respiration rate compared to the control respiration at up to 1000 mg test item/L. A supplemental test was performed at 1000, 2000 and 4000 mg test item/L to investigate potential effects on the respiration rate at 2000 and 4000 mg test item/L, and to confirm the absence of effects on the respiration rate at 1000 mg test item/L as seen in the definitive test. This supplemental test showed no inhibition of total respiration. The results of this study show that the EC20, EC50, EC80 are > 4000 mg test item/L (equivalent to 1004 mg active ingredients/L).
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.
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