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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Ecotoxicological information

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