Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 213-561-3
CAS number: 980-26-7
The abiotic degradation of the substance cannot be determined, because there are no functional groups present in the molecule which could undergo hydrolytic cleavage in aqueous media (e.g. ester, ether or amide functions). Therefore, the study is scientifically not necessary.
In addition, the pigment is practically not soluble in water (water solubility: 5.6 µg/L)
Nevertheless, for the test item, the potential for hydrolytic degradation had been tested according to OECD-guideline for testing of chemicals no. 111 and E.U-method C.7 according to GLP (reliability category 1).
The test could not proceed further as to the first recovery-experiments after preparation of the buffered solutions of the test substance. In spite of trying 4 different co-solvents to increase dissolution of the test item in the buffer solutions all the resulting solutions were too dilute to be detectable by analytics based on HPLC/UV-Vis-spectroscopy after chemical derivatization (LOQ about 0.007 µg/mL).
Therefore, solubility of the test item in buffered solutions is far too low to allow for testing of the potential for hydroyltic degradation.
Biodegradation, screening tests
The ready biodegradability in the Manometric Respirometry Test was determined with a non adapted activated sludge for the test item over a period of 28 days. The study was conducted from 2006-06-20 to 2006-07-18 according to OECD guideline 301 F at DR.U.NOACK-LABORATORIEN, D-31157 Sarstedt. The test item concentration selected as appropriate was 40 mg/L, corresponding to a ThOD of 87.2 mgO2/L in the test vessel. The oxygen was depleted by the respiration of bacteria and the degradation was followed by measuring the oxygen concentration. The biodegradation is therefore expressed as the percentage BOD and was calculated for each study day.
The mean oxygen depletion in the inoculum control came to 33.8 mgO2/L after 28 days. In order to check the activity of the test system sodium benzoate was used as functional control. The pass level > 60 % was reached after 3 days. The biodegradation rate came to 92 % after 28 days.
In the toxicity control containing both test and reference item 39 % degradation occurred within 14 days. The degradation of the reference item was not inhibited by the test item.
The 10 % level (beginning of biodegradation) was not reached until 28 days. The mean biodegradation remained at 0 %.
The validity criteria of the guideline are fulfilled.
The test item must be regarded as not readily biodegradable in the 10-d-window and after 28 days.
In addition, a biodegradation test with a read across substance is available with the same result.
In a ready biodegradability test based upon CO2-evolution (reliability category 1, compliant to GLP) no biodegradation could be observed at the end of the test period (28 days). The reference substance (sodium benzoate) was thoroughly degraded at day 28 and to 79% at day 14 proving the suitability of the activated sludge used. On the other hand, lack of biodegradation was not caused by toxicity of the test item as the toxicity control with both, the test item and the reference substance, showed no inhibition compared to the procedural controls with the reference substance only.
Biodegradation, simulation tests
The testing of biodegradation in water: simulation testing on ultimate degradation in surface water was waived according to "column 2" in Annex IX of REGULATION (EC) No 1907/2006 (CSA does not indicate need for further investigations. Substance considered to be not readily biodegradable, no further relevant information expected from additional testing) In addition the substance is hig´hly insoluble in water.
Regarding sediment simulation testing a second waiver is available, because the substance is not supposed to be directly applied to sediment. Based on the PC properties of the substance (extremely low solubility in water and octanol), a low adsorption potential is indicated. As a consequence, a binding/transfer to sediment is not expected. Therefore, it can be assumed that there is no direct and indirect exposure to the sediment
In addition there the test was waived according to "column 2" in Annex IX of REGULATION (EC) No 1907/2006 (CSA does not indicate need for further investigations. Substance considered to be not readily biodegradable, no further relevant information expected from additional testing)
Biodegradation in soil
The substance is not supposed to be directly applied to soil. Based on the PC properties of the substance (extremely low solubility in water and octanol), a low adsorption potential is indicated. Therefore, binding to sewage sludge is unlikely and as a consequence a transfer to the soil compartment is not expected. Therefore, it can be assumed that there is no direct and indirect exposure to the environment
In addition, the test is waived according to "column 2" in Annex IX of REGULATION (EC) No 1907/2006 (CSA does not indicate need for further investigations. Substance considered to be not readily biodegradable, no further relevant information expected from additional testing)
The study is scientifically not necessary and does not to be conducted because the substance has a low potential for bioaccumulation based on a log Kow < 3.
The study does not need to be conducted because substance has a low octanol water partition coefficient and the adsorption potential of this substance is related to this parameter.
Nevertheless, the estimation of the adsorption coefficient Koc of a read across substance had been applied according to the OECD Guideline 121
The poor solubility of the test item in water as well as in other solvents precluded the deduction of useful results. Using different solvent mixtures, partial dissolution of the test item had been possible. Elution from the HPLC-column, however, proved to be impossible in spite of different solvent systems used. Most probably, the test item had precipitated on the column. Therefore, Koc for the test item cannot be determined using the estimation method based on HPLC.
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.Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
På den här webbplatsen används kakor. Syftet är att optimera din upplevelse av den.
Welcome to the ECHA website. This site is not fully supported in Internet Explorer 7 (and earlier versions). Please upgrade your Internet Explorer to a newer version.
Do not show this message again