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EC number: 203-794-9 | CAS number: 110-71-4
- 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
BIODEGRADATION IN WATER: SCREENINGTESTS
The primary and inherent biodegradability were determined in the Zahn-Wellens-Test / EMPA Test with a non adapted activated sludge for the test itemMonoethylenglykoldimethylether over a period up to 48 days. The study was conducted from 2010-05-05 to 2010-06-22 according to OECD 302 B at Dr. U. Noack-Laboratorien.
For the determination of the primary biodegradation the test item was tested at a concentration of 600 µg/L in duplicates. The primary biodegradation was determined by SPME GC/MS analysis of the test item. For the determination of the inherent biodegradation the test item was tested at a concentration of 95 mg/L in duplicates, corresponding to a DOC of 50.4mg C/L in the test vessel. The inherent biodegradation of the test item was followed by determination of DOC. The ratio of eliminated DOC, corrected for the control at each time interval to the initial DOC value is expressed as the percentage biodegradation at each sampling date.
The physico-chemical elimination (volatilisation) of the test item was monitored in separate sterile controls. At the test item concentration of 95 mg/L a sterile control without inoculum and poisoned with HgCl2was used. For determination of the primary biodegradation sterile controls (with inoculum and poisoned with HgCl2) with a test item concentration of 300 µg/L and 600 µg/L were tested. No physico-chemical elimination (volatilistion) occurred in the sterile controls at 95 mg/L until test end. At the concentration 300 µg/L and 600 µg/L the physico-chemical elimination (volatilisation) was in the range 29 - 34% on day 7. Until test end the mean volatilisation reached a maximum of 37 %.
The primary and inherent biodegradability of the test item in comparison to the degradable functional control and the elimination in the sterile controls is given in the Table below.
For the calculation of the primary biodegradation, the concentration of the test item replicates was corrected for the mean elimination of the sterile control values. The primary degradation started after a long lasting adaptation phase of 39 days. The course of the biodegradation was slow and on day 48 a biodegradation of only 14 % was reached.
The inherent degradation started after a long lasting adaption phase of 26 days. The course of the biodegradation was slow and the biodegradation did not reach the 70 % pass level. After 48 days a biodegradation of 16 % was reached.
Primary and inherent Biodegradability of the Test Item Monoethylenglykoldimethylether in Comparison to the Functional Control and the Sterile Control
Primary and inherent Biodegradation / Elimination [%] | |||||||
Replicate | 7 | 14 | 21 | 26 | 28 | 35 | 48 |
test item 95 mg/L | 5 | 1 | 3 | 10 | 11 | 12 | 16 |
functional control 120 mg/L | 99 | 97 | 100 | 100 | 100 | 98 | 100 |
Sterile control1) 95 mg/Ltest item | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
Test item2) 600 µg/L | -7 | -1 | 2 | - | 5 | - | 14 |
Sterile control1) 300 µg/L test item | 34 | 28 | 22 | - | 38 | - | 37 |
Sterile control1) 600 µg/L test item | 29 | 31 | 46 | - | 35 | - | 36 |
This is supported by two other screening tests (OECD 302B) which shows also no inherent Biodegradability under the test conditions.
BIODEGRADATION IN WATER: SCREENING TESTS
Monoglyme is neither readily nor inherently biodegradable. Stripping from aqueous solution is considerable (almost complete loss from an aqueous solution with 5 g/l Monoglyme during 24 h) which is important for the loss in Sewage treatment plants. It is not expected that the DT90 of Monoglyme in an OECD 308 or 309 would indicate a rapid biodegradation in sediment and surface water e.g. < 100 d. Due to the fact that Monoglyme is classified R62 strict risk reduction measures have to be applied which means that release to the environmental compartments have to be minimized. Based on these facts the simulation tests according OECD 308 and 309 are not warranted.
BIODEGRADATION IN SOIL
The US EPA property estimation program KOCWIN V2.00 calculates for the Koc of Monoglyme 2.4 L/kg (Molecular Connectivity Index) or 4.2 L/kg (beased on Log Kow of -0.21. Due to the low estimated Koc of Monoglyme a transfer to agricultural soil via sewage sludge can be neglected. Indirect exposure via deposition from air is unlikely as Monoglyme is readily photodegrated in air. Because of the low soil exposure by Monoglyme a soil biodegradation study is not warranted. The statement given above fulfills the requirement for waiving as given in 1907/2006/EC Annex IX, Column 2, 9.2.1.3: "The study need not be conducted if direct and indirect exposure of soil is unlikely."
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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