Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
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: 202-571-3 | CAS number: 97-30-3
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2017-03-09 to 2017-05-10
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Version / remarks:
- (1992)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-D (Determination of the "Ready" Biodegradability - Manometric Respirometry Test)
- Version / remarks:
- 30 May, 2008
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): sewage treatment plant Ruhrverband Kläranlage, Sunthelle 6, 57392 Schmallenberg, Germany,
- Laboratory culture: after the arrival at the laboratory kept aerobic until use
- Storage length: freshly prepared
- Preparation of inoculum for exposure: The sludge was left for settlement for ca. one hour. Subsequently the supernatant was discarded and the concentration of suspended solids was measured in the remaining sludge. The concentration was adjusted to 3.2 g/L and verified by dry mass measurement. The concentration used in the test was 29.6 mg dry mass/liter (7.4 mg dry mass/250 mL).
- Water filtered: no, deionized water was used which was free from inhibitory concentrations of toxic substances - Duration of test (contact time):
- 28 d
- Initial conc.:
- 100 mg/L
- Based on:
- test mat.
- Initial conc.:
- 48 mg/L
- Based on:
- test mat.
- Initial conc.:
- 123 mg/L
- Based on:
- ThOD
- Initial conc.:
- 59 mg/L
- Based on:
- ThOD
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- TEST CONDITIONS
- Composition of medium:
( a ) KH PO4 8.50 g/L
K2HPO4 21.75 g/L
Na2HPO4 26.64 g/L
NH4Cl 0.50 g/L
pH 7.4 ± 0.2
( b ) CaCl2 x 2 H2O 36.40 g/L
( c ) MgSO 4 x 7 H2O 22.50 g/L
( d ) FeCl3 x 6 H2O 0.25 g/L.
The mineral medium applied in the test contained 10 mL/L of mineral stock solution a and 1 mL/L of the mineral stock solution b–d, respectively.
- Test temperature: 22°C ± 1°C
- pH: 7.4 ± 0.2
- pH adjusted: yes
- Suspended solids concentration: 29.6 mg dry mass/L
- Continuous darkness: yes
TEST SYSTEM
- Culturing apparatus: 500 mL glass vessels at a medium volume of 250 mL
- Number of culture flasks/concentration: 2
- Measuring equipment: The measurement and recording of the oxygen demand was carried out continuously using a SAPROMAT respirometer (VOITH Inc.)
- Test performed in closed vessels: yes
CONTROL AND BLANK SYSTEM
- Inoculum blank: inoculated mineral medium only
- Toxicity control: test item at 100 mg per liter and reference item (sodium benzoate) at 100 mg per liter mineral test medium (25 mg test item/250 mL and 25 mg reference item/250 mL)
- Procedural control: Vessels containing the reference item (sodium benzoate, 100 mg/L) and inoculum - Reference substance:
- benzoic acid, sodium salt
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 77.3
- St. dev.:
- 4
- Sampling time:
- 14 d
- Remarks on result:
- other: Test suspension A (100 mg/L)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 83
- St. dev.:
- 3.6
- Sampling time:
- 14 d
- Remarks on result:
- other: Test suspension B (48 mg/L)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 71.3
- St. dev.:
- 5.9
- Sampling time:
- 14 d
- Remarks on result:
- other: Toxicity control
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 86.2
- St. dev.:
- 3.5
- Sampling time:
- 28 d
- Remarks on result:
- other: Test suspension A (100 mg/L)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 83
- St. dev.:
- 2.4
- Sampling time:
- 28 d
- Remarks on result:
- other: Test suspension B (48 mg/L)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 82.9
- St. dev.:
- 6.8
- Sampling time:
- 28 d
- Remarks on result:
- other: Toxicity control
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 72.4
- Sampling time:
- 12 d
- Remarks on result:
- other: Test suspension A (100 mg/L)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 78.8
- Sampling time:
- 12 d
- Remarks on result:
- other: Test suspension B (48 mg/L)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 68.3
- Sampling time:
- 12 d
- Remarks on result:
- other: Toxicity control
- Details on results:
- The biodegradation of the test item after 28 days of incubation in the static test was found to be 86 % (SD = 3.5 %) and 83 % (SD = 2.4 %) in the assays with 100 mg/L and 48 mg/L, respectively. The biodegradation within the 10-day-window was 72 % and 81 % in the assays with 100 mg/L and 48 mg/L, respectively. The 10-day-window started at day 2, independent from test item concentration.
The biodegradation of the item mixture in the toxicity control was found to be 71 % after 14 days of incubation. Thus, the demanded threshold value of 25 % is exceeded and the test item can be identified as non-toxic in a ready biodegradability test. The reference item sodium benzoate was degraded to 85 % within the first 14 days. - Results with reference substance:
- The reference item sodium benzoate was degraded to 85 % within the first 14 days. The 10-day-window started at day 2 and the O2 consumption of the reference item was 82.9% at day 12.
- Validity criteria fulfilled:
- yes
- Remarks:
- Validity criteria as specified in guideline were fulfiled, see "any other information on material and methods"
- Interpretation of results:
- readily biodegradable
- Conclusions:
- In the present study according to OECD guideline 301F (1992) alpha methyl glucoside was incubated with activated sludge for 28 days. During that period the oxygen consumption of the inoculum was measured. At day 14 both concentrations (100 and 48 mg test item) exhibited a mean oxygen consumption of 77.3 and 83.0 %, respectively. After 28 days the respective degradation was 86.2 and 83.0%. Thus, the degradation of the substance is > 60% within the 10-days window after achieving 10% degradation. Hence, the test item is considered to be readily biodegradable.
- Executive summary:
The biodegradation in water of alpha methyl glucoside was studied in unfiltered activated sludge (adjusted to pH 7.4, dissolved organic carbon: 3.2%) from the sewage treatment plant Ruhrverband Kläranlage, Schmallenberg, Germany for 28 days under aerated conditions in the dark at 22 °C ± 1°C. The test material was applied at the concentrations of 100 mg and 48 mg/L, equivalent to 123 mg and 59 mg ThOD.
The experiment was conducted in accordance with the OECD guideline 301F (1992) and in compliance with the OECD GLP standards. The test system consisted of 500 mL glass vessels at a medium volume of 250 mL, attached with traps for the collection of CO2 and volatile organic compounds. Samples were analysed at 14 and 28 days of incubation.
For both concentrations ( 100 and 48 mg/L) the mean degradation (oxygen consumption) was 77.3 and 83.0 %, respectively, after 14 days and 86.2 and 83.0% after 28 days. The mean degradation in water of the reference item sodium benzoate at a concentration of 100 mg/L was 85.0 % after 14 days and 88.3 % after 28 days. Based on these results the test was considered valid and the test item was regarded as readily biodegradable.
Reference
Description of key information
- readily biodegradable, OECD TG 301F, GLP, RL1, 77 .3 and 83.0 % degradation for 100 and 48 mg/L, respectively, within the 10 -days-window
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
- Type of water:
- freshwater
Additional information
The biodegradation in water of alpha methyl glucoside was studied in unfiltered activated sludge (adjusted to pH 7.4, dissolved organic carbon: 3.2%) from the sewage treatment plant Ruhrverband Kläranlage, Schmallenberg, Germany for 28 days under aerated conditions in the dark at 22 °C ± 1°C. The test material was applied at the concentrations of 100 mg/L and 48 mg/L, equivalent to 123 mg and 59 mg ThOD.
The experiment was conducted in accordance with the OECD guideline 301F (1992) and in compliance with the OECD GLP standards. The test system consisted of500 mL glass vessels at a medium volume of 250 mL, attached with traps for the collection of CO2 and volatile organic compounds. Samples were analysed at 14 and 28 days of incubation.
For both concentrations (100 and 48 mg/L) the mean degradation (oxygen consumption) was77.3 and 83.0 %, respectively, after 14 days and 86.2 and 83.0% after 28 days. The mean degradation in water of the reference item sodium benzoate at a concentration of 100 mg/L was 85.0 % after 14 days and 88.3 % after 28 days. Based on these results the test was considered valid and the test item was regarded as readily biodegradable.
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.