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EC number: 229-554-3 | CAS number: 6607-34-7
- 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
Toxicity to microorganisms
Administrative data
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1999-11-23
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 999
- Report date:
- 1999
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- GLP compliance:
- yes
Test material
- Reference substance name:
- 2,3,7,8-tetrahydro-2,5,8-benzotrioxacycloundecine-1,9-dione
- EC Number:
- 229-554-3
- EC Name:
- 2,3,7,8-tetrahydro-2,5,8-benzotrioxacycloundecine-1,9-dione
- Cas Number:
- 6607-34-7
- Molecular formula:
- C10H16O5
- IUPAC Name:
- 1,4,7-Trioxacyclotridecane-8,13-dione
- Details on test material:
- - Name of test material (as cited in study report): Adipic acid, Cyclicester with diethylenglycol
- Analytical purity: ca. 90%
- Impurities (identity and concentrations): Diethylenglycol < 10% ; water< 2%
- Purity test date: Report of the sponsor of 18 Feb. 1999
- Lot/batch No.: B47
Constituent 1
Sampling and analysis
- Analytical monitoring:
- no
Test solutions
- Vehicle:
- no
Test organisms
- Test organisms (species):
- activated sludge, domestic
- Details on inoculum:
- - Preparation of inoculum for exposure: The inoculum was washed, brought to a concentration of 5 g/l dry substance and aerated for 24 hours.
- Initial biomass concentration: 50 ml were added to a total volume of 250 ml to obtain a concentration of 1 g/I dry substance in the test.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 30 min
Test conditions
- Test temperature:
- 20 ± 2°C
- pH:
- 7.1-7.2 at test start, 7.3 at test end
- Dissolved oxygen:
- - Oxygen concentration during aeration: >2.5 mg/I
- Oxygen concentration immediately before measurement: >6.5 mg/I - Nominal and measured concentrations:
- 1000 mg/l, in addition a blanc control and a reference control were tested
- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): open
- Material, size, headspace, fill volume: glass, Erlenmeyer-flask (250 ml nominal), liquid volume: 250 ml
- Aeration: sparged with air
- No. of vessels per concentration (replicates; test substance, TS): 1
- No. of vessels per control (replicates; blanc, BC): 3
- No. of vessels per concentration (replicates; positive control, reference substance, RS): 3
TEST MEDIUM / WATER PARAMETERS
- Culture medium: OECD test medium
OTHER TEST CONDITIONS
- Adjustment of pH: no pH adjustments during test
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
O2: on line measurement for 6 min
pH: at test start and test end
- Reference substance (positive control):
- yes
- Remarks:
- 3.5-dichlorophenol (CAS 591-35-5)
Results and discussion
Effect concentrations
- Duration:
- 30 min
- Dose descriptor:
- other: EC20
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Results with reference substance (positive control):
- - Results with reference substance valid? Yes
- Relevant effect levels: EC20 (30 min): 2.2 mg/L (nominal); EC50 (30 min): 6.5 mg/L (nominal); EC80 (30 min): 55 mg/L (nominal)
Any other information on results incl. tables
The EC20 in the activated sludge respiration inhibition test is >1000 mg/l. The inhibition of the degradation activity of activated sludge is not anticipated when introduced in appropriate low concentrations.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Remarks:
- Deviation of blank controls < 15 %; EC50 of 3,5-dichlorophenol in the range of 5-30 mg/I
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