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EC number: 221-221-0 | CAS number: 3033-77-0
- 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 and sediment: simulation tests
Administrative data
- Endpoint:
- biodegradation in water: sewage treatment simulation testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2005-07-01 to 2005-09-30
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to the appropriate OECD test guideline and in compliance with GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 006
- Report date:
- 2006
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 303 A (Simulation Test - Aerobic Sewage Treatment. A: Activated Sludge Units)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 2,3-epoxypropyltrimethylammonium chloride
- EC Number:
- 221-221-0
- EC Name:
- 2,3-epoxypropyltrimethylammonium chloride
- Cas Number:
- 3033-77-0
- Molecular formula:
- C6H14NO.Cl
- IUPAC Name:
- N,N,N-trimethyl(oxiran-2-yl)methanaminium chloride
- Details on test material:
- - Name of test material (as cited in study report): 2,3-epoxypropyltrimethylammonium chloride
- Physical state: Liquid
- Analytical purity: 73.1%
- Impurities (identity and concentrations): 1.4% 3-chloropropryltrimethylammonium chloride (CHPTAC); 19 mg/kg total other impurities; remainder water
- Purity test date: 2005-03-31
- Lot/batch No.: 153897
- Expiration date of the lot/batch: September 2005
- Stability under test conditions: Hydrolyses slowly
- Storage condition of test material: 12-15°C, protected from light
Constituent 1
- Radiolabelling:
- no
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on source and properties of surface water:
- - Details on collection (e.g. location, sampling depth, contamination history, procedure): Domestic sewage was collected from the overflow channel of the primary sedimentation tank or the feed of the activated sludge plant of the municipal sewage treatment plant at D-31137 Hildesheim. Synthetic sewage was prepared according to the test guideline and used for DOC adjustment of the domestic sewage if necessary.
- Storage conditions: Stored at 4°C
- Storage length: Maximum 7 days - Details on source and properties of sediment:
- Not applicable
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): Activated sludge from the municipal sewage treatment plant at D-31137 Hildesheim.
- Storage conditions: Aeration at room temperature
- Concentration of sludge: Starting concentration of dry matter 2.40 to 2.47 g/l - Duration of test (contact time):
- 96 d
Initial test substance concentrationopen allclose all
- Initial conc.:
- 30.1 mg/L
- Based on:
- DOC
- Initial conc.:
- 15.2 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- DOC removal
- test mat. analysis
- Details on study design:
- Simulation test - aerobic sewage treatment according to US EPA, OPPTS 835.3220 April 1996, Porous Pot Test and OECD 302 A.
The degradation was studied in a continously operating porous pot with activated sludge from a municipal sewage treatment plant over a test period of 135 days. The influent was adjusted to 200 mg DOC/l. After 40 days of flow, when the DOC elimination was constant >80 %, the test item was added.
The stock solution was adjusted to pH 9 +/- 0.5 in order to stabilise the test item. Simulation test - aerobic sewage treatment according to US EPA, OPPTS 835.3220 April 1996, Porous Pot Test and OECD 302 A.
The degradation was studied in a continously operating porous pot with activated sludge from a municipal sewage treatment plant over a test period of 135 days. The influent was adjusted to 200 mg DOC/l. After 40 days of flow, when the DOC elimination was constant >80 %, the test item was added.
The stock solution was adjusted to pH 9 +/- 0.5 in order to stabilise the test item. With regard to the low volumes applied the pH value of the porous pot reactor was not markedly influenced. Influent concentration of the test item was 30.1 mg/L DOC which is higher than normal mean test concentration 10-20 mg/l DOC according to OECD quideline (with upper concentration of no more than 50 mg/l).
Activated sludge: pH values were partly outside the specified range 7 to 8. These slight deviations were temporary and found to be negligible. Therefore, no adjustments were made.
Analysis comprised of DOC analysis and specific test item analysis including two known related products CHPTAC and DHPTAC (Di-hydroxypropyl trimethylammonium chloride).
Guideline OECD 303 A does not require substance specific analysis, although it has been performed in this study. Influent concentration of the test item was 30.1 mg/L DOC which is higher than normal mean test concentration 10-20 mg/l DOC according to OECD quideline (with upper concentration of no more than 50 mg/l).
Activated sludge: pH values were partly outside the specified range 7 to 8. These slight deviations were temporary and found to be negligible. Therefore, no adjustments were made.
Analysis comprised of DOC analysis and specific test item analysis including two related products CHPTAC and DHPTAC (Di-hydroxypropyl trimethylammonium chloride).
Guideline OECD 303 A does not require substance specific analysis, although it has been performed in this study.
Reference substance
- Reference substance:
- not required
Results and discussion
% Degradation
- % Degr.:
- ca. 15
- St. dev.:
- 9.7
- Parameter:
- test mat. analysis
- Remarks on result:
- other: Sampling time 61-74 days after test item application
Any other information on results incl. tables
DOC Elimination during the phase of test substance addition
was between 74 and 91%.
The primary degradation of EPTAC was in the range of 0-30 %.
No clear degradation tendency was observed and no plateau
was reached. Mean primary degradation was calculated from 14
(out of total 24) measurements which were done on days
100-113, corresponding to days 61-74 of test item
application.
Based on the combined concentrations of EPTAC, CHPTAC and
DHPTAC the degradation was 15 +- 9.7% expressed as active
ingredient.
Adsorption to sludge was studied in the same study using 6
selected sludge samples during the adaptation.
Koc values ranged from 12 cm3/g to 115 indicating a high to
very high mobility of the test substance and no considerable
absorption to sludge.
Applicant's summary and conclusion
Validity criteria
- Validity criteria fulfilled:
- yes
- Conclusions:
- In an OECD 303A porous pot test, elimination of EPTAC was in the range 0-30%. No clear degradation tendency was observed and no plateau phase was reached. The mean elimination/primary degradation was 15 +/- 9.7% based on measured concentrations of the three substances EPTAC, CHPTAC and DHPTAC in effluent on days 61-74 of test item application.
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