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EC number: 825-246-3 | CAS number: 2098351-38-1
- 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
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 27-01-2017 t/m 01-02-2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Test performed under GLP according guidelines, all quality criteria were met
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Chemical name Sodium cocopropylenediamine glycinate
CAS No. 97659-51-3
Composition See certificate of analysis (Annex 2)
Activity as solids corrected for salt: 30.2% (40.8% dry solids corrected for 10.6% salt)
The substance is a UVCB, purity is equal to activity as solids
Batch/lot No. 1259678
Appearance Yellow liquid
Stability Unknown under test conditions
Solubility Soluble in water
Volatile Expected non-volatile
Storage At ambient temperature in the dark - Analytical monitoring:
- not required
- Vehicle:
- no
- Details on test solutions:
- The highest sodium cocopropylenediamine glycinate concentration was added to the incubation vessels using a 2 g/L stock solution and the other test substance concentrations were dosed from a 1 g/L stock solution. The 1 g/L and 2 g/L stock suspension of sodium cocopropylenediamine glycinate were prepared by dissolving 0.42 g and 2.00 g sodium cocopropylenediamine glycinate in 420 and 1000 mL deionized water, respectively.
The pH of the 1 g/L and 2 g/L stock solution were 7.8 and 8.2, respectively - Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- Unadapted secondary activated sludge was obtained (31-01-2017) from the WWTP Nieuwgraaf in Duiven. The WWTP Duiven is an activated sludge plant treating predominantly domestic wastewater. Prior to use the activated sludge was homogenized with a syringe. The dry weight of the homogenized activated sludge was determined and subsequently concentrated by settlement to the required dry weight concentration. The dry weight of the activated sludge in the incubation vessels was 1.5 g/L.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Test temperature:
- Temperature varied from 20.3 to 20.9°C.
- pH:
- The pH of the reaction mixtures after the incubation period ranged from 7.1 to 7.3.
- Dissolved oxygen:
- aerobic during test
- Details on test conditions:
- -The test was performed in 300 mL Erlenmeyers with a total working volume of 50 mL.
-Prior to use the activated sludge was homogenized with a syringe
-The homogenized activated sludge was incubated in a shaking water bath (100 rpm, 20°C) for 3 hours with various concentrations of the test
compound and synthetic sewage.
-Synthetic sewage was added to the activated sludge (1.6 mL on a total volume of 50 mL).
Synthetic sewage contained per liter: 16 g peptone
11 g meat extract
3 g urea
0.7 g NaCl
0.4 g CaCl2.2H2O
0.2 g MgSO4.7H2O
2.8 g K2HPO4
-Different concentrations (spaced by a factor two) of test compound and reference compound where added using stock solutions
-Tap-water was used to fill up the total test volume to 50 mL.
- The dry weight concentration of the activated sludge in the test was 1.5 g/L.
-The tested concentrations of the reference compound 3,5-dichlorophenol where: 2.5 mg/L, 5.0 mg/L,10.1 mg/L, 20.1 mg/L and 40.2 mg/L
-The tested concentrations of test substance (sodium oleylamphopolycarboxyglycinate) where: 20 mg/L, 40 mg/L, 80 mg/L, 160 mg/L, 320 mg/L, 640 (mg/L), and 1280 (mg/L)
-Controls without test substance (or reference compound) are measured at the beginning and at the end of the test
-The inhibitory effect of the test substance/reference compound is expressed as a percentage of the mean of the two control respiration rates. - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol (p.a. quality 99.7% Aldrich Lot no MKBP6894V)
- Duration:
- 3 h
- Dose descriptor:
- EC10
- Effect conc.:
- 114 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: Active ingredient content 30.2%
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1 745 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: Active ingredient content 30.2%
- Duration:
- 3 h
- Dose descriptor:
- other: EC20
- Effect conc.:
- 290 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC10
- Effect conc.:
- 34.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- inhibition of total respiration
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- 527 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- inhibition of total respiration
- Details on results:
- Test conditions
The pH of the reaction mixtures after the incubation period ranged from 7.1 to 7.3. Temperature varied from 20.3 to 20.9 °C. These conditions allow respiration of the activated sludge used.
Validity of the test
The validity of the test is demonstrated although only two out of three validity criteria were met according the guideline. First, the prescribed oxygen uptake rate of >20 mg O2/g dry weight/hour for the control measurements was not met. The inoculum used was obtained from a treatment plant which is operated at a low organic sludge load and as a consequence has a low oxygen uptake rate. Operating at low organic sludge loads is nowadays very common. Nonetheless the average oxygen uptake rate for the control replicates was 16 mg O2/g dry weight/hour, which is slightly lower than the prescribed rate. This does not influence the sensitivity of the activated sludge as shown by comparable EC50 values of the reference substance 3,5-dichlorophenol at oxygen uptake rates lower and higher than the prescribed rate (AkzoNobel 2012). The lower average oxygen uptake rate does therefore not compromise the test outcome in terms of robustness of the endpoints obtained for the test and reference substance and does not invalidate the test. Second, the coefficient of variation of the replicates of the control oxygen uptake rates was 7%, which shows a high precision and fulfills the maximum prescribed variation of <30%. Third, the EC50 of the reference compound for activated sludge after 3 hours contact time is 12 mg/L, which is within the prescribed range of 2 to 25 mg/L.
Activated sludge respiration inhibition test
The calculated respiration rates and inhibition percentages of sodium cocopropylenediamine glycinate are presented in Table II and the results of the graphical probit analysis are shown in Figure 2. The inhibitory effect of sodium cocopropylenediamine glycinate at a particular concentration is expressed as a percentage of the two controls. From the results EC values were calculated. The EC50 of sodium cocopropylenediamine glycinate for activated sludge after 3 hours contact time is 1745 mg/L. The EC80 value could not be determined and the EC10 and EC20 values were 114 and 290 mg/L, respectively. Sodium cocopropylenediamine glycinate is therefore considered not harmful to activated sludge. - Results with reference substance (positive control):
- The EC50 of the reference compound for activated sludge after 3 hours contact time is 12 mg/L, which is within the prescribed range of 2 to 25 mg/L
- Validity criteria fulfilled:
- yes
- Remarks:
- See validity of test in "details on results"
- Conclusions:
- Test performed under GLP according guidelines meeting the validity criteria of the OECD guideline.
The inhibitory effect of sodium cocopropylenediamine glycinate at a particular concentration is expressed as a percentage of the two controls. From the results EC values were calculated. The EC50 of test substance (sodium cocopropylenediamine glycinate) for activated sludge after 3 hours contact time is 1745 mg/L. The EC80 value could not be determined and the EC10 and EC20 values were 114 and 290 mg/L, respectively. The test substance (Sodium cocopropylenediamine glycinate) is therefore considered not harmful to activated sludge. - Executive summary:
In order to predict effects of chemicals in the environment and in biological waste water treatment plants, an activated sludge respiration inhibition test was performed. The toxicity to activated sludge was determined in accordance with OECD Test Guideline 209, and in compliance with the OECD principles of Good Laboratory Practice.
The test is valid as shown by the EC50of the reference compound 3,5-dichlorophenol (12 mg/L) and the coefficient of variation of the replicates of the control oxygen uptake rates (9%). The average oxygen uptake rate for the control replicates is lower (16 mg O2/g dry weight/hour) than the prescribed rate (>20 mg O2/g dry weight /hour). This does not influence the sensitivity of the activated sludge as shown by comparable EC50 values of the reference substance 3,5-dichlorophenol at oxygen uptake rates lower and higher than the prescribed rate (AkzoNobel 2012). The lower average oxygen uptake rate does therefore not compromise the test outcome in terms of robustness of the endpoints obtained for the test and reference substance and does not invalidate the test.
The toxicity of sodium cocopropylenediamine glycinate to activated sludge was determined at a contact time of 3 hours, using various concentrations of the test substance. The inhibitory effect of sodium cocopropylenediamine glycinate at a particular concentration is expressed as a percentage of the two controls. From the results EC values were calculated. The EC50of sodium cocopropylenediamine glycinate for activated sludge after 3 hours contact time is 1745 mg/L. The EC80 value could not be determined and the EC10 and EC20 values were 114 and 290 mg/L, respectively. Sodium cocopropylenediamine glycinate is therefore considered not harmful to activated sludge.
Reference
Description of key information
One activated sludge respiration test with Amines, N-C8 -18-alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts is available which was performed in accordance with OECD Test Guideline 209, and in compliance with the OECD principles of Good Laboratory Practice.
The toxicity of Amines, N-C8 -18-alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts to activated sludge was determined at a contact time of 3 hours, using various concentrations of the test substance. The EC50 of Amines, N-C8 -18-alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts for activated sludge after 3 hours contact time is 1745 mg/L test substance. The EC10 value was 114 mg/L Amines, N-C8 -18-alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts is therefore considered not harmful to activated sludge.
Based on active ingredient (30.2%) the 3h EC50 =527.0 mg/L. Based on active ingredient the 3h EC10 = 34.4 mg/L.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 527 mg/L
- EC10 or NOEC for microorganisms:
- 34.4 mg/L
Additional information
One activated sludge respiration test with Amines, N-C8 -18-alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts is available.
The toxicity to activated sludge was determined in accordance with OECD Test Guideline 209, and in compliance with the OECD principles of Good Laboratory Practice.
The test is valid as shown by the EC50 of the reference compound 3,5-dichlorophenol (12 mg/L) and the coefficient of variation of the replicates of the control oxygen uptake rates (9%). The average oxygen uptake rate for the control replicates is lower (16 mg O2/g dry weight/hour) than the prescribed rate (>20 mg O2/g dry weight /hour). This does not influence the sensitivity of the activated sludge as shown by comparable EC50 values of the reference substance 3,5-dichlorophenol at oxygen uptake rates lower and higher than the prescribed rate (AkzoNobel 2012). The lower average oxygen uptake rate does therefore not compromise the test outcome in terms of robustness of the endpoints obtained for the test and reference substance and does not invalidate the test.
The toxicity of Amines, N-C8 -18-alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts to activated sludge was determined at a contact time of 3 hours, using various concentrations of the test substance. The inhibitory effect of Amines, N-C8 -18-alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts at a particular concentration is expressed as a percentage of the two controls. From the results EC values were calculated. The EC50 of Amines, N-C8 -18 -alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts for activated sludge after 3 hours contact time is 1745 mg/L. The EC80 value could not be determined and the EC10 and EC20 values were 114 and 290 mg/L, respectively.
Amines, N-C8 -18 -alkyltrimethylenedi-, reaction products with sodium chloroacetate, sodium salts is therefore considered not harmful to activated sludge.
Based on active ingredient (30.2%) the 3h EC50 = 527 mg/L
Based on active ingredient the 3h EC10 = 34.4 mg/L
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