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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 951-773-4 | CAS number: -
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2020-07-16 - 2021-04-26
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- 200116MA1 liquid
- Analytical monitoring:
- yes
- Details on sampling:
- concentrations and the control were taken at the start of the test and at day 1.
For the determination of the stability of the test item under the test conditions and of the maintenance of the test item concentrations during the test period, four samples from the aged test media of all test concentrations and the control were collected at day 1 (after 24 hours of exposure) and at the end of the test by pouring together the contents of the test beakers of each treatment.
One set of duplicate samples of each sampling point was used for the analysis of DCD and Hydantoic acid.
The other set of duplicate samples of each sampling point was used for the determination of total organic carbon (TOC).
All samples remained undiluted. - Vehicle:
- no
- Test organisms (species):
- Daphnia magna
- Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 2.5 mmol/L (= 250 mg/L) as CaCO3
- Test temperature:
- 20.1 to 20.8 °C in the freshly prepared media;
20.2 to 20.8°C in the aged test media - pH:
- 7.7 to 8.0 in the freshly prepared media;
7.9 in the aged test media; and thus the pH-value did not vary by more than 1.5 units - Dissolved oxygen:
- 8.7 to 9.1 mg/L in the freshly prepared media;
7.9 to 8.7 mg/L in the aged test media - Nominal and measured concentrations:
- Nomnal concentrations:
889, 404, 184, 83.5 and 37.9 mg test item/L
equivalent to 160, 72.7, 33.1, 15.0 and 6.83 mg total dissolved solids/L
equivalent to 24.003, 10.908, 4.968, 2.255, 1.023 mg DCD/L
Measured concentrations (% of nominal):
24.003 mg/L: 105
10.908 mg/L: 99
4.968 mg/L: 97
2.255 mg/L: 101
1.023 mg/L: 100 - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 160 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- mg dissolved solids/L
- Basis for effect:
- mortality
- Validity criteria fulfilled:
- yes
- Conclusions:
- The toxic effect of the test item "Solution of By-product from Guanidinoacetic acid manufacturing" to Daphnia magna was assessed in a semi-static concentration-response test. The 48-hour NOEC was determined to be ≥ 889 mg test item/L / ≥ 160 mg dissolved solids/L (based on immobility). The 48-hour LOEC was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L (based on immobility) and the 48-hour EC50 value was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L.
- Executive summary:
The toxic effect of the test item "Solution of By-product from Guanidinoacetic acid manufacturing" to Daphnia magna was assessed in a semi-static concentration-response test. The 48-hour NOEC was determined to be ≥ 889 mg test item/L / ≥ 160 mg dissolved solids/L (based on immobility). The 48-hour LOEC was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L (based on immobility) and the 48-hour EC50 value was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L.
The initial concentrations and the maintenance of the exposure concentrations during the test were determined in the analytical part.
Correct dosage was confirmed by the analysis of the component DCD of the test item because DCD is the component with the highest content in the test item. This component is stable under the experimental conditions and does not undergo any reaction with any other component of the test item. Furthermore, a reference substance is commercially available.
All reported results refer to nominal values since the concentrations of DCD in the test item were within ± 20% of the nominal concentrations during the test and “Solution of By-product from Guanidinoacetic acid manufacturing” is an UVCB substance (Unknown or Variable composition, Complex reaction products or Biological material).
Reference
Description of key information
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Remarks:
- mg dissolved solids / mL
- Effect concentration:
- > 160 mg/L
Additional information
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.