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EC number: 225-306-3 | CAS number: 4767-03-7
- 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
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- Nanomaterial pour density
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- 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:
- 1999-06-15 to 1999-06-17
- 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)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EPA OPPTS 850.1010 (Aquatic Invertebrate Acute Toxicity Test, Freshwater Daphnids)
- GLP compliance:
- yes
- Specific details on test material used for the study:
- - Name of the test material used in the study report: Dimethylolpropionsäure, 2,2-Bis(hydroxymethyl)propansäure
- Batch no.: SE 8069
- Purity: 99.4%
- Storage conditions: storage at room temperature - Analytical monitoring:
- yes
- Details on sampling:
- Samples were taken at 0 hours (fresh media) and 48 hours (expired media) from the control, 12.5 and 100 mg/L test treatments.
Sample preparation: For calibration the test substance was dissolved in demin. water; the stock solutions were diluted with demin. water. Before adjusting the volume a solution of internal standard (dissolved in demin. water and NaOH) was added. Depending on concentration the samples were diluted using carrier prior to addition of internal standard solution. - Vehicle:
- no
- Details on test solutions:
- The test material was stirred in M4 medium for about 10 minutes at 20 ± 2 °C. The nominal concentration of the stock solution was 100 mg/L.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain: Straus 1820
- Source: Institut National de Recherche Chimique Appliqueé, France 1978. From this date on this clone was cultured and bred continuously in the Laboratory of Ecology of BASF AG in Ludwigshafen.
- Age at study initiation (mean and range, SD): 2 - 24h - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- Not applicable
- Hardness:
- 2.2 - 3.2 mmol/L
- Test temperature:
- 19.9 - 20.3°C
- pH:
- 7.5 - 8 (neutralised only)
5.8 - 8 (including non-neutralised)
See tables in results section for further information - Dissolved oxygen:
- 8.2 - 8.8 mg/L
See tables in the results section for further information - Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal: 0 (control) 12.5, 25, 50, 100 mg/L; neutralised: 50, 100 mg/L.
Measured: <5 (control), 12.5, not measured, not measured, 102 mg/L; neutralised: not measured, not measured.
The measured pH in the freshly prepared 50 and 100 mg/L test media were 7.3 and 5.8, therefore additional test vessels were prepared where the pH was neutralised. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- See tabulated data below.
- Results with reference substance (positive control):
- The EC50(24h) of the control substance potassium dichromate was 1,30 mg/L. (Date of the last control experiment: 25 May 1999).
- Reported statistics and error estimates:
- Not applicable
- Validity criteria fulfilled:
- yes
- Conclusions:
- In a 48-hour test with daphnids an EC50 was determined to be >100 mg/L (the highest nominal concentration tested).
- Executive summary:
The 48–hr-acute toxicity of Bis-MPA to Daphnia magna was studied under static conditions. Test species were exposed to control, and test chemical at nominal concentrations of 0, 12.5, 25, 50 and 100 mg a.i./L for 48-hr. Neither immobilisation nor sublethal effects were observed (checked daily). The 48–hour EC50 was >100 mg a.i./L.
This study is classified as acceptable and satisfies the guideline requirements for an acute toxicity study with freshwater invertebrates.
Results Synopsis
Test Organism Age: 2-24 hours
Test Type: Static
NOEL: >100 mg a.i./L
EC50: >100 mg a.i./L
Endpoint Effected: Immobilisation
Reference
Analytical results are presented below:
Nominal Bis-MPA concentration (mg/L) | Measured concentrations (mg/L) | |||
0 hour | 48 hours | Mean | % of nominal | |
Control | <5 | <5, <5 | - | - |
12.5 | 12.4 | 12.3, 12.9 | 12.5 | 100 |
100 | 102 | 102, 104 | 103 | 103 |
The immobility results are presented below:
Nominal Bis-MPA concentration (mg/L) | Number of immobilised Daphnia | |||
24 hours | % immobility | 48 hours | % immobility | |
Control | 0 | 0 | 0 | 0 |
12.5 | 0 | 0 | 0 | 0 |
25 | 0 | 0 | 0 | 0 |
50 | 0 | 0 | 0 | 0 |
100 | 0 | 0 | 0 | 0 |
Neutralised test media | ||||
50 | 0 | 0 | 1 | 5 |
100 | 0 | 0 | 0 | 0 |
The water quality values are presented below:
Nominal Bis-MPA concentration (mg/L) | Parameter | |||
pH | Dissolved oxygen (mg/L) | |||
0 hours | 48 hours | 0 hours | 48 hours | |
Control | 8.0 | 8.0 | 8.4 | 8.8 |
12.5 | 7.9 | 8.0 | 8.5 | 8.7 |
25 | 7.7 | 8.0 | 8.5 | 8.6 |
50 | 7.3 | 7.7 | 8.3 | 8.6 |
100 | 5.8 | 7.6 | 8.3 | 8.6 |
Neutralised test media | ||||
50 | 7.8 | 7.9 | 8.3 | 8.5 |
100 | 7.5 | 7.8 | 8.2 | 8.5 |
Description of key information
A short-term toxicity test with Daphnia magna resulted in an EC50 of >100 mg/L
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Effect concentration:
- > 100 mg/L
Additional information
No adverse effects have been observed at the highest recommended concentration (100 mg/L). Accordingly, the substance is not hazardous in terms of the CLP Regulation.
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.
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