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Diss Factsheets
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EC number: 204-101-2 | CAS number: 115-70-8
- 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:
- toxicity to microorganisms
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 18 Apr - 14 Jun 1991
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- DIN 38412-8 (Pseudomonas Zellvermehrungshemmtest)
- GLP compliance:
- not specified
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
A stock solution of 100 g/L was prepared. Aliquots were transferred into test flasks in amounts resulting in a disolution series separated by a spacing factor of 2. To each flask 10 mL culture medium and 10 mL inoculum with a FNU of 50 at 436 nm are added. Flasks are filled up to a final volume of 100 mL. - Test organisms (species):
- Pseudomonas putida
- Details on inoculum:
- - Laboratory culture: source: Deutsche Sammlung für Mikroorganismen (DSMZ, German Collection of Microorganisms and Cell Cultures)
- Preparation of inoculum for exposure: pre-culture grown for 7 h at 21 °C before inoculation. pre-culture diluted with sterile culture medium, resulting in a FNU (Formazine Nephelometric Units) of 50 - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 16 h
- Remarks on exposure duration:
- 16 ± 1 h
- Test temperature:
- 21 ± 1 °C
- Nominal and measured concentrations:
- nominal: 0, 125, 250, 500, 1000, and 2000 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): closed
- Material, size, headspace, fill volume: 300 mL Erlenmeyer flasks, 100 mL fill volume
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 3
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2x - Reference substance (positive control):
- no
- Duration:
- 16 h
- Dose descriptor:
- EC10
- Effect conc.:
- 300 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
- Duration:
- 16 h
- Dose descriptor:
- EC50
- Effect conc.:
- 640 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
Reference
Table 1: Measured extinction values
Concentration (mg/L) |
Replicate 1 |
Replicate 2 |
Replicate 3 |
Median value |
control |
1.314 |
1.332 |
1.358 |
1.335 |
125 |
1.448 |
1.355 |
1.351 |
1.385 |
250 |
1.362 |
1.401 |
1.309 |
1.357 |
500 |
0.901 |
0.949 |
0.912 |
0.921 |
1000 |
0.135 |
0.142 |
0.135 |
0.137 |
2000 |
0.031 |
0.026 |
0.024 |
0.027 |
Table 2: Inhibition values
Concentration (mg/L) |
% inhibition of cell growth |
125 |
-4 |
250 |
-2 |
500 |
32 |
1000 |
92 |
2000 |
100 |
Description of key information
EC10 = 300 mg/L with Pseudomonas putida (DIN 38412, part 8)
EC50 = 640 mg/L
Key value for chemical safety assessment
- EC50 for microorganisms:
- 640 mg/L
- EC10 or NOEC for microorganisms:
- 300 mg/L
Additional information
There is one microorganism study available for 2-amino-2-ethyl-1,3-propanediol (AEPD), which was used as key study for the assessment. The study was conducted according to the guideline DIN 38412, part 8 (Schopka, 1991). A culture of the bacterium Pseudomonas putida was exposed to AEPD for 16 hours, at the nominal test concentrations 125, 250, 500, 1000, and 2000 mg/L. The obtained EC10 and EC50 values were 300 mg/L and 640 mg/L, respectively.
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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