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EC number: 701-207-5 | CAS number: 1950616-36-0
- 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to the O.E.C.D. test guideline 201 with GLP compliance.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 011
- Report date:
- 2011
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 1-[3-(aminomethyl)phenyl]methanamine; 2,4-bis[({[3-(aminomethyl)phenyl]methyl}amino)methyl]phenol; 2,6-bis[({[3-(aminomethyl)phenyl]methyl}amino)methyl]-4-[(4-hydroxyphenyl)methyl]phenol; 2-[({[3-(aminomethyl)phenyl]methyl}amino)methyl]-4-[(4-hydroxyphenyl)methyl]phenol; 2-[({[3-(aminomethyl)phenyl]methyl}amino)methyl]phenol; phenol
- EC Number:
- 701-207-5
- Cas Number:
- 1950616-36-0
- Molecular formula:
- (C8 H12 N2 . C6 H6 O . C H2 O)x
- IUPAC Name:
- 1-[3-(aminomethyl)phenyl]methanamine; 2,4-bis[({[3-(aminomethyl)phenyl]methyl}amino)methyl]phenol; 2,6-bis[({[3-(aminomethyl)phenyl]methyl}amino)methyl]-4-[(4-hydroxyphenyl)methyl]phenol; 2-[({[3-(aminomethyl)phenyl]methyl}amino)methyl]-4-[(4-hydroxyphenyl)methyl]phenol; 2-[({[3-(aminomethyl)phenyl]methyl}amino)methyl]phenol; phenol
- Test material form:
- other: Liquid at room temperature.
- Details on test material:
- As per IUCLID5 Sections 1.1. 1.2. and 4.1.
Constituent 1
Sampling and analysis
- Analytical monitoring:
- no
Test solutions
- Vehicle:
- yes
- Details on test solutions:
- For test concentrations prepared in the range- finding test, stock solutions were prepared at concentrations of 20, 100 and 200 mg/L by adding the required nominal amount of test substance in the diluent, Algal stock culture medium (Woods Hole) and mixing the solution for approximately 2 hours. For test concentrations prepared in the definitive test, stock solutions were prepared at concentrations of 40, 80 and 160 mg/L by adding the required nominal amount of test substance in the diluent, and mixing the solution for approximately 2 hours.
Test organisms
- Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- Pseudokirchneriellasubcapitata (formerly Selenastrum capricornutum), one of the freshwater alga species specified in the O.E.C.D. guideline was maintained at STILLMEADOW, Inc. Mass algal culture was initiated 3-7 + 1 days prior to dosing. The algae were maintained in Algal stock culture medium (Woods Hole) with EDTA up to 0.300 mg/L, at a temperature of 22-25°C with Continuous lighting approximately 422 fi. c. and continuous aeration.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Post exposure observation period:
- None
Test conditions
- Hardness:
- No data
- Test temperature:
- 22-25°C
- pH:
- 7.9-10
- Dissolved oxygen:
- Saturated
- Salinity:
- No data
- Nominal and measured concentrations:
- 5, 10, 20, 40 and 80 mg/L nominal.
- Details on test conditions:
- Treatment was conducted in 250-mL sterile Erlenmeyer flasks with stoppers and aeration tubing and 50,000 cells/mL. There were three flasks for each test substance concentration and six flasks for the untreated control. A positive control group consisted of three flasks treated with 10 mg/L zinc chloride. The flasks were set on a shaker table for constant agitation at approximately 100 cycles/minute. At 24, 48 and 72 hours following dosing, observations of inhibition were made for each test container by measuring the mean cell density with a hemacytometer. The temperature was recorded daily, and the pH of each container was recorded at study termination.
- Reference substance (positive control):
- yes
- Remarks:
- Zinc chloride at 10 mg/L.
Results and discussion
Effect concentrations
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- ca. 20.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- cell number
- Remarks on result:
- other: 17.6-24.5 mg/L.
- Details on results:
- Little or no increase in cell number was observed at the test substance concentrations of 40 and 80 mg/L throught the study. The relative precent survival at 20 mg/L was 47.9 at 72 hr. The percent survial of the 10 mg/L concentration was 85.9% ay 72 hr and is considered the NOEC.
- Results with reference substance (positive control):
- There was no increase in algal cell number with the positive control zinc chloride.
- Reported statistics and error estimates:
- The NOEC and EC50 values were determined by a commercially available statistical program (ToxCalc Version 5.OTM). The Maximum Likelihood-Logit model was selected for the determination in this case. The 95% confidence Limits on the EC50 value were 17.6-24.5 mg/L.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The estimated EC50 value for the test substance was 20.4 mg/L with 95% confidence Limits of 17.6-24.5 mg/L. This EC50 value is the lowest of the three aquatic species and is therefore the most appropriate value for derivation of PNEC values.
- Executive summary:
The acute toxicity of the test substance, Formaldehyde, polymer with 1,3 -benzenedimethanamine and phenol to algae was determined in an O.E.C.D. test guideline 201 study. The estimated EC50 value for the test substance was 20.4 mg/L with 95% confidence Limits of 17.6-24.5 mg/L following 72 hr of exposure. .
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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