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EC number: 200-834-7 | CAS number: 75-04-7
- 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
- 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
Genetic toxicity: in vivo
Administrative data
- Endpoint:
- in vivo mammalian cell study: DNA damage and/or repair
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- The Testicular DNA-Synthesis Inhibition Test (DSI-Test)
- Author:
- Seiler J.
- Year:
- 1 981
- Bibliographic source:
- In: Stech M. und San R.: Short-Term Tests Chem.Carcinog., Heidelberg
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- - male mice were used
- on the eve of test day: animals received injection of 18,5 kBq (0,5 µCi) (methyl-14C)-thymidine (subcuaneously in the back)
- the next day: prelabeled animals are randomly assigned to test and control groups (receive test substance i.p.)
- 3 hours later: again injection with labeled thymidine subcutaneously (10 µL = 0,37 MBq (10µCi) (methyl-14C)-thymidine
- 45 min later: i.p. injection of 3,0 mg unlabeled thymidine in 0,2 ml physiological saline (provides for a 5x10^4-fold dilution of the radioactive thymidine)
- 30 min later: mice were sacrified and their testes excised
- testes were transferred into 5% trichloroacetic acid (TCA), homogenized and centrifuged
- the pellet was washed twice in 5% TCA, resuspended in fresh 5% TCA, heated for 30 min at 95°C for DNA hydrolysis, cooled and centrifuged
- DNA content was determined photometrically
- radioactivity was determined by liquid scintillation counting - GLP compliance:
- not specified
Test material
- Reference substance name:
- Ethylamine
- EC Number:
- 200-834-7
- EC Name:
- Ethylamine
- Cas Number:
- 75-04-7
- Molecular formula:
- C2H5NH2
- IUPAC Name:
- ethanamine
- Details on test material:
- - Name of test material (as cited in study report): Ethylamine
- Analytical purity: no data
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- not specified
- Sex:
- male
Administration / exposure
- Route of administration:
- intraperitoneal
- Duration of treatment / exposure:
- 3 hours
- Frequency of treatment:
- single application
Doses / concentrationsopen allclose all
- Dose / conc.:
- 5 mg/kg bw/day
- Dose / conc.:
- 15 mg/kg bw/day
- Dose / conc.:
- 50 mg/kg bw/day
- No. of animals per sex per dose:
- no data
- Control animals:
- yes
Examinations
- Statistics:
- nonparametric test (Wilcoxon-rank-test or equivalent)
Results and discussion
Test results
- Sex:
- male
- Genotoxicity:
- negative
- Toxicity:
- not specified
- Vehicle controls validity:
- not specified
- Negative controls validity:
- not specified
- Positive controls validity:
- not specified
Any other information on results incl. tables
Table 1: DSI Test Results of Ethylamine
Compound |
Dose (mg/kg) |
%DSI |
Ethylamine |
5 i.p. |
0 |
15 |
0 |
|
50 |
5,6 |
Applicant's summary and conclusion
- Conclusions:
- Based on the DSI Test results of this publication, the test substance is a Noncarcinogen in mice.
- Executive summary:
Male mice were treated with the test substance intraperitoneal. Three dose levels (5, 15, 50 mg/kb bw) were investigated. The results show that the test substance is a Noncarcinogen under the test conditions chosen.
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