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EC number: 203-782-3 | CAS number: 110-60-1
- 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

Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 14 days
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Not according to OECD guidelines (study in 1978), but very well documented and structural approach.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
- Report date:
- 1978
Materials and methods
- Principles of method if other than guideline:
- Test system: Albino rat, Wistar strain (Institute colony); 5 males and 5 females per group, exposed to single doses of 5.0, 6.0, 7.2, 8.6, or 10.4 ml/kg bw, given by gavage, as a 10% (w/v) suspension in propylene glycol.
The LD50 was calculated according to the method of Weil (Biometrics 8 (1952) 249-263). - GLP compliance:
- not specified
- Test type:
- acute toxic class method
Test material
- Reference substance name:
- Tetramethylenediamine
- EC Number:
- 203-782-3
- EC Name:
- Tetramethylenediamine
- Cas Number:
- 110-60-1
- Molecular formula:
- C4H12N2
- IUPAC Name:
- butane-1,4-diamine
- Details on test material:
- A 200 g sample of the test material was received from the principal in March 1978. It was a colourless solid with a melting-point between 25 and 30 degrees Celcius
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Yong adult albino rats (Wistar-derived) from the Institute's colony were used. The body weights of males varied from 205 to 307 g, those of females from 93 to 145 g.
The rats were housed in groups of five in screen-bottomed stainless steel cages in a well-ventilated room, maintained at 23-25 degrees Celsius. Before dosing the rats fasted overnight.
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- propylene glycol
- Details on oral exposure:
- The test material was giving by gavage, as a 10 per cent (w/v) suspension in propylene glycol.
After treatment the rats received stock diet and tap water ad libitum. - Doses:
- 5.0, 6.0, 7.2, 8.6, and 10.4 ml/kg bw
- No. of animals per sex per dose:
- 5 males, 5 females
- Control animals:
- no
- Details on study design:
- After treatment the rats were observed for signs of intoxication during a 14-day period, after which autopsies were carried out on the survivors.
- Statistics:
- The LD50 was calculated according to the method of Weil (Biometrics 8 (1952), pp 249-263.
Results and discussion
- Preliminary study:
- DAB: LD50 (rat, oral): 740 mg/kg body weight (95% reliability interval: 650 - 850 mg/kg bw), both sexes
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- 740 mg/kg bw
- 95% CL:
- > 650 - < 850
- Clinical signs:
- other: Within one hour of treatment, the rats showed signs of sluggishness and abdominal discomfort. Later on unconsciousness was frequently observed. Black coloured faeces and severe diarrhoea were observed during the first three post-treatment days. Deaths o
- Gross pathology:
- Macroscopic examination of the survivors at autopsy revealed no treatment-related gross alterations.
Applicant's summary and conclusion
- Interpretation of results:
- harmful
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- From the mortality figures the LD50 of 1,4-diaminobutane was calculated to be 0.74 g/kg bw with 0.65 and 0.85 at the 95% confidence limits.
Therefore, the test product can be classified as slightly toxic.
Based on these results and according to the EEC criteria for classification and labeling requirements for dangerous substances and preparations (EEC Directive 91/325/EEC, amendment to annex VI of the EEC Directive 67/548/EEC), DAB is classified as harmful, Xn, R22 Harmful if swallowed. - Executive summary:
Oral gavage study, Wistar albino rats (5 males, 5 females).
LD50 (oral, rats) = 740 mg/kg bw (95% confidence limits: 650 - 850 mg/kg bw).
1,4 -Diaminobutane was classified as slightly toxic;
DAB is classified as harmful, Xn, R22 Harmful if swallowed (EEC Directive 91/325/EEC, amendment to annex VI of the EEC Directive 67/548/EEC).
CLP: Category 4; H302 Harmfull if swallowed
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