Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 203-412-0 | CAS number: 106-58-1
- 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: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- No data
- 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:
- study report
- Title:
- Unnamed
- Year:
- 1 968
- Report date:
- 1968
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Version / remarks:
- (adopted on 1981, 12th may; inhalation hazard test)
- Deviations:
- yes
- Remarks:
- Animals were observed for only 7 days, no details only animal husbandry, exposure period of 8 hours, concentration of test substance in air mixture was not determined analytically
- GLP compliance:
- no
- Test type:
- other: inhalation hazard test (IHT)
Test material
- Reference substance name:
- 1,4-dimethylpiperazine
- EC Number:
- 203-412-0
- EC Name:
- 1,4-dimethylpiperazine
- Cas Number:
- 106-58-1
- Molecular formula:
- C6H14N2
- IUPAC Name:
- 1,4-dimethylpiperazine
- Details on test material:
- - Name of test material (as cited in study report): Jeffcat DMP
Constituent 1
- Specific details on test material used for the study:
- - Name of test material (as cited in study report): N,N´-Dimethylpiperazin
- Analytical purity: 99 %
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 177 g (mean)
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- not specified
- Vehicle:
- air
- Details on inhalation exposure:
- The test demonstrates the toxicity of an atmosphere saturated with vapours of the volatile components of a test substance at the temperature chosen for vapour generation (20 °C). 3 rats (respec. 6 rats in the 8h experiment) per sex were exposed sequentially to the vapours, generated by bubbling 200 l/h air through a substance column of about 5 cm above a fritted glassdisc in a glass cylinder for 1 h, 3 h or 8 h. The documentation of clinical signs was performed over a period of 8 days.
- Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- >= 1 - <= 8 h
- Remarks on duration:
- 1 h, 3 h or 8 h exposure
- Concentrations:
- 1 h and 3 h exposure: 17.2 mg/L (mean); no data concerning 8 h exposure.
(nominal concentrations not verified by analytics). - No. of animals per sex per dose:
- 1 h and 3 h exposure: 6 animals
8 h exposure: 12 animals - Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 7 days
- Frequency of observations: daily
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight
Results and discussion
Effect levels
- Key result
- Sex:
- male/female
- Dose descriptor:
- other: Inhalation Risk Test
- Based on:
- test mat.
- Remarks on result:
- other: exposure of 1, 3 or 8 hours (3 h exposure: 1 rat died within 24 hours; 8 h exposure: 1 animal died within the exposure, 9 animals within 24 h and 1 animal within 72 h after exposure)
- Mortality:
- 1 h exposure: no mortality observed.
3 h exposure: 1 rat died within 24 hours.
8 h exposure: 1 animal died within the exposure, 9 animals within 24 h and 1 animal within 72 h after exposure. - Clinical signs:
- other: Rats showed escape attempts and signs of severe irritation of the mucous membranes. Bloody snout, nose and eye crusts. Lateral position and tumbling in the 8 h exposure group.
- Body weight:
- The surviving animals gained weight.
- Gross pathology:
- 1 h exposure: no abnormalities observed.
3 h exposure: 1 animal showed ruffled fur and slight bloody crusts at the muzzle and orbital cavity. 1 animal had pulmonary emphysema with bronchitis.
8 h exposure: animals showed ruffled fur and bloody crust formation at the nose (4x), muzzles and orbital cavity (1x). 2 animals had pulmonary emphysema.
Any other information on results incl. tables
Mortality:
24 h | 7 days | |
1 h exposure | 0/6 | 0/6 |
3 h exposure | 1/6 | 1/6 |
8 h exposure | 10/12 | 11/12 |
The inhalation of a enriched/saturated vapor-air-mixture caused mortality within 3 h. There is indication that the test substance causes local irritation to exposed tissue including respiratory tract.
Applicant's summary and conclusion
- Interpretation of results:
- study cannot be used for classification
- Conclusions:
- The inhalation of a enriched/saturated vapor-air-mixture caused mortality within 3 h. There is indication that the test substance causes local irritation to exposed tissue including respiratory tract.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.