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EC number: 219-983-4 | CAS number: 2591-76-6
- 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:
- other information
- Study period:
- 1988-04-27 to 1988-05-11
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Basic data given. Only orientating information about the inhalation hazard.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 988
- Report date:
- 1988
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- BASF-Test (IRT = inhalation risk test):
The test was performed in principle as described in OECD test guideline 403. It demonstrates the toxicity of an atmosphere saturated with vapors of the volatile components of the test substance at the temperature chosen for vapor generation (50°C). Rats were exposed to the test substance vapors for 8 hours. Documentation of clinical signs was performed over the 7-day study period. - GLP compliance:
- no
- Test type:
- other: Inhalation hazard test
- Limit test:
- yes
Test material
- Reference substance name:
- N,N-bis(2-methylpropyl)formamide
- EC Number:
- 219-983-4
- EC Name:
- N,N-bis(2-methylpropyl)formamide
- Cas Number:
- 2591-76-6
- Molecular formula:
- C9H19NO
- IUPAC Name:
- N,N-bis(2-methylpropyl)formamide
- Test material form:
- other: liquid
- Details on test material:
- - Name of the test substance used in the study report: Diisobutylformamid
- Purity: 99.7 %
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Dr. K. Thomae GmbH, 7950 Biberach, Germany
- Age at study initiation: about 8 - 9 weeks
- Weight at study initiation (mean): males: 262 g, females: 188 g
- Housing: They were housed in groups of three in type D III wire mesh cages supplied by Becker & Co., without bedding.
- Diet: KLIBA 24-343-4 rat/mouse laboratory diet (10 mm pellets, Klingentalmühle AG, CH-4303 Kaiseraugst, Switzerland), ad libitum in the exposure-free period.
- Water: ad libitum in the exposure-free period
- Acclimation period: At least 5 days
- Animal identification: colour lines on the base of the tail
ENVIRONMENTAL CONDITIONS
- Temperature: 20 - 24 °C
- Humidity: 30- 70 %
- Photoperiod: 12 hours dark/ 12 hours light
Administration / exposure
- Route of administration:
- other: mixture of the vapour of the test substance and air
- Vehicle:
- other: unchanged
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus, filled volume: Glass bottle (fritted glass flask, pore-size 90 - 150 um, diameter 30 mm) filled to a height of 5 cm with the test substance
- Source and rate of air: compressed air, 200 L/h
- Treatment of exhaust air: Disposal
- Temperature in air chamber: Between 19 and 25 °C - Duration of exposure:
- 7 h
- Concentrations:
- The mean concentration of the test substance (calculated for a study duration of 7 hours) was 0.43 mg/L.
- No. of animals per sex per dose:
- 3
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Clinical examinations took place each workday. Lethality was checked each day.
- Necropsy of survivors performed: yes
Results and discussion
- Mortality:
- No mortality was observed.
- Clinical signs:
- other: During exposure: intermittently breathing, increased masticatory movement, snout wiping After exposure: nothing abnormal detected
- Body weight:
- Not determined.
- Gross pathology:
- No treatment related effects were seen during necropsy.
Applicant's summary and conclusion
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.