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EC number: 226-002-3 | CAS number: 5205-93-6
- 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: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Range-finding study, test procedure in accordance with national standard methods with acceptable restrictions.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 973
- Report date:
- 1973
Materials and methods
Test guideline
- Guideline:
- other: Range-finding test
- Principles of method if other than guideline:
- Range-finding study
- GLP compliance:
- not specified
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- N-[3-(dimethylamino)propyl]methacrylamide
- EC Number:
- 226-002-3
- EC Name:
- N-[3-(dimethylamino)propyl]methacrylamide
- Cas Number:
- 5205-93-6
- Molecular formula:
- C9H18N2O
- IUPAC Name:
- N-[3-(dimethylamino)propyl]-2-methylacrylamide
- Test material form:
- liquid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: no data
- Age at study initiation: no data
- Weight at study initiation: 90 to 120 gram.
- Fasting period before study: nonfasted
- Housing: no data
- Diet (e.g. ad libitum): no data
- Water (e.g. ad libitum): no data
- Acclimation period: no data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): room temperature
- Humidity (%): no data
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): no data
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- other: undiluted
- Details on oral exposure:
- MAXIMUM DOSE VOLUME APPLIED: 5.0 ml/kg bw
- Doses:
- 1.25, 2.5 and 5.0 ml/kg
- No. of animals per sex per dose:
- 5
- Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: no data
- Necropsy of survivors performed: yes
Results and discussion
Effect levelsopen allclose all
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- 3 334 mg/kg bw
- Remarks on result:
- other: LD50= 3.54 ml/kg (2.57 to 4.87 ml/kg, oral, rat, original value) Density = 0.94 g/cm³
- Sex:
- male
- Dose descriptor:
- LD100
- Effect level:
- 4 700 mg/kg bw
- Remarks on result:
- other: 5/5 animals died within 2 days
- Sex:
- male
- Dose descriptor:
- LD0
- Effect level:
- 2 350 mg/kg bw
- Remarks on result:
- other: 0/5 animals died
- Mortality:
- Dosage (ml/kg) died
5.0 5/5 animals
2.5 0/5 animals
1.25 0/5 animals - Clinical signs:
- other: Signs of intoxication at 5.0 ml/kg: sluggish, pilo-erection, heavy breathing - 10 min.
- Gross pathology:
- Dead animals: congestion in the lungs, livers, spleens and kidneys mottled,; kidneys congested; adrenals slightly congested; stomachs distended,
liquid and gas filled pylorus hemorrhaged; intestines distended, gas filled, slightly yellow.
Survivors: no abnormal findings
Applicant's summary and conclusion
- Interpretation of results:
- Category 5 based on GHS criteria
- Remarks:
- Migrated information: no Category according REGULATION (EC) No 1272/2008
- Conclusions:
- Dimethylaminopropyl methacrylamide is not listed in annex VI of REGULATION (EC) No 1272/2008. It is of low toxicity and not classified in the
current EU system. Under UN/OECD GHS the substance is Cat. 5 for acute oral toxicity.
Oral LD50 Males = 3334 mg/kg bw
GHS interpretation of the results yield in no Category for Dimethylaminopropyl methacrylamide. - Executive summary:
In an acute oral toxicity study (Range-finding test), groups of 5 male Harlan-Wistar Albino rats (source: no data, age: no data, weight: 90 to 120 gram), were given a single oral dose of undiluted Dimethylaminopropyl methacrylamide (purity: >=98%) at doses of 1.25, 2.5 and 5.0 ml/kg bw. Animals were then observed for 14 days.
Oral LD50 Males = 3.54 (2.57 - 4.87 ml/kg bw) ml/kg bw (original value) equals 3334 mg/kg bw
Dimethylaminopropyl methacrylamide is of low Toxicity based on the oral LD50 in male rats. The substance has no toxicity category according to REGULATION (EC) No 1272/2008 but according to OECD GHS criteria Dimethylaminopropyl methacrylamide has toxicity category V.
There were no treatment related clincal signs, necropsy findings or changes in body weight in surviving animals.
Oral LDL0 Males = 2.5 ml/kg bw
Oral LD100 Males = 5.0 ml/kg bw
This acute oral range-finding study is classified as acceptable. It does satisfy the requirements for an acute oral study in the male rat.
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