Registration Dossier
Registration Dossier
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: 203-336-8 | CAS number: 105-83-9
- 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

Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1996
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: No GLP, no guideline was followed (published literature)
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 996
- Report date:
- 1996
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- , see below in "Principles of method"
- Principles of method if other than guideline:
- Male rabbits generally five per group were examined . Fur was carefully removed from the ventral skin, using an electric clipper . The rabbit was immobilized while 0.01 mL of sample was applied to the ventral skin. The dose site was not occluded during the contact period, which lasted 30 min or, if earlier, until the test material appeared to be completely absorbed or evaporated . At the end of the contact period, any remaining sample residue was removed with moist gauze and the rabbit was returned to its cage. After 18-24 h, the rabbits were again immobilized and the application site was swabbed with cottonwool moistened with lukewarm water (to enhance the visibility of any reaction), and the site was inspected for signs of local injury and inflammation . Additional sets of rabbits were tested using diluted sample, as required, to establish a dose response. The undiluted test material was also tested on occluded rabbit skin . For this procedure 0.5 mL (or 0 .5 g) of test material was applied to the shaven dorsal trunk skin and covered with a 1-in square gauze patch. Polyethylene sheeting was loosely wrapped around the animal's trunk and secured . During a 4-h contact period, the animal was restrained to avoid disturbing the dose site . Excess test material was carefully removed with cleansing tissue . Reactions were recorded at the end of the contact period and at 24 and 48 h following contact.
- GLP compliance:
- no
Test material
- Reference substance name:
- N,N-bis(3-aminopropyl)methylamine
- EC Number:
- 203-336-8
- EC Name:
- N,N-bis(3-aminopropyl)methylamine
- Cas Number:
- 105-83-9
- Molecular formula:
- C7H19N3
- IUPAC Name:
- bis(3-aminopropyl)(methyl)amine
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- not specified
Test system
- Type of coverage:
- other: In the first part of the experiment with the undiluted tets substance the dose site was not occluded. In the second part (new set of animals) using a diluted test substance the dose site was occluded.
- Preparation of test site:
- shaved
- Vehicle:
- other: In the first part of the experiment the undiluted test substance was applied. In the second part the test substance diluted in water was applied
- Controls:
- not required
- Amount / concentration applied:
- In the first part of the experiment 0.01 mL of the undiluted test substance was applied.
in the second part bof teh experiment 0.5 mL of the diluted (10 %) test substance was applied. - Duration of treatment / exposure:
- In the first part (undiluted test substance) exposure duration of 30 minutes or until the test substance was absorbed,
In the second part (diluted test substance) 4 hours exposure duration. - Observation period:
- In the first part (undiluted test substance) - 18 - 24 hours.
In the second part (diluted test substance) - 24 and 48 hours. - Number of animals:
- 5 animals
- Details on study design:
- TEST SITE
- Type of wrap if used: In the second part of the experiment polyethylene sheeting was loosely wrapped around the animal's trunk and secured.
REMOVAL OF TEST SUBSTANCE
- Washing: yes, at the end of the contact/ exposure period, any remaining sample residue was removed with moist gauze.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- other: necrosis
- Basis:
- mean
- Time point:
- other: 24 hours
- Remarks on result:
- other: Necrosis was observed in all animals applied with the undiluted tets substance
- Irritation parameter:
- other: irritaion, necrosis
- Basis:
- mean
- Time point:
- other: 24, 48 hours
- Remarks on result:
- other: No indications were observed when animals were treated with the diluted (10 %) test substance.
Applicant's summary and conclusion
- Interpretation of results:
- corrosive
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
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.
