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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 203-149-1 | CAS number: 103-83-3
- 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: other routes
Administrative data
- Endpoint:
- acute toxicity: other routes
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: No OECD guideline or GLP defined.
Data source
Reference
- Reference Type:
- publication
- Title:
- Comparative acute toxicity and primary irritancy of various classes of amines
- Author:
- Myers R.C. et al.
- Year:
- 1 997
- Bibliographic source:
- Toxic Substance Mechanisms, 16: 151-193 (1997)
Materials and methods
- Principles of method if other than guideline:
- Three- to five month old male New Zealand white rabbits (2.0-3.0 kg) were used, and maintained ad libitum on commercial diet and municipal water, except during the skin preparation and contact periods. Fur was removed from the entire trunk using an electric clipper, avoiding abrasion. Impervious plastic sheeting was wrapped around the trunk and secured. Using a calibrated syringe, test substance was injected under the edge of the plastic sheeting and spread (through gentle massaging) over as large an area as possible (Myers, 1993). Animals were placed into a restraining apparatus for a 24-h contact period. After a dosing, the wrappings and any excess test material were removed (with cleansing tissue), and the animal was returned to its cage for the remainder of a 14-d observation period. Dosed animals were observed frequently during the time of contact, and daily for 13 d after the 24-h contact. Body weights were measured before dosing and at d 14. Necropsy was conducted on decedents and sacrificed survivors. Four male rabbits were used for each dose. Variation in dosages (by a factor of two) was achieved through adjustment of dose volume. LD50 values, and 95% confidence limits, were calculated by the method of Thompson (1947) and Weil (1983).
- GLP compliance:
- not specified
- Limit test:
- no
Test material
- Reference substance name:
- Benzyldimethylamine
- EC Number:
- 203-149-1
- EC Name:
- Benzyldimethylamine
- Cas Number:
- 103-83-3
- Molecular formula:
- C9H13N
- IUPAC Name:
- benzyldimethylamine
- Details on test material:
- Physical state: Pale yellow liquid
Molecular weight: 135.23
Specific gravity : 0.894 (27°C)
Vapor pressure : 1.82 mm Hg (25°C)
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Sex:
- male
Administration / exposure
- Route of administration:
- other: percutaneous
- Vehicle:
- not specified
- Doses:
- no data
- No. of animals per sex per dose:
- 4
- Control animals:
- not specified
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- 1.66 mL/kg bw
- 95% CL:
- 1.35 - 2.04
- Remarks on result:
- other: Time to death: 1-2d
Any other information on results incl. tables
The LD50 value was 1.66 ml/kg. Rabbits died from the test substance after 1 -2 d. Local skin lesionsincluded edema, necrosis, and scabs. At the highest dosage, there was immediate hyperactivity followed by tremors, vocalization, and pupillary dilation (by 4.5 h). The weights were decreased. Pathologic changes included congestion of the liver. In addition, the animals had gray stomachs and congested kidneys.
Applicant's summary and conclusion
- Executive summary:
In an acute percutaneous study, three- to five month old male New Zealand white rabbits (2.0-3.0 kg) were used. Fur was removed from the entire trunk using an electric clipper, avoiding abrasion. Impervious plastic sheeting was wrapped around the trunk and secured. Using a calibrated syringe, test substance was injected under the edge of the plastic sheeting and spread (through gentle massaging) over as large an area as possible (Myers, 1993). Animals were placed into a restraining apparatus for a 24-h contact period. After a dosing, the wrappings and any excess test material were removed (with cleansing tissue), and the animal was returned to its cage for the remainder of a 14-d observation period. Dosed animals were observed frequently during the time of contact, and daily for 13 d after the 24-h contact. Body weights were measured before dosing and at d 14. Necropsy was conducted on decedents and sacrificed survivors. Four male rabbits were used for each dose (no data about doses used given).
Rabbits died from the test substance after 1 -2 d. Local skin lesionsincluded edema, necrosis, and scabs. At the highest dosage, there was immediate hyperactivity followed by tremors, vocalization, and pupillary dilation (by 4.5 h). The weights were decreased. Pathologic changes included congestion of the liver. In addition, the animals had gray stomachs and congested kidneys.
The LD50 value was 1.66 ml/kg.
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.