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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 931-228-7 | CAS number: -
- 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
Dermal absorption
Administrative data
- Endpoint:
- dermal absorption in vivo
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented publication; study report which meets basic scientific principles
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 987
Materials and methods
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Dodecylamine
- EC Number:
- 204-690-6
- EC Name:
- Dodecylamine
- Cas Number:
- 124-22-1
- Molecular formula:
- C12H27N
- IUPAC Name:
- dodecan-1-amine
- Details on test material:
- - Name of test material (as cited in study report): lauryl amine
- Molecular formula (if other than submission substance): C12H27N
- Molecular weight (if other than submission substance): 185.35
- Substance type: primary amine
- Analytical purity: >98%
- Specific activity (if radiolabelling): 14.9 µCi/mg
- Locations of the label (if radiolabelling): C1-position
Constituent 1
- Radiolabelling:
- yes
- Remarks:
- 14-C labeled compounds
Test animals
- Species:
- mouse
- Strain:
- other: HR/De
- Sex:
- not specified
Administration / exposure
- Type of coverage:
- occlusive
- Vehicle:
- other: squalane, castor oil, or triethyl citrate (TEC)
- Duration of exposure:
- 24 h
- Doses:
- concentrations: 50, 5, 05, and 0.05 %
- No. of animals per group:
- 3
- Control animals:
- no
- Details on study design:
- APPLICATION OF DOSE:
patch test plaster
VEHICLE
- Justification for use and choice of vehicle (if other than water): exmination of vehicle influence on absorption
- Amount(s) applied (volume or weight with unit): 2 mL
- Concentration (if solution): 50 - 99.95%
- Purity: reagent grade
TEST SITE
- Preparation of test site: n.a; hairles mice were used
- Area of exposure: 200 mm² (patch test plaster, diameter 16 mm)
- Type of cover / wrap if used: plaster was covered with a thin rubber film to prevent peeling
SITE PROTECTION / USE OF RESTRAINERS FOR PREVENTING INGESTION: yes, plastic film
REMOVAL OF TEST SUBSTANCE
- Washing procedures and type of cleansing agent: no data
- Time after start of exposure: 24 hrs
SAMPLE COLLECTION
- Collection of urine and faeces: yes
- Collection of expired air: yes
- Analysis of organs: yes, skin
ANALYSIS
- Method type(s) for identification ( Liquid scintillation counting)
Results and discussion
- Dermal irritation:
- yes
Any other information on results incl. tables
Percutaneous absorption (approx. percent of dose)
Dodecylamine |
vehicle |
||
Concentration (%) |
Squalane |
Castor oil |
TEC |
50 |
6 |
4 |
5 |
5 |
28 |
22 |
13 |
0.5 |
57 |
5 |
10 |
0.05 |
30 |
6 |
4 |
The dermal absorption and excretion of dodecylamine in hairless mice was examined at various concentrations (50, 5, 0.5, and 0.05%) in different vehicles (squalane, used in cosmetics; castor oil, and triethylcitrate,TEC).
The dermal absorption reached 30 to 57% of the applied dose when dodecylamine was 0.05 to 5% in squalane. The dermal absorption of the amine was higher than that of other C12 compounds (lauryl alcohol, acid, or methyl ester). Approx 80% of the absorbed dose was metabolised and expired as carbon dioxide within 24 h.
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.