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Diss Factsheets
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EC number: 214-684-5 | CAS number: 1185-53-1
- 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
Endpoint summary
Administrative data
Link to relevant study record(s)
- Endpoint:
- dermal absorption in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Principles of method if other than guideline:
- Percutaneous absorption of TRIS HCl was studied in 0.1% and 10% solution in-vitro in 4 samples of human abdominal skin, in a FRANZ diffusion cell.
- GLP compliance:
- not specified
- Radiolabelling:
- yes
- Remarks:
- carbon-14 labelled solution
- Species:
- other: in-vitro, human abdominal skin in a FRANZ diffusion cell
- Strain:
- other: in-vitro, human abdominal skin in a FRANZ diffusion cell
- Sex:
- not specified
- Type of coverage:
- other: not applicable
- Vehicle:
- not specified
- Doses:
- - Concentration: 0.1% (1 g/L) and 10% (100 g/L)
- Dose volume: 100 µL - No. of animals per group:
- not applicable
- Details on in vitro test system (if applicable):
- SKIN PREPARATION
- Source of skin: human skin comes from biopsies obtained after plastic surgery of the abdomen
- Type of skin: human abdominal skin
- Preparative technique: skin is cut with a dermatome
- Thickness of skin (in mm): 0.3
- Storage conditions: stored frozen
PRINCIPLES OF ASSAY
- Diffusion cell: FRANZ diffusion cell
- Flow-through system: jacket with double circulation of water surrounds the lower part
- Test temperature: 37 °C - Key result
- Time point:
- 24 h
- Dose:
- 100 µl of a 10 % solution
- Parameter:
- percentage
- Absorption:
- < 1 %
- Key result
- Time point:
- 24 h
- Dose:
- 100 µl of a 1 % solution
- Parameter:
- percentage
- Absorption:
- < 1 %
Reference
After 24 h, the percutaneous absorption of TRIS-HCl through human abdominal skin in-vitro was very low, regardless of the concentration of the solution. The mean percentages of the applied TRIS HCl dose that had passed into the survival liquid were 0.506 ± 0.765% for the 0.1% solution and 0.797 ± 0.691% for the 10% solution. These differences are not significant.
For both solutions, the maximum value of flux was reached after 4 h and remained essentially constant during the rest of the experiment. However, the value of flux was about 150 times higher for the 10% solution (6.922 ± 6.179 µg/cm2/h) than for the 0.1% solution (0.039 ± 0.052 µg/cm2/h).
After washing, the retention of the test substance in the epidermis and dermis was low: For the 0.1% solution, 0.14 ± 0.19% TRIS HCl remained in the epidermis and 0.69 ± 1.33% in the dermis. For the 10% solution, 0.13 ± 0.21% TRIS HCl was detected in the epidermis and 0.22 ± 0.21% in the dermis. Therefore, the test substance is not retained in the horny layer (epidermis).
The test substance was almost totally eliminated by washing the skin after 24 h. For the 0.1% solution, 91.13 ± 4.67% TRIS HCl was found in the washing waters and for the 10% solution, a quantity of 90.45 ± 4.06%.
However, significant differences in permeability from one skin sample to the other were recorded. (The experiments were carried out on 4 skin samples of different origin: mulatto skin; skin 2 and 3: white skin.) The differences of the individual measurements of the skin samples were lower for the 0.1% solution.
At the end of the 24 h, regardless of the concentration of the solution, the radioactivity found in the epidermis and the dermis was low (less than 1% of the applied dose) and the washing waters contained more than 90% of the applied dose.
Description of key information
percutaneous absorption in-vitro (human abdominal skin placed in a FRANZ diffusion cell): < 1%
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
- Absorption rate - dermal (%):
- 1
Additional information
A quantitative study of percutaneous absorption in-vitro was carried out on human abdominal skin placed in a FRANZ diffusion cell (reference 7.1.2 -1). After 24 h, the percutaneous absorption of TRIS HCl through human skin was very low regardless of the concentration of the TRIS HCl solution (10% and 0.1% TRIS AMINO solutions were tested). Less than 1% of the applied dose was found. For both solutions, the maximum value of flux was reached after 4 h and remained essentially constant during the rest of the experiment (totally 24 h). However, the value of flux was about 150 times higher for the 10% solution (6.922 ± 6.179 µg/cm²/h) than for the 0.1% solution (0.039 ± 0.052 µg/cm²/h). After washing, the retention of TRIS HCl in the epidermis and dermis was also less than 1% of the applied dose. Therefore, TRIS HCl did not retain in the horny layer but was almost totally eliminated by washing the skin. The washing waters contained more than 90% of the applied dose.
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