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EC number: 200-664-3 | CAS number: 67-68-5
- 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 vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Permeability of commercial solvents through living human skin
- Author:
- Ursin C, Hansen CM, Van Dyk JW, Jensen PA, Christensen IJ, Ebbehoej J
- Year:
- 1 995
- Bibliographic source:
- Am Ind Hyg Assoc J, 56:651-660
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Evaluation of the absorption
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Dimethyl sulfoxide
- EC Number:
- 200-664-3
- EC Name:
- Dimethyl sulfoxide
- Cas Number:
- 67-68-5
- Molecular formula:
- C2H6OS
- IUPAC Name:
- dimethyl sulfoxide
- Details on test material:
- Test compound Dimethylsulfoxyde
CAS no.: 67-68-5
Source: Research Industris, Salt Lake City, Utah
Batch : no data
Purity : no data
Constituent 1
- Radiolabelling:
- no
Test animals
- Species:
- human
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- The human skin was removed from healthy females during plastic surgery of the breast. During thinning, most of the dermal tissue was removed from the epidermis using a Downs-Watson dermatome. The thickness of this unstretched "split skin" was about 1 to 2 mm. Split skin samples were stored in the above Dulbecco's medium until used for permeation measurements (<= 10 days).
Administration / exposure
- Type of coverage:
- not specified
- Vehicle:
- unchanged (no vehicle)
- Duration of exposure:
- 0.16, 0.33, 0.5, 1.0, 1.33, and 2 hr
- Doses:
- 0.5 ml of DMSO
- No. of animals per group:
- Females: 3
- Details on study design:
- Permeation measurements were made using a Franz Diffusion Cell, a two-chamber cell with a water jacket and magnetic stirrer in the collection cell. The area of exposed skin in the cell was 0.64 cm². The skin was stretched (area increase of about 3 fold) onto the cell giving a final thickness of about 300 to 600 µm. Water temperature was 37°C, which gave a skin temperature of about 34°. The receptor fluid was isotonic, nourished, saline solution (Dulbecco's medium with gentamycin [50 µg/mL]). A special cap prevented pressure build-up in the challenge half cell, containing solvent.
In all cases [3H] water was run for two hours before the test solvent in order to calibrate the relative permeability of the skin samples and to detect defective (leaky) specimens. [3H] Water permeation was measured by removing 0.5 mL samples from the collection chamber at times of 0.16, 0.33, 0.5, 1.0, 1.33, and 2 hr. The [3H] water was then removed and replaced with the challenge chemical. Its permeation rate was measured by removing 0.5 mL samples at times of 0.16, 0.33, 0.5 (or 0.66), 1.0, 2.0, 4.0, and 6.0 hr. In all the above cases fresh receptor fluid was added to replace the amount used for analysis.
DMSO was analyzed by high pressure liquid chromatography and the detection limits was 0.05 ppm.
Permeability tests and viability tests were not run on the same specimen but were always measured on the same piece of surgically removed skin. Viability tests were started either at the same time or after the permeation tests were started. If the test showed the skin was not viable, all the permeation results for that piece of skin were discarded. Skin viability was determined by measuring the ability of the skin cells to engage in DNA synthesis as measured by their ability to incorporate BrdUrd (5-bromo-2'deoxyuridine), a DNA precursor.
The viability test also was run on skin that had been exposed to solvent for 2 hr (but not used for permeability tests). The results give some insight into how the solvent affects the viability of the skin.
Results and discussion
Percutaneous absorption
- Remarks on result:
- other:
Any other information on results incl. tables
Summary of Data for the Permeability Constants of DMSO through Living Human Skin (Effect of Normalization; Effect of Skin Specimen on Variability; Deviation of steady state region from Linearity).
|
Permeability Constant |
% Error in slope |
|
Skin Donor# |
Un-Normalized |
Normalized |
|
|
|
|
|
4 |
136 |
174 |
9,4 |
4 |
198 |
323 |
10,7 |
4 |
179 |
51 |
9 |
5 |
217 |
427 |
1 |
5 |
138 |
254 |
10,7 |
7 |
112 |
127 |
25,7 |
7 |
208 |
171 |
33,7 |
7 |
220 |
270 |
35,9 |
|
|
|
|
Mean±Std. Dev. |
176 ± 42 |
224 ± 118 |
|
Applicant's summary and conclusion
- Executive summary:
The steady-state rate of permeation of commercial solvents was measured through living human skin. The skin was removed from healthy females during plastic surgery of the breast. The samples were thinned by removing the dermal tissue from the epidermis and then stretched to a thickness of 300 to 600 µm. The permeability rate of DMSO was reported to be 176 g/m2.hour compared to a permeability rate for water of 24 g/m2.hour indicating that DMSO is readily absorbed through the skin. For comparison, N-methyl-2-pyrrolidone, dimethylformamide and methylethylketone present a permeability rate of 171, 98 and 53 g/m2.hour, respectively.
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