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Diss Factsheets
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EC number: 204-317-7 | CAS number: 119-36-8
- 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:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Well-reported non guideline study
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- publication
- Title:
- Percutaneous absorption of salicylates from some commercially available topical products containing methyl salicylate or salicylate salts in rats
- Author:
- Megwa SA, Benson HAE, Roberts MS
- Year:
- 1 995
- Bibliographic source:
- J Pharmacy Pharmacol 47:891-896
Materials and methods
Test guideline
- Qualifier:
- no guideline required
- Principles of method if other than guideline:
- Measurement of dermal absorption
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Methyl salicylate
- EC Number:
- 204-317-7
- EC Name:
- Methyl salicylate
- Cas Number:
- 119-36-8
- Molecular formula:
- C8H8O3
- IUPAC Name:
- methyl salicylate
- Details on test material:
- - Name of test material (as cited in study report):
Metsal Cream (20% MeS)
Dencorub Cream (28.3% MeS)
Biosal Cream (12% MeS)
Deep heat Cream (12.74% MeS)
Goanna Rub (10% MeS)
Constituent 1
- Radiolabelling:
- no
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
Results and discussion
- Signs and symptoms of toxicity:
- no effects
- Dermal irritation:
- no effects
- Absorption in different matrices:
- - Skin test site: MeS was well absorbed
Any other information on results incl. tables
For each of the 5 preparations containing MeS, MeS was absorbed and mainly converted to SA during transport through the skin.
Applicant's summary and conclusion
- Conclusions:
- Topically applied MeS can penetrate deeply into tissues. Local concentrations higher than circulating systemic concentrations are suggestive that direct diffusion and local blood redistribution contribute to this effect
- Executive summary:
In a study to examine dermal penetration of MeS from a topical preparation, dogs (5 male greyhounds) were anaesthetised and microdialysis probes placed in the dermis and gluteal muscle over each coxofemoral (hip) joint.. MeS was applied topically over the left hip joint. Dialysate and plasma (blood samples from the cephalic and femoral veins) were obtained during the subsequent 5 hours. Dogs were euthanatized, and tissue samples and synovial fluid were collected and analyzed for MeS and SA by use of HPLC.
SA and MeS concentrations increased rapidly (<30 minutes after application) in dialysate obtained from treated dermis. SA also appeared in plasma within 30 minutes and reached a plateau concentration after 2 hours, although combined concentrations (SA plus MeS) in plasma obtained from femoral vein samples were twice concentrations (SA only) measured in plasma obtained from the cephalic vain. Treated muscles had a progressive decrease in concentration of SA plus MeS, but it was substantially higher than that in untreated muscle. Substantial amounts of SA and MeS were also measured in synovial fluid of treated joints.
Topically applied MeS can penetrate deeply into tissues. Local concentrations higher than circulating systemic concentrations are suggestive that direct diffusion and local blood redistribution contribute to this effect.
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