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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 209-421-6 | CAS number: 578-36-9
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation, other
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- data is from peer reviewed journals
Data source
Reference
- Reference Type:
- publication
- Title:
- Allergic Contact Dermatitis from Ethylhexyl Salicylate and Other Salicylates
- Author:
- Charlotte Gotthard Mortz, Henrik Thormann, An Goossens, and Klaus Ejner Andersen
- Year:
- 2 010
- Bibliographic source:
- Dermatitis, 21, no. 2 (2010): E7-E10
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Patch test
- Principles of method if other than guideline:
- Patch test were conducted on a patient with allergic contact dermatitis to sunscreen
- GLP compliance:
- not specified
- Remarks:
- Study data from handbook or collection of data
- Type of study:
- patch test
- Justification for non-LLNA method:
- not specified
Test material
- Reference substance name:
- Sodium salicylate
- EC Number:
- 200-198-0
- EC Name:
- Sodium salicylate
- Cas Number:
- 54-21-7
- Molecular formula:
- C7H6O3.Na
- IUPAC Name:
- sodium salicylate
- Test material form:
- solid
- Details on test material:
- - Name of test material (as cited in study report):sodium salicylate- Molecular formula :C7H6O3.Na- Molecular weight : 160.1035 g/mol- Substance type: organic- Physical state: solid- Smilies notation: c1(c(cccc1)O)C(=O)[O-].[Na+]- InChI: 1S/C7H6O3.Na/c8-6-4-2-1-3-5(6)7(9)10;/h1-4,8H,(H,9,10);/q;+1/p-1
Constituent 1
- Specific details on test material used for the study:
- - Name of test material (as cited in study report): Sodium salicylate - Molecular Formula: C7H6O3.Na- Molecular Weight: 160.105 g/mol- Smiles Notation: c1(c(cccc1)O)C(=O)[O-].[Na+]- InChI: 1S/C7H6O3.Na/c8-6-4-2-1-3-5(6)7(9)10;/h1-4,8H,(H,9,10);/q;+1/p-1- Substance Type: Organic- Physical State: Solid
Results and discussion
In vivo (non-LLNA)
Results
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 2% in petrolatum
- No. with + reactions:
- 0
- Total no. in group:
- 1
- Clinical observations:
- no signs of sensitization observed
- Remarks on result:
- no indication of skin sensitisation
Any other information on results incl. tables
Table: Patch test results
Test compound |
CAS |
Test concentration |
Function |
Day 3 reading** |
Day 7 reading** |
Sodium salicylate |
54-21-7 |
2% in petrolatum |
Denaturant and preservative |
- |
- |
**-readings are for the patient in the case report
Applicant's summary and conclusion
- Interpretation of results:
- other: not sensitizing
- Conclusions:
- No dermal reactions were observed on day 3 and day 7 of observation when the patient was tested with 2% sodium salicylate in petrolatum.Hence, sodium salicylate can be considered to be not sensitizing to skin.
- Executive summary:
Patch test were conducted on a patient with allergic contact dermatitis to sunscreen.
A 48 year old woman with a 12 year history of rosacea was advised to use sunscreen. A sample of Anthelios dermo-pediatrics SPF-50+ was given to the patient. Half year later, the patient developed facial dermatitis. She was tested with the European baseline series using panels 1,2, and 3 of the Thin Layer Rapid Use Epicutaneous Test [T.R.U.E Test] supplemented petrolatum-based allergens in Finn chambers on Scanpor tape and with her own topical products including the Anthelios dermo-pediatrics SPF-50+ lotion. The tests were occluded for 2 days and read according to the ICDRG[International Contact Dermatitis Research Group]scoring scale on day 3 and day 7.
The patient was subsequently patch test with individual components of the Anthelios dermo-pediatrics SPF-50+ lotion as provided by the manufacturer.
No dermal reactions were observed on day 3 and day 7 of observation when the patient was tested with 2% sodium salicylate in petrolatum.
Hence, sodium salicylate can be considered to be not sensitizing to skin.
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.