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EC number: 201-714-7 | CAS number: 86-98-6
- 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
Description of key information
The study reports of a series of patch tests performed on process operators operating in a chemical plant using the test chemical. 6 workers developed dermatitis of the face and were employed in jobs involving the charging the test chemical to a hot reaction vessel. The workers were patch tested initially with 50% test chemical in petrolatum. The reactions were read at 72 hours as ++ positive. The patch test was again repeated with 5% test chemical in petrolatum and reactions were observed and scored at 48 and 96 hours. Patch tests on normal controls were negative. Of the 6 workers tested only 4 workers showed positive reactions at 48 as well as at 96 hours. Further investigations indicated that the dermal reactions were only seen in workers charging the test chemical to a hot reaction vessel, but not amongst other workers handling the test chemical. Upon investigation it was observed that the test chemical could sublime at high temperatures, and this property of the chemical could be a possible reason for development of facial dermatitis in workers involved in charging the test chemical. Based on the observations, reactions, it can be considered that the occupational exposure to the test chemical can cause dermatitis to the operators, so the test chemical should be handled with proper care. Hence, it can be considered to be sensitizer to skin.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data from peer reviewed journal
- Qualifier:
- according to guideline
- Guideline:
- other: As mentioned below
- Principles of method if other than guideline:
- Human maximization test was perfiormed to determine the sensitization potential of the test chemical
- GLP compliance:
- not specified
- Type of study:
- patch test
- Justification for non-LLNA method:
- No data available
- Species:
- other: Human
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals and environmental conditions:
- No data available
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 5% in petrolatum
- Adequacy of induction:
- not specified
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 5% in petrolatum
- Adequacy of challenge:
- not specified
- No. of animals per dose:
- 6 workers
- Details on study design:
- RANGE FINDING TESTS:
MAIN STUDY
A. INDUCTION EXPOSURE
- Test groups: 6 workers
- Concentrations: 5% in petrolatum
B. CHALLENGE EXPOSURE
- Test groups: 6
- Concentrations: 5% in petrolatum
- Evaluation (hr after challenge): 48 and 96 hours - Challenge controls:
- No data available
- Positive control substance(s):
- not specified
- Positive control results:
- No data available
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 5%
- No. with + reactions:
- 2
- Total no. in group:
- 4
- Clinical observations:
- reappearance of the original rash in case 1 and 2
- Remarks on result:
- positive indication of skin sensitisation
- Interpretation of results:
- Category 1 (skin sensitising) based on GHS criteria
- Conclusions:
- Based on the observations, reactions, it can be considered that the occupational exposure to the test chemical can cause dermatitis to the operators, so the test chemical should be handled with proper care. Hence, it can be considered to be sensitizer to skin.
- Executive summary:
The study reports of a series of patch tests performed on process operators operating in a chemical plant using the test chemical. 6 workers developed dermatitis of the face and were employed in jobs involving the charging the test chemical to a hot reaction vessel. The workers were patch tested initially with 50% test chemical in petrolatum. The reactions were read at 72 hours as ++ positive. The patch test was again repeated with 5% test chemical in petrolatum and reactions were observed and scored at 48 and 96 hours. Patch tests on normal controls were negative. Of the 6 workers tested only 4 workers showed positive reactions at 48 as well as at 96 hours. Further investigations indicated that the dermal reactions were only seen in workers charging the test chemical to a hot reaction vessel, but not amongst other workers handling the test chemical. Upon investigation it was observed that the test chemical could sublime at high temperatures, and this property of the chemical could be a possible reason for development of facial dermatitis in workers involved in charging the test chemical. Based on the observations, reactions, it can be considered that the occupational exposure to the test chemical can cause dermatitis to the operators, so the test chemical should be handled with proper care. Hence, it can be considered to be sensitizer to skin.
Reference
Results of the patch tests
48hr |
96hr |
|
1 |
++ |
++ |
2 |
++ |
++ |
3 |
+ |
- |
4 |
- |
- |
5 |
Not performed |
|
6 |
Not performed |
|
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (sensitising)
- Additional information:
Various studies have been reviewed to determine the degree of dermal sensitization caused by the test chemical. These include in vivo studies performed on guinea pigs as well as humans for the test chemical. The results are mentioned below:
The study reports of a series of patch tests performed on process operators operating in a chemical plant using the test chemical. 6 workers developed dermatitis of the face and were employed in jobs involving the charging the test chemical to a hot reaction vessel. The workers were patch tested initially with 50% test chemical in petrolatum. The reactions were read at 72 hours as ++ positive. The patch test was again repeated with 5% test chemical in petrolatum and reactions were observed and scored at 48 and 96 hours. Patch tests on normal controls were negative. Of the 6 workers tested only 4 workers showed positive reactions at 48 as well as at 96 hours. Further investigations indicated that the dermal reactions were only seen in workers charging the test chemical to a hot reaction vessel, but not amongst other workers handling the test chemical. Upon investigation it was observed that the test chemical could sublime at high temperatures, and this property of the chemical could be a possible reason for development of facial dermatitis in workers involved in charging the test chemical. Based on the observations, reactions, it can be considered that the occupational exposure to the test chemical can cause dermatitis to the operators, so the test chemical should be handled with proper care. Hence, it can be considered to be sensitizer to skin.
This case study is supported by a guinea pig maximization test performed to evaluate the dermal sensitization potential of the test chemical. 20 male guinea pigs and 10 male guinea pigs were used as test and control animals. The study was carried out according to OECD 406 Guidelines. Dosages were chosen based on the results of dose-finding experiments. 0.1 ml of the test chemical was applied intracutaneously to the skin of the test groups.One week later, topical application of a plaster containing 0.5 ml undiluted test chemical was fixed by alu fole (occlussive condition). 3 weeks after intradermal induction, the guinea pigs were challenged with 0.5 ml of 12%- and 0.5 ml of 25%-solution of the test chemical under semi-occlusive conditions for 24 hours. Afterwards treatment areas were rinsed with physiological saline-solution. Reading were carried out 48 and 72 hours post start of the challenge and the evaluation was done by comparison of the reacting animals between test and control group. No mortality occurred, body weight development was comparable between test and control animals. 14/20 test animals gave positive reactions 48 hours after challenge with 25 % solution, 7/20 test animals gave positive reactions 72 hours after challenge with 25% solution. 3/20 test animals gave positive reactions 48 hours after challenge with 12 % solution, 1/20 test animals gave positive reactions 72 hours after challenge with 12% solution. Control animals showed no reaction at any time point. Based on these readings, the test chemical can be considered to be sensitizing to skin.
Based on the available results the test chemical can be considered to be sensitizing to skin and classified under the category “Skin Sensitizer 1” as per CLP Regulation.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Based on the available results the test chemical can be considered to be sensitizing to skin and classified under the category “Skin Sensitizer 1” as per CLP Regulation.
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