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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 458-930-1 | CAS number: -
- 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
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Genetic toxicity: in vitro
Administrative data
- Endpoint:
- in vitro gene mutation study in bacteria
- Remarks:
- Type of genotoxicity: gene mutation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 004
- Report date:
- 2004
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- bacterial reverse mutation assay
Test material
- Test material form:
- other: clear colourless liquid
- Details on test material:
- - Name of test material (as cited in study report): Ceraphyl 55
- Data of manufacture: 29 July 2003
- Physical state: Clear colourless liquid
- Analytical purity: 99.77%
- Impurities (identity and concentrations): 0.23% as isotridecanol
- Lot/batch No.: P1743
- Expiration date of the lot/batch: January 2006
- Storage condition of test material: Room temperature, in the dark
Constituent 1
Method
Species / strainopen allclose all
- Species / strain / cell type:
- S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
- Species / strain / cell type:
- E. coli WP2 uvr A
- Metabolic activation:
- with and without
- Test concentrations with justification for top dose:
- 0.1 mL volume additions were used for plate-incorporation treatment and 0.05 mL volume additions were used for pre-incubation treatments
Final concentration (µg/plate);
78.13
156.3
312.5
625
1250
2500
5000 - Vehicle / solvent:
- Ethanol
Controls
- Untreated negative controls:
- yes
- Remarks:
- Ethanol
- Negative solvent / vehicle controls:
- yes
- Remarks:
- Ethanol
- Positive controls:
- yes
- Positive control substance:
- 4-nitroquinoline-N-oxide
- 9-aminoacridine
- 2-nitrofluorene
- sodium azide
- benzo(a)pyrene
- other: 2-aminoanthracene
- Details on test system and experimental conditions:
- Toxicity Range-Finder Experiment
Triplicate plates with and without S9 mix were used. Negative (solvent) and positive controls were included in quintuplicate and triplicate, respectively. An initial Range Finder test was performed using TA100 strain only. Ceraphyl 55 was tested at 1.6, 40, 200, 100, 5000 µg/plate with and without metabolic activation (positive and negative controls included). The plating was achieved by adding 2.5 mL molten agar at 46±1C:
- 0.1 mL bacterial culture
- 0.1 mL test article solution
- 0.5 mL 10% S-9 mix or buffer solution
The culture were mixed and placed on agar plates. The plates were incubated at 37±1C in the dark for 3 days and then checked for revertant colonies.
Mutation Experiment
Two experiments were conducted using four strains of Salmonella Typhimurium and one strain Escherichia coli, with and without S9. The first experiment showed negative results; therefore the second experiment included a pre-incubation step. The test article (or control solution), bacteria and S9 mix were mixed together and incubated for 1 hour at 37±1C with shaking, before addition of 2.5 molten agar at 43±1C. Plating followed the normal procedure. In the second experiment, the volume addition in the pre-incubation treatments was reduced to 0.05 mL due to the solvent used (Ethanol).
Ethanol and other organic solvents are toxic at 0.1 mL, therefore 0.05 mL was chosen to minimise the possibility of toxicity.
Experiment 2 was repeated using WP2 uvrA strain with and without S9. - Evaluation criteria:
- The assay was considered valid if:
1. The mean negative control counts fell within the normal ranges (Laboratory database)
2. The positive control chemicals induced clear increase in revertant numbers confirming discrimination between different strains, and an active S9 preparation
3. No more than 5% of the plates were lost due to contamination or other events.
4. A dose related increase in revertant numbers was observed that was at least two times the mean negative control counts for strain TA98, TA100 and WP2 uvrA and at least three times the mean negative control counts for strain TA1535 and TA1537.
5. The positive control has to be reproducible. - Statistics:
- Mean and standard deviations were calculated from all individual plates of all experiments.
Results and discussion
Test results
- Species / strain:
- S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Additional information on results:
- Precipitation of the test article was observed following treatment of the two highest doses, both with and without S9.
- Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative
The test article Ceraphyl 55 does not induce mutation in Salmonella Typhimurium (TA98, TA100, TA1535 and TA1537) and one strain of Escherichia coli ( WP2 uvrA). - Executive summary:
The objective of the study was to evaluate the mutagenic activity of the test material Ceraphyl 55 using four strains of Salmonella Typhimurium (TA98, TA100, TA1535 and TA1537) and one strain of Escherichia coli ( WP2 uvrA), both with and without S9. An initial range finder toxicity study was performed using only TA100 strain. No evidence of toxicity was observed at concentration of 1.6, 8, 40, 200, 1000 and 5000 µg/plate. Precipitation was observed at the two highest doses, with or without S9. The Experiment 1 included all strains and the same doses tested in the range finder test and as previously, no evidence of toxicity was observed at concentration of 1.6, 8, 40, 200, 1000 and 5000µ/plate. Precipitation of the test material was observed at the highest dose, with or without S9. The Experiment 2 was performed using all strains with and without S9 and a dose range from 78.13 to 5000 µg/plate. A pre-incubation step was included to increase the range of mutagenic chemicals able to induce positive responses in this test system. No evidence of toxicity was observed. Test material precipitation was observed at the two highest doses, both with or without S9. The negative and positive controls were included all gave results that fell within the acceptable range. The result of the test shows no increase in revertant numbers in any strain treatment with or without metabolic activation. In conclusion, Ceraphyl 55 is not mutagenic in Salmonella Typhimurium (TA98, TA100, TA1535 and TA1537) and one strain of Escherichia coli ( WP2 uvrA), both with and without S9.
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.
![ECHA](/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/echa_logo.png)
Embora a ECHA disponibilize muito material em linha na sua língua, uma parte desta página está disponível apenas em inglês. Mais informações sobreas práticas de multilinguismo da ECHA.
Bem-vindo ao sítio Web da ECHA O navegador Internet Explorer 7 (e versões anteriores) não é totalmente suportado por este sítio Web. Por favor atualize o seu Internet Explorer para uma versão mais recente.
Este sítio Web utiliza cookies a fim de garantir a melhor experiência possível nos nossos sítios Web.
Saiba mais sobre como utilizar cookies.