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EC number: 215-350-1 | CAS number: 1323-03-1
- 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: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 26 February - 8 April 1976
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study is non-GLP, but well described except for ommissions in experimental conditions like temperature and humidity.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 976
Materials and methods
- Principles of method if other than guideline:
- Landsteiner and Jacobs Guina pig sensitization procedure. The method included ten sensitizing injections (three times weekly) followed by an eleventh (re-test) injection.
- GLP compliance:
- no
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Result are from a study performed in 1976, i.e. before the LLNA requirement.
Test material
- Reference substance name:
- Dodecyl lactate
- EC Number:
- 228-504-8
- EC Name:
- Dodecyl lactate
- Cas Number:
- 6283-92-7
- Molecular formula:
- C15H30O3
- IUPAC Name:
- dodecyl 2-hydroxypropanoate
- Reference substance name:
- Ceraphyl 31
- IUPAC Name:
- Ceraphyl 31
- Test material form:
- solid - liquid: suspension
- Details on test material:
- Ceraphyl 31 (15% active)
Batch # 1441
Received 25 February 1976
Constituent 1
Constituent 2
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- not specified
- Sex:
- male
- Details on test animals and environmental conditions:
- Body weights: 300-500 grams.
Cages: Commercial rabbit pellets and fed with greens, carrots and water.
No further data on test conditions.
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal
- Vehicle:
- physiological saline
- Concentration / amount:
- 0.1%
Challengeopen allclose all
- Route:
- intradermal
- Vehicle:
- physiological saline
- Concentration / amount:
- 0.1%
- No. of animals per dose:
- 10
- Details on study design:
- Injections were performed three times weekly until a total of ten had been applied. The first injection contained 0.05 ml, while the other nine were each 0.1 ml. An eleventh injection was applied as challenge below the area of the ten sensitization injections. Twenty-four hours after each injection, scorings were performed for the diameter, height and redness of the reactions. A comparison of the reaction following the challenge injection was made with the average score for the sensitizing injections. Substantial increase in response after challenging indicates a possible significant sensitization.
- Challenge controls:
- 0.1 % corn oil in physiological saline was employed as a control.
- Positive control substance(s):
- no
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- other: average of ten sensitizing injections
- Group:
- test chemical
- Dose level:
- 0.1% solution
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: other: average of ten sensitizing injections. Group: test group. Dose level: 0.1% solution. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- other: reading after eleventh injection
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 0.1% solution
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: other: reading after eleventh injection. . Hours after challenge: 24.0. Group: test group. Dose level: 0.1% solution. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- other: average of ten sensitizing injections
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: other: average of ten sensitizing injections. . Hours after challenge: 24.0. Group: negative control. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- other: reading after eleventh injection
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: other: reading after eleventh injection. . Hours after challenge: 24.0. Group: negative control. Dose level: 0. No with. + reactions: 0.0. Total no. in groups: 10.0.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: other:
- Conclusions:
- On the challenge injection, none of the test animals exhibited reactions higher than the average of the original scores. Although the test method is not equivalent to the method described in international guidelines, the total lack of response indicates that the test material is not sensitizing.
- Executive summary:
CERAPHYL® 31 (15% active) was not a sensitizer to guinea pig skin. Ten white male guinea pigs were treated using intracutaneous injections of 0.1% CERAPHYL® 31 (15% active) three times a week for a total of ten injections. The first injection was 0.5 ml and the remaining injections were 0.1 ml. Sterile saline was used as the control and the same amounts as test material were injected. Two weeks following the tenth injection, all animals were challenged with 0.05 ml CERAPHYL® 31 on a virgin site. The test sites were scored 24 hours after each injection. No dermal reactions were exhibited during either the induction phase or challenge phase of the study.
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