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EC number: 938-828-8 | CAS number: 1463474-95-4
- 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
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Endpoint summary
Administrative data
Description of key information
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
- Study period:
- February 1996
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Principles of method if other than guideline:
- In the report, it had not been clearly mentioned whether the epidermal application during induction was semi-occlusive or occlusive. Additional information from the test lab learnt that it was occlusive.
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Several tests have been carried out with the structurally related read across substances, including the LLNA. The guinea pig tests were carried out long before there was the requirement to perform a LLNA or in vitro tests.
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Charles River, Germany
- Age at study initiation: approximately 5 weeks
- Weight at study initiation: 361 - 407 g
- Housing: 1 or 2 animals per cage with wire-mesh floors
- Diet (e.g. ad libitum): free access to standard guinea pig diet
- Water (e.g. ad libitum): free access to tap water
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21
- Humidity (%): 50
- Air changes (per hr): 15 air changes per hour
- Photoperiod (hrs dark / hrs light): 12 hours artificial fluorescent light and 12 hours dark per day
IN-LIFE DATES: From: February 5, 1996 To: February 29, 1996 - Route:
- other: intradermal and epicutaneous, occlusive
- Vehicle:
- water
- Concentration / amount:
- Induction: 5% (intradermal), 50% test material concentration (epicutaneous)
- Day(s)/duration:
- 7 days after the intradermal injection the sites were treated with the test sample for 48 h
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- water
- Concentration / amount:
- Challenge: 50%, 25% and 10% test material concentrations and the vehicle (distilled water)
- Day(s)/duration:
- 24 h
- No. of animals per dose:
- - Main test:
Experimental group: 10 females
Control group: 5 females
- Preliminary test: 4 animals in total - Details on study design:
- RANGE FINDING TESTS:
- By intradermal route tested concentrations: in 1 animal a 25% and a 10% concentration (0.1 mL each injected), in another animal a 5% and a 2% concentration
- By epidermal route:
1. after intradermal injection: in 1 animal 50% (0.5 mL), in the other animal 25% concentration
2. 50%, 25%, 10% and 5% (0.05 mL each) in two other animals
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures:
Intradermal injections (3 pairs and 0.1 ml/site):
1. FCA, 50:50 with water
2. test material at 5% concentration
3. test material in a 50:50 mixture of FCA
Topical application: After treatment with SDS a patch with 0.5 mL of 50% test material was applied
Controls: treated as experimental animals except that vehicle only was administered
- Exposure period: topical application 48 hours
- Test groups: test material
- Control group: vehicle (distilled water)
- Site: (clipped) scapular region
- Frequency of applications: 7 days after the intradermal injection the sites were treated with the test sample for 48 h
- Duration: from injection till topical application was 7 days
- Concentrations: 5% intradermal and 50% epidermal
B. CHALLENGE EXPOSURE
- No. of exposures:
Topical application: on day 22 all animals were challenged by a cutaneous application of the test material. 4 concentrations were applied and maintained for 24 hours.
- Day(s) of challenge: 24 hours (3 weeks after the first intradermal injection)
- Exposure period: 24 h
- Test groups: test material
- Control group: test material
- Site: a clipped flank
- Concentrations: 50%, 25%, 10% and the vehicle, as occlusive applications
- Evaluation (hr after challenge): evaluated approximately 24 and 48 hours after removal of the dressing
Grading system:
Score
No visible change 0
Discrete or patchy erythema 1
Moderate and confluent erythema 2
Moderate erythema and swelling 3
Intense erythema and swelling 4
OTHER: - Challenge controls:
- Yes, treated with test material.
- Positive control substance(s):
- yes
- Remarks:
- Alpha-Hexylcinnamicaldehyde, tech. 85%
- Positive control results:
- - Test material:
ALPHA-HEXYLCINNAMICALDEHYDE, TECH. 85% (CAS no. 101-86-0) was fabricated under lot no. 80281 and the purity was 99.4% (GLC) (Aldrich Chemicals Co., Germany).
- Results: The skin reactions in the experimental animals observed in response to the 50% and 25% test substance concentrations in the challenge phase were considered indicative of sensitisation, based on the absence of any response in the control animals.
These results lead to a sensitisation rate of 100 per cent for the 50% concentration and to a sensitisation rate of 60 per cent for the 25% concentration.
From these results, it was concluded that the Albino Dunkin Hartley strain of guinea pig is an appropriate animal model for the performance of studies designed to evaluate the sensitising potential of a substance in a Maximisation type of test. - Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 25%
- No. with + reactions:
- 1
- Total no. in group:
- 10
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 10%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 0%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 25%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 10%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 25%
- No. with + reactions:
- 1
- Total no. in group:
- 10
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 10%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 25%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 10%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- 24 h respectively 48 h after challenge, the test and control animals did not show specific primary skin irritations or a reference to a specific sensitive effect. The test material FeEDDHMANa should not be classified as sensitizing to the skin.
- Executive summary:
A Guinea Pig Maximisation test was conducted with a group of 10 Dunkin Hartley guinea pigs and a negative control group of 5 Dunkin Hartley guinea pigs. They were used to investigate the skin sensitising properties of the FeEDDHMANa (trade name Bolikel FE). The study was performed in accordance with the method of B. Magnusson and A. M Kligman (OECD-guidelines: Guideline 406 ‘Skin Sensitisation’). The study was designed and performed according to Good Laboratory Practice Standards.
The test group received first intradermal injections with 5% test substance. After 7 days a topical application of 10% SDS in vaseline was performed. On Day 8 the animals were treated with a 48 h occlusive epicutaneous application of 50% concentration in distilled water. Two weeks after the last application, the test animals received a 24 h occlusive epicutaneous application (concentrations 50%, 25%, 10% and 0%). After 24 h and 48 h skin reactions were scored. Controls were treated with vehicle (distilled water) during induction and similar as the treated group during challenge.
No clinical signs and no deaths were noted during the study.
After the induction phase some skin effects were seen, like brown staining of the skin, small scabs, erythema and necrosis. The reactions were considered to be enhanced by SDS treatment.
After the challenge application, a discrete erythema was recorded in 1/10 animals of the 25% treated group at the 24- and 48-hour reading. The response to the 25% concentration was considered non-specific, since no response was observed to the higher concentration (50%) in this animal. No skin reactions were evident in the control animals.
24 h respectively 48 h after challenge, the test and the control animals did not show specific primary skin irritations or a reference to a specific sensitive effect. The test material FeEDDHMANa should not be classified as sensitizing to the skin.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
It is concluded that the structurally related substances EDDHMA-Fe and EDDHA-Fe are not a skin sensitiser. In addition it is noted that HBED-Fe, EDDHMA-Fe and EDDHA-Fe do not interact with protein, which is considered a requirement for sensitization (needed for haptenisation). Finally, also decades of use of EDDHMA-Fe and EDDHA-Fe did not result in any reports of people becoming sensitized.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
- Additional information:
Decades of use of the structurally related substances EDDHMA-Fe and EDDHA-Fe did not result in any reports of people becoming sensitized.
Justification for classification or non-classification
One key study (OECD 406 and GLP) did not indicate sensitising properties of the structurally related substanxce EDDHMA-Fe. This was supported by other studies with this substance and by studies with EDDHA-Fe. HBED-Fe (UVCB) should not be classified with regard to sensitisation according to Directive 67/548/EEC (DSD) and to Regulation (EC) No 1272/2008 (CLP), respectively.
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.
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