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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 946-282-7 | 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
Endpoint summary
Administrative data
Description of key information
Skin sensitisation (OECD 406): not sensisiting
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:
- 20 Sep - 30 Oct 2004
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Version / remarks:
- adopted in July 1992
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Version / remarks:
- 96/54/EC
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Behörde für Arbeit, Gesundheit und Soziales, Hamburg, Germany
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- The test was done before LLNA as first-choice method for in-vivo testing was set into force.
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- male
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Age at study initiation: 27 days
- Weight at study initiation: 247 - 315 g
- Housing: in pairs in MAKROLON cages (type IV) on granulated textured wood
- Diet: ssniff Ms-H V2233 (ssniff Spezialdiäten GmbH, Soest, Germany), ad libitum
- Water: tap water, ad libitum, analysis was performed
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 ± 3
- Humidity (%): 40 - 70
- Photoperiod (hrs dark / hrs light): 12/12 - Route:
- intradermal
- Vehicle:
- other: sesame oil
- Concentration / amount:
- 10%
- Day(s)/duration:
- Day 0 / single injections
- Adequacy of induction:
- highest concentration used causing mild-to-moderate skin irritation and well-tolerated systemically
- Route:
- epicutaneous, occlusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- 100%
- Day(s)/duration:
- Day 7 / 48 h
- Adequacy of induction:
- highest concentration used causing mild-to-moderate skin irritation and well-tolerated systemically
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: sesame oil
- Concentration / amount:
- 50%
- Day(s)/duration:
- Day 21 / 24 h
- Adequacy of challenge:
- highest non-irritant concentration
- No. of animals per dose:
- 5 (controls), 10 (test groups)
- Details on study design:
- RANGE FINDING TESTS:
A range finding study was performed to determine the appropriate dose level of the test substance following intradermal and epicutaneous administrations. 8 animals were used: 6 animals for the topical and 2 for the intracutaneous administration.
For the intradermal administration 3 concentrations of the test item (0.01, 0.1 and 1%) were injected intradermally into one and 3 further concentrations (5, 10 and 50%) into a second animal. Solutions up to 1% did not reveal any skin reactions, a concentration of 5% revealed a discrete or patchy erythema, a concentration of 10% revealed a moderate and confluent erythema, a concentration of 50% revealed an intense erythema and swelling 24, 48 and 72 hours after start of administration.
For the epicutaneous administration 2 concentrations each (1% and 5%, 10% and 25%, 50% and 100%) were applied to the shaved or depilated flanks of 3 animals each.
Administration of a 50% solution to the shaved skin revealed a discrete or patchy erythema, a concentration of 100% revealed a moderate and confluent erythema 48 and 72 hours after start of administration.
Administration of a 50% solution to the depilated skin revealed no skin reaction, a concentration of 100% revealed a discrete or patchy erythema 24, 48 and 72 hours after start of administration.
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 2 (intradermal and epicutaneous, respectively)
- Exposure period: single injection (intradermal) and 48 h (epicutaneous)
- Test group:
Intradermal (3 pairs of injections):
Injection 1: a 1:1 mixture (v/v) FCA/0.9% NaCI
Injection 2: test substance in sesame oil
Injection 3: test substance in a 1:1 mixture (v/v) FCA/physiological saline
Epicutaneous: undiluted test substance
- Control group:
Injection 1: a 1:1 mixture (v/v) FCA/0.9% NaCI
Injection 2: sesame oil
Injection 3: sesame oil in a 1:1 mixture (v/v) FCA/physiological saline
Epicutaneous: sesame oil
- Site: shoulder region (intradermal + epicutaneous)
- Duration: Days 0-7
- Concentrations: intradermal 10%, epicutaneous 100%
B. CHALLENGE EXPOSURE
- No. of exposures: 1 (challenge)
- Day of challenge: 21 (challenge)
- Exposure period: 24 h
- Test groups: test substance in sesame oil and sesame oil
- Control group: test substance in sesame oil and sesame oil
- Site: left flank (test substance in sesame oil) and right flank (sesame oil)
- Concentrations: 50%
- Evaluation: 24 and 48 h after patch removal - Challenge controls:
- The control group is actually a challenge control.
- Positive control substance(s):
- yes
- Remarks:
- benzocaine was dissolved in 40% ethanolic 0.9% sodium chloride solution, Induction: intradermal 2% (w/v), epicutaneous 5% (w/v), challenge: 5% (w/v)
- Positive control results:
- The positive control substance induced positive reactions in 20/20 animals (100%), thus meeting the reliability criteria for the Guinea Pig Maximisation Test (≥ 30% positive response). The positive control group was not carried out concurrently with this study but is a historical background data group from a study performed during April/May 2004.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- Induction intradermal: 0%; challenge: 50%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- Induction intradermal: 10%, challenge: 50%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- Induction intradermal: 2%; challenge: 5%
- No. with + reactions:
- 20
- Total no. in group:
- 20
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- Induction intradermal: 0%; challenge: 50%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- Induction intradermal: 10%, challenge: 50%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- Induction intradermal: 2%; challenge: 5%
- No. with + reactions:
- 20
- Total no. in group:
- 20
- Interpretation of results:
- other: CLP/EU GHS criteria not met, no classification required according to Regulation (EC) No 1272/2008
- Conclusions:
- Under the conditions of the guinea pig maximisation test the test substance revealed no sensitising properties.
- Executive summary:
The skin sensitising potential of the test substance was investigated in a guinea pig maximisation test (GPMT test) according to OECD Guideline 406 and in compliance with GLP (2004). A range finding study was performed to determine the appropriate dose level of the test substance in sesame oil following intradermal and epicutaneous administrations. For the intradermal administration 3 concentrations of the test item (0.01, 0.1 and 1%) were injected intradermally into one and 3 further concentrations (5, 10 and 50%) into a second animal. For the epicutaneous administration 2 concentrations each (1% and 5%, 10% and 25%, 50% and 100%) were applied to the shaved or depilated flanks of 3 animals each. Based on the results of the preliminary study, a 10% solution of the test substance in sesame oil for the first induction stage (intradermal) on Day 0, the undiluted test substance for the second induction stage (epicutaneous) on Day 7 and a 50% concentration for the challenge on Day 21 were selected.
In the main study, 10 animals were used to investigate the skin sensitising potential of the test substance. In addition, 5 animals treated with sesame oil only served as vehicle reference. The 10% solution of the test substance used for the first induction stage on Day 0 revealed a moderate and confluent erythema in 5 animals 25 hours after administration, a discrete or patchy erythema in 5 animals 25 hours and in 7 animals 48 hours after administration. In the second induction stage on Day 7, 2 mL of the undiluted test substance revealed a moderate and confluent erythema in 6 animals 49 hours after start of administration, a discrete or patchy erythema in 4 animals 49 hours and in 6 animals 72 hours after start of administration. The challenge with 2 mL of the 50% solution of the test substance in sesame oil on Day 21 revealed no skin irritation in any animal. The body weight gain of animals treated with test substance was within the expected range during the experiment. The vehicle reference revealed no skin reactions per se. Based on the results of this GPMT test, the test substance was not regarded as a skin sensitizer under the conditions of the test.
Reference
A 10% solution of test substance in sesame oil chosen for the intradermal induction stage revealed a moderate and confluent erythema in 5 animals 25 h after administration, a discrete or patchy erythema in 5 animals 25 h and in 7 animals 48 h after administration.
2 mL of 100% test substance chosen for the epicutaneous induction revealed a moderate and confluent erythema in 6 animals 49 h after start of administration, a discrete or patchy erythema in 4 animals 49 h and in 6 animals 72 h after start of administration.
The challenge with 2 mL of a 50% solution of the test substance in sesame oil revealed no skin irritation in any animal.
The body weight gain of the animals treated with test substance was within the range of the vehicle reference during the experiment. The behaviour remained unchanged.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
The skin sensitising potential of the test substance was investigated in a guinea pig maximisation test (GPMT test) according to OECD Guideline 406 and in compliance with GLP (2004). A range finding study was performed to determine the appropriate dose level of the test substance in sesame oil following intradermal and epicutaneous administrations. For the intradermal administration 3 concentrations of the test item (0.01, 0.1 and 1%) were injected intradermally into one and 3 further concentrations (5, 10 and 50%) into a second animal. For the epicutaneous administration 2 concentrations each (1% and 5%, 10% and 25%, 50% and 100%) were applied to the shaved or depilated flanks of 3 animals each. Based on the results of the preliminary study, a 10% solution of the test substance in sesame oil for the first induction stage (intradermal) on Day 0, the undiluted test substance for the second induction stage (epicutaneous) on Day 7 and a 50% concentration for the challenge on Day 21 were selected.
In the main study, 10 animals were used to investigate the skin sensitising potential of the test substance. In addition, 5 animals treated with sesame oil only served as vehicle reference. The 10% solution of the test substance used for the first induction stage on Day 0 revealed a moderate and confluent erythema in 5 animals 25 hours after administration, a discrete or patchy erythema in 5 animals 25 hours and in 7 animals 48 hours after administration. In the second induction stage on Day 7, 2 mL of the undiluted test substance revealed a moderate and confluent erythema in 6 animals 49 hours after start of administration, a discrete or patchy erythema in 4 animals 49 hours and in 6 animals 72 hours after start of administration. The challenge with 2 mL of the 50% solution of the test substance in sesame oil on Day 21 revealed no skin irritation in any animal. The body weight gain of animals treated with test substance was within the expected range during the experiment. The vehicle reference revealed no skin reactions per se. Based on the results of this GPMT test, the test substance was not regarded as a skin sensitizer under the conditions of the test.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
The available data on skin sensitisation of the test substance do not meet the criteria for classification according to Regulation (EC) No 1272/2008, and are therefore conclusive but not sufficient for classification.
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.