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EC number: 907-434-8 | 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 23 July 1997 - 22 August 1997
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted in accordance with EPA, EC and OECD test guidelines, and in compliance with GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 998
- Report date:
- 1998
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EPA OTS 798.4100 (Skin Sensitisation)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Notification Yakushin 1 No. 24 11 September 1989, Pharmaceutical Affairs Bureau, MOHW "Skin Sensitization Tests".
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- no
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- The study was conducted long before the LLNA existed and the requirement was present
Test material
- Reference substance name:
- Benzoflex 2-45
- IUPAC Name:
- Benzoflex 2-45
- Reference substance name:
- Oxydiethylene dibenzoate
- EC Number:
- 204-407-6
- EC Name:
- Oxydiethylene dibenzoate
- Cas Number:
- 120-55-8
- Molecular formula:
- C18H18O5
- IUPAC Name:
- 2-[2-(benzoyloxy)ethoxy]ethyl benzoate
- Details on test material:
- - Name of test material (as cited in study report): Benzoflex 2-45 (Diethylene glycol dibenzoate DEGDB)
- Physical state: Clear colourless liquid
- Storage condition of test material: Room temperature.
Constituent 1
Constituent 2
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- male
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: D. Hall, Newchurch, Staffordshire, England
- Age at study initiation: Approximately four to seven weeks
- Weight at study initiation: 316 - 436 g
- Housing: Housed in groups of five in suspended metal cages with wire mesh floors.
- Diet: Vitamin C enriched guinea-pig diet FD2 was provided ad libitum.
- Water: mains drinking water provided ad libitum.
- Acclimation period: Five days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19 to 28.5°C
- Humidity (%): 44 to 66%
- Air changes (per hr): 15
- Photoperiod (hrs dark / hrs light): 12 hours light per 24 hour period.
IN-LIFE DATES: From: 23 July 1997 To: 22 August 1997
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal and epicutaneous
- Vehicle:
- other: None for induction injection and application; Alembicol D for the challenge application.
- Concentration / amount:
- Used as supplied for topical and intradermal injection induction exposures; Used as supplied and as 50% (v/v) in Alembicol D for the topical challenge exposure.
Challengeopen allclose all
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- other: None for induction injection and application; Alembicol D for the challenge application.
- Concentration / amount:
- Used as supplied for topical and intradermal injection induction exposures; Used as supplied and as 50% (v/v) in Alembicol D for the topical challenge exposure.
- No. of animals per dose:
- 20 for test substance group and test substance vehicle control group; 10 for positive control group and vehicle control group to positive control group.
- Details on study design:
- RANGE FINDING TESTS:
The intradermal and topical irritancy of a range of dilutions of the test substance was investigated to identify where possible (a) concentrations of the test substance that would produce irritation suitable for the induction phase of the main study and (b) a maximum non-irritant concentration by the topical route of administration for the challenge phase. Animals for these investigations were pre treated with an intradermal injection of Freund's complete adjuvant (FCA) 50:50 with water for irrigation (Ph Eur) at least one week prior to the start of the preliminary investigations.
The procedure employed for these investigations was as follows:
Intradermal injections - Intradermal injections (0.1 mL/site) were made into the clipped flank of a total of four guinea pigs, using a range of concentrations of the test material in a suitable vehicle. As no adverse reactions were observed for the first two guinea pigs receiving concentrations 0.1 - 10% v/v, further concentrations (20-100% v/v) were investigated. The resulting dermal responses were assessed approximately 24 and 72 hours later.
Topical application - Approximately 0.5 mL of each of a range of concentrations of the test substance in a suitable vehicle was applied to patches of surgical gauze (20 x 20mm). These were placed on the clipped and shaved flanks of each of four guinea pigs. The patches were covered by a strip of "Blenderm" and firmly secured by "Elastoplast" wound round the trunk and covered with "Sleek impervious" plastic adhesive tape. After an exposure period of approximately 6 hours, the dressings were removed and the reaction sites were assessed for erythema and oedema on a numerical basis according to the system given. Further examination ofthe sites was carried out approximately 24 and 48 hours after removal of the dressings.
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 2 (One by intradermal injections, one by topical application)
- Exposure period: 8 days (6 days following injections plus two days following dermal application).
- Test groups: 1)FCA in water (50/50 v/v); 2) Test substance as supplied; 3) Test substance in FCA (50/50 v/v).
- Control group: Vehicle control for test substance, Positive control (hexyl cinnamic aldehyde (HCA)), Vehicle control for positive control.
- Site: Scapular region
- Frequency of applications: As noted above.
B. CHALLENGE EXPOSURE
- No. of exposures: 1
- Day(s) of challenge: One day, two weeks after topical induction.
- Exposure period: 24 hours
- Test groups: Test group and vehicle control group were exposed to 0.2 mL test substance and 0.2 mL test substance in Alembicol D (50% v/v).
- Control group: Positive control groups were exposed to HCA and HCA 50% in Alembicol D
- Site: Test substance or HCA as supplied was applied to an anterior site; test substance or HCA in Alembicol D was applied to the posterior site.
- Evaluation (hr after challenge): 24 and 48 - Positive control substance(s):
- yes
- Remarks:
- Hexyl Cinnamic Aldehyde
Results and discussion
- Positive control results:
- Dermal reactions were seen in all ten test animals compared to none in the controls. Therefore all ten test animals gave positive responses.
In vivo (non-LLNA)
Resultsopen allclose all
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 0.2 mL, material as supplied or 50% in Alembicol
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- No signs of ill health or toxicity were recorded.
- Remarks on result:
- no indication of skin sensitisation
- Remarks:
- Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: 0.2 mL, material as supplied or 50% in Alembicol. No with. + reactions: 0.0. Total no. in groups: 20.0. Clinical observations: No signs of ill health or toxicity were recorded..
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0.2 mL, material as supplied or 50% in Alembicol
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- No signs of ill health or toxicity were recorded.
- Remarks on result:
- no indication of skin sensitisation
- Remarks:
- Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: 0.2 mL, material as supplied or 50% in Alembicol. No with. + reactions: 0.0. Total no. in groups: 20.0. Clinical observations: No signs of ill health or toxicity were recorded..
- Key result
- Reading:
- other: All animals
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 50%
- No. with + reactions:
- 10
- Total no. in group:
- 10
- Clinical observations:
- moderate erythema
- Remarks on result:
- positive indication of skin sensitisation
- Key result
- Reading:
- other:
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 50:50 FCA and water
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Remarks:
- None
Applicant's summary and conclusion
- Interpretation of results:
- other:
- Remarks:
- EU-GHS criteria not met
- Conclusions:
- In this study, DEGDB did not produce evidence of skin sensitization (delayed contact hypersentisivity) in any of the twenty test animals.
Evidence of skin sensitization was produced by hexyl cinnamic aldehyde (HCA) in all of the ten positive control test animals thus confirming the sensitivity of the method. - Executive summary:
A study was performed to determine the potential for skin sensitization to guinea pigs of the test substance DEGDB. The study was conducted according to EPA, OECD and EC test guidelines, and in compliance with GLP. Evidence of skin sensitization was seen in all animals treated by the positive control substance, Hexyl cinnamic aldehyde, confirming the sensitivity of the method. DEGDB did not produce evidence of skin sensitization (delayed contact hypersensitivity) in any of the animals tested.
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