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EC number: 700-960-7 | CAS number: 68512-30-1
- 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 (LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2010
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.42 (Skin Sensitisation: Local Lymph Node Assay)
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- mouse local lymph node assay (LLNA)
Test material
- Reference substance name:
- Oligomerisation and alkylation reaction products of 2-phenylpropene and phenol
- EC Number:
- 700-960-7
- Cas Number:
- 68512-30-1
- Molecular formula:
- not applicable
- IUPAC Name:
- Oligomerisation and alkylation reaction products of 2-phenylpropene and phenol
- Test material form:
- liquid: viscous
- Details on test material:
- - Manufacturers identification: Novares LA 300
- Substance type: organic
- Test material is 'Oligomerisation and alkylation reaction products of 2-phenylpropene and phenol' (OAPP), EC list number 700-960-7 (assigned manually to validated substances from inquiries by ECHA). Originally the substance phenol, methylstyrenated, CAS No. 68512-30-1, EC No. 270-966-8 was submitted for registration. Subsequent to substance validation, the identity of the substance was changed by ECHA.
- for additional information see respective study record
1
- Specific details on test material used for the study:
- - Name of test material (as cited in study report): Novares LA 300 (phenol, methylstyrenated)
- Lot/batch No.: 28166
- Composition of test material: composition is specified in IUCLID Sect. 13 - Assessment reports under Certificate of Analysis_Novares LA 300_phenol, methylstyrenated
- Stability under test conditions: no measured data; based on chemical structure assumed to be stable
- Storage condition of test material: room temperature, exclusion of light
In vivo test system
Test animals
- Species:
- mouse
- Strain:
- Balb/c
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Breeding farm VELAZ s.r.o., Koleč u Kladna, Czech Republic
- Age at study initiation: 8 - 10 wks
- Weight at study initiation: 17 - 19 g
- Housing: macrolon cages
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +- 3
- Humidity (%): 30 – 70
- Photoperiod (hrs dark / hrs light): 12 / 12
Study design: in vivo (LLNA)
- Vehicle:
- other: DAE 433
- Concentration:
- mixture of 40% dimethylacetamide, 30% acetone and 30% ethanol
- No. of animals per dose:
- 5
- Details on study design:
- RANGE FINDING TESTS:
- Compound solubility: dispersion
- Irritation: no
- Lymph node proliferation response: not examined
MAIN STUDY
ANIMAL ASSIGNMENT AND TREATMENT
- Criteria used to consider a positive response:
Stimulation index (SI) is ≥ 3
Response increases in dose-related manner
Criteria for irritation potential: individual and mean ear weight
TREATMENT PREPARATION AND ADMINISTRATION:
Days 1-3: 25 µL test suspension in DAE 433 , 1x on day 1, 2, and 3
Days 4 and 5: no treatment
Day 6: Injection of 250 μL of phosphate-buffered saline (PBS) containing 7.5 x105 Bq (c. 21 µCi) of 3H-methyl thymidine
into all test and control mice via the tail vein. Five hours later, the animals were killed.
- Positive control substance(s):
- other: DNCB (dinitrochlorbenzene, 0.5% (w/v) solution)
- Statistics:
- Non-parametric Kruskal-Wallis test, and then the non-parametric two-group Mann-Whitney rank test (probability level 0.05) was applied to all two-group comparisons [using software Statgraphic ® Centurion (version XV, USA)].
Results and discussion
In vivo (LLNA)
Resultsopen allclose all
- Key result
- Parameter:
- EC3
- Value:
- 3.63
- Parameter:
- SI
- Value:
- 2.36
- Test group / Remarks:
- 0.3% test substance in vehicle; 5 animals
- Parameter:
- SI
- Value:
- 2.68
- Test group / Remarks:
- 3% test substance in vehicle; 5 animals
- Parameter:
- SI
- Value:
- 16.35
- Test group / Remarks:
- 30% test substance in vehicle; 5 animals
Any other information on results incl. tables
Table 1: Individual and mean radioactivity in cell suspensions (Report Table 4)
Activity (DPM) |
|||||
Animal No. |
NC (1-5) |
PC (6-10) |
30% (11-15) |
3% (16-20) |
0.3% (21-25) |
1 |
550.98 |
11374.69 |
9354.53 |
1425.77 |
1232.24 |
2 |
485.39 |
10401.94 |
9984.31 |
1475.60 |
1484.48 |
3 |
568.93 |
10347.82 |
11634.71 |
1367.08 |
1128.80 |
4 |
526.30 |
8837.38 |
9107.79 |
1301.28 |
1222.94 |
5 |
596.74 |
9493.34 |
4517.77 |
1748.67 |
1091.42 |
Group mean |
545.67 |
10091.03 |
8919.82 |
1463.68 |
1231.98 |
SI |
1.00 |
18.49 |
16.35 |
2.68 |
2.26 |
NC = vehicle control; PC = positive control
Table 2: Individual and average ear weights (Report Table 5)
Weight of ear biopsies (milligrams) |
|||||
Animal No. |
NC (1-6) |
PC (7-12) |
30% (13-18) |
3% (19-24) |
0.3% (25-30) |
1 |
24.5 |
27.4 |
32.7 |
25.0 |
21.8 |
2 |
25.2 |
27.5 |
28.4 |
23.0 |
23.1 |
3 |
23.8 |
26.5 |
34.2 |
21.4 |
21.4 |
4 |
23.4 |
26.7 |
29.4 |
21.5 |
21.0 |
5 |
24.7 |
27.2 |
41.2 |
21.7 |
25.0 |
Group mean |
24.32 |
27.06* |
33.18* |
22.52 |
22.46 |
SD |
0.72 |
0.44 |
5.07 |
1.53 |
1.62 |
NC = vehicle control; PC = positive control
* statistically significant with p =< 0.05, Mann-Whitney test
Table 3: Summary table (Report Table 6)
Group |
Radioisotope incorporation in lymph nodes |
Ear weight |
|
Mean DPM |
SI |
Mean (mg) |
|
NC |
545.67 |
1.0 |
24.32 |
PC |
10091.03 |
18.49+ |
27.06 |
30% |
8919.82 |
16.35+ |
33.18 |
3% |
1463.68 |
2.68 |
22.52 |
0.3% |
1231.98 |
2.26 |
22.46 |
Bold figures with + = values >= 3
Applicant's summary and conclusion
- Interpretation of results:
- Category 1B (indication of skin sensitising potential) based on GHS criteria
- Conclusions:
- In this LLNA according to OECD TG 429, an EC3 of 3.63 was determined for the substance oligomerisation and alkylation reaction products of 1-phenylpropene and phenol. Resulting EU/GHS classification is skin sensitising Cat. 1B (EC3 > 2).
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