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EC number: 630-324-3 | CAS number: 861229-15-4
- 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
Endpoint summary
Administrative data
Description of key information
Skin sensitization: positive
Respiratory sensitization: no study available
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:
- January 11, 1994 - February 11, 1994
- 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 July, 1997
- Qualifier:
- according to guideline
- Guideline:
- other: EEC directive 92/69, Methods for the determination of toxicity, Publication No. L383A, B.6.: Acute Toxicity-Skin Sensitization
- Version / remarks:
- December 29, 1992
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- The Guinea Pig Maximazitation Test met the previous requirements before the entry into force of REACH. The GPMT is suitable and reliable to cover this endpoint. For this reason and for animal welfare reasons, no further in vivo study (LLNA test) needs to be performed.
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- batch No.of test material: 5007
- sample No.:1505E
- Expiration date of the lot/batch: March 1993
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: 4°C in the dark - Species:
- guinea pig
- Strain:
- Pirbright-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Charles River GmbH - Wiga, Sulzfeld, FRG
- Age at study initiation: young adult animals
- Weight at study initiation: 296 -355 g
- Housing: Makrolon cage, type IV; 5 animals per cage
- Bedding: Granulat Typ 3/4, SSNIFF
- Diet: ad libitum, Kliba Labordiät 341, Klingentalmühle AG, Kaiseraugst, Switzerland
- Water: ad libitum, tap water; about 2 g of ascorbic acid per 10 L water was added to the drinking water twice a week
- Acclimation period: 7 days
- Indication of any skin lesions:
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-24°C
- Humidity (%): 30-70%
- Photoperiod (hrs dark / hrs light):12h light/12h dark
Clipping of the test animals: about 3 h prior application of test substance at the appropriate application sites - Route:
- intradermal
- Vehicle:
- other: olive oil DAB 10 or Freund´s adjuvant/0.9% aqueous NaCl-solution (1:1) or olive oil
- Concentration / amount:
- 5%
- Day(s)/duration:
- 48 hours
- Route:
- epicutaneous, occlusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- 0.3 g (unchanged test substance)
- Day(s)/duration:
- 48 hours
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- unchanged test substance
- Day(s)/duration:
- 24 hours
- No.:
- #2
- Route:
- epicutaneous, occlusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- unchanged test substance
- Day(s)/duration:
- 24 hours
- No. of animals per dose:
- number of animals per control group 10
number of animals of the test group 20 - Details on study design:
- PRETEST (Dose finding)
- Amount applied: filter paper soaked in test substance or test substance formulations; animal was exposed to about 0.15 g of the test substance formulations
- Application: 2 x 2 cm filter paper strips were applied to the skin of the flanks under occlusive dressing (bandage consists of rubberized linen patches 4 x 4 cm from Russka, test patch 5 x 5 cm of Idealbinde from Pfälzische Verbandstoff-Fabrik,and Fixomull Strech adhesive fleece)
- Exposure period: test substance was applied 2 times for 24 h within a period of 96 h in order to detect non-specific phenomena that are not caused by a sensitization reaction but could possibly be attributed to a shift in the irritation threshold
- Site of application: flank, respective on the same area
- Number of test animals: 4 per test concentration (unchanged, 75%, 50% and 25%)
- Readings: about 24 and 48 h after the beginning of application
- Assessment of skin findings: scores according to Draize et al. 1959:
Erythema and eschar formation:
No erythema 0
Very slight erythrema (barely perceptible) 1
well-defined erythema 2
Moderate to severe erythema 3
Severe erythema (beet redness) to slight eschar formation (injuries in depth) 4
Oedema formation:
No oedema 0
Very slight oedema (barely perceptible) 1
Slight oedema (edges of area well-defined by definite raising) 2
Moderate oedema (raised approximately 1 millimetre) 3
Severe oedema (raised more than 1 millimetre and extending beyond the area of exposure) 4
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 6 intradermal injections in groups of two per animal
- Test groups: 20 animals
- Control group: 10 animals
- Site: shoulder
A.front row with 2 injections each of 0.1 mL Freund´s adjuvant without test substance emulsified with 0.9% aqueous NaCl-Solution in a ratio of 1:1
B.middle row with 2 injections each of 0.1 mL of the test substance formulation
C.back row with 2 injections each of 0.1 mL Freund´s adjuvant /0.9% aqueous NaCl-solution (1:1) with test substance
- Injections for control groups 1 and 2:
The animals were given the same injections (A,B,C) but without test substance, only with the formulating agent
- Readings: 24 h after application
- Assessment of skin findings: analogous to the pretest
Percutaneous induction: one week after intradermal induction
- Amount applied: 2 x 4 cm filter paper strips to the skin of the shoulder under occlusive dressing; the filter paper strip was soaked in the test substance and exposed to about 0.3 g of the test substance
-control groups not treated, since the test substance was applied unchanged and thus no solvent was used
- Duration of exposure; 48 h
- Site: shoulder, same area as in the case of the previous intradermal application
- Readings: 48 h after the beginning of application
- Assessment of skin findings: analogous to the pretest
B. CHALLENGE EXPOSURE
First challenge 21 days after intradermal induction. To clarify the results obtained in the first challende, a second challenge was carried out after the first one.
- amount applied: 2 x 2 cm filter paper strips to the skin of the flank under occlusive dressing; the filter paper strip was soaked in the test substance
- 1st challenge: treatment of the test group and of the control group 1 with the test substance (control group 2 remained untreated)
- 2nd challenge: treatment of the test group and of the control groups 1 and 2 with the test substance
- Duration of exposure: 24 h
- Site: intact flank
- Readings: 24 h and 48 h after the removal of the patch
- Assessment of skin findings: analogous to the pretest - Challenge controls:
- yes
- Positive control substance(s):
- yes
- Remarks:
- 1-chloro-2,4-dinitrobenzene (not included in this study, but seperate study was performed and results presented; Project no. 30H0383/912273)
- Positive control results:
- The positive control with 1-chloro-2,4-dinitrobenzene showed that the test system was able to detect sensitizing compounds under the laboratory conditions chosen.
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- unchanged substance
- No. with + reactions:
- 8
- Total no. in group:
- 20
- Clinical observations:
- 5 animals with very slight erythema and 3 animals with well-defined erythema
- Remarks on result:
- positive indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 0.5% in ethanol
- No. with + reactions:
- 15
- Total no. in group:
- 20
- Clinical observations:
- well-defined erythema in 8 animals and very slight erythema in 7 animals observed
- Remarks on result:
- positive indication of skin sensitisation
- Key result
- Reading:
- rechallenge
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- unchanged substance
- No. with + reactions:
- 3
- Total no. in group:
- 20
- Clinical observations:
- 2 animals with very slight erythema and 1 animal with well.defined erythema
- Key result
- Reading:
- rechallenge
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- rechallenge
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 0.5% in ethanol
- No. with + reactions:
- 19
- Total no. in group:
- 20
- Clinical observations:
- 17 animals with very slight erythema and 2 animals with well-defined erythema
- Remarks on result:
- positive indication of skin sensitisation
- Interpretation of results:
- Category 1B (indication of skin sensitising potential) based on GHS criteria
- Conclusions:
- Based on the results of the study under the test conditions chosen MCPP-P 2-EHE has a sensitizing effect on the skin of the guinea pigs in the Maximization Test.
- Executive summary:
A GLP study according OECD 406 was performed based on the method of Magnusson and Kligman to test for its skin sensitization potential of MCPP-P 2-EHE. A pretest was carried out to detect non-specific phenomena that are not caused by a sensitization reaction but could possibly be attributed to a shift in the irritation threshold. Based on this test, concentrations for intradermal (5%) and percutaneous (unchanged) induction and challenge (unchanged) were selected.
In the main test, after intradermal induction with 5% test substance, slight to well-defined signs of irritation could be observed in the treated animals. The percutaneous induction with the unchanged test substance led to increstation, partially open (caused by the intradermal induction), in addition to well-defined erythema and slight edema. The challenges with the unchanged test substance caused very slight to well-defined erythema. After the 1st challenge (21 days after intradermal induction) with the unchanged test substance, 8 out of 20 animals of the test group were observed with skin findings (40%). Most of the skin findings were mild (erythema grad 1), only three cases grad 2 erythema were noted 24h after removal of the patch. The control group did not show any skin reactions. After the 2nd challenge (28 days after intradermal induction), three animals out of 20 (15%) showed skin reactions in form of very slight erythema (2) and well defined erythema (1). Again, the control groups did not show any skin reactions. A significant lowering of the incidence of skin findings after a second challenge is a rare event with chemicals causing only mild sensitization. The positive control with 1 -chloro-2, 4 -dinitrobenzene showed that the test system was able to detect sensitizing compounds under the laboratory conditions chosen. Based on the results of the study under the test conditions chosen MCPP-P 2-EHE has a sensitizing effect on the skin of the guinea pigs in the Guinea Pig Maximization Test. The evaluation "sensitizing" results because more than 30% of the experiment animals exhibit skin reactions.
Reference
Table 1: Number of animals with skin findings after the 1st challenge and after the 2nd challenge.
|
1st challenge |
2nd challenge |
unchanged test substance |
unchanged test substance |
|
Control group 1 |
0 / 10 |
0 / 10 |
Control group 2 |
No application of test substance |
|
Test group |
8 / 20 |
3 / 20 |
x/y: number of positive reactions/number of animals tested; readings 24 h after the removal of the patch
Table 2: Number of animals with visual skin findings after the 1st challenge and after the 2nd challenge
|
1st challenge |
2nd challenge |
||
Positive ctr 0.5% in ethanol conc. |
Ethanol conc. |
Positive ctr 0.5% in ethanol conc. |
Ethanol conc. |
|
Control group 1 |
0 / 10 |
0 / 10 |
5 / 10 |
0 / 10 |
Control group 2 |
No application of test substance |
0 / 10 |
0 / 10 |
0 / 10 |
Test group |
15 / 20 |
0 / 20 |
19 / 20 |
0 / 20 |
x/y: number of positive reactions/number of animals tested; readings 24 h after the removal of the patch
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (sensitising)
- Additional information:
Skin sensitization
A GLP study according OECD TG 406 (Version 1997) was performed based on the method of Magnusson and Kligman to test for the skin sensitization potential of MCPP-P 2-EHE. A pretest was carried out to detect non-specific phenomena that are not caused by a sensitization reaction but could possibly be attributed to a shift in the irritation threshold. Based on this test, concentrations for intradermal (5% dilution) and percutaneous (unchanged substance) induction and challenge (unchanged substance) were selected. In the main test, after intradermal induction with 5% test substance, slight to well-defined signs of irritation could be observed in the treated animals. The percutaneous induction with the unchanged test substance led to increstation, partially open (caused by the intradermal induction), in addition to well-defined erythema and slight edema. The challenges with the unchanged test substance caused very slight to well-defined erythema. After the 1st challenge (21 days after intradermal induction) with the unchanged test substance, 8 out of 20 animals of the test group were observed with skin findings (40%). Most of the skin findings were mild (erythema grad 1), only three cases grad 2 erythema were noted 24h after removal of the patch. The control group did not show any skin reactions. After the 2nd challenge (28 days after intradermal induction), three animals out of 20 (15%) showed skin reactions in form of very slight erythema (2) and well defined erythema (1). Again, the control groups did not show any skin reactions. A significant lowering of the incidence of skin findings after a second challenge is a rare event with chemicals causing only mild sensitization, but no explanation causing this effect was provided. The positive control 1 -chloro-2, 4 -dinitrobenzene proofed, that the test system was able to detect sensitizing compounds under the laboratory conditions chosen. Based on the results of the study under the test conditions chosen MCPP-P-2 -EHE has a sensitizing effect on the skin of the guinea pigs in the Guinea Pig Maximization Test (BASF 30H0383/912273; 1995).
A Buehler test was performed in compliance with EPA OPP 81 -6 (Version 1984) to investigate the skin sensitization potential of MCPP-P 2-EHE in guinea pigs. Both, the induction and challenge were performed with the unchanged test substance. No reactions occurred in the animals of the control group treated at challenge (0/10), while 7/10 animals of the test group showed skin reactions mostly restricted to a small area of the challenge site. Non-localized reactions were only observed in animals at the 24 h reading after patch removal, while at later intervals only localized reactions occurred. Only in 3 animals, the localized reactions persisted at the 72h reading. At the 2nd challenge neither the previously treated control group nor the test treated animals had a positive skin reaction. The reason for the difference between the two challenge applications is unclear and makes the overall interpretation of the study difficult. However, based on the results of the first challenge, which were clearly greater than the controls, MCPP-P 2 -EHE has a sensitizing effect on the skin of the guinea pigs in the Buehler test (BASF 920881D7JE L 78/SS; 1993).
In conclusion, it was shown in a Guinea Pig Maximization Test as well as in a Buehler test that MCPP-P 2-EHE has a sensitizing potential on the skin.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Classification,
Labelling, and Packaging Regulation (EC) No 1272/2008
The available experimental test data are reliable and suitable for classification purposes under Regulation (EC) No 1272/2008. The substance is considered to be classified for skin sensitisation Cat 1B (H317" May cause an allergic skin reaction.") under Regulation (EC) No 1272/2008, as amended for the tenth time in Regulation (EU) No 2017/776.
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