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EC number: 939-487-8 | 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
Endpoint summary
Administrative data
Description of key information
In the key skin sensitisation study, conducted according to OECD Test
Guideline 406 and in compliance with GLP, the test material was not
sensitising to guinea pigs skin. Twenty male guinea pigs exhibited no
reactions indicative of skin sensitisation when treated with test
material (Dow Corning Corporation, 1997).
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:
- 7 November 1995 to 30 September 1997
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- The restrictions were deviations from the guideline: temperature and humidity were sometimes slightly higher than recommended; sodium lauryl sulphate was not applied to the skin prior to induction 2.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- yes
- Remarks:
- (relative humidity range was 52 to 75% (not recommended to exceed 70%), temperature range of 21 to 25 °C (19 to 23 °C recommended), sodium lauryl sulphate not applied to skin prior to induction 2 (recommended for non-irritants))
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- An LLNA study was not performed because there is an existing reliable study for skin sensitisation using the Guinea Pig Maximisation test method. Furthermore, the LLNA test method is not considered to be suitable for substances that contain silicon. Please refer to the attached document for further details.
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- male
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Sasco, Inc., Madison, WI
- Age at study initiation: ~6 weeks
- Weight at study initiation: 321 to 485 g
- Housing: individually in stainless steel wire cages
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: ~3 weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21 to 25
- Humidity (%): 52 to 75
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 21 November 1995 To: 18 December 1995 - Route:
- intradermal and epicutaneous
- Vehicle:
- other: Dow Corning(R) 360 Medical Fluid
- Concentration / amount:
- 5% (first induction and challenge), 100% (second induction)
- No.:
- #1
- Route:
- intradermal and epicutaneous
- Vehicle:
- other: Dow Corning(R) 360 Medical Fluid
- Concentration / amount:
- 5% (first induction and challenge), 100% (second induction)
- No. of animals per dose:
- 20 (and 10 positive and 10 vehicle control animals)
- Details on study design:
- RANGE FINDING TESTS: 0.1 ml intradermal injections of 2.5 and 5% test material with Freund's complete adjuvant and 0.9% saline were tolerated locally and systemically by two guinea pigs. 0.3 ml of various concentrations of test material applied under Hill Top Chambers to shaved skin for 48 hours produced different levels of erythema among four guinea pigs (see Table 1 in "Any other information on results incl. tables").
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 2
- Exposure period: n/a (first induction, intradermal injection), ~48 hours (second induction, topical application)
- Test groups:
- Induction #1: six intradermal injections of 0.1 ml (2 x test material, 2 x saline/Freund's complete adjuvant, 2 x test material/saline/Freund's complete adjuvant).
- Induction #2: 1.5 ml topical test material, wrapped in elastic adhesive bandage for approximately 48 hours.
- Control group: as above, but vehicle and positive control groups administered undiluted Dow Corning(R) 360 Medical Fluid and 0.1% 1-chloro-2,4-dinitrobenzene (in propylene glycol) respectively instead of test material
- Site: skin over the scapula (shaved)
- Frequency of applications: weekly (day 1 and day 8)
- Concentrations: 5% (first induction - intradermal), 100% (second induction - topical)
B. CHALLENGE EXPOSURE
- No. of exposures: 1
- Day(s) of challenge: day 22
- Exposure period: 24 hours
- Test groups: 0.3 ml test material on left flank, 0.3 ml vehicle on the right
- Vehicle control group: 0.3 ml test material on right flank, 0.3 ml vehicle on the left
- Positive control group: 0.3 ml 1-chloro-2,4-dinitrobenzene (DNCB) in propylene glycol (PG) on left flank, 0.3 ml PG on the right flank
- Site: upper flank (shaved)
- Concentrations: 5% test substance, 0.1% DNCB, vehicles (including PG) undiluted
- Evaluation (hr after challenge): 24 and 48 hours after patch removal (48 and 72 hours after application) (See "Any other information on materials and methods incl. tables" for information on scoring of skin effects)
OTHER
- Guinea pigs were observed daily for mortality and morbidity during treatment
- Animals were weighed weekly (i.e. prior to dosing on dosing days) - Challenge controls:
- Vehicle control animals treated with test material and vehicle, positive control animals treated with DNCB in propylene glycol, and propylene glycol.
- Positive control substance(s):
- yes
- Remarks:
- 1-chloro-2,4-dinitrobenzene (in propylene glycol)
- Positive control results:
- All animals treated with the positive control substance exhibited reactions indicative of sensitisation (i.e. erythema scores of at least 1) on the first (24-hour) and second (48-hour) readings after challenge patch removal.
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 5% test material
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- none of the test animals exhibited a positive response at any time during the study
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 5% test material
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- none of the test animals exhibited a positive response at any time during the study
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0.3 ml vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- none of the vehicle control animals exhibited a positive response at any time during the study
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0.3 ml vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- none of the vehicle control animals exhibited a positive response at any time during the study
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 1-chloro-2,4-dinitrobenzene (in propylene glycol)
- No. with + reactions:
- 10
- Total no. in group:
- 10
- Clinical observations:
- All animals treated with the positive control substance exhibited a positive response at the first and second reading, with severity indices of 3.30 and 3.20 respectively
- Remarks on result:
- positive indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 1-chloro-2,4-dinitrobenzene (in propylene glycol)
- No. with + reactions:
- 10
- Total no. in group:
- 10
- Clinical observations:
- All animals treated with the positive control substance exhibited a positive response at the first and second reading, with severity indices of 3.30 and 3.20 respectively
- Remarks on result:
- positive indication of skin sensitisation
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In a GLP-compliant guinea pig maximisation test, performed in accordance with OECD Test Guideline 406, twenty male guinea pigs exhibited no reactions indicative of skin sensitisation when treated with the test material.
- Executive summary:
A guinea pig maximisation test was carried out according to OECD Test Guideline 406 and in compliance with GLP to assess the skin sensitising potential of the test material.
In the induction phase of the study, on day one, the shaved fur over the scapulae of twenty male guinea pigs were given two lots of 0.1 ml intradermal injections of the test material (at 5% in Dow Corning® 360 Medical Fluid), the 5% test material with saline and Freund’s complete adjuvant, and saline and Freund’s complete adjuvant. One week later (day eight), the same region was shaved again and saturated with 1.5 ml of neat test material, applied topically, and wrapped with an elastic adhesive bandage for 48 hours. Groups of 10 control animals were treated similarly with the vehicle (Dow Corning® 360 Medical Fluid) or the positive control substance (1-chloro-2,4-dinitrobenzene in propylene glycol).
On day 22 a challenge application of 0.3 ml 5% test material and 0.3 ml of the undiluted vehicle were each applied to one shaved flank of both the test and vehicle control animals. Positive control animals instead received 0.1% DNCB and undiluted propylene glycol. The application sites were covered with an adhesive bandage for 24 hours, with reactions read 48 and 72 hours after application (24 and 48 hours after bandage removal).
All positive control animals exhibited reactions indicative of sensitisation at both the 24- and 48-hour readings. There were no skin reactions seen at either time point for any of the test or vehicle control animals.
Under the conditions of this study, the test material was not sensitising to the skin of male guinea pigs.
Reference
Table 1: Irritant/corrosive response data for each animal at each observation time in the preliminary test
Test substance concentration (topically applied) |
Erythema (24-hour) |
Erythema (48-hour) |
Max. score: 4 |
Max. score: 4 |
|
100% |
2/2/2/1 |
1/1/1/1 |
75% |
2/2/1/0 |
1/1/0/0 |
50% |
2/1/0/0 |
1/0/0/0 |
25% |
2/1/0/0 |
0/0/0/0 |
All animals gained weight over the course of the study.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
A guinea pig maximisation test was carried out according to OECD Test Guideline 406 and in compliance with GLP to assess the skin sensitising potential of the registered substance (Dow Corning Corporation,1997). All positive control animals exhibited reactions indicative of sensitisation at both the 24- and 48-hour readings. There were no skin reactions seen at either time point for any of the test or vehicle control animals. Under the conditions of this study, the test material was found not sensitising to the skin of male guinea pigs.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Based on the available information on the lack of sensitisation potential of phenyl silsesquioxanes, no classification is required in accordance with Regulation (EC) No 1272/2008.
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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