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EC number: 221-906-4 | CAS number: 3277-26-7
- 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
There are no skin sensitisation data for the registered substance, 1,1,3,3-tetramethyldisiloxane (CAS 3277-26-7). Therefore data for the structural analogue, hexamethyldisiloxane (HMDS; CAS 107-46-0) have been read across. A human patch test study on the related hexamethyldisiloxane (CAS 107-46-0), reported no evidence of sensitising potential (Dow Corning Corporation, 1992).
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:
- 02.12.1991 to 10.01.1992
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Principles of method if other than guideline:
- Human Patch test to determine whether the test material was capable of sensitising the skin of humans under controlled patch test conditions.
- GLP compliance:
- not specified
- Type of study:
- patch test
- Justification for non-LLNA method:
- An LLNA study was not performed because there is an existing reliable study for skin sensitisation using Human Patch 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:
- human
- Sex:
- male/female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Not applicable
- Age at study initiation: 18 to 78 years
- Weight at study initiation: Not applicable
- Housing: Not applicable
- Diet (e.g. ad libitum): Not applicable
- Water (e.g. ad libitum): Not applicable
- Acclimation period: Not applicable
ENVIRONMENTAL CONDITIONS: Not applicable
IN-LIFE DATES: From: 02.12.1991 to 10.01.1992 - Route:
- epicutaneous, semiocclusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- Undiluted
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- Undiluted
- No. of animals per dose:
- 100
- Details on study design:
- 1st application: Induction undiluted semiocclusive
(0.2ml)
2nd application: Challenge undiluted semiocclusive (0.2ml)
One hundred subjects were employed in this study. Semi-occlusive, 2 cm x 2 cm Webril pad patches were applied to the infrascapular area of the back, either to the right or left of the midline. The induction phase consisted of application of the test material every 48 hours for a total of nine applications (applications made on Friday were not evaluated until Monday, prior to the re-application of test material) with the occlusive patch being removed after 24 hours. The test sites were evaluated prior to each application. Following the ninth evaluation, the subjects were dismissed for a 14-day rest period. After the rest period, identical patches were applied to sites previously unexposed to test material. These patches were removed 24 hours after application and were evaluated 48 hours and 72 hours after application. Each person was considered a complete case and used for evaluation of the material if they had six or more applications and subsequent readings during the first phase and at least one reading during the final phase.
Test Subjects
* 11 males and 97 females.
Following the second application of the test material, a significant number of subjects developed superficial epidermal erosion. It was decided to change the occlusive patch condition to semi-occlusive, applying the material to the same site beginning with the third application. - Challenge controls:
- None
- Positive control substance(s):
- no
- Positive control results:
- No positive control.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0.2 ml undiluted
- No. with + reactions:
- 0
- Total no. in group:
- 100
- Clinical observations:
- Under the conditions employed in this study, there was no evidence of skin sensitization to the test material.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 0.2 ml undiluted
- No. with + reactions:
- 0
- Total no. in group:
- 100
- Remarks on result:
- other:
- Group:
- positive control
- Remarks on result:
- other: No positive control was used.
- Group:
- negative control
- Remarks on result:
- other: Not specified
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In a well conducted human patch test hexamethyldisiloxane was not sensitising to the skin of human volunteers.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
In a well conducted human patch test, hexamethyldisiloxane (HMDS) was not sensitising to the skin of human volunteers. At induction and challenge, 0.2 ml of the undiluted test substance was applied onto the skin of 100 human volunteers under semiocclusive dressing. The challenge application was performed in a similar way. No skin reactions were observed in any of the human volunteers (Dow Corning Corporation, 1992).
Justification for classification or non-classification
Based on the available data, no classification is proposed for sensitisation according to Regulation (EC) No 1272/2008.
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