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EC number: 453-230-2 | CAS number: 406679-89-8
- 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:
- 2002-02-13 until 2002-04-12
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: OECD test under GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 002
- Report date:
- 2002
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- LLNA has not been available/mandatory in 2002.
Test material
- Reference substance name:
- -
- EC Number:
- 453-230-2
- EC Name:
- -
- Cas Number:
- 406679-89-8
- Molecular formula:
- Hill formula: C5H11NO3Si CAS formula: C5H11NO3Si
- IUPAC Name:
- (isocyanatomethyl)dimethoxymethylsilane
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Harlan Winkelmann GmbH, D-33178 Borchen
- Age at study initiation: not stated in the report
- Weight at study initiation: 300-500 g
- Housing: The animals were barrier maintained (semi-barrier) in an air conditioned
room
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: Adequate
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 3°C
- Humidity (%): 55 +/- 10%
- Air changes (per hr): at least 10 x / hour
- Photoperiod (hrs dark / hrs light): 12/12
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal and epicutaneous
- Vehicle:
- cotton seed oil
- Concentration / amount:
- For the intradermal injection (induction - first stage) the test item was applied at a concentration of 1% (diluted in Cotton Seed Oil).
For the topical application (induction - second stage) the test item was applied at a 100% concentration.
For the topical application (challenge) the test item was applied at a 100% concentration.
Challengeopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- cotton seed oil
- Concentration / amount:
- For the intradermal injection (induction - first stage) the test item was applied at a concentration of 1% (diluted in Cotton Seed Oil).
For the topical application (induction - second stage) the test item was applied at a 100% concentration.
For the topical application (challenge) the test item was applied at a 100% concentration.
- No. of animals per dose:
- Test group: 10
Negative control group: 5 - Details on study design:
- RANGE FINDING TESTS:
For the justification of dose levels a preliminary test was performed. Three animals were topically treated with 25% / 50% and 100% concentration of
the test item. No signs of irritation and systemic toxicity were recorded for any of the concentrations.
Therefore the 100% concentration was chosen for the topical induction and for the challenge, respectively.
Two animals were intradermally treated with 1% / 2.5% and 5% concentration of the test item. Signs of erythema grade 4 were recorded 24, 48 and 72 h after application of the 5% concentration as well as 2.5% concentration. Signs of erythema grade 1 were recorded 24, 48 and 72 h after application of the 1% concentration.
Therefore the concentration of 1 % was chosen for the intradermal induction
MAIN STUDY
A. INDUCTION EXPOSURE
First Stage, Intradermal InJection
Three pairs of intradermal injections of 0.1 ml volume were given in the shoulder region which was cleared of hair by clipping so that one of each
pair lies on each side of the midline.
Test group: Day 0
Injection 1: Freund's Adjuvant complete, 1 + 1 (v/v) diluted with isotonic saline
Injection 2: Prepared Test item
Injection 3: Prepared Test item at a concentration of 50% (VN) in Freund's Adjuvant complete, 1 + 1 (v/v) diluted with isotonic saline
Control group : Day 0
Injection 1: Freund's Adjuvant complete, 1 + 1 (v/v) diluted with isotonic saline
Injection 2: Vehicle
Injection 3: Vehicle at a concentration of 50% (V/V) in Freund's Adjuvant complete, 1 + 1 (v/v) diluted with isotonic saline
Injections 1 and 2 were given close to each other and nearest to the head, while 3 is given toward the caudal part of the test area.
Second Stage, Topical Application
Test and Control Group: Day 6
Approximately twenty-four hours before the topical induction application the test area was closely clipped.
Test Group: Day 7
A patch was loaded with 0.5 ml of the test item, applied to the test area and held in contact by an occlusive dressing for 48 hours.
Control Group: Day 7
A patch was loaded with 0.5 ml of the vehicle and applied to the test area and held in contact by an occlusive dressing for 48 hours.
B. CHALLENGE EXPOSURE
The flanks of treated and control animals were cleared of hair by closely clipping and the use of a depilation creme.
Test and Control Group: Day 20
A patch loaded with 0.5 ml of the prepared test item was applied to the left flank of the animals and, a patch loaded with 0.5 ml vehicle to the right flank
(intraspecific control), respectively. The patches were held in contact by an occlusive dressing for 24 hours. At the end of the challenge skin was cleaned
with the aid ofmoistened gauze patches.
Observation
Approximately 21 hours after removing the patch the challenge area was cleaned and cleared of hair. Approximately 24 hours after removing of the
patch the skin reaction was observed and recorded according to the grades shown below. Two more observations were recorded 48 and 72 hours after
patch removal. - Positive control substance(s):
- no
- Remarks:
- but historical positive controls for the laboratory reported.
Results and discussion
- Positive control results:
- Positive control substance: Mercaptobenzothiazole, Purity> 98%, CAS No. 149-30-4, Lot 117H3487, Sigma Chemicals Co.
Concentrations:
2% induction I phase
25% induction 11 phase
15% challenge
The sensitization rate after application of the positive control substance Mercaptobenzothiazole (15% in Vaseline) was 60 %, confirming the reliability of the test system.
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 100 %
- No. with + reactions:
- 7
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: 100 %. No with. + reactions: 7.0. Total no. in groups: 10.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 100 %
- No. with + reactions:
- 7
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: 100 %. No with. + reactions: 7.0. Total no. in groups: 10.0.
- Reading:
- other: 3rd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 100 %
- No. with + reactions:
- 7
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: other: 3rd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 100 %. No with. + reactions: 7.0. Total no. in groups: 10.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 100 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: negative control. Dose level: 100 %. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 100 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: negative control. Dose level: 100 %. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- other: 3rd reading
- Hours after challenge:
- 72
- Group:
- negative control
- Dose level:
- 100 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- other: Reading: other: 3rd reading. . Hours after challenge: 72.0. Group: negative control. Dose level: 100 %. No with. + reactions: 0.0. Total no. in groups: 5.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 15
- No. with + reactions:
- 3
- Total no. in group:
- 5
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 15
- No. with + reactions:
- 3
- Total no. in group:
- 5
Applicant's summary and conclusion
- Interpretation of results:
- sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Considering the reported data of this sensitization test it can be stated that the test item caused skin reactions identified as sensitization.
- Executive summary:
During the induction phase the guinea pigs (10 test group, 5 control group all females, strain: Hsd Poc: DH) were intradermally injected with 1% test item (diluted in Cotton Seed Oil) and topically treated with 100% test item. After a latency of 2 weeks - to allow a potential reaction of the immune system - the animals were challenged with 100% test item on the flank. The grade of skin reactions was compared to control animals, which were treated with Cotton Seed Oil during the induction stage, and during challenge phase with 100% test item, respectively.
The sensitization rate after application of the test item was 70 %.
Under the test conditions described below the test item showed clear sensitizing properties. According to the EC criteria for classification and labelling requirements for dangerous substances and preparations (Guidelines in Commission Directive
93/21 EEC) labelling is necessary as the sensitization rate was more than 30%.
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