Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 947-972-0 | 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin corrosion: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- The experimental start date was 16 April 2018, and the experimental completion date was 20 April 2018.
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 018
- Report date:
- 2018
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 431 (In Vitro Skin Corrosion: Human Skin Model Test)
- Version / remarks:
- 29 July 2016
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: EC Guideline No. 440/2008. Part B: Methods for the Determination of Toxicity and other health effects, Guideline B.40 BIS: "In Vitro Skin Corrosion: Human Skin Model Test". Official Journal of the European Union No. L142.
- Version / remarks:
- 31 May 2008
- Deviations:
- no
- GLP compliance:
- yes
- Remarks:
- Analyses conducted to support the information cited in the Certificate of Analysis for the test item were not conducted in compliance with the GLP or GMP regulations but under a sponsor or sponsor subcontractor quality system.
Test material
- Reference substance name:
- 2,4,4 TMDI function group 1 + mercaptan, mono-reacted
- IUPAC Name:
- 2,4,4 TMDI function group 1 + mercaptan, mono-reacted
- Reference substance name:
- 2,4,4 TMDI function group 2 + mercaptan, mono-reacted
- IUPAC Name:
- 2,4,4 TMDI function group 2 + mercaptan, mono-reacted
- Reference substance name:
- 2,2,4 TMDI function group 1 + mercaptan, mono-reacted
- IUPAC Name:
- 2,2,4 TMDI function group 1 + mercaptan, mono-reacted
- Reference substance name:
- 2,2,4 TMDI function group 2 + mercaptan, mono-reacted
- IUPAC Name:
- 2,2,4 TMDI function group 2 + mercaptan, mono-reacted
- Reference substance name:
- 2,2,4 bi-reacted compound
- IUPAC Name:
- 2,2,4 bi-reacted compound
- Reference substance name:
- 2,4,4 bi-reacted compound
- IUPAC Name:
- 2,4,4 bi-reacted compound
- Reference substance name:
- 2,4,4-trimethylhexa-1,6-diyl diisocyanate
- EC Number:
- 239-714-4
- EC Name:
- 2,4,4-trimethylhexa-1,6-diyl diisocyanate
- Cas Number:
- 15646-96-5
- Molecular formula:
- C11H18N2O2
- IUPAC Name:
- 1,6-diisocyanato-2,4,4-trimethylhexane
- Reference substance name:
- 2,2,4-trimethylhexa-1,6-diyl diisocyanate
- EC Number:
- 241-001-8
- EC Name:
- 2,2,4-trimethylhexa-1,6-diyl diisocyanate
- Cas Number:
- 16938-22-0
- Molecular formula:
- C11H18N2O2
- IUPAC Name:
- 1,6-diisocyanato-2,2,4-trimethylhexane
- Test material form:
- liquid
Constituent 1
Constituent 2
Constituent 3
Constituent 4
Constituent 5
Constituent 6
Constituent 7
Constituent 8
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: BZA11014
- Expiration date of the lot/batch: 21 April 2018
- Manufacturing date: 21 March 2018
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: At room temperature under nitrogen
- Not stable at higher temperatures
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing: No correction was made for purity/composition of the test item. The weighed amount of test item was flushed with nitrogen. The liquid item was applied undiluted.
In vitro test system
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Cell source:
- other: Human donors. Tissue is obtained by MatTek Corporation from accredited institutions.
- Justification for test system used:
- The test is based on the experience that corrosive chemicals show cytotoxic effects following short-term exposure to the stratum corneum of the epidermis. The test is designed to predict and classify the skin corrosion potential of a test item by assessment of its effect on a three-dimensional human epidermis model.
- Vehicle:
- unchanged (no vehicle)
- Details on test system:
- RECONSTRUCTED HUMAN EPIDERMIS (RHE) TISSUE
- Model used: EpiDerm
- Tissue batch number(s): 28326
- Delivery date: 18 April 2018
- Date of initiation of testing: 16 April 2018
TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: all incubations, with the excepton of the test item incubation of 3 minutes at room temperature, were carried out at 37 +/- 1ºC.
REMOVAL OF TEST MATERIAL AND CONTROLS
-Volume and number of washing steps: After the exposure period, the tissues were washed with phosphate buffered saline (Invitrogen Corporation, Breda, The Netherlands) to remove residual test item. Due to the characteristics of the test item it was difficult to remove and therefore some residual test item could still be left on the skin. The skin inserts were carefully dried. Rinsed tissues were kept in 24 well plates on 300 μL DMEM until 6 tissues (= one application time) were dosed and rinsed.
MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: MTT concentrate (5 mg/mL) diluted (1:5) with MTT diluent (supplemented DMEM). Both supplied by MatTek Corporation.
- Incubation time: 3 hours
- Spectrophotometer: TECAN Infinite® M200 Pro Plate Reader
- Wavelength: 570 nm
FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
- Viability: Acceptance criteria: OD (540-570 nm) 1.0 - 3.0. Pass (value: 2.124 +/- 0.066)
- Barrier function: Acceptance criteria: ET-50 3.68 - 8.02 h. Pass (value: 6.13 h)
- No contamination
NUMBER OF REPLICATE TISSUES: Two tissues for a 3-minute exposure and 2 tissues for a 1-hour exposure
NUMBER OF INDEPENDENT TEST SEQUENCES / EXPERIMENTS TO DERIVE FINAL PREDICTION: 1
PREDICTION MODEL / DECISION CRITERIA (choose relevant statement)
- The test substance is considered to be corrosive to skin if the viability after 3 minutes exposure is less than 50%, or if the viability after 3 minutes exposure is greater than or equal to 50 % and the viability after 1 hour exposure is less than 15%.
- The test substance is considered to be non-corrosive to skin if the viability after 3 minutes exposure is greater than or equal to 50% and the viability after 1 hour exposure is greater than or equal to 15%. - Control samples:
- yes, concurrent negative control
- yes, concurrent positive control
- Amount/concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 50 µL
NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 50 µL
POSITIVE CONTROL
- Amount(s) applied (volume or weight): 50 µL
- Concentration (if solution): 8N - Duration of treatment / exposure:
- 3 minutes and 1 hour
- Duration of post-treatment incubation (if applicable):
- Not applicable
- Number of replicates:
- 2 replicates for each test condition
Results and discussion
In vitro
Resultsopen allclose all
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 3-minutes incubation
- Value:
- >= 102
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- no indication of irritation
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 1-hour incubation
- Value:
- >= 81
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- no indication of irritation
- Other effects / acceptance of results:
- - OTHER EFFECTS:
- Direct-MTT reduction: Not observed
- Colour interference with MTT: Not observed
ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: yes. The absolute mean OD570 of the two tissues of the negative control is within the laboratory historical control data range.
- Acceptance criteria met for positive control: yes . The mean relative tissue viability following 1-hour exposure to the positive control is < 15% (observed value = 6.8%).
- Acceptance criteria met for variability between replicate measurements: yes. In the range 20-100% viability, the coefficient of variation between tissue replicates is <= 30% (obtained value = <=22%).
Any other information on results incl. tables
Mean tissue viability:
3 -minute application, % viability | 1 -hour application, % viability | |
Negative control | 100 | 100 |
Test item | 102 | 81 |
Positive control | 14 | 6.8 |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The Thio Isocyanate Adduct is not corrosive in the in vitro skin corrosion test under the experimental conditions described in this report.
- Executive summary:
The study was performed to evaluate Thio Isocyanate Adduct for its ability to induce skin corrosion on a human three dimensional epidermal model (EpiDerm (EPI-200)). The possible corrosive potential of Thio Isocyanate Adduct was tested through topical application for 3 minutes and 1 hour. The study procedures were based on OECD guideline 431 and performed according to GLP. Thio Isocyanate Adduct was applied undiluted (50 μL) directly on top of the skin tissue. The positive control had a mean relative tissue viability of 6.8% after the 1-hour exposure. The absolute mean OD570 (optical density at 570 nm) of the negative control tissues was within the acceptance limits of OECD 431 (lower acceptance limit ≥0.8 and upper acceptance limit <=2.8) and the laboratory historical control data range. In the range of 20 - 100% viability the Coefficient of Variation between tissue replicates was <= 22%, indicating that the test system functioned properly.
Skin corrosion is expressed as the remaining cell viability after exposure to the test item. The relative mean tissue viability obtained after 3-minute and 1-hour treatments with Thio Isocyanate Adduct compared to the negative control tissues was 102% and 81%, respectively. Because the mean relative tissue viability for Thio Isocyanate Adduct was not below 50% after the 3-minute treatment and not below 15% after the 1-hour treatment Thio Isocyanate Adduct is considered to be not corrosive.
In conclusion, Thio Isocyanate Adduct is not corrosive in the in vitro skin corrosion test under the experimental conditions described in this report.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.