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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 284-461-5 | CAS number: 84896-44-6
- 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 irritation / corrosion
- Remarks:
- other: in vitro
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Study period:
- 28th to 30th April 2010
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study conducted to GLP. Used for read across purposes so reliability reduced to 2.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: OECD 431 “In Vitro Skin Corrosion: Human Skin Model Test” (adopted 13 April 2004)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 2-ethylhexyl 4,4-dibutyl-10-ethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate
- EC Number:
- 234-186-1
- EC Name:
- 2-ethylhexyl 4,4-dibutyl-10-ethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate
- Cas Number:
- 10584-98-2
- Molecular formula:
- C28H56O4S2Sn
- IUPAC Name:
- 2-ethylhexyl 4,4-dibutyl-10-ethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecan-1-oate
- Details on test material:
- Sponsor's identification: CAS No 10584-98-2
Description: clear colourless liquid
Batch number: 20100409995
Date received: 26 March 2010
Expiry date: 26 March 2012
Storage conditions: approximately 4°C in the dark under nitrogen
The integrity of supplied data relating to the identity, purity and stability of the test material is the responsibility of the Sponsor.
Constituent 1
Test animals
- Species:
- other: Reconstituted Human Epidermis (RHE)
- Strain:
- other: Not applicable
- Details on test animals or test system and environmental conditions:
- The EPISKIN model is a three-dimensional reconstituted human epidermis model consisting of adult human-derived epidermal keratinocytes seeded on a dermal substitute consisting of a collagen type I matrix coated with type IV collagen. A highly differentiated and stratified epidermis model is obtained after a 13 day culture period comprising the main basal, supra basal, spinous and granular layers and a functional stratum corneum.
EPISKIN Model Kit 0.38 cm2
Supplier: SkinEthic Laboratories, Nice, France
Date received: 27 April 2010
Test system
- Type of coverage:
- other: Not applicable
- Preparation of test site:
- other: Not applicable
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: Duplicate tissues, treated with 50 µl of 0.9% w/v sodium chloride solution served as negative controls. Duplicate tissues, treated with 50 µl of glacial acetic acid served as positive controls.
- Amount / concentration applied:
- 50 µl of the test material was applied
- Duration of treatment / exposure:
- Duplicate tissues were treated with the test material for exposure periods of 3, 60 and 240 minutes.
- Observation period:
- 3, 60 and 240 minutes.
- Number of animals:
- Not applicable
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- other: Relative mean viability (%)
- Basis:
- other: n/a
- Time point:
- other: 3 minutes
- Score:
- 102.9
- Reversibility:
- other: n/a
- Irritation parameter:
- other: Relative mean viability (%)
- Basis:
- other: n/a
- Time point:
- other: 60 minutes
- Score:
- 108.2
- Reversibility:
- other: n/a
- Irritation parameter:
- other: Relative mean viability (%)
- Basis:
- other: n/a
- Time point:
- other: 240 minutes
- Score:
- 96.6
- Reversibility:
- other: n/a
- Irritant / corrosive response data:
- Direct MTT Reduction:
An assessment found the test material was able to directly reduce MTT. Therefore, an additional procedure using water-killed tissues was performed during the determination of skin corrosion potential. However, the results obtained showed that no degree of interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water-killed tissues for quantitative correction of results or for reporting purposes.
Test Material, Positive Control Material and Negative Control Material:
Mean OD540 values and viabilities for the negative control, positive control and test material are given in Table 1.
The relative mean viability of the test material treated tissues was as follows:
240 minutes exposure: 96.6%
60 minutes exposure: 108.2%
3 minutes exposure: 102.9%
The qualitative evaluation of tissue viability is given in Table 2.
Following the 3, 60 and 240 Minute exposure periods the test material treated tissues appeared blue which was considered to be indicative of viable tissue.
Quality Criteria:
The relative mean tissue viability for the positive control treated tissues was 4.8% relative to the negative control treated tissues following the 240-minute exposure period. The positive control acceptance criterion was therefore satisfied.
Any other information on results incl. tables
The test material was considered to be Non-Corrosive to the skin and accredited the EU risk phrase of No label and a UN packing group Non-Corrosive.
Table 1: Mean OD540Values and Viabilities for the Negative Control Material, Positive Control Material and Test Material
Material |
Exposure Period |
Mean OD540of duplicate tissues |
Relative mean viability (%) |
|
Negative Control Material |
240 Minutes |
0.207 |
100* |
|
Positive Control Material |
240 Minutes |
0.010 |
4.8 |
|
Test Material |
240 Minutes |
0.200 |
96.6 |
|
60 Minutes |
0.224 |
108.2 |
||
3 Minutes |
0.213 |
102.9 |
* = The mean viability of the negative control tissues is set at 100%
Table 2 Qualitative Evaluation of Tissue Viability (MTT uptake visual evaluation)
Material |
Exposure Period |
Tissue 1 |
Tissue 2 |
Negative Control Material |
240 Minutes |
- |
- |
Positive Control Material |
240 Minutes |
++ |
++ |
Test Material |
240 Minutes |
- |
- |
60 Minutes |
- |
- |
|
3 Minutes |
- |
- |
MTT Visual Scoring Scheme of EpiSkin Tissues
- = Blue tissue (viable)
+ = Blue/white tissue (semi-viable)
++ = Tissue completely white (dead)
Applicant's summary and conclusion
- Interpretation of results:
- other: Non-Corrosive to the skin
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- The test material was considered to be Non-Corrosive to the skin and accredited the EU risk phrase of No label and a UN packing group Non-Corrosive.
- Executive summary:
The purpose of this test is to evaluate the corrosivity potential of the test material using the EPISKINTM in vitro Reconstituted Human Epidermis (RHE) Model after treatment periods of 3, 60 and 240 minutes. This method was designed to meet the requirements of the OECD Guideline for the Testing of Chemicals No. 431 “In Vitro Skin Corrosion: Human Skin Model Test” (adopted 13 April 2004).
The EPISKIN model is able to distinguish between corrosive and non-corrosive chemicals for all of the chemical types studied, and is also able to distinguish between known R35 (UN packing group I) and R34 (UN packing group II & III) chemicals.
Duplicate tissues were treated with the test material for exposure periods of 3, 60 and 240 minutes. At the end of the exposure period the test material was rinsed from each tissue before each tissue was taken for MTT-loading. After MTT loading a total biopsy of each epidermis was made and placed into micro tubes containing acidified isopropanol for extraction of formazan crystals out of the MTT-loaded tissues.
At the end of the formazan extraction period each tube was mixed thoroughly and duplicate 200 µl samples were transferred to the appropriate wells of a pre-labelled 96 well plate. The optical density was measured at 540 nm.
Data are presented in the form of percentage viability (MTT reduction in the test material treated tissues relative to negative control tissues).
The relative mean viability of the test material treated tissues was:
240 minutes exposure: 96.6%
60 minutes exposure: 108.2%
3 minutes exposure: 102.9%
The quality criteria required for acceptance of results in the test were satisfied.
The test material was considered to be Non-Corrosive to the skin and accredited the EU risk phrase of No label and a UN packing group Non-Corrosive.
Read across from DBT-2EHMA (CAS: 10584-98-2)
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.