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EC number: 309-886-6 | CAS number: 101316-84-1 A tar obtained from low temperature carbonization and low temperature gasification of brown coal. Composed primarily of aliphatic, naphthenic and cyclic aromatic hydrocarbons, heteroaromatic hydrocarbons and cyclic phenols.
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2.9.2010 - 30.9.2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Although the study was not performed under GLP principles, it was carried out according to generally valid and internationally accepted testing guideline.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: OECD Test Guideline No. 437, Bovine Corneal Opacity and Permeability Test Method for Identifying Ocular Corrosives and Severe Irritants, Adopted 7th September 2009.
- Principles of method if other than guideline:
- The Bovine Corneal Opacity and Permeability test method (BCOP) is an in vitro test method that can be used to classify substances as 'ocular corrosives and severe irritants'. The BCOP uses isolated corneas from the eyes of cattle slaughtered for commercial purposes, thus avoiding the use of laboratory animals. Each treatment group (test substance, negative/positive controls) consists of a minimum of three eyes where the cornea has been excised and mounted to a holder. Depending on the physical nature and chemical characteristics of the test substance, different methods can be used for its application since the critical factor is ensuring that the test substance adequately covers the epithelial surface. Effects to the cornea are measured as opacity and permeability, which when combined gives an In Vitro Irritancy Score (IVIS) for each treatment group. A substance that induces an IVIS superior or equal to 55.1 is defined as a corrosive or severe irritant.
- GLP compliance:
- no
Test material
- Reference substance name:
- Tar, brown-coal, low-temp.
- EC Number:
- 309-886-6
- EC Name:
- Tar, brown-coal, low-temp.
- Cas Number:
- 101316-84-1
- Molecular formula:
- Not known - the substance is complex of hundreds organic compounds.
- IUPAC Name:
- Tar, brown-coal, low-temp.
- Details on test material:
- - Name of test material (as cited in study report): Tar, brown-coal, low-temp.
- Molecular formula: not known - UVCB substance
- Molecular weight: not known - UVCB substance
- Smiles notation: not known - UVCB substance
- InChl: not known - UVCB substance
- Substance type: technical product
- Physical state: viscous liquid
- Lot/batch No.: T201E
- Expiration date of the lot/batch: 31.3.2011
- Stability under test conditions: stable
- Storage condition of test material: The substance was stored in closed vessel in dry room at the temperature bellow 25ºC in dark
Constituent 1
Test system
- Vehicle:
- unchanged (no vehicle)
- Details on study design:
- Procedure scheme:
Selection of corneas, mounting in holders → incubation with EMEM (Eagle`s Minimum Essential Medium 1hour (32 ± 1°C) → removed EMEM, measurement of baseline opacity → treatment by positive and negative control substance and test substance (incubation 10 min.) → washing epithelium, incubation 2 hour (32 ± 1°C), measurement of opacity after application → application of sodium fluorescein (4 mg/ml), incubation 1.5 hour (32 ± 1°C) → measurement of absorbance (490 nm).
Treatment groups:
The test was performed using nine isolated bovine corneas. Three corneas for each group – positive control group, negative control group and test substance group.
Control substances
Concurrent negative controls and positive controls were included in experiment. The control group was included in the BCOP test method so that nonspecific changes in the test system could be detected and to provide a baseline for the assay endpoints
Negative control substance: 0.9% sodium chloride solution
Positive control substance: 1% NaOH solution
Aplication of the substance:
Open-chamber method was used, because the test substance was viscous liquid. The test substance (enough test substance to completely cover the cornea) was applied directly to the epithelial surface of the cornea using the micropipet. After dosing, the glass window was replaced on the anterior chamber to recreate a closed system.
Endpoints Measured
Opacity - the amount of light transmission through the cornea. Corneal opacity was measured quantitatively with the aid of an opacitometer (Opacitometer, MC2 - Le spécialiste du laboratoire – France) resulting in opacity values measured on a continuous scale.
Permeability - the amount of sodium fluorescein dye that penetrates all corneal cell layers (i.e., the epithelium on the outer cornea surface through the endothelium on the inner cornea surface) measured indirectly using UV/VIS visible light spectrophotometry (at 490 nm).
Evaluation of results
Once the opacity and mean permeability (A490 ) values had been corrected for background opacity and the negative control permeability A490 values, the mean opacity and permeability A490 values for each treatment group was combined in an empirically-derived formula to calculate an in vitro irritancy score (IVIS) for each treatment group as follows:
IVIS = mean opacity value + (15 x mean permeability A490 value)
Results and discussion
In vivo
Results
- Irritation parameter:
- other: IVIS (In Vitro Irritancy Score ) - see section Details on study design
- Basis:
- other: see section Details on study design
- Time point:
- other: 10 min.
- Score:
- 27.03
- Reversibility:
- not specified
Any other information on results incl. tables
Opacity values
Application substance |
Cornea No. |
Baseline opacity |
Opacity after treatment |
Opacity difference |
Mean |
Negative control (0.9% sodium chloride solution) |
1 |
7 |
8 |
1 |
0.33 |
4 |
7 |
7 |
0 |
||
12 |
6 |
6 |
0 |
||
Positive control (1%NaOH solution) |
2 |
7 |
118 |
111 |
107.00
|
7 |
5 |
104 |
99 |
||
11 |
7 |
118 |
111 |
||
Test substance (Tar, brown-coal, low-temp.) |
5 |
7 |
28 |
21 |
22.67 |
10 |
5 |
26 |
21 |
||
15 |
7 |
33 |
26 |
Absorbance values
Application substance |
Cornea No. |
Absorbance (490 nm) |
Mean |
Negative control (0.9% sodium chloride solution) |
1 |
0.022 |
0.021 |
4 |
0.014 |
||
12 |
0.027 |
||
Positive control (1%NaOH solution) |
2 |
2.129 |
2.21 |
7 |
2.305 |
||
11 |
2.194 |
||
Test substance (Tar, brown-coal, low-temp.) |
5 |
1.110 |
1.00 |
10 |
0.948 |
||
15 |
0.943 |
IVIS (In Vitro Irritancy Score)
Application substance |
IVIS |
Negative control (0.9% sodium chloride solution) |
0.65 |
Positive control (1%NaOH solution) |
139.51* |
Test substance (Tar, brown-coal, low-temp.) |
27.03 |
* IVIS >55.1 – positive response
Applicant's summary and conclusion
- Interpretation of results:
- other: The substance is not defined as a corrosive or severe irritant
- Remarks:
- Criteria used for interpretation of results: EU
- Executive summary:
The test was performed according to the OECD Test Guideline No. 437, Bovine Corneal Opacity and Permeability Test Method for Identifying Ocular Corrosives and Severe Irritants, Adopted 7th September 2009.
The BCOP test method is an organotypic model that provides short term maintenance of normal physiological and biochemical function of the bovine cornea in vitro. In this test method, damage by the test substance is assessed by quantitative measurements of changes in corneal opacity and permeability with an opacitometer and visible light spectrophotometer, respectively. Both measurements are used to calculate an IVIS (In Vitro Irritancy Score), which is used to assign an in vitro irritancy hazard classification category for prediction of an in vivo ocular irritation of the test substance.
The test was performed using nine isolated bovine corneas. Three corneas for each group - positive group, negative group and treatment group. Open-chamber method was used, because the substance is viscous liquid.
Results:
The In Vitro Irritancy Score (IVIS) is stated in the following table. IVIS of the test substance was found: 27.03. A substance that induces an IVIS ≥ 55.1 is defined as a corrosive or severe irritant.
IVIS (In Vitro Irritancy Score)
Application
substance
IVIS
Negative control
(0.9% sodium chloride solution)
0.65
Positive control
(1%NaOH solution)
139.51*
Test substance
(Tar, brown-coal, low-temp.)
27.03
* IVIS >55.1 – positive response
The substance - Tar, brown-coal, low-temp - was not identified as an corrosive and severe irritant.
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