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EC number: 203-459-7 | CAS number: 107-07-3
- 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: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- no data
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was performed pre-GLP and according to methods similar to OECD404.
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- publication
- Title:
- Tissue Reactions to 2-Chloroethanol in Rabbits
- Author:
- Guess, W.L.
- Year:
- 1 970
- Bibliographic source:
- Toxicol. Appl. Pharamcol., 16, pp 382-390,
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Principles of method if other than guideline:
- Method: Draize Test (1944)
- skin was exposed to 0.2ml under occlusion and for 2 hours
- only the average score for 6 animals per concetration was shown, not the animal individual data. - GLP compliance:
- no
Test material
- Reference substance name:
- 2-chloroethanol
- EC Number:
- 203-459-7
- EC Name:
- 2-chloroethanol
- Cas Number:
- 107-07-3
- Molecular formula:
- C2H5ClO
- IUPAC Name:
- 2-chloroethan-1-ol
- Details on test material:
- Anhydrous 2-chloroethanol was obtained from J. T. Baker Company.
Confirmation of purity was further accomplished by infrared analysis and index of refraction. These tests failed, however, to reveal traces of HCl
which altered the pH of the solutions of 2-chloroethanol in normal saline. This HCl was detected by silver nitrate test solution; on titration with 0.1 N NaOH solution, the hydrogen ion concentration was found to be 0.011 mole/liter. The HCl present in the 2- chloroethanol probably originates from hydrolysis of the compound in the presence of moisture. It was felt that chloroacetic acid was not the source of the acidic reaction since
the conditions necessary for the oxidation of the alcohol to the acid were not present.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: normal and abraded
- Vehicle:
- physiological saline
- Controls:
- no
- Amount / concentration applied:
- 0.2 ml
- Duration of treatment / exposure:
- 2 hours
- Observation period:
- 72 hours
- Number of animals:
- 6
- Details on study design:
- For the skin irritation study, the method of Draize et al. (1944) was used with the following deviations: It was found impractical in view of the large numbers of animals in this study to use the rubber sleeve covering described by Draize. Instead, the animals were anesthetized with pentobarbital iv, the necessary incisions were made, and glass wells (1 cm id, x3 mm) were sealed to the skin over the desired areas of application with Dow-Corning silicone grease. The test liquids were added to the glass wells in a volume of 0.2 ml per well and sealed with a round microscope coverslip. These were allowed to remain on the site for 2 hours, thereby maintaining the test liquids at the site for a standard time and in known concentration. The sites of exposure were scored for degree of erythema and edema, 24, 48, and 72 hours after exposure.
Results and discussion
In vivo
- Irritant / corrosive response data:
- 2-chloroathanol caused only barely perceptible reaction on normal and abraded skin under the conditions of this test. In this regard, only the pure material caused even a transient reaction to intact skin, see table 1.
Any other information on results incl. tables
Table 1. Skin reactions
|
|
Rabbit skin |
|
|||
|
|
Intact |
Abraded |
|
||
Compound |
Dilution |
24 hr |
72 hr |
24 hr |
72 hr |
Combined average 72 hr score |
2-chloroethanol |
Undiluted |
0.6 |
0 |
1.0 |
1.0 |
0.5 |
|
1:5 |
0 |
0 |
0.6 |
0.3 |
0.15 |
|
1:10 |
0 |
0 |
0 |
0.3 |
0.15 |
|
1:100 |
0 |
0 |
0.3 |
0.3 |
0.15 |
Saline control |
- |
0 |
0 |
0 |
0 |
0 |
Ethanol |
95% |
0 |
0 |
0.3 |
0 |
0 |
|
1:10 |
0 |
0 |
0.3 |
0 |
0 |
-Score (each score represents an average of 6 rabbits used for each)
1, barely perceptibl erythema;
2, well-defined erythema;
3, moderate erythema;
4, severe (beet red) erythema.
No oedema observed
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: OECD GHS
- Conclusions:
- 2-chloroethanol caused only barely perceptible reaction on normal and abraded skin under the conditions of this test. In this regard, only the pure material caused even a transient reaction to intact skin. The maximun average score is 0.6 for the undiluted compound after 24 hours. This was fully reversible within 72 hours. No further effects observed.
- Executive summary:
This paper reports on the effect of pure 2-chloroethanol, and various dilutions of this material, on several of the tissue types with which a tracheotomy tube might come into contact in a patient. It was found that pure 2-chloroethanol is quite destructive to most of the tissues, including ophthalmic, mucosal, muscular, and subcutaneous tissues; however, on dilution, the toxicity potential decreased sharply. Dilutions of 1:10 were still toxic, but in most cases, dilutions of 1:100 were practically innocuous. A cell culture evaluation correlated almost perfectly with in vivo techniques.
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