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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
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- 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 vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was performed prior to the implementation of GLP and OECD Guidelines, but meets the principles of an eye irritation study.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 973
- Report date:
- 1973
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- 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:
- no details
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or tissues and environmental conditions:
- 2 males, initial weight 3.39 kg and 2.83 kg.
Source: Fa. Gaukler
no further details
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: NaCl-solution treated adjacent eye served as a control.
- Amount / concentration applied:
- ca. 0.05 ml or 60 mg undiluted test substance instilled into the conjunctival sac
- Duration of treatment / exposure:
- The eyes were not washed out after 24 hour.
- Observation period (in vivo):
- The animals were observed several times on the treatment day and up to 8 days afterwards, and findings were recorded on working days.
- Number of animals or in vitro replicates:
- 2 males
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- other: 24h, 48h, 72h (mean)
- Score:
- 1
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 8 days
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- other: 24h, 48h, 72h (mean)
- Score:
- 2.33
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- other: 24, 48h, 72h (mean)
- Score:
- 2.67
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- other: 24h, 48h, 72h (mean)
- Score:
- 1
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 8 days
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- other: 24h, 48h, 72h (mean)
- Score:
- 2.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Time point:
- other: 24h, 48h, 72h (mean)
- Score:
- 2.33
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Irritant / corrosive response data:
- Details presented in the Table below. Irreversible damage has been shown in both treated rabbits.
- Other effects:
- Post exposure day 3: one rabbit with loss of appetite.
Weight loss was observed. The terminate weight was 2.9 kg (at the beginning 2.85 kg) and 3.47 kg (at the beginning 3.39 kg).
Any other information on results incl. tables
Eye irritation in rabbits after instillation of ca. 60 mg ethylene chlorohydrin
Time after instillation |
Animal 1 |
Animal 2 |
1 hour |
Slight redness, marked edema, opacity of the cornea and cornea exfoliated |
Slight redness, marked edema, opacity of the cornea with smeary overlay |
1 day |
Slight redness, marked edema, opacity of the cornea with smeary overlay |
Slight redness, marked edema, opacity of the cornea and with smeary overlay |
2 days |
Slight edema; opacity of the cornea and with smeary overlay; nictating membrane whitish |
Slight edema; opacity of the cornea and with smeary overlay |
3 days |
Slight edema; opacity of the cornea and with bloody & smeary overlay; nictating membrane partly whitish |
Slight edema; opacity of the cornea & smeary overlay; blood |
6 days |
Ulcerations, whitish nictating and mucous membrane with blood; corneal opacity; proliferation of blood vessels from the periphery |
Slight edema; opacity of the cornea & smeary overlay; ablation of cornea; secretion; nictating membrane partly whitish |
8 days |
Iritis; crusty lids, scar formation; corneal opacity, smeary overlay & blood; proliferation of blood vessels from the periphery; |
proliferation of blood vessels from the periphery; corneal opacity; blood |
No effects were detected in the left eye treated with NaCl-solution (control) |
Applicant's summary and conclusion
- Conclusions:
- Irreversible damage on the eyes in rabbits instilled with undiluted test substance.
- Executive summary:
The study is comparable to OECD Guideline 405 with acceptable restrictions (partly limited documentation, e.g. no details about the test substance; 50 µl instead of 100 µl test substance instilled; scoring system not according to OECD405).
An amount of ca. 60 mg test substance was instilled into the right eye of rabbits; the left eye served as control (physiological saline instilled). No effects were detected in the control eyes but irreversible damage of the treated eye in both rabbits.
Conclusion: Irreversible damage on the eyes in rabbits instilled with undiluted test substance.
Conclusion: Irreversible damage on the eyes.
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