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EC number: 221-022-9 | CAS number: 2976-74-1
- 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
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- Solubility in organic solvents / fat solubility
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- Flash point
- Auto flammability
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- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
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- Stability: thermal, sunlight, metals
- pH
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- 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
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- Nanomaterial surface chemistry
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- Nanomaterial pour density
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- Endpoint summary
- Stability
- Biodegradation
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- 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:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study had been performed in accordance with OECD Guideline No.: 405.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 006
- Report date:
- 2006
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 2,3-dichlorophenoxyacetic acid
- EC Number:
- 221-022-9
- EC Name:
- 2,3-dichlorophenoxyacetic acid
- Cas Number:
- 2976-74-1
- Molecular formula:
- C8H6Cl2O3
- IUPAC Name:
- (2,3-dichlorophenoxy)acetic acid
- Test material form:
- solid: crystalline
- Details on test material:
- - Name of test material (as cited in study report): Dichlorophenoxyacetic acid
- Physical state: light beige powder
- Purity test date: 26. 09. 2005
- Lot/batch No.: 10
- Expiration date of the lot/batch: : 07. 2006
- Storage condition of test material: at room temperature, protected from light
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Breeder: Ferenc Sándor, address: Császár street 135, Kartal, H-2173, Hungary
- Age at study initiation: 11 weeks
- Weight at study initiation: 2584-2903 g
at study termination: 3015-3234 g
- Housing: individually in metal cages
- Diet (e.g. ad libitum): ad libitum, PURINA Base - Lap gr. diet for rabbits (produced by AGRIBRANDS Europe)
- Water (e.g. ad libitum): ad libitum, tap water (for human cosumption) from automatic self supplying watering system
- Acclimation period: 8 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 ± 3 °C
- Humidity (%): 30 - 70 %
- Photoperiod (hrs dark / hrs light): 12-12
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the contralateral eye served as control
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 g of test item Dichlorophenoxyacetic acid in pure state in a single dose - Duration of treatment / exposure:
- The eyes of the test animals were not washed out after the application of the test item.
- Observation period (in vivo):
- 14 days (1, 24, 48, 72 hours and then one and two weeks after the treatment)
- Number of animals or in vitro replicates:
- 3
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
The eyes of the test animals were not washed out after the application of the test item.
SCORING SYSTEM:
Draize (1959)
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- conjunctivae score
- Basis:
- animal: 1, 2, 3
- Time point:
- other: 1, 24, 48, 72 hours after the treatment
- Score:
- 0 - 18
- Max. score:
- 20
- Reversibility:
- fully reversible within: 2 weeks
- Irritation parameter:
- iris score
- Basis:
- animal: 1, 2, 3
- Time point:
- other: 1, 24, 48 and 72 hours after the treatment
- Score:
- 0
- Max. score:
- 10
- Irritation parameter:
- cornea opacity score
- Basis:
- animal: 1, 2, 3
- Time point:
- other: 1, 24, 48 and 72 hours after the treatment
- Score:
- 0 - 30
- Max. score:
- 80
- Reversibility:
- fully reversible within: 2 weeks
- Irritant / corrosive response data:
- One hour after treatment the vessels were diffuse beefy red (score 3) in two animals (5140, 5135), as well as were diffuse and the individual vessels were not easily discernible (score 2) in one animal (5129).
In all animals some swelling above normal was observed (score 1) at this time.
The discharge moistened lids and hairs on considerable area around the treated eye (score 3) were found in all animals.
In two animals (5140, 5135) diffuse areas of opacity were observed on the cornea, but the details of iris were clearly visible (score 1). In animal No.: 5129 easily discernible translucent areas of the cornea were observed and the details of iris were slightly obscured (score 2). The area of cornea involved was greater than three quarters, up to the whole area (score 4).
There were no effects observed in the iris alterations during the study period.
24 hours after treatment in all animals the vessles were diffuse beefy red (score 3) and the discharge with moistening of the lids and hairs on considerable area around the eye (score 3) was found.
The conjunctival swelling with lids about half closed (score 3) was seen in animal No.: 5129, conjunctival sweeling with partial eversion of the lids (score 2) was observed in animal No.: 5135, as well as swelling above normal (score 1) was found in animal No.: 5140.
In two animals (5135, 5129) easily discernible translucent areas of the cornea were observed and the details of iris were slightly obscured (score 2). In animal No.: 5140 diffuse areas of opacity were observed on the cornea, but the details of iris were clearly visible (score 1). The area of cornea involved was greater than three quarters, up to the whole area (score 4).
48 hours after treatment
The eye irritation symptoms became slighter at this time. In all animals the irritation of conjunctive decreased (score 2) when compared to the previous observation.
Discharge was not observable in the treated animals.
In two animals (5135, 5129) conjunctival sweeling with partial eversion of the lids (score 2) was observed.
In animal No.: 5129 the degree and extension of cornea opacity did not change when compared to the previous observation. In two animals (5140, 5135) diffuse areas of opacity were observed on the cornea, but the details of iris were clearly visible (score 1). Area of cornea involved was greater than three quarters, up to the whole are (score 4).
72 hours after treatment redness of the conjunctivae and corneal alteration did not change compared to the previous observation.
In two animals (5135, 5129) some swelling above normal was observed (score 1).
One week after the treatment in two animals 8No.: 5135, 5129) were found corneal alterations. Diffuse areas of opacity were observed on the cornea but the details of iris were clearly visible (scores 1). The area of cornea involved was greater than three quarters, up to the whole areas (scores 4). However, in animal No.: 5135 some blood vessles were hyperaemic (score 1) occurred.
The animal No.: 5140 became free of irritation symptoms by this time.
Two weeks after the treatment the study was terminated, since no primary irritation symptoms remained.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The test item DICHLOROPHENOXYACETIC ACID, applied to the rabbit's eye mucosa, caused conjunctival and corneal irritant effects, fully reversible within two weeks. According to the EC criteria for classification and labelling requirements for dangerous substances and preparations the test item does not have to be classified and has no obligatory labelling requirement for eye irritation.
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