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EC number: 444-040-0 | CAS number: 52950-18-2
- 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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP Guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 003
- Report date:
- 2003
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Principles of method if other than guideline:
- A dermal irritation/corrosion test in White New Zealand rabbits was performed according to the method described in OECD guideline 404.
- GLP compliance:
- yes
Test material
- Reference substance name:
- (2R)-2-(2-chlorophenyl)-2-hydroxyethanoic acid
- EC Number:
- 444-040-0
- EC Name:
- (2R)-2-(2-chlorophenyl)-2-hydroxyethanoic acid
- Cas Number:
- 52950-18-2
- Molecular formula:
- Hill formula: C8H7ClO3 CAS formula: C8H7CLO3
- IUPAC Name:
- (2R)-2-(2-chlorophenyl)-2-hydroxyacetic acid
- Details on test material:
- - Name of test material (as cited in study report): (R)-2-Chlormandelsäure
- Physical state: Solid, crystalline 1 white to slight yellowish;
- Analytical purity: 99.7 area-%
- Lot/batch No.: TI 38-02-01
- Stability: The stability under storage conditions over the exposure period was guaranteed by the sponsor.
- Storage condition of test material: Room temperature
- Homogeneity: The test substance was homogeneous by visual inspection.
- Other: pH-value of a 10% aqueous suspension: about 1.0
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Centre Lago S.A., 01540 Vonnas, France
- Age at study initiation: 7 - 9 months
- Weight at study initiation: 3.55 kg - 3.86 kg
- Housing: Single housing
- Diet: Kliba-Labordiät, Provimi Kuba SA, Kaiseraugst, Switzerland (about 130 g/animal per day)
- Water: Tap water ad libitum
- Acclimation period: At least 5 days before the beginning of the study.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-24
- Humidity (%): 30-70
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- water
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 g moistened in water - Duration of treatment / exposure:
- 4 hour(s)
- Observation period:
- 14 days
- Number of animals:
- 6
- Details on study design:
- TEST SITE
- Area of exposure: 2.5 x 2.5 cm
- semiocclusive dressing consisting of a test patch (Idealbinde, Pfälzische Verbandstoff-Fabrik, Kaiserslautern) and FixomuII-stretch (adhesive fleece), Beiersdorf AG
REMOVAL OF TEST SUBSTANCE
- Washing (if done): Lutrol concentrated and Lutrol/water (1:1)
- Time after start of exposure: 4 hours
SCORING SYSTEM: The Draize scoring system was used
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- 1-3
- Time point:
- other: 24,48,72 h
- Score:
- 0.8
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- 1-3
- Time point:
- other: 24,48,72 h
- Score:
- 0
- Max. score:
- 4
Any other information on results incl. tables
Results summary
After the exposure period of 3 minutes, no skin findings were observed in all animals. The average score (24 to 72 hours) for irritation was calculated to be 0.0 for erythema and edema.
After the exposure period of 1 hour slight to moderate erythema was observed in all animals during the course of the study. The cutaneous reactions were reversible in all animals within 7 days after removal of the patch. The average score (24 to 72 hours) for irritation was calculated to be 1.3 for erythema and 0.0 for edema.
After the exposure period of 4 hours slight to marked erythema was observed in all animals during the course of the study. The cutaneous reactions were reversible in all animals within 72 hours after removal of the patch at latest. The average score (24 to 72 hours) for irritation was calculated to be 0.8 for erythema and 0.0 for edema.
Considering the described cutaneous reactions as well as the average score for irritation, (R)-2-Chlormandelsäure does not show a skin irritation potential under the test conditions chosen.
Results details
ANALYSES
Food analyses:
In view of the aim and duration of the study the contaminants occurring in commercial food should not influence the results.
Drinking water analyses:
In view of the aim and duration of the study there are no special requirements exceeding the specification of drinking water.
CLINICAL EXAMINATIONS AND ASSESSMENT OF SKIN FINDINGS
After the exposure period of 3 minutes, no skin findings were noted in all animals. The average score (24 to 72 hours) for irritation was calculated to be 0.0 for erythema and edema.
After the exposure period of 1 hour the following findings were observed:
Moderate erythema (grade 2) was observed in all animals 1 hour after removal of the patch and decreased in all animals to slight erythema (grade 1) 24, 48 or 72 hours after removal of the patch, respectively and persisted in all animals until 72 hours after removal of the patch.
No other cutaneous reactions were observed during the study. The cutaneous reactions were reversible in all animals within 7 days after removal of the patch.
Mean scores over 24, 48 and 72 hours for each animal were 1.3, 1.0 and 1.7 for erythema and 0.0 for edema.
After the exposure period of 4 hours the following findings were noted:
Marked erythema (grade 3) was observed in two animals and slight erythema (grade 1) in one animal 1 hour after removal of the patch. Marked erythema decreased in the two animals to moderate erythema (grade 2) after 24 hours and to slight erythema (grade 1) 48 hours after removal of the patch. Slight erythema persisted in the third animal until the24 hour reading.
The cutaneous reactions were reversible in one animal within 48 hours and in two animals within 72 hours after removal of the patch.
Mean scores over 24, 48 and 72 hours for each animal were 1.0, 1.0 and 0.3 for erythema and 0.0 for edema.
Readings |
Animal |
Exposure period: 3 min |
||
Erythema |
Edema |
Additional findings |
||
1 h |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
24 h |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
48 h |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
72 h |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
7 d |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
Mean 24, 48, 72 h |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
Mean 24, 48, 72 h |
1-3 |
0 |
0 |
|
Readings |
Animal |
Exposure period: 1 h |
||
Erythema |
Edema |
Additional findings |
||
1 h |
1 |
2 |
0 |
|
2 |
2 |
0 |
|
|
3 |
2 |
0 |
|
|
24 h |
1 |
2 |
0 |
|
2 |
1 |
0 |
|
|
3 |
2 |
0 |
|
|
48 h |
1 |
1 |
0 |
|
2 |
1 |
0 |
|
|
3 |
2 |
0 |
|
|
72 h |
1 |
1 |
0 |
|
2 |
1 |
0 |
|
|
3 |
1 |
0 |
|
|
7 d |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
Mean 24, 48, 72 h |
1 |
1.3 |
0 |
|
2 |
1.0 |
0 |
|
|
3 |
1.7 |
0 |
|
|
Mean 24, 48, 72 h |
1-3 |
1.3 |
0 |
|
Readings |
Animal |
Exposure period: 4 h |
||
Erythema |
Edema |
Additional findings |
||
1 h |
1 |
3 |
0 |
|
2 |
3 |
0 |
|
|
3 |
1 |
0 |
|
|
24 h |
1 |
2 |
0 |
|
2 |
2 |
0 |
|
|
3 |
1 |
0 |
|
|
48 h |
1 |
1 |
0 |
|
2 |
1 |
0 |
|
|
3 |
0 |
0 |
|
|
72 h |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
7 d |
1 |
0 |
0 |
|
2 |
0 |
0 |
|
|
3 |
0 |
0 |
|
|
Mean 24, 48, 72 h |
1 |
1 |
0 |
|
2 |
1 |
0 |
|
|
3 |
0.3 |
0 |
|
|
Mean 24, 48, 72 h |
1-3 |
0.8 |
0 |
|
(Calculation of the mean according to 83/467/EEC criteria of July 29th, 1983)
(Calculation of the mean according to 93/21/EEC criteria of April 27th, 1993)
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information
- Conclusions:
- Classification: not irritating
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