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EC number: 221-486-2 | CAS number: 3115-49-9
- 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:
- October 13, 1983 - October 20, 1983
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non-GLP study following OECD guideline 404 performed under GLP-like QAU surveillance.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 983
- Report date:
- 1983
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- (1981)
- GLP compliance:
- no
Test material
- Reference substance name:
- (4-nonylphenoxy)acetic acid
- EC Number:
- 221-486-2
- EC Name:
- (4-nonylphenoxy)acetic acid
- Cas Number:
- 3115-49-9
- Molecular formula:
- C17H26O3
- IUPAC Name:
- 2-(4-nonylphenoxy)acetic acid
- Details on test material:
- - Physical state: viscous liquid
- Analytical purity: commercial grade
- Storage condition of test material: room temperature
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Kleintierfarm Madoerin AG, CH-4414 Fuellinsdorf
- Age at study initiation: 12 - 14 weeks
- Weight at study initiation: 211 - 2440 g
- Housing: Animals were housed individually in metal cages.
- Diet: Rabbit food, NAFAG, No. 814 Tox, NAFAG AG,Gossau, SG (Switzerland), ad libitum
- Water: ad libitum
- Acclimation period: 4 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 +/- 3
- Humidity (%): 30 - 70
- Air changes (per hr): 15
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 ml - Duration of treatment / exposure:
- 4 h
- Observation period:
- Skin reaction was evaluated after 1, 24, 48, 72 hours.
- Number of animals:
- 3 females
- Details on study design:
- TEST SITE
- Area of exposure: 6 sq. cm
- Type of wrap if used: A gauze patch bearing 0.5 ml of the test substance was applied to the skin and loosely held in place by adhesive but non irritating tape
REMOVAL OF TEST SUBSTANCE
- Time after start of exposure: 4h
SCORING SYSTEM:
Erythema and Eschar Formation
No erythema = 0
Very slight erythema = 1
Well defined erythema = 2
Moderate to severe erythema = 3
Severe erythema (beet redness) to slight eschar formation = 4
Corrosion = +
Oedema Formation
No oedema = 0
Very slight oedema = 1
Slight oedema (edges of area well defined by definite raising) = 2
Moderate oedema (appr. 1 mm) = 3
Severe oedema (raised more than 1 mm, extended beyond appl. site) = 4
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 1, 24, 48, 72 h
- Score:
- 5.92
- Max. score:
- 8
- Remarks on result:
- other: considered as severly irritant
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 3.6
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 3
- Max. score:
- 4
- Irritant / corrosive response data:
- The test article caused severe irritant and corrosive reactions when applied to the rabbit skin; there was no tendency of recovery towards the end of the observation period. Due to extreme irritation in the skin the animals were killed after the 72 h scoring out of animal protection reasons.
- Other effects:
- The animals showed a normal body weight development.
Any other information on results incl. tables
Table 1 - Evaluation of the dermal reactions
Animal No. /Sex | 1h | 24h | 48h | 72h | |
Erythema and eschar formation | |||||
78/F | 2 | 3 | 4+ | 4+ | |
79/F | 2 | 3 | 4+ | 4+ | |
80/F | 2 | 2 | 4+ | 4+ | |
Total | 6 + 8 + 12 + 12 = 38 |
||||
Oedema formation | |||||
78/F | 2 | 3 | 3 | 3 | |
79/F | 2 | 3 | 3 | 3 | |
80/F | 2 | 3 | 3 | 3 | |
Total | 6 + 9 + 9 + 9 = 33 |
+ = corrosion
INDEX of skin irritation : 38 + 33 = 71 : 12 = 5.92 (= severly irritant)
Applicant's summary and conclusion
- Interpretation of results:
- corrosive
- Remarks:
- Migrated information
- Conclusions:
- Under the conditions of the present experiment the test substance was found to be severely irritant and corrosive when applied to the rabbit skin.
- Executive summary:
In a skin irritation study following OECD guideline 404 (1981) and performed under GLP-like QAU surveillance, 0.5 ml of the test article was applied to the rabbit skin under semiocclusive conditions for 4 hours. After removal of the dressings the skin reaction was assessed after 1, 24, 48 and 72 hours according to the Draize scoring scheme presented in the OECD guideline. The test substance was found to be severely irritant and corrosive when applied to the rabbit skin; there was no tendency of recovery towards the end of the observation period. Due to extreme irritation in the skin the animals were killed after the 72 h scoring out of animal protection reasons. Based on these results, the test substance was considered to be corrosive to the skin and requires classification.
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