Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 939-487-8 | CAS number: -
- 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:
- 21 August 1995 to 30 September 1997
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 997
- Report date:
- 1997
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
Test material
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Kuiper Rabbit Ranch, Gary, IN
- Age at study initiation: 2.5 months
- Weight at study initiation: 1.74-2.23 kg
- Housing: stainless steel cages with mesh floors, 61.0 x 45.5 x 41.0 cm
- Diet (e.g. ad libitum): 150 g/day, Purina Lab Rabbit Chow HF #5326
- Water (e.g. ad libitum): ad libitum, reverse osmosis-purified water
- Acclimation period: 9 weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 23-34
- Humidity (%): 41-55
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12:12
IN-LIFE DATES: From: 29 August 1995 to 1 September 1995
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
- Concentration (if solution): undiluted - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72 hours
- Number of animals:
- 3
- Details on study design:
- TEST SITE
- Area of exposure: not stated, but test site covered with 6.25 cm2 patch (shaved area was 240 cm2)
- % coverage: no data
- Type of wrap if used: 2.5 x 2.5 cm 12-ply cotton gauze patch secured with porous tape; mid-section of each rabbit wrapped in lint-free cloth secured by an elastic adhesive bandage.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): not done (no residual test material visible) - area wiped with gauze
- Time after start of exposure: 4 hours
SCORING SYSTEM: Primary Dermal Irritation Score:
Erythema and eschar formation:
no erythema 0
very slight erythema 1
well-defined erythema 2
moderate-severe erythema 3
severe erythema (beet redness) to slight eschar formation (injuries in depth) 4
Oedema formation:
no oedema 0
very slight oedema 1
slight oedema 2
moderate oedema 3
severe oedema 4
Descriptive rating:
0 non-irritating (grade 0)
0.1-1.5 minimally irritating (grade 1)
1.6-3.0 mildly irritating (grade 2)
3.1-5.0 moderately irritating (grade 3)
5.1-8.0 severely irritating (grade 4)
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 30-60min, 24 h, 48 h, 72 h
- Score:
- 0
- Max. score:
- 8
- Remarks on result:
- other: All animals, all endpoints, all timepoints - score 0
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritant / corrosive response data:
- Non-irritant - see table 1
- Other effects:
- No deaths
Any other information on results incl. tables
Table 1: Irritant/corrosive response data for each animal at each observation time up to removal of each animal from the test
One male and 2 female rabbits:
Score at time point / Reversibility |
Erythema |
Edema |
Max. score: 0 |
Max. score: 0 |
|
30-60 min |
0/0/0 |
0/0/0 |
24 h |
0/0/0 |
0/0/0 |
48 h |
0/0/0 |
0/0/0 |
72 h |
0/0/0 |
0/0/0 |
Average 24h, 48h, 72h |
0/0/0 |
0/0/0 |
Erythema: 0=none, 1=very slight, 2=well defined, 3=moderate to severe 4=severe erythema to slight eschar formation
Edema; 0=none, 1=very slight, 2=slight, 3=moderate, 4 =severe
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In the skin irritation study, which was conducted according to OECD Test Guideline 404 and in compliance with GLP, the undiluted test material was not irritating to the skin of rabbits, following 4 hours semi-occlusive contact.
- Executive summary:
In a study performed according to OECD Test Guideline 404 (Acute dermal irritancy/corrosivity) and in compliance with GLP, the test material was tested for its potential to induce skin irritation in rabbits.
A 0.5 ml volume of the test material was applied undiluted for 4 hours to the shaved backs of three (two male and one female) New Zealand White rabbits, semi-occluded. All test sites were examined for signs of dermal irritation (i.e. oedema, erythema and/or eschar formation) and corrosivity (i.e. ulceration and/or necrosis) 30-60 minutes and 24, 48 and 72 hours following removal of the patch. The primary Dermal Irritation Index (PDII) was calculated according to Draize criteria.
No signs of dermal irritation or corrosivity were observed in the three rabbits at any timepoint. The PDII for the test material was 0.
Under the conditions of the test, the test material was not irritating to rabbit skin.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

Welcome to the ECHA website. This site is not fully supported in Internet Explorer 7 (and earlier versions). Please upgrade your Internet Explorer to a newer version.
This website uses cookies to ensure you get the best experience on our websites.
Find out more on how we use cookies.