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EC number: 269-144-1 | CAS number: 68188-18-1
- 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
- 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:
- May - June 1991
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 991
- Report date:
- 1991
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- GLP compliance:
- yes
Test material
- Reference substance name:
- Paraffin oils, sulfochlorinated, saponified
- EC Number:
- 269-144-1
- EC Name:
- Paraffin oils, sulfochlorinated, saponified
- Cas Number:
- 68188-18-1
- Molecular formula:
- typical example: C15H31Na03S
- IUPAC Name:
- n-C14-C17 alkanes, secondary monosulphonic acids, sodium salts
- Reference substance name:
- Water
- EC Number:
- 231-791-2
- EC Name:
- Water
- Cas Number:
- 7732-18-5
- Molecular formula:
- H2O
- IUPAC Name:
- water
- Reference substance name:
- Sodium chloride
- EC Number:
- 231-598-3
- EC Name:
- Sodium chloride
- Cas Number:
- 7647-14-5
- Molecular formula:
- ClNa
- IUPAC Name:
- sodium chloride
- Reference substance name:
- Glycerides, mixed decanoyl and octanoyl
- EC Number:
- 277-452-2
- EC Name:
- Glycerides, mixed decanoyl and octanoyl
- Cas Number:
- 73398-61-5
- IUPAC Name:
- 73398-61-5
- Reference substance name:
- Sodium hydroxide
- EC Number:
- 215-185-5
- EC Name:
- Sodium hydroxide
- Cas Number:
- 1310-73-2
- Molecular formula:
- HNaO
- IUPAC Name:
- sodium hydroxide
- Test material form:
- solid
Constituent 1
impurity 1
impurity 2
impurity 3
impurity 4
- Specific details on test material used for the study:
- Information from study report:
- Name of test material: Emulgator E30, Fest
- CAS number: 5896-54-8
The CAS number in report (5896-54-8) is misleading, since this CAS number does only represent 1-Penta-decanesulfonic acid, sodium salt (1:1), but it is confirmed that the substance used is correctly assigned to CAS 68188-18-1.
- Appearance/Further information: The test substance was supplied as white wax-like leaf-let and was received at the test institute on March 06, 1991.
- Batch No. of test material: 210291
- Purity: 95 %
- Analysis reference: TGL 39237
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Strain: NZW rabbits
- Sex: male
- Source: Thomae, Biberach, Germany
- Weight at study initiation (mean): 2.5 kg ± 0.047
- Housing: singly in steel wire cages
- Diet and water: ad libitum
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21 ± 2
- Humidity (%): 28 - 41
- Air changes (per hr): 12-15
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not specified
- Amount / concentration applied:
- 500 g
- Duration of treatment / exposure:
- 4 h
- Observation period:
- 14 days
- Number of animals:
- 3
- Details on study design:
- One day before the application the fur was carefully removed by shaving an area approximately 10 x 20 cm of the dorsal trunk.
On day of application 0.5 g of the test substance was placed on a 2 x 3 cm gauze patch and wetted for one hour with 0.4 mL water (Ampuwa, Fresenius, Bad Homburg) to make the emulgator soft. This patch was then positioned on the rabbit so that the test substance was in contact with the shaved skin, just left of the dorsal midline. The patch was held in place by a wrapping of gauze which was secured and semioccluded by a wrapping of blendderm and Leukoplast. After a 4-hour exposure period, wrappings were removed and the test substance was gently washed away with water.
SCORING SYSTEM: Draize
The treated area was scored 0.5, 1, 6, 24, 48, and 72 hours after patch removal, and then periodically until day 14.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- >= 2 - <= 3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 14 days. A slight redness(score 1) was still present by Day 14.
- Remarks on result:
- other: mean score: 2.7; at 48 and 72 h leathery and red skin was reported
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 12 days
- Remarks on result:
- other: at 48 and 72 h leathery and red skin was reported
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- >= 2 - <= 3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 12 days
- Remarks on result:
- other: mean score: 2.7; at 72 h leathery skin was reported
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- >= 0 - <= 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 5 days
- Remarks on result:
- other: mean score: 0.3
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- >= 0 - <= 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 5 days
- Remarks on result:
- other: mean score: 0.7
- Irritant / corrosive response data:
- The substance caused initial slight to mild erythema of the treated skin, progressing to moderate erythema in all rabbits by 48 hours after treatment. The severity of the redness decreased slowly thereafter, but was in one animal still present as a slight redness by study day 14. All rabbits also exhibited slight to mild oedema during the first four days.
- Other effects:
- No animal died during the observation period of 14 days. In all animals, the body weight development was apparently normal, unaffected by treatment. No adverse clinical observations were made in any animal. At necropsy, all animals were essentially normal.
Applicant's summary and conclusion
- Executive summary:
In a skin irritation/corrosion study according to OECD TG 404 the test substance was applied under semiocclusive dressings for 4 hours to the previously shorn skin of three male rabbits. The treated areas were assessed after 0.5, 1, 6, 24, 48, and 72 hours and then periodically until Day 14 using the Draize scale. The substance caused local irritation of exposed skin, but no evidence of systemic toxicity. In detail, the substance caused initial slight to mild erythema of the treated skin, progressing to moderate erythema in all rabbits by 48 hours after treatment. Additionally for some time points leathery and red skin was reported. The severity of the redness decreased slowly thereafter, but was still present in one animal as a slight redness by study day 14. All rabbits also exhibited slight to mild oedema during the first four days. Mean erythema scores after 24, 48 and 72 hours were 3 (1/3 rabbits) and 2.7 (2/3 rabbits), mean edema scores were 0, 1.3, and 1.7 (each 1/3).
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