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EC number: 939-607-9 | CAS number: 1474044-65-9
- 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:
- July, 1995
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to OECD Guideline 404 and EU Method B.4 in compliance with GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 995
- Report date:
- 1995
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Quaternary ammonium compounds, C12-14 (even-numbered)-alkylethyldimethyl, ethyl sulphates
- EC Number:
- 939-607-9
- Cas Number:
- 1474044-65-9
- Molecular formula:
- C18 H41 N1 O4 S1
- IUPAC Name:
- Quaternary ammonium compounds, C12-14 (even-numbered)-alkylethyldimethyl, ethyl sulphates
- Test material form:
- other: solid
- Details on test material:
- - Name of test material (as cited in study report): N-alkyl "coco" diméthyl éthyl ammonium ethosulfate
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Elevage cunicole da Val de Selle, 80160 Prouzel, France
- Weight at study initiation: 2.6 +/- 0.2 kg
- Housing: individually housed
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18 +/- 3°C
- Humidity (%): 30 to 70%
- Photoperiod (hrs dark / hrs light): 12 h dark/ 12 h light
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): 500 mg - Duration of treatment / exposure:
- 3 minutes or 4 h
- Observation period:
- 14 days
- Number of animals:
- 3 animals
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): Residual test material was removed by gentle swabbing with compress soaked in water
- Time after start of exposure: 3 minutes or 4 h
SCORING SYSTEM: Draize scoring system
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24, 48 and 72 h
- Score:
- 4
- Reversibility:
- not fully reversible within: 14 d
- Remarks on result:
- other: exposure period: 3 minutes
- Irritation parameter:
- edema score
- Basis:
- other: range of scores
- Time point:
- other: 24, 48 and 72 h
- Score:
- >= 2 - <= 2.7
- Max. score:
- 2.7
- Reversibility:
- not fully reversible within: 14 d
- Remarks on result:
- other: exposure period: 3 minutes
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24, 48 and 72 h
- Score:
- 4
- Reversibility:
- not fully reversible within: 14 d
- Remarks on result:
- other: exposure period: 4 hours
- Irritation parameter:
- edema score
- Basis:
- other: range of scores
- Time point:
- other: 24, 48 and 72 h
- Score:
- >= 2.7 - <= 4
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 14 d
- Remarks on result:
- other: exposure period: 4 hours
- Irritant / corrosive response data:
- Exposure period: 3 minutes
- severe erythema was noted at the treated skin site at 24, 48 and 72 h
- slight edema was noted at the treated skin site at 24, 48 and 72 h
Exposure period: 4 h
- severe erythema was noted at the treated skin site at 24, 48 and 72 h
- slight to severe edema was noted at the treated skin site at 24, 48 and 72 h
Any other information on results incl. tables
Table 1: Individual skin reactions following 3 minutes exposure
Rabbit number | Skin reaction | Scores |
Mean irritation score | Scores |
|||||||||||||
1h / Day 1 | 24h / Day 2 | 48 h / Day 3 | 72h / Day 4 | Day 5 | Day 6 | Day 7 | Day 8 | Day 9 | Day 10 | Day 11 | Day 12 | Day 13 | Day 14 | Day 15 | |||
# 1 | Erythema | 3 | 4 | 4 | 4 | 4.0 | 4 | LN | LN | LN | LN | LN | LN | DT | DT | LA | LA |
Edema | 0 | 2 | 2 | 2 | 2.0 | 2 | LN | LN | LN | LN | LN | LN | DT | DT | LA | LA | |
Other | * | N | N | N | N/A | N | N | N | N | N | N | A | A | A/S | A/S | ||
# 2 | Erythema | 2 | 4 | 4 | 4 | 4.0 | 4 | 4 | 4 | 4 | LN | LN | LN | LN | LA | LA | LA |
Edema | 0 | 2 | 2 | 2 | 2.0 | 2 | 0 | 0 | 0 | LN | LN | LN | LN | LA | LA | LA | |
Other | * | * | * | * | N | N | N | N | N | N | N | N | A/S | A/S | A/S | ||
# 3 | Erythema | 2 | 4 | 4 | 4 | 4.0 | 4 | 4 | 4 | 4 | LN | LN | LN | LN | LA | LA | LA |
Edema | 0 | 4 | 2 | 2 | 2.7 | 2 | 0 | 0 | 0 | LN | LN | LN | LN | LA | LA | LA | |
Other | * | * | * | N | N | N | N | N | N | N | N | N | A | A | A |
* no reaction
N = necrosis
S = dry skin
A = crust
DT = tissue destruction
LN = reading masked by necrosis
LA = reading masked by crust
Table 2: Individual skin reactions following 4 hours exposure
Rabbit number | Skin reaction | Scores |
Mean irritation score | Scores |
|||||||||||||
1h /Day 1 | 24h /Day 2 | 48 h / Day 3 | 72h / Day 4 | Day 5 | Day 6 | Day 7 | Day 8 | Day 9 | Day 10 | Day 11 | Day 12 | Day 13 | Day 14 | Day 15 | |||
# 1 | Erythema | 4 | 4 | 4 | 4 | 4.0 | 4 | LN | LN | LN | LN | LN | LN | LN | LN | DT | DT |
Edema | 4 | 4 | 4 | 4 | 4.0 | 4 | LN | LN | LN | LN | LN | LN | LN | LN | DT | DT | |
Other | N | N | N | N | N | N | N | N | N | N | N | N | N | A/S | A/S | ||
# 2 | Erythema | 4 | 4 | 4 | 4 | 4.0 | LN | LN | LN | LN | LN | LN | LN | LN | LA | LA | LA |
Edema | 4 | 4 | 2 | 2 | 2.7 | LN | LN | LN | LN | LN | LN | LN | LN | LA | LA | LA | |
Other | N | N | N | N | N | N | N | N | N | N | N | N | A/S | A/S | A/S | ||
# 3 | Erythema | 4 | 4 | 4 | 4 | 4.0 | 4 | 4 | 4 | 4 | LN | LN | LN | LN | LA | LA | LA |
Edema | 4 | 4 | 3 | 2 | 3.0 | 4 | 0 | 0 | 0 | LN | LN | LN | LN | LA | LA | LA | |
Other | N | N | N | N | N | N | N | N | N | N | N | N | A/S | A/S | A/S |
* no reaction
N = necrosis
S = dry skin
A = crust
DT = tissue destruction
LN = reading masked by necrosis
LA = reading masked by crust
Applicant's summary and conclusion
- Interpretation of results:
- Category 1C (corrosive)
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Under the test conditions, the erythema and edema scores of the test substance was calculated to be 4.0 and ranged from 2.0 to 2.7 (3-minute exposure) and 2.7 to 4.0 (4 h exposure), respectively.
- Executive summary:
A OECD guideline study was performed to assess the skin irritation potential of C12-14 ADMAES in New Zealand White rabbits. The test substance (500 mg) was applied to the shaved skin area on the back of each animal under semi-occlusive dressing. A single 3-minute or 4-hour application of the test substance to the intact skin of three rabbits produced severe erythema and oedema. Under the test conditions, the mean erythema and oedema scores were 4.0 (3-minute and 4-hour exposure), and ranged from 2.0 to 2.7 (3-minute exposure) and 2.7 to 4.0 (4-hour exposure), respectively. Effects were not fully reversible within the 14 day observation period. The test substance was considered corrosive to the skin of rabbits.
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