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EC number: 931-294-7 | CAS number: 1334422-17-1
- 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:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- 1997/10/17-1998/03/02
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to the appropriate OECD test guideline, and in compliance with GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 998
- Report date:
- 1998
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:
- Alcohols, C16-19-branched
- EC Number:
- 297-790-4
- EC Name:
- Alcohols, C16-19-branched
- Cas Number:
- 93762-74-4
- IUPAC Name:
- 93762-74-4
- Details on test material:
- - Name of test material (as cited in study report): Development Detergent Alcohol 23731-52. Equivalent to Alcohols, C16-17, monobranched, type 2
- Substance type:
- Physical state: Clear, colourless liquid.
- Analytical purity: Purity data are the responsibility of the sponsor
- Storage condition of test material: Stored under nitrogen in the original container at 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: Covance Research Products, Inc., Denver, PA
- Age at study initiation: Young adults.
- Weight at study initiation: 3686 - 3790g
- Housing: Individual suspended wire mesh cages.
- Diet: PMI Feeds, Inc. Certified Rabbit LabDiet 5322, at ca. 150 g per day during the study
- Water: Reverse osmosis treated municipal water (ad libitum)
- Acclimation period: minimum of 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°F): 66-67.6
- Humidity (%): 41.3-45.9%
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- not specified
- Controls:
- not specified
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5ml
- Duration of treatment / exposure:
- 1h and 4 h
- Observation period:
- 15 days
- Number of animals:
- 3 females
- Details on study design:
- TEST SITE
- Area of exposure: The back
- coverage: 2.5x2.5cm
- Type of wrap if used: The dose was applied under a two-ply gauze patch secured in place with Micropore tape. The patches were overwrapped with a gauze binder and secured with Dermiform tape.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): The test site was wiped with a disposable paper towel moistened with tepid tap water.
- Time after start of exposure: 1h or 4 hours.
SCORING SYSTEM: Draize
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 23/48/72h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- fully reversible within: 12 days
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24/48/72h
- Score:
- 0.9
- Max. score:
- 2
- Reversibility:
- fully reversible within: 12 days
- Irritant / corrosive response data:
- There were no mortalities during this study. Slight to moderate erythema, very slight oedema and desquamation were noted on all three 4 hour exposure sites. There were no other dermal findings. Oedema completely subsided by day 4 or earlier for all animals. Erythema completely subsided by day 12 or earlier for two rabbits. Very slight erythema with desquamation persisted through day 15 (termination) for the remaining animal.
- Other effects:
- There were no remarkable changes or differences observed in body weights during the study.
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
Score at time point / Reversibility |
Erythema |
Edema |
Max. score: 4 |
Max. score: 2 |
|
60 min |
2/2/1 |
1/1/0 |
24 h |
3/2/2 |
2/2/1 |
48 h |
2/2/2 |
1/1/0 |
72 h |
2/1/2 |
1/0/0 |
Average 24h, 48h, 72h |
2.3/1.7/2.0 |
1.3/1.0/0.3 |
Reversibility*) |
c |
c |
Average time (unit) for reversion |
12 days or less |
12 days or less |
*) Reversibility: c. = completely reversible; n.c. = not completely reversible; n. = not reversible
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on EU criteria, the test material is not considered to be a skin irritant as determined in a reliable study conducted according to an appropriate test protocol, and in compliance with GLP.
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