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EC number: 246-677-8 | CAS number: 25155-23-1
- 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:
- September 29 1982 to January 25 1983
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non GLP, carried out according to recognised (older) guideline, results fully documented. Considered appropriate for use based on data available and animal welfare concerns.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 984
- Report date:
- 1984
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Consistent with Environmental Protection Agency's Guidelines for registering pesticides in the U.S.: Hazard evaluation: Humans and Domestic Animals, Fed. Reg. 43:163 37336-37402 (1978); test exceeds the protocol recommended in the OECD Guidelines (1981)
- Deviations:
- no
- Principles of method if other than guideline:
- The primary irritation of the skin was measured by a patch-test technique on the abraded and intact skin of six Stauffland albino rabbits. Half a milliliter of the test substance was introduced under a one inch square gauze patch. The patches were secured in place by adhesive tape and wrapped with rubberized damming for a period of four hours. After 4 hours of exposure, the patches and test material were removed, and the resulting reactions were given a score. Readings were also made after 24 and 72 hours and the final score represents an avaerage of all the readings. The scoring and evaluation criteria are those described by Draize (1965).
- GLP compliance:
- no
Test material
- Reference substance name:
- Trixylenyl phosphate
- IUPAC Name:
- Trixylenyl phosphate
- Reference substance name:
- Fyrquel EHC
- IUPAC Name:
- Fyrquel EHC
- Details on test material:
- - Name of test material (as cited in study report): Fyrquel EHC (Trixylenyl phosphate)
- Molecular formula (if other than submission substance): not applicable
- Molecular weight (if other than submission substance): not applicable
- Smiles notation (if other than submission substance): not applicable
- InChl (if other than submission substance): not applicable
- Structural formula attached as image file (if other than submission substance): not applicable
- Substance type: not specified
- Physical state: liquid
- Analytical purity: not specified
- Impurities (identity and concentrations): not specified
- Composition of test material, percentage of components: not specified
- Isomers composition: not specified
- Purity test date: not specified
- Lot/batch No.: #9221-J-1-1X
- Expiration date of the lot/batch: not specified
- Radiochemical purity (if radiolabelling): not applicable
- Specific activity (if radiolabelling): not applicable
- Locations of the label (if radiolabelling): not applicable
- Expiration date of radiochemical substance (if radiolabelling): not applicable
- Stability under test conditions: not specified
- Storage condition of test material: not specified
- Other:
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- other: Stauffland albino
- Details on test animals or test system and environmental conditions:
- Animals used for this study were purchased from Phillips Rabbitry, Soquel, California.
No details on environmental conditions are provided.
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: abraded and intact
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- 0.5 mL
- Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72 hours
- Number of animals:
- 6
- Details on study design:
- The primary irritation of the skin was measured by a patch-test technique on the abraded and intact skin of six Stauffland albino rabbits. Half a milliliter of the test substance was introduced under a one inch square gauze patch. The patches were secured in place by adhesive tape and wrapped with rubberized damming for a period of four hours. After 4 hours of exposure, the patches and test material were removed, and the resulting reactions were given a score. Readings were also made after 24 and 72 hours and the final score represents an avaerage of all the readings. The scoring and evaluation criteria are those described by Draize (1965).
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- overall irritation score
- Basis:
- animal #1
- Time point:
- 72 h
- Score:
- 0.5
- Max. score:
- 1
- Reversibility:
- fully reversible within: 72 hours
- Irritation parameter:
- overall irritation score
- Basis:
- animal #2
- Time point:
- 72 h
- Score:
- 0.67
- Max. score:
- 1
- Reversibility:
- fully reversible within: 72 hours
- Irritation parameter:
- overall irritation score
- Basis:
- animal #3
- Time point:
- 72 h
- Score:
- 0.33
- Max. score:
- 1
- Reversibility:
- fully reversible within: 24 hours
- Irritation parameter:
- overall irritation score
- Basis:
- animal #4
- Time point:
- 72 h
- Score:
- 0.67
- Max. score:
- 1
- Reversibility:
- fully reversible within: 72 hours
- Irritation parameter:
- overall irritation score
- Basis:
- animal #5
- Time point:
- 72 h
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- not fully reversible within: 72 hours
- Remarks on result:
- other: score attributed to erythema / eschar presence
- Irritation parameter:
- overall irritation score
- Basis:
- animal #6
- Time point:
- 72 h
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- not fully reversible within: 72 hours
- Remarks on result:
- other: score attributed to erythema / eschar presence
- Irritant / corrosive response data:
- Fyrquel EHC Trixylenyl phosphate produced mild erythema in intact and abraded skin of 6 rabbits following 4 hour exposure. By the 24 hour observation irritation decreased in 2 rabbits. At 72 hours irritation had cleared in 4 rabbits and 2 rabbits had mild erythema.
- Other effects:
- None noted
Any other information on results incl. tables
Results
|
Skin type |
Erythema-eschar Observation |
Edema Observation |
Sum Total |
Score* |
||||
Rabbit No |
|||||||||
|
|
4 hr. |
24 hr. |
72 hr. |
4 hr. |
24 hr. |
72 hr. |
||
83-F-l |
Intact |
1 |
0 |
0 |
0 |
0 |
0 |
3.0 |
0.50 |
|
|
|
|
|
|
|
|||
Abraded |
1 |
1 |
0 |
0 |
0 |
0 |
|||
|
|
|
|
|
|
|
|
|
|
83-F-2 |
Intact |
1 |
1 |
0 |
0 |
0 |
0 |
4.0 |
0.67 |
|
|
|
|
|
|
|
|||
Abraded |
1 |
1 |
0 |
0 |
0 |
0 |
|||
|
|
|
|
|
|
|
|
|
|
83-F-3 |
Intact |
1 |
0 |
0 |
0 |
0 |
0 |
2.0 |
0.33 |
|
|
|
|
|
|
|
|||
Abraded |
1 |
0 |
0 |
0 |
0 |
0 |
|||
|
|
|
|
|
|
|
|
|
|
83-F-4 |
Intact |
1 |
1 |
0 |
0 |
0 |
0 |
4.0 |
0.67 |
|
|
|
|
|
|
|
|||
Abraded |
1 |
1 |
0 |
0 |
0 |
0 |
|||
|
|
|
|
|
|
|
|
|
|
83-F-5 |
Intact |
1 |
1 |
1 |
0 |
0 |
0 |
6.0 |
1.0 |
|
|
|
|
|
|
|
|||
Abraded |
1 |
1 |
1 |
0 |
0 |
0 |
|||
|
|
|
|
|
|
|
|
|
|
83-F-6 |
Intact |
1 |
1 |
1 |
0 |
0 |
0 |
6.0 |
1.0 |
|
|
|
|
|
|
|
|||
Abraded |
1 |
1 |
1 |
0 |
0 |
0 |
|||
Primary Irritant Score |
|
0.70 |
*Score = Sum of individual values for each rabbit divided by six.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Fyrquel EHC (Trixylenyl phosphate) was a mild irritant to intact and abraded skin of albino rabbits after a 4 hour exposure. This formulation produced mild erythema in intact and abraded skin of 6 rabbits following 4 hour exposure. By the 24 hour observation irritation decreased in 2 rabbits. At 72 hours irritation had cleared in 4 rabbits and 2 rabbits had mild erythema.
- Executive summary:
Fyrquel EHC (Trixylenyl phosphate) was a mild irritant to intact and abraded skin of albino rabbits after a 4 hour exposure. This formulation produced mild erythema in intact and abraded skin of 6 rabbits following 4 hour exposure. By the 24 hour observation irritation decreased in 2 rabbits. At 72 hours irritation had cleared in 4 rabbits and 2 rabbits had mild erythema.
On the basis of EU Criteria, the substance is not classified as a skin irritant.
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