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EC number: 615-086-0 | CAS number: 70225-05-7
- 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:
- 1981
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Conducted to sound scientific principles. GLP
Data source
Referenceopen allclose all
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 981
- Reference Type:
- publication
- Title:
- TRIS(2-ETHYLHEXYL)BENZENE-1,2,4-TRICARBOXYLATE
- Author:
- OECD SIDS
- Year:
- 2 002
- Bibliographic source:
- SIDS Initial Assessment Report for Siam 14: TRIS(2-ETHYLHEXYL)BENZENE-1,2,4-TRICARBOXYLATE
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- GLP compliance:
- yes
Test material
- Reference substance name:
- Tris(2-ethylhexyl)benzene-1,2,4-tricarboxylate
- IUPAC Name:
- Tris(2-ethylhexyl)benzene-1,2,4-tricarboxylate
- Reference substance name:
- Tris(2-ethylhexyl) benzene-1,2,4-tricarboxylate
- EC Number:
- 222-020-0
- EC Name:
- Tris(2-ethylhexyl) benzene-1,2,4-tricarboxylate
- Cas Number:
- 3319-31-1
- Molecular formula:
- C33H54O6
- IUPAC Name:
- tris(2-ethylhexyl) benzene-1,2,4-tricarboxylate
- Reference substance name:
- Nuoplaz 6959
- IUPAC Name:
- Nuoplaz 6959
- Details on test material:
- Source: Nouplaz TOTM(Tenneco Chemicals, Inc.)
Purity: 98.95%
Constituent 1
Constituent 2
Constituent 3
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- Temperature - 70 ± 2 degree F
Relative Humidity - 45% ± 5%
Light - 12 hour light/dark cycle
Diet - Wayne 15% Rabbit Ration and tap water are provided ad libitum.
Based on our current knowledge no contaminants are known to
be in this diet or water that might be expected to interfere with
the objectives of the study.
Caging - Stainless steel with elevated wire mesh flooring 1 rabbit/cage
Bedding - Techbord
Shepherd Products Company
Kalamazoo, Michigan 49005
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: intact and abraded
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.5 mL 100% w/w
- Duration of treatment / exposure:
- 24h
- Observation period:
- immediately after removal of patch and 48 hours later (24 and 72 hours after initial application)
- Number of animals:
- 6 rabbits
- Details on study design:
- A 0.5 mL portion of material was applied to an abraded and an intact akin site on the same rabbit. Gauze patches were then placed over the treated areas and an impervious material was wrapped snugly around the trunks of the animals to hold the patches in place. The wrapping was removed at the end of the twenty-four hour period and the treated areas were examined. Readings were also made after seventy-two hours. The Draize method of scoring was employed.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Remarks:
- for intact skin
- Basis:
- mean
- Time point:
- other: 24h after application
- Score:
- 1.5
- Max. score:
- 2
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- edema score
- Remarks:
- for intact skin
- Basis:
- mean
- Time point:
- other: 24 h after application
- Score:
- 0.33
- Max. score:
- 1
- Reversibility:
- fully reversible
- Irritation parameter:
- erythema score
- Remarks:
- for intact skin
- Basis:
- mean
- Time point:
- other: 72 h after application
- Score:
- 0.17
- Max. score:
- 1
- Reversibility:
- fully reversible
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 72 h after application
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- fully reversible
- Irritation parameter:
- erythema score
- Remarks:
- for abraded skin
- Basis:
- mean
- Time point:
- other: 24 h after application
- Score:
- 1.5
- Max. score:
- 2
- Reversibility:
- not fully reversible within: 48 h
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 h after application
- Score:
- 0.33
- Max. score:
- 1
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 72 h after application
- Score:
- 0.33
- Max. score:
- 1
- Reversibility:
- fully reversible
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: Total Score
- Score:
- 1.04
- Remarks on result:
- other: 4.16/4 = 1.04
- Irritant / corrosive response data:
- see Table 1 below
Any other information on results incl. tables
Table 1 – Individual Animal Results
Primary Irritation Score : 4.16/4 =1.04
Reading – Individual (#1-6) Rabbit Score - Average
Erythema and Eschar Formation (Hours)
Intact skin 24 - 2 1 2 1 2 1 – Average 1.50
Intact skin 72 - 0 0 1 0 0 0 – Average 0.17
Abraded skin 24 - 2 1 2 1 2 1 – Average 1.50
Abraded skin 72 - 0 0 1 1 0 0 – Average 0.33
Subtotal 3.50
Oedema Formation
Intact skin 24 - 1 0 0 0 1 0 – Average 0.33
Intact skin 72 - 0 0 0 0 0 0 – Average 0.00
Abraded skin 24 - 1 0 0 0 1 0 – Average 0.33
Abraded skin 72 - 0 0 0 0 0 0 – Average 0.00
Subtotal 0.66
Total 4.16
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on the results of the study, the test material is not a demal irritant to rabbits. Classification as a dermal irritant is not warranted under the new Regulation (EC) 1272/2008 on classification, labeling and packaging of substances and mixtures (CLP) or under Directive 67/548/EEC for dangerous substances and Directive 1999/45/EC for preparations.
- Executive summary:
Dermal irritation was evaluated in a similar manner to OECD TG 404 Guideline study using 0.5 mL of tris(2-ethylhexyl)benzene-1,2,4-tricarboxylate. The 1-48 h mean erythema score was 0.835 and the 1-48 h mean edema score was 0.165 for intact skin.
Based on the results of the study, the test material is not a demal irritant to rabbits. Classification as a dermal irritant is not warranted under the new Regulation (EC) 1272/2008 on classification, labeling and packaging of substances and mixtures (CLP) or under Directive 67/548/EEC for dangerous substances and Directive 1999/45/EC for preparations.
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