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Diss Factsheets
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EC number: 813-272-8 | CAS number: 309721-49-1
- 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
Endpoint summary
Administrative data
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP- and guideline-conformant study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- testing lab.
- Type of study:
- mouse local lymph node assay (LLNA)
- Species:
- mouse
- Strain:
- CBA
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Envigo RMS B.V., Inc. (Netherlands)
- Age at study initiation: 11-12 weeks (pre-test), 8-9 weeks (main study)
- Weight at study initiation: 19.4 +/- 1 g (main study)
- Housing: by group
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 2
- Humidity (%): 45-65
- Photoperiod (hrs dark / hrs light): 12/12 - Vehicle:
- propylene glycol
- Remarks:
- purity 99%
- Concentration:
- Based on a pre-test with concentrations of 25% and 10% substance, 10% was the highest concentration that could be achieved whilst avoiding local skin irritation. Therefore, the main study was conducted at concentrations of 2, 5, and 10% test substance.
- No. of animals per dose:
- 5
- Parameter:
- SI
- Value:
- 1.74
- Test group / Remarks:
- 2% test substance
- Parameter:
- SI
- Value:
- 4.25
- Test group / Remarks:
- 5% test substance
- Parameter:
- SI
- Value:
- 7.67
- Test group / Remarks:
- 10% test substance
- Parameter:
- EC3
- Value:
- 3.3
Reference
The following data were obtained in the local lymph node assay (calculated per group):
Test substance concentration |
mean DPM per animal (2 lymph nodes)$ |
SD |
S.I. |
Vehicle control |
1169.2 |
281.5 |
1.00 |
2% 1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3) |
2035.0 |
800.8 |
1.74 |
5%1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3) |
4965.4 |
1516.4 |
4.25 |
10%1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3) |
8969.8* |
4310.1 |
7.67 |
DPM, Radioactive disintegrations per minute
S.I., stimulation index
$Mean DPM/animal was determined by dividing the sum of the measured values from lymph nodes of all animals within a group by the number of animals in that group (5 animals)
* mean DPM value for the group was significantly higher than the corresponding control value (ANOVA Dunnett-test, p=0.000)
Calculation of the EC3 value:
|
Test substance concentration |
S.I. |
Test group 2 |
1.58% (a) |
1.74 (b) |
Test group 3 |
5%(c) |
4.25 (d) |
EC3 = (a-c) [(3-d)/(b-d)] + c = 3.3% (w/w) |
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (sensitising)
- Additional information:
1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3) was tested in the LLNA at concentrations of 2, 5, and 10%, resulting in stimulation indices of 1.74, 4.25, and 7.67. The calculated EC3 value was 3.3% (w/w).
Migrated from Short description of key information:
LLNA (OECD 429, BASF SE, 2015): positive
Justification for selection of skin sensitisation endpoint:
GLP- and guideline-conformant study
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Testing of 1,3,5 -Benzenecarboxylic acid, copper (2 +) salt (2:3) derived an EC3 value of 3.5% in the LLNA. According to Regulation (EU) 1272/2008, classification as skin sensitizer (Cat. 1B, H317) is warranted.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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