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Diss Factsheets
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EC number: 252-552-9 | CAS number: 35415-27-1
- 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
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- For details on endpoint specific justification please see read-across report in section 13 or find a link in cross-reference “assessment report”.
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- assessment report
- GLP compliance:
- yes
- Key result
- Duration:
- 4.75 h
- Dose descriptor:
- EC10
- Effect conc.:
- > 915 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: corrected for the molecular weight of the target substance: maximum weight source substance: 630.94 g/mol
- Duration:
- 4.75 h
- Dose descriptor:
- EC10
- Effect conc.:
- > 1 060 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: corrected for the molecular weight of the target substance: minimum weight: source substance: 543.76 g/mol;
- Validity criteria fulfilled:
- yes
- Conclusions:
- The test substance was not toxic under test conditions in the range of water solubility.
- Executive summary:
The study used as source investigated bacteriotoxicity of 1,2,4-Benzenetricarboxylic acid, mixed decyl and octyl triesters according to a method developed by the testing laboratory. The test substance did not affect the bacterial respiration and derived effect concentration were: 4.75h-EC10 > 0.9 g a.i./L, 4.75h-EC50 > 915 -1060 mg a.i./L (corrected for the molecular weight of the target substance). Results of the source compound were considered applicable to the target compound. Justification and applicability of the read-across approach (structural analogue) is outlined in the read-across report in section 13 or find a link in cross-reference “assessment report”.
Reference
Description of key information
No microorganism toxicity data for the submission substance is available. However adequate and reliable data for structural analogues is available (i.e. C8C10TM, for read-across justification please see read-across report in section 13).The derived 4.75h-EC10 (Pseudomonas putida, respiration) > 915 -1060 mg a.i./L (corrected for the molecular weight of the target substance).
Key value for chemical safety assessment
Additional information
No microorganism toxicity data for the submission substance is available. However adequate and reliable data for structural analogues (i.e. C8C10TM, for read-across justification please see read-across report in section 13) are reported below.
In a reliable toxicity study on microorganism (non-guideline study and in compliance with GLP, Huels AG, 1994, RL2), no effect on respiration (biochemical oxygen demand) was observed during 4.75 hours of exposure to three concentrations up to 980 mg a.i./L test substance (nominal 1000 mg/L, use of solubilizer, analogue substance: 1,2,4-benzenetricarboxylic acid, mixed decyl and octyl triesters, C8C10TM, CAS no. 90218-76-1) (corresponding to 915 - 1060 mg/L of the target substance). No analytical verification of the test concentrations was performed. No toxicity to microorganisms is expected below the water solubility of the analogue and submission substance.
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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