Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
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

PBT assessment
Administrative data
PBT assessment: overall result
- PBT status:
- the substance is not PBT / vPvB
- Justification:
Persistent/very Persistent
The substance displays properties that indicate persistency within the environment, based on low ready biodegradability. Trixylyl phosphate displays a low ready biodegradability in that it achieved 14% biodegradation in a 28-day study closed bottle test.
The substance is also not expected to hydrolyse under normal environmental conditions. Experimental studies on hydrolytic effects demonstrated that the substance was stable to hydrolysis at environmentally relevant temperature and pH’s, with a half life of > 1year at pH 7. As such, negligible to nil degradation is anticipated via this route. Studies on direct phototransformation in water are not available but it is assumed on the basis of chemical structure that the substance is not degraded by direct photolysis. It is concluded, therefore, that abiotic processes would not contribute significantly to the depletion of the substance within the environment.
A study was conducted to assess the potential mineralization and transformation of Trixylyl Phosphate in aerobic water systems. HPLC/β-RAM analyses of samples from the live and sterile 200 μg/L treatment groups showed that the parent compound Trixylyl Phosphate remained substantially intact in all live and sterile vessels throughout the course of this study. Additionally there were no transformation products of the parent compound found. The DT50 and DT90 values are reported as >60 days, the duration of the study, confirming that the substance does not undergo mineralization in water.
Due to being not readily biodegradable, and having no significant mechanism of hydrolysis the substance is considered to be persistent. As such, the substance fulfills the requirements of Annex XIII, Para 1.1 based on evaluation of available data, and can be considered to be “P” and “vP” based on this data.
Bioaccumulative/very Bioaccumulative
An assessment of the propensity towards bioaccumulation was undertaken, utilizing appropriate techniques such as:
· Read across to structural analogues.
· QSAR derivation, using recognized tools
· Literature data
The results are as follows:
Read across to Structural Analogues:
Phenol, isopropylated, phosphate (3:1).
As a recently conducted study, this is considered as the key substance for evaluation. The highest BCF of 922 is assigned to the substance from read across to this study.
The substance is not considered to be bioaccumulative, and all BCF’s are less than 1000.
Tricresyl phosphate.
This data is listed on the World Health Organisation website. The paper contains various bioaccumulation assessment studies on this structural analogue and demonstrate thattricresyl phosphate does not demonstrate a propensity towards bioaccumulation, based on the measured values within the studies.
As a weight of evidence approach, it is considered that on structural grounds, the same conclusion can be applied to trixylyl phosphate.
QSARs for substance:
QSAR prediction using BCF model (CAESAR) (Version 2.1.1.11) = BCF 36.0 L/kg based on log(L/kg) 1.56
QSAR prediction using BCF model (Meylan) (version 1.0.0) (CAESAR).= BCF 669.24 L/kg Based on log(L/kg) 2.83
QSAR prediction using BCF Read-Across (version 1.0.0) (CAESAR) = BCF >=118.0 - <=126.0 Based on log(L/kg) 2.07-2.1
QSAR prediction using US EPA On-Line EPI Suite™ v4.0 model BCFBAF = BCF 669.09 L/kg Based on Estimated Log BCF = 2.817
Literature data:
Two studies by Bengtsson et al are presented.
Conclusion:
On the basis of a weight of evidence approach, there is sufficient information available to state that the substance is not bioaccumulative without the need for further testing as requested by ECHA. Results observed across the data available indicate that the substance, as part of the phosphates group, is unlikely to be bioaccumulative within the aquatic environment.
Overall
On the basis of a weight of evidence approach, there is sufficient information available to state that the substance is not bioaccumulative.
Toxicity
On the basis of effects noted in fish and Daphnia, the substance is deemed to be classified according to Regulation (EC) No 1272/2008 the substance is also classified as:
- H400: Very toxic to aquatic life with long lasting effects;: Aquatic Acute and Chronic Category 1.
- H410: Very Toxic to aquatic life with long lasting effects.
No chronic NOEC for the substance currently is available, so determination of this value is not applicable. However, the substance is also classified as having concern for reproductive toxicity. The results triggered classification under the CLP Regulation (EC No 1272/2008) as follows:
Repr. Cat. 1B:
H360f: May damage fertility <testicular effects > <oral>.
H373: May cause damage to organs <or state all organs affected, if known> through prolonged or repeated exposure <state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard>. (adrenals, testes, epididymides, ovaries, liver (females only))
As such, the substance fulfils the requirements of Annex XIII, Para 1.3 based on evaluation of available data, and can be considered as “T” for the purposes of the assessment.
Conclusion
Although the substance can be considered to fulfil the criteria for Persistency and Toxicity, it does not fulfil the criteria for Bioaccumulation, as specified in REACH Annex XIII. As such, the substance cannot be considered as a PBT or vPvB substance, based on the available data.
PBT/vPvB criteria: Not classified.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
