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EC number: 223-622-6 | CAS number: 3982-91-0
- 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
Key value for chemical safety assessment
Additional information
There are no data for genotoxicity in bacteria (Ames test, in vitro), or in mamalian cells in vitro available.
Thiophosphoryl trichloride hydrolyses in aqueous medium rapidly.
The hydrolysis of a 30% aqueous thiophosphoryl chloride solution in CD3CN was evaluated by NMR spectroscopy. After 2.5 h as main components S=P(OH)2Cl and S=P(OH)3 and minor amounts of O=P(OH)2Cl and H3PO4 were found.
After 9 hours as main component S=P(OH)3 and minor amounts of O=P(OH)2Cl and H3PO4 were detected.
Due to analytical limitations of the method used, hydrogen chloride can not be detected, but the formation of HCl is predicted based on the stoichiometry of the hydrolysis reaction.
Phosphoric acid and hydrogen chloride are strong acids and according Regulation (EC) No 1272/2008 Annex VI Table 3.2 hydrogen chloride is corrosive (C; R35) as well as phosphoric acid (C; R34), (C > 25%). Due to the rapid hydrolysis and corrosivity of hydrolyses products a study with thiophosphoryl trichloride is scientifically not justified.
With phosphoric acid consistent negative results have been obtained in the bacterial systems, while positive results have been obtained in the non-bacterial systems. The positive results were observed at high concentration, but they were considered to be artifacts due to low pH (OECD SIDS for phosphoric acid).
For HCl, a negative result has been shown in the Ames test. A positive result, which is considered to be an artifact due to the low pH, has been obtained in a chromosome aberration test using Hamster ovary cells (OECD SIDS for HCl).
No chromosome aberration test in vitro is available is thiophosphoryl trichloride.
Short description of key information:
No in-vitro genotoxicity studies are available for thiophosphoryl trichloride.
Endpoint Conclusion:
Justification for classification or non-classification
From the available results of in-vitro genotoxicity studies with phosphoric acid and hydrogenchloride (H3PO4 + 3 HCl) a genotoxicity classification for thiophosphoryl trichloride is not justified.
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