Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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: 215-245-0 | CAS number: 1314-85-8
- 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
The substance is not skin irritant but it causes serious eye damage.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irreversible damage)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin irritation/corrosion
Tetraphosphorus trisulphide was tested for its skin irritation potential with an in vitro test according to OECD TG 439 Reconstructed human epidermis model. The mean cell viability of test item treated tissues was 106 % after 15 minutes exposure period and 42 hours of post-exposure incubation period. No classification for skin irritation of this substance is required according to the CLP Regulation (EC.n.1272/2008).
Eye damage
Tetraphosphorus trisulphide was tested for its eye irritation potential with an in vitro test according to OECD TG 492 Reconstructed human Cornea-like Epithelium (RhCE) test method. After 6 hours of exposure followed by product washing and a post incubation of 18 hours a residual cell viability (mean of two replicates) of 15.1 % has been quantified for test item. This results did not allow discrimination between eye irritation/reversible effects on the eye (Category 2) and serious eye damage/irreversible effects on the eye (Category 1). For this purpose, further investigation were performed. Tetraphosphorus trisulphide was tested for its eye damage potential with an in vitro test according to OECD TG 437 Bovine Corneal opacity and Permeability test (BCOP). The test item was incubated on the cornea for 4 hours at 32 ± 1 °C and, after removal of the test item, opacity and permeability values were measured. The calculated IVIS value for the test item was 95.56 (> 55) and so it is possible to conclude that Tetraphosphorus trisulphide causes serious eye damage on the cornea of the bovine eye and it is classified H318 (eye damage cat.1) according to the CLP Regulation (EC. n.1272/2008).
Justification for classification or non-classification
According to the OECD TG 439 (EpiSkinTM/MTT Method) the test item is classified not irritant to skin if the mean relative viability is higher than 50 % according to the CLP Regulation (EC n.1272/2008). Tetraphosphorus trisulphide was tested for skin irritation according to OECD TG 439: the mean cell viability of the test item treated tissues was 106 % and therefore no classification for skin irritation/corrosion is required according to the CLP Regulation (EC n.1272/2008).
According to OECD TG 437 Bovine Corneal Opacity and Permeability (BCOP) Test, a substance with an IVIS > 55 induces serious eye damage and it is classified UN GHS Category I or H318 (eye damage cat.1) according to the CLP Regulation (EC n.1272/2008). IVIS of Tetraphosphorus trisulphide is 95.56 and it satisfies the criteria for the classification H318 (eye damage cat.1) according to the CLP Regulation (EC n.1272/2008).
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.