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EC number: 203-812-5 | CAS number: 110-88-3
- 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
No signs of skin irritation in a OECD 404 GLP study on rabbits.
No signs of eye irritation in a OECD 405 GLP study with rabbits.
Transient signs of local respiratory tract irritation following repeated dose inhalation applications.
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:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Additional information
Skin irritation
In an OECD 404 GLP study the semioccclusive application of trioxane to the skin of rabbits for 4h did not result in signs indicative for skin irritation (Hoechst, 1989). Erythema and edema scores were reported as 0, however no data regarding individual Draize scores are available.
In a further incompletely reported skin irritation study with rabbits, no apparent irritation was reported following occlusive application of trioxane for 24h (IHFA, 1962). According to this study no classification for skin irritation is indicated, although the only result reported is a primary irritation score of 0.
Additionally data from a guinea pig maximization test indicated no skin irritation within 96h following 2 x 24h occlusive applications of a 75% trioxane solution (BASF AG, 1989).
Based on the Hoechst-study (1989) trioxane was not legally classified for skin irritation (reported erythema and edema scores of 0) (C&L 2002).
Eye irritation:
In an OECD 405 GLP study trioxane was reported to be not irritating to the eyes of rabbits (Hoechst, 1989). Instillation of trioxane in the eyes for 24 h did only result in mild reversible irritation of the conjunctivae and slight reversible chemosis (mean values: conjunctivae 1.7, chemosis 0.7, cornea 0, iris 0.1, fully reversible after 72 h).
In an incompletely reported eye irritation study with rabbits, reversible signs of mild eye irritation were observed (mild iritis, corneal opacity, conjunctivitits). According to the results of this study no classification according to Directive 67/548/EEC would be required but classification as a mild eye irritant (Cat.2B) according to GHS.
Additional data indicates only mild eye irritant properties of trioxane in rabbit eyes (BASF AG, 1968). No classification would be required according to this study. In this study a smaller amount of test substance was instilled into the eyes of 2 animals only and no rinsing was performed.
Based on the Hoechst (1989) study trioxane was not legally classified for eye irritation (C&L 2002).
Respiratory irritation:
Due to transient signs of local respiratory tract irritation observed in repeated dose inhalation studies, trioxane was classified as a respiratory tract irritant.
EU: R37, GHS: STOTsinglecategory 3 (H335, may cause respiratory irritation).
Effects on respiratory irritation: irritating
Justification for classification or non-classification
No classification for skin and eye irritation according to Directive 67/548/EEC and Directive 1272/2008.
Trioxane was classifid as a respiratory tract irritant. EU: R37, GHS: STOTsingle category 3 (H335, may cause respiratory irritation).
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