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Diss Factsheets
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EC number: 201-058-1 | CAS number: 77-78-1
- 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
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
Additional information
EU RISK ASSESSMENT – DIMETHYL SULPHATE
Toxico-kinetics, metabolism, and distribution
DMS can be absorbed via respiratory and oral routes. For oral absorption this is concluded from toxicodynamic data. No information is provided on the metabolism of DMS in animals following oral administration. The information on inhalatory or dermal exposure is limited and no quantitative conclusion can be drawn.
In an inhalatory study in rats a rapid disappearance of DMS from the exposure chamber was reported (40 minutes after exposure to 4.7-127 mg/m3). Blank chambers (DMS, no animal) were run as controls. At the higher dose levels (50.3 and 127 mg/m3) the disappearance rate was decreased, probably due to a decreased minute volume caused by DMS (Mathison, 1995). This study provides information on uptake of DMS, however does not allow quantification of the percentage of absorption.
In the urine of mice exposed by inhalation to3H-DMS (average concentration 16.3 mg/m³ and 0.32 mg/m³ for 135 and 60 min resp.) 84-94% of the radiolabel was collected from urine at 48 hours. Less than 0.5% of estimated dose was recovered in the urine as labelled methylated purines (Löfroth, 1974). Due to the limited report this study is considered not suitable for quantitative evaluation.
After an intravenous injection of 75 mg/kg bw in the rat, DMS was no longer detectable in the blood after 3 minutes (Swann, 1968B).
After inhalatory and dermal exposure DMS is reported to be slowly hydrolysed to methanol and sulphuric acid in the tissues, however no quantitative data are provided (Kühn, 1994). Other minor metabolites may be methylsulphate, formaldehyde, and formate. Methylsulphate is stated not to decompose to sulphate (Mathison, 1995), however this statement is not understandable.
When rat liver- and nasal microsomes were incubated with DMS (2 mM in water) only minor amounts of formaldehyde were found with liver microsomes and traces with rat nasal microsomes (Dahl, 1983).
Conclusion
The data are insufficient to quantify the kinetic behaviour of DMS after inhalatory exposure, however, apparently absorption is high. No quantitative information on absorption via the oral and dermal route of exposure is available.
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