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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
Description of key information
EU RISK ASSESSMENT – DIMETHYL SULPHATE
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 106 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Dose descriptor:
- LC50
- Value:
- 45 mg/m³ air
Additional information
Several studies have been carried out with different species and by different routes.
All data on acute toxicity of DMS are of limited quality. DMS has to be classified as toxic after oral treatment (based on the study of BASF, 1968). In inhalation studies the compound is found to be very toxic.
No signs of toxicity other than death are reported, except in the studies of Druckrey (1966), BASF (1968), and Batsura et al. (1980). Druckrey reports convulsions and dyspnoea in rats exposed to DMSand i.v. Autopsy revealed pulmonary oedema, hepatic congestion and intestinal bleedings. In the BASF study rats (p.o.) and mice (i.p.) were reported to experience dyspnoea and convulsions, rats were apathic and remained in a hunched posture. Autopsy showed gastrectasy and terminal lung oedema (BASF, 1968).
In an inhalation study by BASF (1968) rats (6-12 per group) were exposed to saturated DMS vapour (according to the rapporteur 592 ppm≈3100 mg/m3l, 20°C. However, this study of BASF is not suitable for the determination of a LC50.
In rats the LC50level after a 4 hr-inhalative exposure to DMS is reported to be 45 mg/m3. Groups of animals were sacrificed immediately following exposure and at intervals thereafter. The rats were dyspnoeic with cyanosis of the mucosae, hyperemia of the lung, and hemorrhage in the internal organs. Some animals had nasal discharge. Histological and electron microscopic examination of lung tissue revealed hemorrhage and coagulated proteins in the alveoli. After a latent period of 5-6 hr, accumulation of edematous fluid in the air spaces developed progressively over 24-48 hr (Batsura et al., 1980).
Justification for classification or non-classification
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.
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