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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 200-664-3 | CAS number: 67-68-5
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- A toxicologic study of dimethyl sulfoxide
- Author:
- Willson JE, Brown DE and Timmens EK
- Year:
- 1 965
- Bibliographic source:
- Toxicol. Appl. Pharmacol. 7: 104-112
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- GLP compliance:
- no
- Test type:
- standard acute method
Test material
- Reference substance name:
- Dimethyl sulfoxide
- EC Number:
- 200-664-3
- EC Name:
- Dimethyl sulfoxide
- Cas Number:
- 67-68-5
- Molecular formula:
- C2H6OS
- IUPAC Name:
- dimethyl sulfoxide
- Details on test material:
- Test compound: Dimethylsulfoxyde
Source: Crown Zellerbach Corp.
Batch : no data
Purity : no data
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: Carworth CFN
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Initial body weight: 112-130 g
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- unchanged (no vehicle)
- Details on oral exposure:
- Animals were fasted for 16-18 hr prior to DMSO administration.
- Doses:
- 10, 20, and 40 g/kg
- No. of animals per sex per dose:
- 5 males and 5 females
- Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 14 days
- Statistics:
- Median lethal dose (LD50), 95% confidence limit, and probit slopes were determined by the Cornfield-Mantel modifications of Karber's method
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- 28 300 mg/kg bw
- Remarks on result:
- other: Lethal doses caused ataxia, myasthenia, decreased motor activity, and bradypnea
- Mortality:
- With one exception, all deaths occurred within the first 24 hours.
- Clinical signs:
- other: Lethal doses caused ataxia, myasthenia, decreased motor activity, and bradypnea shortly after administration. Non-lethal doses of DMSO produced decreased motor activity, although polydipsia and polyuria were noted in rats following doses of 20 g/kg.
- Gross pathology:
- no data
Applicant's summary and conclusion
- Interpretation of results:
- study cannot be used for classification
- Remarks:
- Migrated information
- Conclusions:
- Under these experimental conditions, a LD50 of 28500 mg/kg has been calculated in rats.
- Executive summary:
- The Acute oral toxicity of Dimethylsulfoxide (DMSO) was evaluated in rats
according to a protocol similar to the OECD N°401 guideline (Acute Toxic
Standard Method). Groups of 5 males and 5 females Carworth CFN rats were
given a single oral dose of DMSO at doses of 10000, 20000 and 40000 mg/kg.
Following treatment, rats were observed during 14 days.
With one exception, all deaths occurred within the first 24 hours.
Lethal doses caused ataxia, myasthenia, decreased motor activity, and bradypnea shortly after administration.
Non-lethal doses of DMSO produced decreased motor activity, although polydipsia and polyuria were noted in rats following doses of 20 g/kg.
Under these experimental conditions, the oral LD50 of DMSO is 28500 mg/kg in Carworth CFN rats.
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.