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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: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 998
- Report date:
- 1998
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Deviations:
- no
- GLP compliance:
- yes
- Test type:
- standard acute method
- Limit test:
- yes
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
- Test material form:
- liquid
- Details on test material:
- Chemical registery number : CAS 67-68-5 / EC 200-664-3
Chemical name : dimethyl sulfoxide (DMSO)
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Sprague-Dawley, Charles River UK Ltd, anston Road, argate, Kent, UK
- Age at study initiation: 8-9 weeks old
- Weight at study initiation: 210-245 g (males) and 185-211 g (females)
- Fasting period before study:
- Housing: by sex in group of 5 in wire-wesh cages
- Diet (e.g. ad libitum): SDS RM1 ad libitum
- Water (e.g. ad libitum): tap water ad libitum
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21+/-2
- Humidity (%): 55+/-10
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: To: no data
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- nose only
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
The vapour generator was designed to produce and maintain an atmosphere containing the vapour of DMSO at the saturation concentration in air by evaporation of the test substance from a fritted glass disc with a countercurrent of air. The test substance was delivered to the generator at a constant flow rate from a syringe driven by a syringe pump and the air supplied to the generator was dried, filtered and oil free.
The snout-only exposure chambers (ADG Developments ) used for the exposures were of cylindrical form (30 cm i.d., 45 cm height) and made of aluminium alloy. The chambers have an enclosed volume of approximately 30 litres. The rats were held for exposure in moulded polycarbonate restraining tubes which were attached at evenly spaced ports in the cylindrical section of the chamber, and were designed to allow only the snout to project into the chamber. Each rat was restrained in a forward position by an adjustable foamed plastic stopper which also provided a seal for the tube.
Rats were held for exposure in nose-only molded polycarbonate restraining tubes which were attached to a central exposure chamber.
The test atmosphere entered through a port at the top centre of the chamber and passed out through a port at the base section below the level of the rats. Each chamber was positioned in a large cabinet equipped with an extract fan exhausting to atmosphere through an absolute filter.
TEST ATMOSPHERE
- Brief description of analytical method used: At least five air samples were taken from the chamber during the exposure to determine the concentration of test substance in the air chamber. The samples were taken at approximately 30, 60, 95, 120, 180, and 230 minutes alter the start of exposure.
Each air sample was withdrawn, at 2 liters per minute, into a gas absorption trap (gas bubbler) containing 2-butanone as the trapping solvent. The volume of the air sample was measured with a wet-type gas meter.
Two additional air samples were taken during the Group 3 exposure using a May impinger.
The May impinger is used for particle size distribution analysis of droplet aerosol atmospheres. The device has a three stage particle size discrimination and is intended to simulate some of the characteristics if the respiratory tract, where similar processes of inertial collection of particles operate. At a constant flow rate of 10 liters per minute the particles are distributed between the stages according to equivalent aerodynamic diameter (EAD) as follows (the approximate size ranges for which collection efficiencies exceed 10% are shown):
Chamber 1 4 µm and above (50% cut-off EAD approximately 6 µm)
Chamber 2 remainder down to 2 µm (50% cut-off EAD approximately 3 µm)
Chamber 3 remainder down to 0.5 !am (50% cut-off EAD approximately 1 µm)
5 minutes if the theoretical time required for the concentration of the aerosol in the chamber to reach 90% of its final value under the conditions of the exposure employed May, K.R., Multistage Liquid Impingers., Bacteriol: Rev. 30, 1966, 559-570
- Samples taken from breathing zone: yes - Analytical verification of test atmosphere concentrations:
- yes
- Duration of exposure:
- 4 h
- Concentrations:
- 0, 0.9 and 5.33 mg/l
- No. of animals per sex per dose:
- 5 males and 5 females
- Control animals:
- yes
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Rats were observed continuously for reaction to the test atmosphere during exposure, at one and two hours after exposure, and at least twice daily during the post-exposure interval. Body weight, food and water consumption were measured daily for all rats, from day of delivery until the end of the observation interval.
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight,organ weights, histopathology, other: Rats were sacrificed and subjected to a detailed macroscopic examination at the end of the 14-day observation interval. Lungs were processed and examined microscopically.
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LC0
- Effect level:
- > 5.33 mg/L air
- Exp. duration:
- 4 h
- Remarks on result:
- other: No mortality and clinical sings
- Mortality:
- There were no deaths during or following exposure to DMSO.
- Clinical signs:
- other: There were no clinical signs related to exposure to DMSO during exposure. Soiling of the fur with excreta, as a consequence of the method of restraint, was seen in all test and control rats during and immediately after exposure. Normal appearance and beh
- Body weight:
- Rate of body weight gain, and food and water consumption in rats exposed to DMSO were similar to controls.
- Gross pathology:
- There were no macroscopic abnormalities in test or control rats.
- Other findings:
- - Organ weights: Lung to body weight ratios in test animals were similar to controls
- Histopathology: There were no treatment-related histopathologic changes in the lungs of test animals that could be ascribed to DMSO exposure. Only minor changes were reported and these of similar incidence in control and test rats : foamy alveolar macrophages (10/10 in high dose, 4/5M and 3/5 F in mid dose group, 4/5M & 5/5F in controls)
- Other observations: The analyzed concentration of DMSO in the exposure chamber during exposure was 5.33 mg/l (sd 0.475 mg/l). Analysis of aerosol determined that 32% of the particles were less than 4 microns in size, and 20% were less than 0.5 microns. The remainder were greater than 4 microns. The respirable fraction of DMSO in the test aerosol was 52%.
Any other information on results incl. tables
The mean analyzed concentrations of DMSO in the chamber air, the standard deviation (sd) of the means and the nominal concentrations were:
Group Analyzed sd Nominal
concentration concentration
(mg/l) (mg/l)
2 0.90 0.043 2.9
3 5.33 0.475 35.6
The nominal concentration was calculated from the amount of DMSO dispersed and the total volume of air supplied to the exposure system.
Chamber air temperature and relative humidity
The mean chamber air temperature, the relative humidity and the standard deviation (sd) of the means during exposure of the groups were:
Group Temperature Relative Humidity
(°C) (°/U)
Mean sd Mean sd
1 (Control) 22 0.3 48 1.2
2 (0.90 mg/1) 22 0.3 48 2.3
3 (5.33 mg/1) 24 0.4 41 4.8
There were no extremes of chamber air temperature or relative humidity considered likely to have influenced the results of the study.
Applicant's summary and conclusion
- Interpretation of results:
- study cannot be used for classification
- Conclusions:
- Under these experimental conditions, the LC0 of DMSO was higher than 5.3 mg/l in Sprague Dawley rats exposed nose-only for a 4-hour period.
- Executive summary:
The acute inhalation toxicity of DMSO was evaluated in a 4-hour, single-exposure study in rats according to OECD Guideline 403 (May 12th 1981). DMSO was initially administered to a single group of five male and five female Sprague Dawley rats via nose only vapor exposure at concentrations of 0, 0.9 or 5.33 mg/l. Rats were held for exposure in nose-only molded polycarbonate restraining tubes which were attached to a central exposure chamber.
Rats were observed continuously for reaction to the test atmosphere during exposure, at one and two hour after exposure, and at least twice daily during the post-exposure interval. Body weight, and food and water consumption were measured daily for all rats, from day of delivery until the end of the observation interval. Rats were sacrificed and subjected to a detailed macroscopic examination at the end of the 14-day observation interval. Lungs were processed and examined microscopically.
There were no deaths during or following exposure to DMSO.
There were no clinical signs related to exposure to DMSO during exposure. Soiling of the fur with excreta, as a consequence of the method of restraint, was seen in all test and control rats during and immediately after exposure. Normal appearance and behaviour was observed in all animals during the 14-day observation interval
Rate of body weight gain, and food and water consumption in rats exposed to DMSO were similar to controls. There were no macroscopic abnormalities in test or control rats.
Based on the results of this study, the LC0 of DMSO was higher than 5.3 mg/l when male and female Sprague Dawley rats were exposed nose-only to a vapor of the test article for a single, 4-hour period.
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