Flammable liquids, Category 2
H225 Highly flammable liquid and vapour
P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
P233 Keep container tightly closed.
P240 Ground and bond container and receiving equipment.
P241 Use explosion-proof [electrical/ventilating/lighting/...] equipment.
P242 Use non-sparking tools.
P243 Take action to prevent static discharges.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P303+P361+P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse affected areas with water [or shower].
P370+P378 In case of fire: Use ... to extinguish.
P403+P235 Store in a well-ventilated place. Keep cool.
P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
no data available
Fresh air, rest. Refer for medical attention.
Remove contaminated clothes. Rinse and then wash skin with water and soap.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Give one or two glasses of water to drink. Refer for medical attention .
Inhalation causes moderate irritation of upper respiratory system. Contact of liquid with eyes causes moderate irritation. Repeated contact with skin may extract oils and result in irritation. Ingestion causes nausea and irritation of mouth and stomach. (USCG, 1999)
Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. Sulfur and related compounds
Use CO2, dry chemical.
Special Hazards of Combustion Products: Toxic and irritating sulfur dioxide is formed. Behavior in Fire: Vapor is heavier than air and may travel considerable distance to source of ignition and flash back. (USCG, 1999)
Use powder, foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Evacuate danger area! Consult an expert! Personal protection: filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Collect leaking and spilled liquid in sealable containers as far as possible. Do NOT wash away into sewer.
Evacuate danger area! Consult an expert! Personal protection: filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Collect leaking and spilled liquid in sealable containers as far as possible. Do NOT wash away into sewer.
SRP: Wastewater from contaminant suppression, cleaning of protective clothing/equipment, or contaminated sites should be contained and evaluated for subject chemical or decomposition product concentrations. Concentrations shall be lower than applicable environmental discharge or disposal criteria. Alternatively, pretreatment and/or discharge to a permitted wastewater treatment facility is acceptable only after review by the governing authority and assurance that "pass through" violations will not occur. Due consideration shall be given to remediation worker exposure (inhalation, dermal and ingestion) as well as fate during treatment, transfer and disposal. If it is not practicable to manage the chemical in this fashion, it must be evaluated in accordance with EPA 40 CFR Part 261, specifically Subpart B, in order to determine the appropriate local, state and federal requirements for disposal.
NO open flames, NO sparks and NO smoking. Closed system, ventilation, explosion-proof electrical equipment and lighting. Do NOT use compressed air for filling, discharging, or handling. Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Fireproof. Separated from strong oxidants. Cool.Before entering confined space where this chemical may be present, check to make sure that an explosive concentration does not exist. Store in tightly closed containers in a cool, well ventilated area. Metal containers involving the transfer of this chemical should be grounded and bonded. Where possible, automatically pump liquid from drums or other storage containers to process containers. Drums must be equipped with self-closing valves, pressure vacuum bungs, and flame arresters. Use only non-sparking tools and equipment, especially when opening and closing containers of this chemical. Sources of ignition, such as smoking and open flames, are prohibited where this chemical is used, handled, or stored in a manner that could create a potential fire or explosion hazard. Wherever this chemical is used, handled, manufactured, or stored, use explosion-proof electrical equipment and fittings.
TLV: 10 ppm as TWA
no data available
Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear safety spectacles.
Protective gloves.
Use local exhaust or breathing protection.
no data available
Dimethyl sulfide is a clear colorless to straw colored liquid with a disagreeable odor. Flash point less than 0°F. Less dense than water and slightly soluble in water. Vapors are heavier than air.
Colorless, volatile liquid
UNPLEASANT ODOR OF WILD RADISH, CABBAGE-LIKE
-95°C(lit.)
37°C
Highly flammable. Gives off irritating or toxic fumes (or gases) in a fire.
Lower flammable limit: 2.2% by volume; Upper flammable limit: 19.7% by volume
-34°C(lit.)
403° F (USCG, 1999)
no data available
no data available
Less than 32.6 Saybolt unit sec
Soluble in alcohol, ether; soluble in water at concentrations below 300 mM
log Kow = 0.92 (est)
26.24 psi ( 55 °C)
0.84
2.1 (vs air)
no data available
Decomposes on burning. This produces toxic and corrosive fumes of sulfur oxides. Reacts violently with oxidants. This generates fire and explosion hazard.
no data available
Highly flammableThe vapour is heavier than air and may travel along the ground; distant ignition possible.Organosulfides, such as DIMETHYL SULFIDE, are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Dimethyl sulfide rapidly decomposes dibenzoyl peroxide explosively in the absence of solvent, [J. Org. Chem., 1972, 37, 2885]. The sulfide also decomposes xenon difluoride explosively at ambient temps, [J, Chem Soc., 1984, 2827]. Interaction of dimethyl sulfide and oxygen is explosive at 210°C and above, [Atmos. Environ., 1967, 1, 491-497]. A delayed explosion occurred in a system containing nitric acid, dimethyl sulfide, and 1, 4-dioxane, even with cooling with liquid nitrogen, [Chem. Abs., 1972, 76, 13515].
no data available
Can react vigorously with oxidizing materials.
Thermal decomposition in sulfur dioxide, carbon monoxide, and carbon dioxide.
no data available
no data available
no data available
no data available
no data available
no data available
The substance is irritating to the eyes and skin.
no data available
A harmful contamination of the air can be reached rather quickly on evaporation of this substance at 20°C.
AEROBIC: Dimethyl sulfide was initially present in a wastewater/recycled sludge mixture at 150 (ug/kg)/(ug/L); following activated sludge treatment, effluent concns were below the detection limit(7). Radiolabeled-dimethyl sulfide added to the head space over 1 ml of freshwater lake sediment was metabolized to methane and carbon dioxide; 33 and 5% radiolabeled carbon was converted to methane and carbon dioxide, respectively, in 8 hours(2). No degradation of dimethyl sulfide occurred in sterilized (heat killed - 70 deg C, 1 hr) samples of sediment(2). Addition of dimethyl sulfide to various anoxic aquatic sediments (e.g. fresh water, estuarine, alkaline/hypersaline) stimulated methane production(3). The yield of methane from dimethyl sulfide typically ranged between 52-63%, although high concns of dimethyl sulfide inhibited methanogenesis in sediment from alkaline lakes(3). Metabolism resulted in appearance of methanethiol as a transient intermediate(3). Dimethyl sulfide was completely biodegraded in anoxic salt marsh sediments within 11 days with the production of methanethiol and methane(4). Biological consumption rates of dimethyl sulfide, in seawater samples collected in the eastern Pacific Ocean, ranged from 1.1 nM/day to 18.0 nM/day, giving turnover times of 0.6 to 4.6 days(5). The conversion efficiency from added dimethyl sulfide to methane of an algal mat and sediments obtained from a hypersaline pond was 11.2%(6).
An estimated BCF of 3.2 was calculated in fish for dimethyl sulfide(SRC), using a water solubility of 22,000 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Koc of dimethyl sulfide is estimated as 6.3(SRC), using a water solubility of 22,000 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that dimethyl sulfide is expected to have very high mobility in soil.
no data available
The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.
ADR/RID: UN1164 (For reference only, please check.)
IMDG: UN1164 (For reference only, please check.)
IATA: UN1164 (For reference only, please check.)
ADR/RID: DIMETHYL SULPHIDE (For reference only, please check.)
IMDG: DIMETHYL SULPHIDE (For reference only, please check.)
IATA: DIMETHYL SULPHIDE (For reference only, please check.)
ADR/RID: 3 (For reference only, please check.)
IMDG: 3 (For reference only, please check.)
IATA: 3 (For reference only, please check.)
ADR/RID: II (For reference only, please check.)
IMDG: II (For reference only, please check.)
IATA: II (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available