Acute toxicity - Category 4, Dermal
Eye irritation, Category 2
Acute toxicity - Category 4, Inhalation
Reproductive toxicity, Category 1B
H312 Harmful in contact with skin
H319 Causes serious eye irritation
H332 Harmful if inhaled
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P264 Wash ... thoroughly after handling.
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P271 Use only outdoors or in a well-ventilated area.
P203 Obtain, read and follow all safety instructions before use.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P317 Get medical help.
P321 Specific treatment (see ... on this label).
P362+P364 Take off contaminated clothing and wash it before reuse.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P318 IF exposed or concerned, get medical advice.
P405 Store locked up.
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. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Do NOT induce vomiting. Refer for medical attention .
Irritation of eyes, skin and nose. May cause nausea. (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. Organic acids and related compounds
Wear self contained breathing apparatus for fire fighting if necessary.
Special Hazards of Combustion Products: Vapors are irritating (USCG, 1999)
Use water spray, powder, alcohol-resistant foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Personal protection: complete protective clothing including self-contained breathing apparatus. Ventilation. Remove all ignition sources. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Personal protection: complete protective clothing including self-contained breathing apparatus. Ventilation. Remove all ignition sources. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Use personal protective equipment. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Remove all sources of ignition. Evacuate personnel to safe areas. Beware of vapors accumulating to form explosive concentrations. Vapors can accumulate in low areas.
NO open flames, NO sparks and NO smoking. NO contact with oxidizing agents. Above 58°C use a closed system and ventilation. 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.
Separated from incompatible materials. See Chemical Dangers.Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Handle and store under inert gas.
TLV: 5 ppm as TWA; (skin); A3 (confirmed animal carcinogen with unknown relevance to humans); BEI issued.MAK: 15 mg/m3, 5 ppm; peak limitation category: II(2); skin absorption (H); carcinogen category: 4; pregnancy risk group: B.EU-OEL: 15 mg/m3, 5 ppm as TWA; 30 mg/m3, 10 ppm as STEL; (skin)
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 goggles or eye protection in combination with breathing protection.
Barrier cream. Protective gloves. Protective clothing.
Use ventilation, local exhaust or breathing protection.
no data available
Liquid.
Colourless.
Fishy odor
-61.4 - -61 °C.
152 - 153 °C. Atm. press.:1 013 hPa.
Class II Combustible Liquid: Fl.P. at or above 100°F and below 140°F.
Lower flammable limit: 2.2% by volume at 212 deg F (100 deg C); Upper flammable limit: 15.2% by volume
57.5 °C. Atm. press.:1 013.25 hPa.
435 °C. Atm. press.:1 013.25 hPa.
no data available
pH = 6.7 (0.5 molar solution in water)
dynamic viscosity (in mPa s) = 0.79 - 0.805. Temperature:25.0°C.
Miscible with water
log Pow = -1.01.
3.08 hPa. Temperature:20 °C.
0.94 - 0.95. Temperature:20 °C.
2.5 (vs air)
no data available
Decomposes on heating. This produces toxic fumes including nitrogen oxides. Reacts violently with strong oxidants, halogens, halogenated hydrocarbons and nitrates. Attacks some plastics and rubber.
DMF is stable. It is hygroscopic and easily absorbs water form a humid atmosphere and should therefore be kept under dry nitrogen. High purity DMF, required for acrylic fibers, is best stored in aluminum tanks. DMF dose not change under light or oxygen and does not polymerize spontaneously. Temperatures >350 deg C may cause decomposition to form dimethylamine and carbon dioxide, with pressure developing in closed containers.
CombustibleN,N-DIMETHYLFORMAMIDE may react violently with a broad range of chemicals, e.g.: alkaline metals (sodium, potassium), azides, hydrides (sodium borohydride, lithium aluminum hydride), bromine, chlorine, carbon tetrachloride, hexachlorocyclohexane, phosphorus pentaoxide, triethylaluminum, magnesium nitrate, organic nitrates. Forms explosive mixtures with lithium azide [Bretherick, 5th ed., 1995, p. 453]. Oxidation by chromium trioxide or potassium permanganate may lead to explosion [Pal B. C. et al., Chem. Eng. News, 1981, 59, p. 47].
no data available
Can react vigorously with oxidizing agents, halogenated hydrocarbons, & inorg nitrates.
When heated to decomposition it emits toxic fumes of /nitrogen oxides/.
no data available
no data available
no data available
no data available
Evaluation: There is inadequate evidence in humans for the carcinogenicity of dimethylformamide. There is evidence suggesting the lack of carcinogenicity of dimethylformamide in experimental animals. Overall evaluation: Dimethylformamide is not classifiable as to its carcinogenicity in humans (Group 3).
Only one study is available on the reproductive effects of dimethylformamide in humans. This study reported an increased rate of spontaneous abortion among pregnant women occupationally exposed to dimethylformamide. However, these results cannot be attributed solely to dimethylformamide, as these women were exposed to a number of additional chemicals. Dimethylformamide is embryotoxic in animals; reduced implantation efficiency, decreased mean fetal weight, and increased abortions have been reported in rats exposed by inhalation. In rabbits exposed to dimethylformamide by gavage (experimentally placing the chemical in the stomach), decreased mean fetal weight and increased percentage of malformed live fetuses per litter and increased percentage of litters with malformed fetuses were observed in the high-dose group.
The substance is irritating to the eyes and respiratory tract. The substance may cause effects on the liver. This may result in tissue lesions. The effects may be delayed. Medical observation is indicated. See Notes. If swallowed the substance easily enters the airways and could result in aspiration pneumonitis.
The substance may have effects on the liver. This may result in impaired functions. Tumours have been detected in experimental animals but may not be relevant to humans. Animal tests show that this substance possibly causes toxic effects upon human reproduction.
A harmful contamination of the air will be reached rather slowly on evaporation of this substance at 20°C.
AEROBIC: Aerobic unacclimated and acclimated river die-away tests showed that N,N-dimethylformamide at an initial concentration of 30 mg/L completely disappeared within 6 and 3 days, respectively(1). However, 24 to 48 hours was required before any degradation was observed among unacclimated samples(1). N,N-Dimethylformamide, present at 100 mg/L, reached 4.4% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(2). Aerobic grab sample data for N,N-dimethylformamide in sea water showed a mineralization rate of <3% in 24 hours for initial concentration of 10 ug/L and 100 ug/L(3). However, 20% of N,N-dimethylformamide at a concentration of 0.1 ug/L was mineralized in 24 hrs(3). All samples were adjusted to sterilized controls(3). Aqueous screening test data demonstrated that dimethylformamide was easily removed by sewage treatment facilities upon acclimation(4). Wastewater from a polyimide synthesis operation at Kansas City, MO contained N,N-dimethylformamide at a concentration of 65,500 mg/L before entering a bench scale biological treatment system(5). At feed rates of 90 lb/day/1000 cu ft, effluent from the biological reactor contained N,N-dimethylformamide at a concentration of <10 mg/L(5). The concentration of N,N-dimethylformamide in the reactor sludge was not documented(5).
BCFs of 0.3-1.2 and 0.3-0.8 were reported in carp (Cyprinus carpio) when exposed to 2 and 20 ppm of N,N-dimethylformamide over a 2-week period, respectively(1). According to a classification scheme(2), these BCFs suggest the potential for bioconcentration in aquatic organisms is low(SRC).
Using a structure estimation method based on molecular connectivity indices(1), the Koc of N,N-dimethylformamide can be estimated to be 1(SRC). According to a classification scheme(2), this estimated Koc value suggests that N,N-dimethylformamide 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: UN2265 (For reference only, please check.)
IMDG: UN2265 (For reference only, please check.)
IATA: UN2265 (For reference only, please check.)
ADR/RID: N,N-DIMETHYLFORMAMIDE (For reference only, please check.)
IMDG: N,N-DIMETHYLFORMAMIDE (For reference only, please check.)
IATA: N,N-DIMETHYLFORMAMIDE (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: III (For reference only, please check.)
IMDG: III (For reference only, please check.)
IATA: III (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
The symptoms of poisoning do not become manifest until a few hours or even days have passed.Use of alcoholic beverages enhances the harmful effect.