Flammable liquids, Category 2
Acute toxicity - Category 4, Oral
Skin corrosion, Sub-category 1B
Acute toxicity - Category 4, Inhalation
H225 Highly flammable liquid and vapour
H302 Harmful if swallowed
H314 Causes severe skin burns and eye damage
H332 Harmful if inhaled
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/...
P264 Wash ... thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P260 Do not breathe dust/fume/gas/mist/vapours/spray.
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P271 Use only outdoors or in a well-ventilated area.
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.
P301+P317 IF SWALLOWED: Get medical help.
P330 Rinse mouth.
P301+P330+P331 IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P363 Wash contaminated clothing before reuse.
P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P316 Get emergency medical help immediately.
P321 Specific treatment (see ... on this label).
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P317 Get medical help.
P403+P235 Store in a well-ventilated place. Keep cool.
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. Half-upright position. Artificial respiration may be needed. Refer for medical attention.
First rinse with plenty of water for at least 15 minutes, then remove contaminated clothes and rinse again. 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 .
Inhalation of vapors causes irritation, sometimes with nausea and vomiting; can also cause burns to the respiratory system. Ingestion causes irritation of mouth and stomach. Vapor irritates eyes; liquid causes severe burn, like caustic. Contact with skin causes irritation. (USCG, 1999)
Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary . Monitor for shock and treat if necessary . Anticipate seizures and treat if necessary . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patent can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal . Cover skin burns with dry sterile dressings after decontamination . /Organic bases/amines and related cmpds/
Use dry chemical, "alcohol resistant" foam, carbon dioxide, or water spray. Water may be ineffective. Use water spray to keep fire-exposed containers cool. Approach fire from upwind to avoid hazardous vapors and toxic decomposition products.
Special Hazards of Combustion Products: Toxic oxides of nitrogen may form in fires. Behavior in Fire: Vapor is heavier than air and may travel to a source of ignition and flash back. (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. Collect leaking liquid in sealable containers. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations. Wash away remainder with plenty of water. Do NOT wash away into sewer.
Personal protection: complete protective clothing including self-contained breathing apparatus. Collect leaking liquid in sealable containers. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations. Wash away remainder with plenty of water. Do NOT wash away into sewer.
1. remove all ignition sources. 2. ventilate area of spill or leak. 3. for small quantities, absorb on paper towels. evaporate in safe place (such as fume hood). allow sufficient time for evaporating vapors to completely clear hood ductwork. burn paper in suitable location away from combustible materials. large quantities can be reclaimed or collected and atomized in a suitable combustion chamber equipped with an appropriate effluent gas cleaning device.
NO open flames, NO sparks and NO smoking. NO contact with oxidizing agents. Closed system, ventilation, explosion-proof electrical equipment and lighting. Prevent build-up of electrostatic charges (e.g., by grounding). 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 strong oxidants and strong acids. Cool. Well closed. Keep in a well-ventilated room.Store in a cool, dry, well-ventilated location. Separate from acids; oxidizing material, plastics.
TLV: 5 ppm as TWA; (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 spectacles or eye protection in combination with breathing protection.
Protective clothing.
Use ventilation, local exhaust or breathing protection.
no data available
Diisopropylamine is a clear colorless liquid with an ammonia-like odor. Flash point 30°F. Less dense than water. Vapors heavier than air. Toxic oxides of nitrogen produced during combustion. Used to make other chemicals.
Colorless liquid ...
... Ammonia or fish-like odor.
36°C(lit.)
84°C(lit.)
Class IB Flammable Liquid: Fl.P. below 73°F and BP at or above 100°F.
Lower flammable limit: 1.1% by volume; Upper flammable limit: 7.1% by volume
-13°C(lit.)
600° F (USCG, 1999)
no data available
Strongly alkaline
0.40 cP @ 25 deg C
Slightly soluble (NTP, 1992)
log Kow= 1.4
50 mm Hg ( 20 °C)
0.716
3.5 (vs air)
no data available
Decomposes on heating. This produces toxic fumes of nitrogen oxides. The substance is a strong base. It reacts with acid and is corrosive. Reacts with oxidants. This generates fire and explosion hazard. Attacks some forms of plastic.
Decomposes on heating and on burning. This produces toxic gases of nitrogen oxides. The solution in water is a medium strong base. Reacts with strong acids. Reacts violently with strong oxidants. This generates fire and explosion hazard.
VOLATILE
Flammable; severe fire hazardThe vapour is heavier than air and may travel along the ground; distant ignition possible.,Dust explosion possible if in powder or granular form, mixed with air.DIISOPROPYLAMINE can react violently with oxidizing agents and strong acids. Readily eutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
no data available
Strong oxidizers, strong acids.
When heated to decomposition it emits toxic fumes of nitroxides.
no data available
no data available
no data available
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no data available
Lachrymation. The vapour is corrosive to the eyes and respiratory tract. Inhalation of the vapour may cause lung oedema. See Notes. Contact of the vapour with the eyes may cause visual disturbances. Exposure could cause death. The effects may be delayed. Medical observation is indicated.
Repeated or prolonged contact with skin may cause dermatitis.
A harmful contamination of the air can be reached very quickly on evaporation of this substance at 20°C.
Diisopropylamine achieved 1% of the theoretical BOD over an incubation period of 5 days in an aerobic screening study at 20 deg C using sewage inoculum(1). In a second run of the same screening study using acclimated sewage seed, 43% of the theoretical BOD was achieved after 5 days(1). At an initial concn of 10 ppm diisopropylamine, 0% of the theoretical BOD was observed after an incubation period of 14 days in a screening study using sludge inoculum(2). In the same study using acclimated sludge inoculum, 31.5% of the theoretical BOD was observed after 15 days using the same initial concn of diisopropylamine(2). Furthermore, in the same study, initial concns of 50 and 100 ppm diisopropylamine appeared to be inhibitory to microbial growth(2).
An estimated BCF of 2 was calculated for diisopropylamine(SRC), using a log Kow of 1.4(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 diisopropylamine was estimated as 140(SRC), using a log Kow of 1.4(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that diisopropylamine is expected to have high mobility in soil(SRC). The pKa of diisopropylamine is 11.07(4), indicating that the protonated form will be the predominant species in moist soils and cationic molecules generally adsorb to organic carbon and clays more strongly than their neutral counterparts(SRC).
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: UN1158 (For reference only, please check.)
IMDG: UN1158 (For reference only, please check.)
IATA: UN1158 (For reference only, please check.)
ADR/RID: DIISOPROPYLAMINE (For reference only, please check.)
IMDG: DIISOPROPYLAMINE (For reference only, please check.)
IATA: DIISOPROPYLAMINE (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
Other reported melting points: -91°C and -96°C.The symptoms of lung oedema often do not become manifest until a few hours have passed and they are aggravated by physical effort.Rest and medical observation are therefore essential.Immediate administration of an appropriate inhalation therapy by a doctor or a person authorized by him/her, should be considered.