Oxidizing solids, Category 3
H272 May intensify fire; oxidizer
P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
P220 Keep away from clothing and other combustible materials.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P370+P378 In case of fire: Use ... to extinguish.
none
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. Refer for medical attention .
Exposure can cause mild irritation of eyes, nose and throat. (USCG, 1999)
Maintain an open airway and assist ventilation if necessary. Administer supplemental oxygen. Treat hypotension with supine positioning, intravenous crystalloid fluids, and a low dose -pressor if needed. Monitor vital signs and ECG for 4 to 6 hours. Symptomatic methemoglobinemia may be treated with methylene blue. ... Administer activated charcoal. Gastric emptying is not necessary for small ingestions if activated charcoal can be given promptly . Hemodialysis and hemoperfusion are not effective. Severe methemoglobinemia in infants not responsive to methylene blue therapy may require exchange transfusion. Nitrates and Nitrites
If material on fire or involved in fire: Flood with water. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible.
Special Hazards of Combustion Products: May produce toxic nitrogen oxides upon decomposition. Behavior in Fire: Strong oxidizer which may react explosively when mixed with reducing agents. Mixture may detonate by heat or shock. Increases the flammability of any combustible material. (USCG, 1999)
In case of fire in the surroundings, use appropriate extinguishing media.
Sweep spilled substance into plastic or glass containers. Wash away remainder with plenty of water.
Sweep spilled substance into plastic or glass containers. Wash away remainder with plenty of water.
Sweep spilled substance into plastic or glass containers. Wash away remainder with plenty of water.
NO contact with combustible substances or reducing agents. 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 combustible substances and reducing agents.Separated from combustible and reducing substances.
Component | Potassium nitrate | |||
---|---|---|---|---|
CAS No. | 7757-79-1 | |||
Limit value - Eight hours | Limit value - Short term | |||
ppm | mg/m3 | ppm | mg/m3 | |
Latvia | ? | 5 | ? | ? |
Remarks |
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.
Protective gloves.
Use local exhaust or breathing protection.
no data available
Potassium nitrate is a white to dirty gray crystalline solid. Water soluble. Noncombustible, but accelerates the burning of combustible materials. If large quantities are involved in fire or the combustible material is finely divided an explosion may result. May explode under prolonged exposure to heat or fire. Toxic oxides of nitrogen are produced in fires. Used in solid propellants, explosives, fertilizers.
Colorless, rhombic or trigonal crystals
Odorless
334°C
400°C
Not combustible but enhances combustion of other substances. Gives off irritating or toxic fumes (or gases) in a fire.
no data available
400°C
no data available
400°C
4,5-8,5 (5?% solution)
no data available
Sol in water, glycerol; slightly sol in alcohol
no data available
no data available
2.109
no data available
no data available
Decomposes on heating. This increases fire hazard. The substance is a strong oxidant. It reacts with combustible and reducing materials.
no data available
Not combustible but enhances combustion of other substances ... Risk of fire and explosion on contact with reducing agents.POTASSIUM NITRATE mixed with alkyl esters may explode, owing to the formation of alkyl nitrates; mixtures with phosphorus, tin (II) chloride, or other reducing agents may react explosively [Bretherick 1979. p. 108-109]. Powdered antimony mixed with potassium nitrate explodes when heated [Mellor 9:282 1946-47]. A mixture of antimony trisulfide and potassium nitrate explodes at a red heat [Mellor 9:524. 1946-47]. Arsenic disulfide forms explosive mixtures when mixed with potassium nitrate, [Mellor 9:270.1946-47]. A mixture of sodium acetate and potassium nitrate may cause an explosion [Pieters 1957. p. 30]. A mixture of potassium nitrate and sodium hypophosphite constitutes a powerful explosive [Mellor 8:881. 1946-47]. A mixture of powdered zirconium and potassium nitrate explodes when heated above the melting point [Mellor 7:116. 1946-47].
no data available
A micro Parr calorimeter exploded when the wrong proportions of these ingredients were used. The intended mixture was 4.0 g sodium peroxide, 0.2 g dextrose, and 0.2 g potassium nitrate; actual proportions were 0.35 g, 2.59 g, and 0.2 g respectively. There was insufficient sodium peroxide to dissolve decomposition gases, hence a rapid temp and pressure build-up caused the Parr bomv to burst.
When heated to decomp it emits very toxic fumes of /nitrogen oxides & dipotassium oxide/.
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, skin and respiratory tract. Ingestion could cause effects on the blood. This may result in the formation of methaemoglobin. The effects may be delayed. Medical observation is indicated.
no data available
Evaporation at 20°C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed.
no data available
no data available
no data available
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: UN1486 (For reference only, please check.)
IMDG: UN1486 (For reference only, please check.)
IATA: UN1486 (For reference only, please check.)
ADR/RID: POTASSIUM NITRATE (For reference only, please check.)
IMDG: POTASSIUM NITRATE (For reference only, please check.)
IATA: POTASSIUM NITRATE (For reference only, please check.)
ADR/RID: 5.1 (For reference only, please check.)
IMDG: 5.1 (For reference only, please check.)
IATA: 5.1 (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
Rinse contaminated clothing with plenty of water because of fire hazard.Specific treatment is necessary in case of poisoning with this substance; the appropriate means with instructions must be available.