Oxidizing solids, Category 2
Acute toxicity - Category 4, Oral
Hazardous to the aquatic environment, short-term (Acute) - Category Acute 1
Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 1
Reproductive toxicity, Category 2
H272 May intensify fire; oxidizer
H302 Harmful if swallowed
H410 Very toxic to aquatic life with long lasting effects
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/...
P264 Wash ... thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P273 Avoid release to the environment.
P203 Obtain, read and follow all safety instructions before use.
P370+P378 In case of fire: Use ... to extinguish.
P301+P317 IF SWALLOWED: Get medical help.
P330 Rinse mouth.
P391 Collect spillage.
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. Half-upright position. Artificial respiration may be needed. Refer immediately for medical attention.
Wear protective gloves when administering first aid. First rinse with plenty of water for at least 15 minutes, then remove contaminated clothes and rinse again. Refer for medical attention .
Rinse with plenty of water for several minutes (remove contact lenses if easily possible). Refer immediately for medical attention.
Rinse mouth. If within a few minutes after ingestion, one small glass of water may be given to drink. Do NOT induce vomiting. Refer immediately for medical attention.
Burns and stains the skin dark brown. If ingested will cause severe distress of gastro-intestinal system. May be fatal if over 4 oz. are consumed. (USCG, 1999)
Following ingestion of tablets, gastric lavage & supervision on surgical unit is proposed. operation should be conservative if digestive perforation is present, although it is extremely rare.
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.
Behavior in Fire: May cause fire on contact with combustibles. Containers may explode. (USCG, 1999)
In case of fire in the surroundings, use appropriate extinguishing media.
Personal protection: chemical protection suit including self-contained breathing apparatus. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. Carefully collect remainder. Then store and dispose of according to local regulations. Do NOT absorb in saw-dust or other combustible absorbents.
Personal protection: chemical protection suit including self-contained breathing apparatus. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. Carefully collect remainder. Then store and dispose of according to local regulations. Do NOT absorb in saw-dust or other combustible absorbents.
Environmental considerations: Land spill: Dig a pit, pond, lagoon, holding area to contain liquid or solid material. /SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner./ Cover solids with a plastic sheet to prevent dissolving in rain or fire fighting water. Add sodium bisulfite (NaHSO3).
NO contact with combustible substances. 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, reducing agents and powdered metals. Well closed. Provision to contain effluent from fire extinguishing. Store in an area without drain or sewer access.
TLV: (as Mn): 0.2 mg/m3, as TWA.EU-OEL: (as Mn, inhalable fraction): 0.2 mg/m3 as TWA.EU-OEL: (as Mn, respirable fraction): 0.05 mg/m3 as TWA.MAK: (as Mn, inhalable fraction): 0.2 mg/m3; (as Mn, respirable fraction): 0.02 mg/m3; peak limitation category: II(1); pregnancy risk group: C; (DFG 2016)
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 face shield or eye protection in combination with breathing protection.
Protective gloves. Protective clothing.
Avoid inhalation of dust. Use local exhaust or breathing protection.
no data available
Potassium permanganate is a purplish colored crystalline solid. Noncombustible but accelerates the burning of combustible material. If the combustible material is finely divided the mixture may be explosive. Contact with liquid combustible materials may result in spontaneous ignition. Contact with sulfuric acid may cause fire or explosion. Used to make other chemicals and as a disinfectant.
Dark purple or bronze-like crystals; Almost opaque by transmitted light and of a blue metallic luster by reflected air.
Odorless
240°C
no data available
Not combustible but enhances combustion of other substances. Gives off irritating or toxic fumes (or gases) in a fire.
no data available
no data available
Not flammable (USCG, 1999)
240°C
no data available
no data available
Soluble in many organic solvents; also by concentrated acids with the liberation of oxygen.
1.73 (calculated)
at 20°C: negligible
1.01g/mLat 25°C
no data available
no data available
500 mg/cu m Manganese compounds and fume (as Mn)
Decomposes on heating. This produces toxic gases and irritating fumes. The substance is a strong oxidant. It reacts with combustible and reducing materials. This generates fire and explosion hazard. Reacts violently with powdered metals. This generates fire hazard.
Stable in air and light; soln are unstable
MODERATE, BY CHEMICAL REACTION.POTASSIUM PERMANGANATE is a very powerful oxidizing agent, particularly in acidic surroundings. Reacts with incandescence with aluminum carbide [Mellor 5:872. 1946-47]. Grinding with antimony or arsenic causes ignition of the metals [Mellor 12:322. 1946-47]. Mixtures with acetic acid or acetic anhydride may explode if not kept cold [Von Schwartz 1918. p. 34]. Explosions can occur when acidified solutions come in contact with benzene, carbon disulfide, diethyl ether, ethyl alcohol, petroleum, or organic matter. Contact with glycerol may produce an explosion [Pieters 1957. p. 30]. Contact with concentrated hydrogen peroxide solution can produce an explosion [Haz. Chem. Data 1973. p. 230]. Contact with solid hydroxylamine produces an immediate white flame [Mellor 8:294. 1946-47]. Transport through a polypropylene tube ignited the tube [MCA Case History 1842. 1972]. Mixing with concentrated sulfuric acid in a vessel containing moisture caused an explosion (due to formation of manganese heptoxide) [Delhez 1967].
no data available
Caution: take great care in handling as explosions may occur if it is brought into contact with org or other readily oxidizable substances, either in soln or in dry state.
Decomp at about 240 deg c with evolution of oxygen; decomp by alcohol & many other org solvents, also by concn acids with liberation of oxygen; with hydrochloric acid, chlorine liberated; readily decomp by many reducing substances, such as ferrous salts, iodides, oxalates, etc, esp in presence of an acid
no data available
no data available
no data available
no data available
no data available
no data available
The substance is corrosive to the eyes, skin and respiratory tract. Corrosive on ingestion. Inhalation of dust may cause lung oedema, but only after initial corrosive effects on eyes and/or airways have become manifest. The effects may be delayed. Medical observation is indicated.
The substance may have effects on the lungs. This may result in bronchitis and pneumonia. Animal tests show that this substance possibly causes toxicity to human reproduction or development.
A harmful concentration of airborne particles can be reached quickly when dispersed, especially if powdered.
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: UN1490 (For reference only, please check.)
IMDG: UN1490 (For reference only, please check.)
IATA: UN1490 (For reference only, please check.)
ADR/RID: POTASSIUM PERMANGANATE (For reference only, please check.)
IMDG: POTASSIUM PERMANGANATE (For reference only, please check.)
IATA: POTASSIUM PERMANGANATE (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: II (For reference only, please check.)
IMDG: II (For reference only, please check.)
IATA: II (For reference only, please check.)
ADR/RID: Yes
IMDG: Yes
IATA: Yes
no data available
no data available
Rinse contaminated clothing with plenty of water because of fire hazard.