Explosives, Division 1.1
Oxidizing solids, Category 1
H201 Explosive; mass explosion hazard
H271 May cause fire or explosion; strong oxidizer
P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
P230 Keep wetted with ...
P234 Keep only in original packaging.
P240 Ground and bond container and receiving equipment.
P250 Do not subject to grinding/shock/friction/….
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P220 Keep away from clothing and other combustible materials.
P283 Wear fire resistant or flame retardant clothing.
P370+P372+P380+P373 In case of fire: Explosion risk. Evacuate area. DO NOT fight fire when fire reaches explosives.
P306+P360 IF ON CLOTHING: Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
P371+P380+P375 In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
P370+P378 In case of fire: Use ... to extinguish.
P401 Store in accordance with…
P420 Store separately.
P503 Refer to manufacturer/supplier… for information on disposal/recovery/recycling.
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.
First rinse with plenty of water for at least 15 minutes, then remove contaminated clothes and rinse again.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Give one or two glasses of water to drink.
Irritating to skin and mucous membranes. (USCG, 1999)
Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). 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 signs of pulmonary edema and treat if necessary . Monitor for shock and treat if necessary . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with 0.9% saline (NS) during transport . Do not use emetics. For ingestion, rinse mouth and administer 5 mg/kg up to 200 ml of water for dilution if the patent can swallow, has a strong gag reflex, and does not drool . Do not attempt to neutralize. Ammonia and related compounds
If material on fire or involved in fire: Dangerously explosive. Do not fight fires in a cargo of explosives. Evacuate area and let burn. Explosives
Special Hazards of Combustion Products: Toxic gases are produced in a fire. Behavior in Fire: May explode when involved in fire or exposed to shock or friction. (USCG, 1999)
In case of fire in the surroundings, use appropriate extinguishing media. In case of fire: keep drums, etc., cool by spraying with water. Combat fire from a sheltered position.
Evacuate danger area! Consult an expert! Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. If appropriate, moisten first to prevent dusting. Sweep spilled substance into covered containers. Then store and dispose of according to local regulations. Do NOT absorb in saw-dust or other combustible absorbents.
Evacuate danger area! Consult an expert! Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. If appropriate, moisten first to prevent dusting. Sweep spilled substance into covered containers. Then store and dispose of according to local regulations. Do NOT absorb in saw-dust or other combustible absorbents.
Ion exchange is an ex situ technology used to remove perchlorate from drinking water, groundwater, surface water, and environmental media at full scale. ... The most commonly used ion exchange media are synthetic, strongly basic, anion exchange resins. Ion exchange has been used at sites to reduce perchlorate concentrations to less than 4 ug/L. Its effectiveness is sensitive to a variety of untreated water contaminants and characteristics. It has also been used as a polishing step for other water treatment processes such as biological treatment of perchlorate. Ion exchange of perchlorate in environmental media and drinking water is commercially available. Information is available on 15 full-scale applications, including 11 applications for environmental media, and four applications for drinking water. Three pilot-scale applications for groundwater also have been identified. ...For the 14 groundwater projects (11 full scale and three pilot scale), influent perchlorate concentrations ranged from 10 ug/L to 350,000 ug/L. Effluent concentrations of perchlorate ranged from non-detectable at a detection limit of 0.35 ug/L to 2,000 ug/L. Of the four drinking water projects, performance data were available for only one project. The initial concentration of perchlorate in this project ranged from 20 to 50 ug/L, while the final concentration was below the detection limit of 4 ug/L. ...Cleanup goals varied by site and type of project. Perchlorates
NO contact with combustible substances, reducing agents or organic materials. Do NOT expose to heat, friction or shock. 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 combustible substances, reducing agents and metals. See Chemical Dangers. Well closed.Separate from acids, alkalies reducing agents, combustible materials. Store in cool, dry, well-ventilated location.
no data available
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 if powder.
Protective gloves. Protective clothing.
Use local exhaust or breathing protection.
no data available
Solid. Powder.
White.
No odor
Remarks:Decomposition of pure AP may begin at a temperature higher than 150°C.
no data available
Not combustible but enhances combustion of other substances. Many reactions may cause fire or explosion. Gives off irritating or toxic fumes (or gases) in a fire. See Notes.
no data available
no data available
464° F (USCG, 1999)
>200°C
no data available
no data available
In water, 2.0X10+5 mg/L at 25 deg C
log Pow = -5.84. Temperature:25 °C.
< 0 Pa. Remarks:The calculated vapour pressure is 8.3 E-12 Pa at 25°C.
1.95 g/mL. Temperature:20 °C.
no data available
no data available
May decompose on shock, friction, concussion or heating. The substance is a strong oxidant. It reacts violently with combustible and reducing materials and metals. This produces toxic and corrosive fumes including ammonia and hydrogen chloride. This generates fire and explosion hazard.
no data available
IGNITES VIOLENTLY WITH COMBUSTIBLES.AMMONIUM PERCHLORATE is a strong oxidizing agent. Decomposes at 130°C and explodes at 380°C [Mellor 2 Supp. 1:608 1956]. Explosions have occurred in propellant formulations containing ammonium perchlorate to which ferrocene has been added as a burning rate catalyst. Although the cause was not been definitely established, it was most probably frictional heating from dragging a spatula through the mixture [ASESB Expl. Report 211 1966]. Can explode when mixed with sugar, charcoal or on contact with hot copper pipes. Becomes impact-sensitive when contaminated by powdered carbon, ferrocene, sulfur, or other reducing materials such as organic matter or powdered metals.
no data available
Ammonium perchlorate decomposes at 130 DEG C and explodes at 380 DEG C
Oxides of nitrogen (except nitrous oxide), hydrogen chloride, and ammonia /are/ emitted on decomposition of ammonium perchlorate...
no data available
no data available
no data available
no data available
no data available
no data available
The aerosol is irritating to the eyes, skin and respiratory tract.
The substance may have effects on the thyroid. This may result in reduced levels of thyroid hormones.
A harmful concentration of airborne particles can be reached quickly when dispersed.
ANAEROBIC: Microorganisms isolated from soil have been found to reduce perchlorates under anaerobic conditions using laboratory tests(1). Perchlorate applied to Yolo loam at a concentration of 180 mg/L and incubated anaerobically under flooded conditions was completely biodegraded after 30 days(1). No loss was observed using a Columbia loam soil(1). The facultative anaerobes belonging to the genera Riemerella, Acidovorax and Azoarcus together may be capable of perchlorate reduction(2). However, nitrate does interfere with perchlorate reduction(3). Using sediment and soil samples obtained from two Texas sites associated historically with perchlorate discharge, anaerobic microcosms studies indicate that rapid perclorate degradation did not occur until nitrate was degraded to a relatively low level(3).
Using a plant-mediated treatment of perchlorate-contaminated water, perchlorate uptake occurred in eastern cottonwoods (Populus deltoides and hybrid populus), Eucalyptus cineria, and willow (Salix nigra) in sand bioreactors. Perchlorate uptake in willows was found initially rapid at a rate that was linear with the volume of water evapotranspired by the tree until a plateau was reached. From an initial application of 88.8 mg (96.4 mg/L), the total amounts of perchlorate in root, lower stem, upper stem, and leaf after 26 days were 0.04, 0.18, 0.34 and 0.48 mg, respectively. 11% of the perchlorate was not accounted for and believed to be degraded in the leaves(1).
Ammonium perchlorate readily dissolves and dissociates to the perchlorate ion(1). The perchlorate ion is only weakly absorbed to mineral surfaces of moderate ionic strength(1). The ion exhibits high aqueous solubility and together these properties contribute to its ability to readily migrate in groundwater systems(2).
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: UN0402 (For reference only, please check.)
IMDG: UN0402 (For reference only, please check.)
IATA: UN0402 (For reference only, please check.)
ADR/RID: AMMONIUM PERCHLORATE? (For reference only, please check.)
IMDG: AMMONIUM PERCHLORATE? (For reference only, please check.)
IATA: AMMONIUM PERCHLORATE? (For reference only, please check.)
ADR/RID: 1.1D (For reference only, please check.)
IMDG: 1.1D (For reference only, please check.)
IATA: 1.1D (For reference only, please check.)
ADR/RID: (For reference only, please check.)
IMDG: (For reference only, please check.)
IATA: (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
Different decomposition temperatures are given in the literature, and the unstabilized substance may explode on heating.Health effects of exposure to the substance have not been investigated adequately.Rinse contaminated clothing with plenty of water because of fire hazard.