| Section 1. Identification | |||
|---|---|---|---|
| Chemical Name | Potassium Bromate | CAS No. | 7758-01-2 |
| Synonyms | bromicacidpotassiumsalt; potassiumbromate | Chinese Name | 溴酸钾 |
| Molecular Formula | KBrO3 | Molecular Weight | 167.01 |
| UN No. | 1484 | Data Source | PubChem (NIH/NLM) |
| GHS Hazard Classification | |
|---|---|
| Signal Word | DANGER |
| Pictograms | GHS03 · Oxidizer GHS06 · Acute Toxic GHS07 · Irritant GHS08 · Health Hazard |
| Hazard Statements | H271H301H350H272H341H370H372H302H320H335H351H316H319 |
| Precautionary Statements | P203P210P220P264P270P280P283P301+P316P306+P360P318P321P330P370+P378P371+P380+P375P405P420P501P260P308+P316P319P261P264+P265P271P301+P317P304+P340P305+P351+P338P337+P317P403+P233P332+P317 |
| Contents | |||
|---|---|---|---|
| Section 2 | Hazards Identification | Section 4 | First-Aid Measures |
| Section 5 | Fire-Fighting Measures | Section 6 | Accidental Release Measures |
| Section 7 | Handling and Storage | Section 8 | Exposure Controls / Personal Protection |
| Section 9 | Physical and Chemical Properties | Section 10 | Stability and Reactivity |
| Section 11 | Toxicological Information | Section 12 | Ecological Information |
| Section 13 | Disposal Considerations | Section 14 | Transport Information |
H271: May cause fire or explosion; strong Oxidizer [Danger Oxidizing liquids; Oxidizing solids]
H301: Toxic if swallowed [Danger Acute toxicity, oral]
H350: May cause cancer [Danger Carcinogenicity]
P203, P210, P220, P264, P270, P280, P283, P301+P316, P306+P360, P318, P321, P330, P370+P378, P371+P380+P375, P405, P420, and P501 (click each P-code to see the statement)
H271 (99.5%): May cause fire or explosion; strong Oxidizer [Danger Oxidizing liquids; Oxidizing solids]
H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]
H350 (97.9%): May cause cancer [Danger Carcinogenicity]
Aggregated GHS information provided per 190 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
H272: May intensify fire; oxidizer [Danger Oxidizing liquids; Oxidizing solids]
H341: Suspected of causing genetic defects [Warning Germ cell mutagenicity]
H370: Causes damage to organs [Danger Specific target organ toxicity, single exposure]
H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure]
P203, P210, P220, P260, P264, P270, P280, P301+P316, P308+P316, P318, P319, P321, P330, P370+P378, P405, and P501 (click each P-code to see the statement)
H302: Harmful if swallowed [Warning Acute toxicity, oral]
H320: Causes eye irritation [Warning Serious eye damage/eye irritation]
H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
H351: Suspected of causing cancer [Warning Carcinogenicity]
P203, P210, P220, P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P304+P340, P305+P351+P338, P308+P316, P318, P319, P321, P330, P337+P317, P370+P378, P403+P233, P405, and P501 (click each P-code to see the statement)
H316: Causes mild skin irritation [Warning Skin corrosion/irritation]
H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]
P203, P210, P220, P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P304+P340, P305+P351+P338, P308+P316, P318, P319, P321, P330, P332+P317, P337+P317, P370+P378, P403+P233, P405, and P501 (click each P-code to see the statement)
Fresh air, rest. 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. Give a slurry of activated charcoal in water to drink. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention .
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. IMMEDIATELY call a hospital or poison control center even if no symptoms (such as redness or irritation) develop. IMMEDIATELY transport the victim to a hospital for treatment after washing the affected areas.
INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. IMMEDIATELY call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.
INGESTION: DO NOT INDUCE VOMITING. Corrosive chemicals will destroy the membranes of the mouth, throat, and esophagus and, in addition, have a high risk of being aspirated into the victim's lungs during vomiting which increases the medical problems. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. IMMEDIATELY transport the victim to a hospital. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. Transport the victim IMMEDIATELY to a hospital.
OTHER: Since this chemical is a known or suspected carcinogen you should contact a physician for advice regarding the possible long term health effects and potential recommendation for medical monitoring. Recommendations from the physician will depend upon the specific compound, its chemical, physical and toxicity properties, the exposure level, length of exposure, and the route of exposure. (NTP, 1992)
General First Aid:
· Call 911 or emergency medical service.
· Ensure that medical personnel are aware of the material(s) involved, take precautions to protect themselves and avoid contamination.
· Move victim to fresh air if it can be done safely.
· Administer oxygen if breathing is difficult.
· If victim is not breathing:
-- DO NOT perform mouth-to-mouth resuscitation; the victim may have ingested or inhaled the substance.
-- If equipped and pulse detected, wash face and mouth, then give artificial respiration using a proper respiratory medical device (bag-valve mask, pocket mask equipped with a one-way valve or other device).
-- If no pulse detected or no respiratory medical device available, provide continuous compressions. Conduct a pulse check every two minutes or monitor for any signs of spontaneous respirations.
· Remove and isolate contaminated clothing and shoes.
· For minor skin contact, avoid spreading material on unaffected skin.
· In case of contact with substance, remove immediately by flushing skin or eyes with running water for at least 20 minutes.
· For severe burns, immediate medical attention is required.
· Effects of exposure (inhalation, ingestion, or skin contact) to substance may be delayed.
· Keep victim calm and warm.
· Keep victim under observation.
· For further assistance, contact your local Poison Control Center.
· Note: Basic Life Support (BLS) and Advanced Life Support (ALS) should be done by trained professionals.
Specific First Aid:
· Contaminated clothing may be a fire risk when dry.
In Canada, an Emergency Response Assistance Plan (ERAP) may be required for this product. Please consult the shipping paper and/or the "ERAP" section.
Excerpt from ERG Guide 140 [Oxidizers]:
SMALL FIRE: Use water. Do not use dry chemicals or foams. CO2 or Halon® may provide limited control.
LARGE FIRE: Flood fire area with water from a distance. Do not move cargo or vehicle if cargo has been exposed to heat. If it can be done safely, move undamaged containers away from the area around the fire.
FIRE INVOLVING TANKS, RAIL TANK CARS OR HIGHWAY TANKS: For ammonium nitrate products: Do not fight cargo fire. Withdraw, evacuate and isolate area for at least 1600 meters (1 mile). Treat as an explosive (ERG Guide 112). Do not enter area for 24 hours or until expert advice has been provided. Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. ALWAYS stay away from tanks in direct contact with flames. For massive fire, use unmanned master stream devices or monitor nozzles; if this is impossible, withdraw from area and let fire burn. (ERG, 2024)
Use water in large amounts. In case of fire: keep drums, etc., cool by spraying with water.
Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Advice for firefighters: Wear self-contained breathing apparatus for firefighting if necessary.
Use water spray to cool unopened containers.
This chemical is a combustible solid. Use water only. Do not use chemical or carbon dioxide extinguishers. Poisonous gases are produced in fire including bromine, potassium oxide, and oxygen, which increases fire hazard. If materials or contaminated reunoff enters waterways, notify downstream users of potentially contaminated waters. Notify local healty and fire officials and pollution control agencies. Containers may explode in fire. From a secure, explosion-proof location, use water spray to cool exposed containers. If cooling streams are ineffective (venting sound increases in volume and pitch, tank discolors, or shows any signs of deforming), withdraw immediately to a secure position.
For more Fire Fighting Procedures (Complete) data for POTASSIUM BROMATE (6 total), please visit the HSDB record page.
· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.
· Keep unauthorized personnel away.
· Stay upwind, uphill and/or upstream.
· Ventilate closed spaces before entering, but only if properly trained and equipped.
· Keep combustibles (wood, paper, oil, etc.) away from spilled material.
· Do not touch damaged containers or spilled material unless wearing appropriate protective clothing.
· Stop leak if you can do it without risk.
· Do not get water inside containers.
Small Dry Spill
· With clean shovel, place material into clean, dry container and cover loosely; move containers from spill area.
Small Liquid Spill
· Use a non-combustible material like vermiculite or sand to soak up the product and place into a container for later disposal.
Large Spill
· Dike far ahead of liquid spill for later disposal.
Excerpt from ERG Guide 140 [Oxidizers]:
IMMEDIATE PRECAUTIONARY MEASURE: Isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.
LARGE SPILL: Consider initial downwind evacuation for at least 100 meters (330 feet).
FIRE: If tank, rail tank car or highway tank is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. If ammonium nitrate products are in a tank, rail car or truck and involved in a fire, ISOLATE for 1600 meters (1 mile) in all directions; also, initiate evacuation including emergency responders for 1600 meters (1 mile) in all directions. (ERG, 2024)
Immediate precautionary measure
· Isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.
· Consider initial downwind evacuation for at least 100 meters (330 feet).
· If tank, rail tank car or highway tank is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.
· If ammonium nitrate products are in a tank, rail car or truck and involved in a fire, ISOLATE for 1600 meters (1 mile) in all directions; also, initiate evacuation including emergency responders for 1600 meters (1 mile) in all directions.
Sweep spilled substance into covered sealable containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations. Do NOT absorb in saw-dust or other combustible absorbents. Personal protection: P3 filter respirator for toxic particles.
ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Wear respiratory protection. Avoid dust formation. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. Environmental precautions: Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Methods and materials for containment and cleaning up: Sweep up and shovel. Contain spillage, and then collect with an electrically protected vacuum cleaner or by wetbrushing and place in container for disposal according to local regulations. Keep in suitable, closed containers for disposal.
Evacuate and restrict persons not wearing protective equipment from area of spill or leak until cleanup is complete. Remove all ignition sources. Collect powdered material in the most convenient and safe manner and deposit in sealed containers. Ventilate area of spill or leak after clean-up is complete. Keep potassium bromate out of confined space, such as sewer, because of the possiblity of an explosion, unless the sewer is designed to prevent the build-up of explosive concentrations. It may be necessary to contain and dispose of this chemical as a hazardous waste. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Contact your Department of Environmental Protection or your regional office of the federal EPA for specific recommendations. If employees are required to clean-up spills, they must be properly trained and equipped.
PRECAUTIONS FOR "CARCINOGENS": A high-efficiency particulate arrestor (HEPA) or charcoal filters can be used to minimize amt of carcinogen in exhausted air ventilated safety cabinets, lab hoods, glove boxes or animal rooms ... Filter housing that is designed so that used filters can be transferred into plastic bag without contaminating maintenance staff is avail commercially. Filters should be placed in plastic bags immediately after removal ... The plastic bag should be sealed immediately ... The sealed bag should be labelled properly ... Waste liquids ... should be placed or collected in proper containers for disposal. The lid should be secured & the bottles properly labelled. Once filled, bottles should be placed in plastic bag, so that outer surface ... is not contaminated ... The plastic bag should also be sealed & labelled. ... Broken glassware ... should be decontaminated by solvent extraction, by chemical destruction, or in specially designed incinerators. /Chemical Carcinogens/
SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
SRP: Wastewater from contaminant suppression, cleaning of protective clothing/equipment, or contaminated sites should be contained and evaluated for subject chemical or decomposition product concentrations. Concentrations shall be lower than applicable environmental discharge or disposal criteria. Alternatively, pretreatment and/or discharge to a permitted wastewater treatment facility is acceptable only after review by the governing authority and assurance that "pass through" violations will not occur. Due consideration shall be given to remediation worker exposure (inhalation, dermal and ingestion) as well as fate during treatment, transfer and disposal. If it is not practicable to manage the chemical in this fashion, it must be evaluated in accordance with EPA 40 CFR Part 261, specifically Subpart B, in order to determine the appropriate local, state and federal requirements for disposal.
Product: Burn in a chemical incinerator equipped with an afterburner and scrubber but exert extra care in igniting as this material is highly flammable. Offer surplus and non-recyclable solutions to a licensed disposal company. Contact a licensed professional waste disposal service to dispose of this material. Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber; Contaminated packaging: Dispose of as unused product.
Cautiously acidify a 3% soln or a suspension of the material to pH 2 with sulfuric acid. Gradually add a 52% excess of aqueous sodium bisulfite with stirring at room temp. An incr in temp indicates that a reaction is taking place. If no reaction is observed on the addition of about 10% of the sodium bisulfite soln initiate it by cautiously adding more acid. If manganese, chromium, or molybdenum is present, adjust the pH of the soln to 7 and treat with sulfide to precipitate for burial in a chemical landfill. Destroy excess sulfide and neutralize /the material/.
For more Disposal Methods (Complete) data for POTASSIUM BROMATE (9 total), please visit the HSDB record page.
ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Wear respiratory protection. Avoid dust formation. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. Environmental precautions: Prevent further leakage or spillage if safe to do so. Do not let product enter drains.
Precautions for safe handling: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Provide appropriate exhaust ventilation at places where dust is formed. Keep away from sources of ignition - No smoking.
Appropriate engineering controls: Avoid contact with skin, eyes and clothing. Wash hands before breaks and immediately after handling the product.
Gloves must be inspected prior to use. Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands.
For more Preventive Measures (Complete) data for POTASSIUM BROMATE (19 total), please visit the HSDB record page.
Excerpt from ERG Guide 140 [Oxidizers]:
Keep combustibles (wood, paper, oil, etc.) away from spilled material. Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Do not get water inside containers.
SMALL DRY SPILL: With clean shovel, place material into clean, dry container and cover loosely; move containers from spill area.
SMALL LIQUID SPILL: Use a non-combustible material like vermiculite or sand to soak up the product and place into a container for later disposal.
LARGE SPILL: Dike far ahead of liquid spill for later disposal. (ERG, 2024)
Separated from combustible substances, reducing agents, powdered metals and incompatible materials. See Chemical Dangers.
Keep container tightly closed in a dry and well-ventilated place.
Prior to working with this chemical you should be trained on its proper handling and storage. Potassium bromate must be stored to avoid contact with oxidizers (such as perchlorates, peroxides, premangantes, chlorates, and nitrates) and other incompatible materials listed above, since violent reactions can occur. Protect storage containers against physical damage. Avoid storage on wood floors. Where possible, automatically transfer material from drums or other storage containers to process containers. Sources of ignition such as smoking and open flames are prohibited where this chemical is handled, used, or stored. Metal containers involving the transfer of this chemical should be grounded and bonded. Wherever this chemical is used, handled, manufactured, or stored, use explosion-proof electrical equipment and fittings.
PRECAUTIONS FOR "CARCINOGENS": Storage site should be as close as practical to lab in which carcinogens are to be used, so that only small quantities required for ... expt need to be carried. Carcinogens should be kept in only one section of cupboard, an explosion-proof refrigerator or freezer (depending on chemicophysical properties ...) that bears appropriate label. An inventory ... should be kept, showing quantity of carcinogen & date it was acquired ... Facilities for dispensing ... should be contiguous to storage area. /Chemical Carcinogens/
· Wear positive pressure self-contained breathing apparatus (SCBA).
· Wear chemical protective clothing that is specifically recommended by the manufacturer when there is NO RISK OF FIRE.
· Structural firefighters' protective clothing provides thermal protection but only limited chemical protection.
0.30 [mg/m3]
5.2 [mg/m3]
31 [mg/m3]
Small Fire
· Use water. Do not use dry chemicals or foams. CO2 or Halon® may provide limited control.
Large Fire
· Flood fire area with water from a distance.
· Do not move cargo or vehicle if cargo has been exposed to heat.
· If it can be done safely, move undamaged containers away from the area around the fire.
Fire Involving Tanks, Rail Tank Cars or Highway Tanks
· For ammonium nitrate products: Do not fight cargo fire. Withdraw, evacuate and isolate area for at least 1600 meters (1 mile). Treat as an explosive (GUIDE 112). Do not enter area for 24 hours or until expert advice has been provided.
· Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles.
· Cool containers with flooding quantities of water until well after fire is out.
· ALWAYS stay away from tanks in direct contact with flames.
· For massive fire, use unmanned master stream devices or monitor nozzles; if this is impossible, withdraw from area and let fire burn.
Workplace Environmental Exposure Level (WEEL): 8-hr Time-weighted Average (TWA) 0.1 mg/cu m. Last Revised: 2004.
Evaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed, especially if powdered.
The substance is irritating to the eyes, skin and respiratory tract. Ingestion could cause effects on the kidneys and central nervous system. This may result in renal failure, respiratory depression and hearing loss. The effects may be delayed.
This substance is possibly carcinogenic to humans.
Excerpt from ERG Guide 140 [Oxidizers]:
Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer when there is NO RISK OF FIRE. Structural firefighters' protective clothing provides thermal protection but only limited chemical protection. (ERG, 2024)
Eye/face protection: Face shield and safety glasses Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection: Handle with gloves.
Body Protection: Complete suit protecting against chemicals. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection: Where risk assessment shows air-purifying respirators are appropriate use a full-face particle respirator type N100 (US) or type P3 (EN 143) respirator cartridges as a backup to engineering controls. If the respirator is the sole means of protection, use a full-face supplied air respirator. Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
For more Personal Protective Equipment (PPE) (Complete) data for POTASSIUM BROMATE (7 total), please visit the HSDB record page.
NO contact with combustible substances or reducing agents.
PREVENT DISPERSION OF DUST!
Use local exhaust or breathing protection.
Protective gloves.
Wear safety goggles or eye protection in combination with breathing protection if powder.
Do not eat, drink, or smoke during work. Wash hands before eating.
Potassium bromate appears as a white crystalline solid.
White solid; [Merck Index] White odorless crystalline solid; Soluble in water; [MSDSonline]
WHITE CRYSTALS OR POWDER.
White hexagonal crystal
White crystalline powder
White crystals or granules
White or colorless, hexagonal crystals, or powder
Odorless
Tasteless
Decomposes at 698 °F (NTP, 1992)
662 °F (NTP, 1992)
350 °C; decomposes at 370 °C with evolution of oxygen.
MP: 370 °C (decomposes)
MP: 434 °C
10 to 50 mg/mL at 66 °F (NTP, 1992)
Solubility (g/100 g water): 3.1 at 0 °C; 6.9 at 20 °C; 13.1 at 40 °C; 22.2 at 60 °C; 33.9 at 80 °C; 49.7 at 100 °C
Soluble in 12.5 ppm water, 2 parts boiling water
Soluble in boiling water
Insoluble in ethanol
Sparingly soluble in ethanol; insoluble in acetone
Solubility in water, g/100ml at 25 °C: 7.5
3.27 (NTP, 1992) - Denser than water; will sink
3.27 g/cu cm at 17.5 °C
3.27 g/cm³
3.27 @25 °C
Stable under recommended storage conditions.
/Potassium bromate/ mixtures with sulfur are unstable, and may ignite some hours after preparation, depending on the state of subdivision and atmospheric humidity.
When heated to decomposition it emits very toxic fumes of bromate anion and K2O.
The pH of a 1:20 aqueous solution is between 5 and 9
Standard molar enthalpy of formation at 298.15 K: -360.2 kJ/mol; molar heat capacity at constant pressure at 298.15 K: 105.2 J/mol K
Strong oxidizing agent
The enthalpy (heat content) difference for KBr03 (crystalline solid) between 298.15 deg K (25 °C) and 0 deg K is 5.593 deg K.
The virtual or "thermal" entropy of KBr03 (crystalline solid) in the standard state at 298.15 K (25 °C) is 35.65 cal/deg mol
The enthalpy (heat content) and Gibbs energy (formerly the free energy) of formation of KBr03 when one gram formula weight in the crystalline solid state is formed isothermally at 298.15K (25 °C) is -86.10 kcal/mole and -64.82 kcal/mole, respectively.
dielectric constant
satellite line
pyroelectric constant
crystal structure
dielectricity
paraelectricity
Water soluble.
Oxidizing Agents, Strong
Strong Oxidizing Agent
CSL00132
WATER + Ammonium cerium(IV) nitrate + MALONIC ACID + POTASSIUM BROMATE
Chemical & Engineering News (15 Jun 1998) Vol. 76, No. 24, pp. 4. We wish to point out a safety hazard with a widely performed standard chemical demonstration that caused significant damage recently in a teaching laboratory in the chemistry department at the University of Tennessee, Knoxville. The Belousov-Zhabotinsky oscillator reaction described in Bassam Shakhashiri's" Chemical Demonstrations: A Handbook for Teachers of Chemistry," Vol. 2, involves the cerium ammonium nitrate-catalyzed redox reaction of potassium bromate with malonic acid. This reaction was carried out in an honors general chemistry laboratory without incident during the afternoon, but a fire was discovered in the lab two hours after everyone had left. It destroyed the wooden drawers beneath a stone benchtop before being extinguished by the fire department. Investigation revealed that the three chemicals used are stable when mixed dry, and react as expected when in dilute solution. However, when 0.5 g of each are mixed together, and between one drop and 3 mL of water added, a very exothermic reaction occurs with considerable fuming. All three chemicals are needed for this to initiate. When carried out on a piece of filter paper, ignition of the paper occurred. We suspect that in the teaching laboratory, dry chemicals were spilled during weighing, and, rather than being disposed of in the aqueous heavy-metal waste container, were placed in a trash can. This was stored under a sink with a leaky drainpipe, and the critical amount of moisture set off the reaction after everyone had left the room. There is a safety warning in the experimental procedure regarding bromates being strong oxidizing agents and indicating that mixtures with finely divided organic materials are easily ignited. The catalytic nature of the cerium salt on this is not indicated, however. We alert people to the hazardous nature of this particular mixture, under conditions that are not unusual.
Flammable,Oxidizer
Not Available
oxidation
ACS Safety Letters
POTASSIUM BROMATE is a strong oxidizing agent. Forms very flammable mixtures with combustible materials. Such mixtures may be explosive if the combustible material is finely divided and are often ignitable by friction. A mixture with finely divided aluminum can explode by heat, percussion, and friction [Mellor 2:310. 1946-47]. Reacts explosively with selenium [Mellor 2 Supp1:763. 1956].
Incompatible materials: Strong reducing agents, powdered metals.
A strong oxidizer. Reacts violently with combustibles, organics, and reducing agents, powdered metals, metal sulfides, carbon, sulfur, phosphorus, ammonium salts, oxidizers. Incompatible with aluminum, copper.
Potassium bromate reacts violently with disulfur dibromide; ignition occurs at 125 °C.
Potassium bromate reacts violently in the presence of water and disulfur dibromide (3-4%); ignition occurs at 20 °C.
For more Hazardous Reactivities and Incompatibilities (Complete) data for POTASSIUM BROMATE (16 total), please visit the HSDB record page.
Based upon the data included in this report the CIR Expert Panel concludes that Sodium Bromate and Potassium Bromate may be used in cosmetic permanent wave formulations at concentrations not to exceed 10.17%, measured as Sodium Bromate.
Safe for use in cosmetics, with qualifications
IDENTIFICATION AND USE: Potassium bromate forms white hexagonal crystals. It is used as laboratory reagent, oxidizing agent, permanent-wave compounds, maturing agent in flour, dough conditioner, food additive. HUMAN EXPOSURE AND TOXICITY: Potassium bromate dust is irritating to the mucous membranes of the upper respiratory tract, but there was no evidence of any cumulative effect on the lung of workers after 18 years of exposure to levels as high as 15 mg/cu m. In children 1.5-3 years of age, ingestion of 2-4 oz (57-133 g) of a 2% solution of potassium bromate caused nausea and vomiting, usually with epigastric and/or abdominal pain; diarrhea and hematemesis occurred in some cases. Potassium bromate is possibly carcinogenic to humans. In human peripheral blood lymphocytes potassium bromate induced chromosomal aberrations. Micronucleus formation was induced by potassium bromate. Significant dose-dependent increases in the frequency of DNA single-strand breaks and alkali-labile sites were obtained after a 20-hr exposure of primary cultures of human thyroid cells to the potassium bromate. ANIMAL STUDIES: Although adverse effects are not evident in animals fed bread-based diets made from flour treated with KBrO3, the agent is carcinogenic in rats and nephrotoxic in both man and experimental animals when given orally. It has been demonstrated that KBrO3 induces renal cell tumors, mesotheliomas of the peritoneum, and follicular cell tumors of the thyroid. In addition, experiments aimed at elucidating the mode of carcinogenic action have revealed that KBrO3 is a complete carcinogen, possessing both initiating and promoting activities for rat renal tumorigenesis. However, the potential seems to be weak in mice and hamsters. In contrast to its weak mutagenic activity in microbial assays, KBrO3 showed relatively strong potential inducing chromosome aberrations both in vitro and in vivo. Glutathione and cysteine degrade KBrO3 in vitro; in turn, the KBrO3 has inhibitory effects on inducing lipid peroxidation in the rat kidney. Active oxygen radicals generated from KBrO3 were implicated in its toxic and carcinogenic effects, especially because KBrO3 produced 8-hydroxydeoxyguanosine in the rat kidney. KBrO(3) also induces mesotheliomas which may secrete hormones or similar substances, such as parathyroid hormone related protein, phosphatonins or melanocyte stimulating hormone. Several multigeneration studies in which rats or mice were fed bread made from flour treated with potassium bromate. However, because most potassium bromate added to flour is converted to bromide during the bread baking process it is unlikely that the animals in these studies were actually exposed to bromate. ECOTOXICITY STUDIES: The order of sensitivity to the toxic effects of bromate was Daphnia magna, Moina > Scenedesmus obliquus > zebrafish > Chlorella vulgaris, luminescent bacteria.
Bromine is a powerful oxidizing agent and is able to release oxygen free radicals from the water in mucous membranes. These free radicals are also potent oxidizers and produce tissue damage. In additon, the formation of hydrobromic and bromic acids will result in secondary irritation. The bromide ion is also known to affect the central nervous system, causing bromism. This is believed to be a result of bromide ions substituting for chloride ions in the in actions of neurotransmitters and transport systems, thus affecting numerous synaptic processes. (L626, L627, A543)
Evaluation: There is inadequate evidence in humans for the carcinogenicity of potassium bromate. There is sufficient evidence in experimental animals for the carcinogenicity of potassium bromate. Overall evaluation: Potassium bromate is possibly carcinogenic to humans (Group 2B).
Under the current Guidelines for Carcinogen Risk Assessment (U.S. EPA, 1986), bromate would be classified as B2, probable human carcinogen. Under the Proposed Guidelines for Carcinogen Risk Assessment (U.S. EPA, 1996), bromate should be evaluated as a likely human carcinogen by the oral route of exposure. Insufficient data are available to evaluate the human carcinogenic potential of bromate by the inhalation route. /Based on former classification guidelines/
Potassium bromate
Group 2B: Possibly carcinogenic to humans
Volume Sup 7: Overall Evaluations of Carcinogenicity: An Updating of IARC Monographs Volumes 1 to 42, 1987; 440 pages; ISBN 92-832-1411-0 (out of print)
Volume 73: (1999) Some Chemicals that Cause Tumours of the Kidney or Urinary Bladder in Rodents and Some Other Substances
2B, possibly carcinogenic to humans. (L135)
Bromine vapour causes irritation and direct damage to the mucous membranes. Elemental bromine also burns the skin. The bromide ion is a central nervous system depressant and chronic exposure produces neuronal effects. This is called bromism and can result in central reactions reaching from somnolence to coma, cachexia, exicosis, loss of reflexes or pathologic reflexes, clonic seizures, tremor, ataxia, loss of neural sensitivity, paresis, papillar edema of the eyes, abnormal speech, cerebral edema, delirium, aggressiveness, and psychoses. Bromate is also a potential carcinogen. (L625, L626, L627, L638)
The substance can be absorbed into the body by inhalation of its aerosol and by ingestion.
Oral (L96) ; inhalation (L96) ; dermal (L96)
Cough. Sore throat.
Redness.
Redness. Pain.
Abdominal pain. Diarrhoea. Nausea. Vomiting.
Bromine vapour causes irritation and direct damage to the mucous membranes. Symptoms include lacrimation, rhinorrhoea, eye irritation with mucous secretions from the oropharyngeal and upper airways, coughing, dyspnoea, choking, wheezing, epistaxis, and headache. The bromide ion is a central nervous system depressant producing ataxia, slurred speech, tremor, nausea, vomiting, lethargy, dizziness, visual disturbances, unsteadiness, headaches, impaired memory and concentration, disorientation and hallucinations. This is called bromism. (L626, L627)
Neurotoxin - Other CNS neurotoxin
Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Nephrotoxin - The chemical is potentially toxic to the kidneys in the occupational setting.
Methemoglobinemia - The presence of increased methemoglobin in the blood; the compound is classified as secondary toxic effect
IARC Carcinogen - Class 3: Chemicals are not classifiable by the International Agency for Research on Cancer.
LD50: 321 mg/kg (Oral, Rat) (T14)
LD50: 177 mg/kg (Intraperitoneal, Mouse) (T14)
LD50 Rat oral 321 mg/kg
LD50 Rat (F344, male) oral 400 mg/kg /From table/
LD50 Rat (F344, female) oral 495 mg/kg /From table/
LD50 Rat (Wistar) oral 160 mg/kg /From table/
For more Non-Human Toxicity Values (Complete) data for POTASSIUM BROMATE (13 total), please visit the HSDB record page.
EYES: irrigate opened eyes for several minutes under running water.
INGESTION: do not induce vomiting. Rinse mouth with water (never give anything by mouth to an unconscious person). Seek immediate medical advice.
SKIN: should be treated immediately by rinsing the affected parts in cold running water for at least 15 minutes, followed by thorough washing with soap and water. If necessary, the person should shower and change contaminated clothing and shoes, and then must seek medical attention.
INHALATION: supply fresh air. If required provide artificial respiration.
Potassium bromate (KBrO3) is an oxidizing agent used as a food additive which causes kidney damage as a potent nephrotoxic agent, and the mechanism may be explained by the generation of oxygen free radicals. ... Single intraperitoneal administration of 200 mg/kg KBrO3 could induce serious kidney damage, with an increase in serum blood urea nitrogen (BUN) and creatinine levels. Five-day oral administration of bilberry (Vaccinium myrtillus L.) extract at 50, 100, and 200 mg/kg resulted in a reversal in serum BUN and creatinine to normal levels and decreased kidney malondialdehyde (MDA), nitric oxide (NO), and xanthine oxidase (XOD) levels. Also, bilberry extract improved oxygen radical absorbance capacity (ORAC) levels in kidney tissue, which showed that bilberry extract reduced the degree of oxidative stress and kidney damage induced by KBrO3. These findings demonstrate that the protective effect of bilberry extract is attributed to its free radical scavenging activity and lipid peroxidation inhibitory effect.
... The protective effect of the antioxidants melatonin, resveratrol, vitamin E, butylated hydroxytoluene and 2-mercaptoethylamine, and the spin-trapping compound alpha-phenyl-N-tert-butyl nitrone (PBN) against oxidative DNA damage was studied in the kidney of rats treated with the kidney-specific carcinogen potassium bromate (KBrO3). KBrO3 was given to rats previously treated with melatonin, resveratrol, PBN, vitamin E, butylated hydroxytoluene, or 2-mercaptoethylamine. Oxidative damage to kidney DNA was estimated 6 hours afterwards by measuring 8-oxo-7,8-dihydro-2'-deoxyguanosine (oxo8dG) referred to deoxyguanosine (dG) by means of high performance liquid chromatography with electrochemical-coulometric and ultraviolet detection. Levels of oxo8dG in the renal genomic DNA significantly increased by more than 100% after the KBrO3 treatment. This increase was completely abolished by the treatment with resveratrol and was partially prevented by melatonin, PBN and vitamin E. Resveratrol and PBN also prevented the increase in relative kidney weight induced by KBrO3. These results show that various different antioxidants and a free radical trap, working in either the water-soluble or the lipid-soluble compartments, can prevent the oxidative DNA damage induced in the kidney by the carcinogen KBrO3.
... The aim of the study was to compare protective effects of melatonin, indole-3-propionic acid (IPA), and propylthiouracil (PTU) against lipid peroxidation in the kidneys and blood serum and, additionally, in the livers and the lungs, collected from rats, pretreated with KBrO(3). Male Wistar rats were administered KBrO(3) (110 mg/kg bw, ip, on the 10th day of the experiment) and/or melatonin, or IPA (0.0645 mmol/kg bw, ip, twice daily, for 10 days), or PTU (0.025% solution in drinking water, for 10 days). The level of lipid peroxidation products-malondialdehyde + 4-hydroxyalkenals (MDA + 4-HDA)-was measured spectrophotometrically in thyroid homogenates. KBrO(3), when injected to rats, significantly increased lipid peroxidation in the kidney homogenates and blood serum, but not in the liver and the lung homogenates. Co-treatment with either melatonin or with IPA, but not with PTU, decreased KBrO(3)-induced oxidative damage to lipids in the rat kidneys and serum...
... Treatment of rats with Nymphaea alba (100 and 200 mg/kg body weight) one hour before KBrO3 (125 mg/kg body weight, ip) resulted in significant decreases in xanthine oxidase (P < 0.05), lipid peroxidation, gamma-glutamyl transpeptidase, H202 generation, blood urea nitrogen, serum creatinine, renal ODC activity and DNA synthesis (P < 0.001). Renal glutathione content, glutathione metabolizing enzymes and antioxidant enzymes were also recovered to significant levels (P < 0.001). These results show that Nymphaea alba acts as chemopreventive agent against KBrO3-mediated renal injury and hyperproliferative response.
For more Interactions (Complete) data for POTASSIUM BROMATE (35 total), please visit the HSDB record page.
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. /Bromates and Related Compounds/
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. Anticipate seizures and treat if necessary ... . Monitor for 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 mL/kg up to 200 mL of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . /Bromates and Related Compounds/
Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious or is in severe respiratory distress. Positive-pressure ventilation techniques with a bag valve mask device may be beneficial. Start IV administration of D5W /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's (LR) if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Bromates and Related Compounds/
Emergency and supportive measures. 1. Maintain an open airway and assist ventilation if necessary. 2. Treat coma and seizures if they occur. 3. Replace fluid losses, treat electrolyte disturbances caused by vomiting and diarrhea, and monitor renal function. Perform hemodialysis as needed for support of renal failure. /Bromates/
LC50; Species: Eisenia fetida (Earthworm) adult, age >2 months, weight 300-400 mg; dermal (ground spray on artificial soil) 393 mg/kg soil for 14 days (1 dose per study)
LC50; Species: Eisenia fetida (Earthworm) adult, age >2 months, weight 300-400 mg; dermal (filter paper) 530 ug/sq cm for 48 hr (1 dose per study)
/AQUATIC SPECIES/ Acute toxic effects of potassium bromate, sodium bromate and potassium bromide on luminescent bacteria, water flea, green alga and zebrafish were studied using standard toxic testing methods. The results showed that the pollutants had no effect on the luminous intensity of luminescent bacteria. The 96 hr EC50. of potassium bromate on Scenedesmus obliquus was 738.18 mg/L, 48 hr EC50 on Daphnia magna and Moina was 154.01 mg/L was 161.80 mg/L, while 48 hr LC50 was 198 52 mg/L, 175.68 mg/L, and 96 hr LC50 on zebrafish was 931.4 mg /L. The 96 hr EC50 of sodium bromate on Scenedesmus obliquus was 540.26 mg/L, 48 hr EC50 Daphnia magna and Moina was 127.90 mg/L, 111.07 mg/L, while 48 hr LC50 was 161.80 mg/L, 123.47 mg/L, and 96 hr LC50 on zebrafish was 1065.6 mg/L. But the effects of potassium bromide on the above several kinds of aquatic organisms were far smaller than those of potassium bromate and sodium bromate. The toxic effects on test organisms were due to the impacts of bromate after the comparison of different pollutants, and the effects were more obvious with the increase of exposure time. The order of sensitivity to the toxic effects of bromate was Daphnia magna, Moina > Scenedesmus obliquus > zebrafish > Chlorella vulgaris, luminescent bacteria.
Potassium bromate's production and use in flour treatment, hair wave solutions, in cheese making and as an analytical standard(1) may result in its release to the environment through various waste streams(SRC).
Public attention was aroused when mutagenicity was found in potassium bromate (KBrO3) which has been used as an oxidizing agent in baking bread. Ion chromatography was found to be very useful for analyzing bromide and bromate ions in food. The residual condition of potassium bromate added to bread in the baking process was clarified. It was found that the residual rate of bromate ions in bread was approximately 30% at the added level of 100 ug/g, but it decreased markedly when the added levels went down. At 40 ug/g no residue was detected.
NIOSH (NOES Survey 1981-1983) has statistically estimated that 26,562 workers (11,090 of these are female) were potentially exposed to potassium bromate in the US(1).
skin, eye and usouc membrane irritant
SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
SRP: Wastewater from contaminant suppression, cleaning of protective clothing/equipment, or contaminated sites should be contained and evaluated for subject chemical or decomposition product concentrations. Concentrations shall be lower than applicable environmental discharge or disposal criteria. Alternatively, pretreatment and/or discharge to a permitted wastewater treatment facility is acceptable only after review by the governing authority and assurance that "pass through" violations will not occur. Due consideration shall be given to remediation worker exposure (inhalation, dermal and ingestion) as well as fate during treatment, transfer and disposal. If it is not practicable to manage the chemical in this fashion, it must be evaluated in accordance with EPA 40 CFR Part 261, specifically Subpart B, in order to determine the appropriate local, state and federal requirements for disposal.
Product: Burn in a chemical incinerator equipped with an afterburner and scrubber but exert extra care in igniting as this material is highly flammable. Offer surplus and non-recyclable solutions to a licensed disposal company. Contact a licensed professional waste disposal service to dispose of this material. Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber; Contaminated packaging: Dispose of as unused product.
Cautiously acidify a 3% soln or a suspension of the material to pH 2 with sulfuric acid. Gradually add a 52% excess of aqueous sodium bisulfite with stirring at room temp. An incr in temp indicates that a reaction is taking place. If no reaction is observed on the addition of about 10% of the sodium bisulfite soln initiate it by cautiously adding more acid. If manganese, chromium, or molybdenum is present, adjust the pH of the soln to 7 and treat with sulfide to precipitate for burial in a chemical landfill. Destroy excess sulfide and neutralize /the material/.
For more Disposal Methods (Complete) data for POTASSIUM BROMATE (9 total), please visit the HSDB record page.
/GUIDE 140 OXIDIZERS/ Fire or Explosion: These substances will accelerate burning when involved in a fire. Some may decompose explosively when heated or involved in a fire. May explode from heat or contamination. Some will react explosively with hydrocarbons (fuels). May ignite combustibles (wood, paper, oil, clothing, etc.). Containers may explode when heated. Runoff may create fire or explosion hazard.
/GUIDE 140 OXIDIZERS/ Health: Inhalation, ingestion or contact (skin, eyes) with vapors or substance may cause severe injury, burns or death. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may cause pollution.
/GUIDE 140 OXIDIZERS/ Public Safety: CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number listed on the inside back cover. As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind, uphill and/or upstream. Ventilate closed spaces before entering.
/GUIDE 140 OXIDIZERS/ Protective Clothing: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing will only provide limited protection.
For more DOT Emergency Guidelines (Complete) data for POTASSIUM BROMATE (8 total), please visit the HSDB record page.
UN 1484; Potassium bromate
IMO 5.1; Potassium bromate
49 187 36; Potassium bromate
No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance ... and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by ... /the hazardous materials regulations (49 CFR 171-177)./
The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials. Potassium bromate is included on the dangerous goods list.
The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article. Potassium bromate is included on the dangerous goods list.
PRECAUTIONS FOR "CARCINOGENS": Procurement ... of unduly large amt ... should be avoided. To avoid spilling, carcinogens should be transported in securely sealed glass bottles or ampoules, which should themselves be placed inside strong screw-cap or snap-top container that will not open when dropped & will resist attack from the carcinogen. Both bottle & the outside container should be appropriately labelled. ... National post offices, railway companies, road haulage companies & airlines have regulations governing transport of hazardous materials. These authorities should be consulted before ... material is shipped. /Chemical Carcinogens/
PRECAUTIONS FOR "CARCINOGENS": When no regulations exist, the following procedure must be adopted. The carcinogen should be enclosed in a securely sealed, watertight container (primary container), which should be enclosed in a second, unbreakable, leakproof container that will withstand chem attack from the carcinogen (secondary container). The space between primary & secondary container should be filled with absorbent material, which would withstand chem attack from the carcinogen & is sufficient to absorb the entire contents of the primary container in the event of breakage or leakage. Each secondary container should then be enclosed in a strong outer box. The space between the secondary container & the outer box should be filled with an appropriate quantity of shock-absorbent material. Sender should use fastest & most secure form of transport & notify recipient of its departure. If parcel is not received when expected, carrier should be informed so that immediate effort can be made to find it. Traffic schedules should be consulted to avoid ... arrival on weekend or holiday ... /Chemical Carcinogens/
Oxidizer
Symbol: O, T; R: 45-9-25; S: 53-45; Note: E
UN Hazard Class: 5.1; UN Pack Group: II