BROMINE PENTAFLUORIDE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Bromine pentafluoride is a highly corrosive chemical. Severe burns of the eyes and skin can result from direct contact. Ingestion can produce severe irritation or burns of the mouth, throat, esophagus, or gastrointestinal tract.
- Vapor exposure can cause severe burns or irritation of the respiratory tract mucosa, excessive salivation and lacrimation, swelling of the eyelids, and corneal clouding. Chronically exposed experimental animals have developed hepatotoxicity and nephrotoxicity.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
TOXIC; inhalation or contact with vapor, substance, or decomposition products may cause severe injury or death. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may cause pollution.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. Contaminated clothing may be a fire risk when dry. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. Keep victim warm and quiet. Keep victim under observation. Effects of contact or inhalation may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
GENERAL - Move victims of inhalation exposure from the toxic environment and administer 100 percent humidified supplemental oxygen with assisted ventilation as required. Exposed eyes and skin should be copiously flushed with water. In ingestion exposures, emesis should not be induced and gastric lavage done only with caution. Immediate dilution with milk or water may be beneficial.
ORAL EXPOSURE - Because of potential serious esophageal irritation or burns, emesis should not be induced. DILUTION: If no respiratory compromise is present, administer milk or water as soon as possible after ingestion. Dilution may only be helpful if performed in the first seconds to minutes after ingestion. The ideal amount is unknown; no more than 8 ounces (240 mL) in adults and 4 ounces (120 mL) in children is recommended to minimize the risk of vomiting. Significant esophageal or gastrointestinal tract irritation or burns may occur following ingestion. The possible benefit of early removal of some ingested material by cautious gastric lavage must be weighed against potential complications of bleeding or perforation. GASTRIC LAVAGE: Consider after ingestion of a potentially life-threatening amount of poison if it can be performed soon after ingestion (generally within 1 hour). Protect airway by placement in the head down left lateral decubitus position or by endotracheal intubation. Control any seizures first. Observe patients with ingestion carefully for the possible development of esophageal or gastrointestinal tract irritation or burns. If signs or symptoms of esophageal irritation or burns are present, consider endoscopy to determine the extent of injury. Carefully observe patients with ingestion exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary. A number of chemicals produce abnormalities of the hematopoietic system, liver, and kidneys. Monitoring complete blood count, urinalysis, and liver and kidney function tests is suggested for patients with significant exposure.
INHALATION EXPOSURE - INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm. Respiratory tract irritation, if severe, can progress to pulmonary edema which may be delayed in onset up to 24 to 72 hours after exposure in some cases. ACUTE LUNG INJURY: Maintain ventilation and oxygenation and evaluate with frequent arterial blood gases and/or pulse oximetry monitoring. Early use of PEEP and mechanical ventilation may be needed. If respiratory tract irritation or respiratory depression is evident, monitor arterial blood gases, chest x-ray, and pulmonary function tests. Carefully observe patients with inhalation exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary.
EYE EXPOSURE - DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility. Because of the potential for severe caustic injury if this material is splashed directly into the eye, prolonged initial flushing and early ophthalmologic consultation are advisable.
DERMAL EXPOSURE - DECONTAMINATION: Remove contaminated clothing and jewelry and place them in plastic bags. Wash exposed areas with soap and water for 10 to 15 minutes with gentle sponging to avoid skin breakdown. A physician may need to examine the area if irritation or pain persists (Burgess et al, 1999). Treat dermal irritation or burns with standard topical therapy. Patients developing dermal hypersensitivity reactions may require treatment with systemic or topical corticosteroids or antihistamines. Some chemicals can produce systemic poisoning by absorption through intact skin. Carefully observe patients with dermal exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
Experimental animals exposed to 500 ppm immediately developed gasping respirations, corneal clouding, excessive lacrimation and salivation, and acute distress (ACGIH, 1986). Experimental animals chronically exposed to 3 ppm developed hepatotoxicity, nephrotoxicity, and severe respiratory irritation (ACGIH, 1986).
- Carcinogenicity Ratings for CAS7789-30-2 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Bromine pentafluoride EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed ; Listed as: Bromine pentafluoride MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS7789-30-2 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS7789-30-2 (American Conference of Governmental Industrial Hygienists, 2010):
Editor's Note: The listed values are recommendations or guidelines developed by ACGIH(R) to assist in the control of health hazards. They should only be used, interpreted and applied by individuals trained in industrial hygiene. Before applying these values, it is imperative to read the introduction to each section in the current TLVs(R) and BEI(R) Book and become familiar with the constraints and limitations to their use. Always consult the Documentation of the TLVs(R) and BEIs(R) before applying these recommendations and guidelines.
- AIHA WEEL Values for CAS7789-30-2 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS7789-30-2 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS7789-30-2 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS7789-30-2 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS7789-30-2 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS7789-30-2 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS7789-30-2 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS7789-30-2 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS7789-30-2 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS7789-30-2 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS7789-30-2 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1745 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1745 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS7789-30-2 (NFPA, 2002):
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
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 provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
- Closed spaces should be ventilated before entry. Avoid breathing vapors from this material (AAR, 1987).
- Avoid any contact with this material (CHRIS , 1985; AAR, 1987). Spilled material must not be touched without proper protective equipment. Immediately wash off any material that comes in contact with the body (AAR, 1987). Do not attempt to handle broken or leaking containers without proper protective equipment (AAR, 1987).
Wear appropriate chemical protective clothing including goggles, long rubber gloves, an acid suit, and a self-contained positive pressure breathing apparatus (CHRIS , 1985; AAR, 1987; NFPA, 1986; ITI, 1985; Sittig, 1985).
RESPIRATORY PROTECTION
- Wear appropriate chemical protective clothing including goggles, long rubber gloves, an acid suit, and a self-contained positive pressure breathing apparatus (CHRIS , 1985; AAR, 1987; NFPA, 1986; ITI, 1985; Sittig, 1985).
- Refer to "Recommendations for respirator selection" in the NIOSH Pocket Guide to Chemical Hazards on TOMES Plus(R) for respirator information.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 7789-30-2.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004) May ignite combustibles (wood, paper, oil, clothing, etc.). React vigorously and/or explosively with water. Produce toxic and/or corrosive substances on contact with water. Flammable/toxic gases may accumulate in tanks and hopper cars. Some may produce flammable hydrogen gas upon contact with metals. Containers may explode when heated. Runoff may create fire or explosion hazard.
Bromine pentafluoride is not combustible or flammable itself, but it is highly reactive and may start a fire if in contact with combustible materials (CHRIS , 1985; NFPA, 1986). Bromine pentafluoride is very reactive, usually causing a fire (Windholz et al, 1983). DO NOT USE WATER on SPILLED MATERIAL NOT INVOLVED IN A FIRE (AAR, 1987; NFPA, 1986).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS7789-30-2 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
DRY sand, dry chemical, soda ash or lime or withdraw from area and let fire burn. Move containers from fire area if you can do it without risk.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire.
- NFPA Extinguishing Methods for CAS7789-30-2 (NFPA, 2002):
- DO NOT USE WATER or FOAM ON ADJACENT FIRES or ON FIRES INVOLVING THIS MATERIAL (CHRIS , 1985; AAR, 1987; NFPA, 1986).
- If large quantities of this material are involved in a fire, water may be used as spray and fog in flooding quantities (AAR, 1987),
- Water can be used if large amounts of combustible materials are involved in a fire with bromine pentafluoride, but fire fighters should apply the water from as far away as possible or from behind barriers to protect themselves from the violent reaction that may occur (NFPA, 1986).
- Use dry chemical or carbon dioxide to fight fire (AAR, 1987; CHRIS , 1985; NFPA, 1986).
Bromine pentafluoride reacts violently with water, forming irritating and corrosive hydrogen fluoride gas (CHRIS , 1985; Sax & Lewis, 1989). Irritating and toxic hydrogen fluoride and bromine fumes may be evolved if bromine pentafluoride is involved in a fire (CHRIS , 1985; Sax & Lewis, 1989). This release occurs when the material is heated to decomposition (860 degrees F, 460 degrees C) or on contact with acid or acid fumes (NFPA, 1986; ITI, 1985).
EXPLOSION HAZARD
- Containers may explode violently if exposed to the heat of a fire (CHRIS , 1985). Stay away from the ends of containers or tanks. Cylinders may rocket or rupture violently if they are exposed to the heat of a fire (AAR, 1987).
- Bromine pentafluoride may cause an explosion on contact with water (Windholz et al, 1983).
DUST/VAPOR HAZARD
- Bromine pentafluoride reacts violently with water, forming irritating and corrosive hydrogen fluoride gas (CHRIS , 1985; Sax & Lewis, 1989).
- Irritating and toxic hydrogen fluoride and bromine fumes may be evolved if bromine pentafluoride is involved in a fire (CHRIS , 1985; Sax & Lewis, 1989). This release occurs when the material is heated to decomposition (860 degrees F, 460 degrees C) or on contact with acid or acid fumes (NFPA, 1986; ITI, 1985).
REACTIVITY HAZARD
- Bromine pentafluoride reacts violently with water, forming irritating and corrosive hydrogen fluoride gas (CHRIS , 1985; Sax & Lewis, 1989).
- Irritating and toxic hydrogen fluoride and bromine fumes may be evolved if bromine pentafluoride is involved in a fire (CHRIS , 1985; Sax & Lewis, 1989). This release occurs when the material is heated to decomposition (860 degrees F, 460 degrees C) or on contact with acid or acid fumes (NFPA, 1986; ITI, 1985).
- Bromine pentafluoride is a strong oxidizing agent and may cause a fire if in contact with organic materials such as straw, cotton, or wood (CHRIS , 1985; NFPA, 1986).
- Bromine pentafluoride can react violently with a variety of metals and with construction materials such as glass, wood, and some plastics (CHRIS , 1985).
- Bromine pentafluoride reacts with all known elements except the inert gases, oxygen, and nitrogen (Sax & Lewis, 1987).
Bromine pentafluoride forms a fluoride film when copper, stainless steel, nickel, and monel are exposed to the gas (ACGIH, 1986).
- Bromine pentafluoride may cause an explosion on contact with water (Windholz et al, 1983).
- Bromine pentafluoride does not attack quartz when dry (Windholz et al, 1983).
- Bromine pentafluoride explodes or ignites on contact with hydrogen-containing compounds, including (Sax & Lewis, 1989):
Acetic acid Ammonia Benzene Ethanol Hydrogen Hydrogen Sulfide Methane Cork Grease Paper Wax Chloromethane
- Bromine pentafluoride can react violently and may ignite on contact with (Sax & Lewis, 1989):
- Bromine pentafluoride is a storable fluorinating agent and oxidizer which is stable to electric sparks, heat, and shock (ACGIH, 1986).
- Bromine pentafluoride may have a violent reaction with fuels.
EVACUATION PROCEDURES
- Initial Isolation and Protective Action Distances (ERG, 2004)
Data presented from the Emergency Response Guidebook Table of Initial Isolation and Protective Action Distances are for use when a spill has occurred and there is no fire. If there is a fire, or if a fire is involved, evacuation information presented under FIRE - PUBLIC SAFETY EVACUATION DISTANCES should be used. Generally, a small spill is one that involves a single, small package such as a drum containing up to approximately 200 liters, a small cylinder, or a small leak from a large package. A large spill is one that involves a spill from a large package, or multiple spills from many small packages. Suggested distances to protect from vapors of toxic-by-inhalation and/or water-reactive materials during the first 30 minutes following the spill.
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 50 meters (150 feet) for liquids and 25 meters (75 feet) for solids in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
If tank, rail car or tank truck 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.
- PUBLIC SAFETY MEASURES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004)
CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number: MEXICO: SETIQ: 01-800-00-214-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5559-1588; For calls originating elsewhere, call: 011-52-555-559-1588.
CENACOM: 01-800-00-413-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5550-1496, 5550-1552, 5550-1485, or 5550-4885; For calls originating elsewhere, call: 011-52-555-550-1496, or 011-52-555-550-1552; 011-52-555-550-1485, or 011-52-555-550-4885.
ARGENTINA: CIQUIME: 0-800-222-2933 in the Republic of Argentina; For calls originating elsewhere, call: +54-11-4613-1100.
BRAZIL: PRÓ-QUÍMICA: 0-800-118270 (Toll-free in Brazil); For calls originating elsewhere, call: +55-11-232-1144 (Collect calls are accepted).
COLUMBIA: CISPROQUIM: 01-800-091-6012 in Colombia; For calls originating in Bogotá, Colombia, call: 288-6012; For calls originating elsewhere, call: 011-57-1-288-6012.
CANADA: UNITED STATES:
For additional details see the section entitled "WHO TO CALL FOR ASSISTANCE" under the ERG Instructions. 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. Keep out of low areas. Ventilate closed spaces before entering.
- If a container is exposed directly to flames or if a fire becomes uncontrollable, consider evacuation of an area one-third mile in all directions (AAR, 1987).
- If bromine pentafluoride is leaking but not on fire, consider evacuation in a downwind direction (AAR, 1987). The size of the evacuation area should be based on location, the amount of material spilled, and the weather conditions (AAR, 1987).
- AIHA ERPG Values for CAS7789-30-2 (AIHA, 2006):
- DOE TEEL Values for CAS7789-30-2 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Bromine pentafluoride TEEL-0 (units = ppm): 0.1 TEEL-1 (units = ppm): 0.15 TEEL-2 (units = ppm): 1.0 TEEL-3 (units = ppm): 33 Definitions: TEEL-0: The threshold concentration below which most people will experience no adverse health effects. TEEL-1: The airborne concentration (expressed as ppm [parts per million] or mg/m(3) [milligrams per cubic meter]) of a substance above which it is predicted that the general population, including susceptible individuals, could experience notable discomfort, irritation, or certain asymptomatic, nonsensory effects. However, these effects are not disabling and are transient and reversible upon cessation of exposure. TEEL-2: The airborne concentration (expressed as ppm or mg/m(3)) of a substance above which it is predicted that the general population, including susceptible individuals, could experience irreversible or other serious, long-lasting, adverse health effects or an impaired ability to escape. TEEL-3: The airborne concentration (expressed as ppm or mg/m(3)) of a substance above which it is predicted that the general population, including susceptible individuals, could experience life-threatening adverse health effects or death.
- AEGL Values for CAS7789-30-2 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; United States Environmental Protection Agency Office of Pollution Prevention and Toxics, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS7789-30-2 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Use water spray to reduce vapors or divert vapor cloud drift. Avoid allowing water runoff to contact spilled material. DO NOT GET WATER on spilled substance or inside containers.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004) 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 provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
Water spray may be used to knock down or reduce vapors, but should not be allowed to get inside containers (AAR, 1987). Spilled material may be neutralized with lime, soda ash, or crushed limestone (AAR, 1987).
SMALL SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 144 (ERG, 2004) The spill area may be flushed with flooding amounts of water (CHRIS , 1985). Allow the gas to flow into a solution of mixed slaked lime and caustic soda (ITI, 1985; Sittig, 1985). If it is possible, the leaking cylinder is best kept in a hood until this process is accomplished and the cylinder is emptied (ITI, 1985).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- No information found at the time of this review.
ABIOTIC DEGRADATION
- No information found at the time of this review.
ENVIRONMENTAL TOXICITY
- The effect of low concentrations of bromine pentafluoride on aquatic life is not known, but the material may be harmful if in enters water intakes (CHRIS , 1985).
Notify appropriate local health and wildlife officials as well as operators of water intakes in the vicinity of water spills (CHRIS , 1985). This material should be kept out of water sources and sewers (AAR, 1987).
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- At temperatures below 40.3 degrees C, bromine pentafluoride is a colorless to pale yellow colored liquified gas which fumes in air and has a highly irritating odor (CHRIS , 1985; Sax & Lewis, 1987; Windholz et al, 1983; ACGIH, 1986).
At temperatures above 40.3 degrees C, bromine pentafluoride is a colorless, pungent, corrosive gas which is about 6 times heavier than air (ACGIH, 1986). Bromine pentafluoride is only shipped in cylinders without any type of safety release device (AAR, 1987).
VAPOR PRESSURE
- 7 psia (at 21.1 degrees C) (Sax & Lewis, 1987)
DENSITY
- NORMAL TEMPERATURE AND PRESSURE
(25 degrees C; 77 degrees F and 760 mmHg) LIQUID: 2.47 g/mL (ITI, 1985) LIQUID: 2.466 g/mL (Sax & Lewis, 1987)
- OTHER TEMPERATURE AND/OR PRESSURE
FREEZING/MELTING POINT
-60 degrees C; -76 degrees F (CHRIS , 1985) -61 degrees C (Sax & Lewis, 1987)
BOILING POINT
- 40.5 degrees C (Sax & Lewis, 1987)
- 41 degrees C; 106 degrees F (CHRIS , 1985)
- 104 degrees F (NFPA, 1986)
OTHER/PHYSICAL
-REFERENCES
GENERAL BIBLIOGRAPHY- 40 CFR 372.28: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Lower thresholds for chemicals of special concern. National Archives and Records Administration (NARA) and the Government Printing Office (GPO). Washington, DC. Final rules current as of Apr 3, 2006.
- 40 CFR 372.65: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Chemicals and Chemical Categories to which this part applies. National Archives and Records Association (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Apr 3, 2006.
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