BROMOTRIFLUOROMETHANE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
BROMOFLUOROFORM BROMOTRIFLUOROMETHANE CARBON MONOBROMIDE TRIFLUORIDE DAIFLON 13B1 F 13B1 F-13B1 FC 13B1 FE 1301 FLUGEX 13B1 FLUOROCARBON 1301 FREON 13B1 HALOCARBON 13B1 HALON 1301 KHALDON 13B1 METHANE, BROMOTRIFLUORO- MONOBROMOTRIFLUOROMETHANE R13B1 R 13B1 REFRIGERANT 13B1 TRIFLUOROBROMOMETHANE TRIFLUOMETHYL BROMIDE TRIFLUOROMONOBROMOMETHANE
IDENTIFIERS
SYNONYM REFERENCE
- (HSDB , 2000; Lewis, 1996; RTECS , 2000)
USES/FORMS/SOURCES
This compound is used primarily as a refrigerant and in fire extinguishing. It has also been reportedly used for the following: chemical intermediate; metal hardening; ionization studies (special purposes in bubble chambers); quark detection; radiation counters; erosion inhibitor (during manufacture of hydraulic fluids) (Lewis, 1997; HSDB , 2000; Sittig, 1991).
Bromotrifluoromethane can be produced by the bromination of chlorotrifluoromethane, trifluoromethane, or perfluoropropane (Ashford, 1994; HSDB , 2000; Lewis, 1997).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Humans exposed to up to 100,000 ppm developed light-headedness, paresthesia, and diminished performance. A feeling of impending unconsciousness developed at 150,000 ppm.
- In experimental animals exposed by inhalation, a negative cardiac inotropic effect, tremors, seizures, lethargy, unconsciousness, and a lowering of the myocardial threshold to the arrhythmogenic action of injected epinephrine have been noted.
- Exposure to thermal decomposition products may cause irritation of the eyes, nose, throat, and respiratory tract, and could lead to chemical pneumonitis or noncardiogenic pulmonary edema.
- Simple asphyxiants displace oxygen from the breathing atmosphere primarily in enclosed spaces and result in hypoxemia. Air hunger, fatigue, decreased vision, mood disturbances, numbness of extremities, headache, confusion, decreased coordination and judgment, cyanosis, and unconsciousness may be noted.
- Direct contact with the liquid or escaping compressed gas may cause defatting of the skin and frostbite injury.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004)
Vapors may cause dizziness or asphyxiation without warning. Vapors from liquefied gas are initially heavier than air and spread along ground. Contact with gas or liquefied gas may cause burns, severe injury and/or frostbite. Fire may produce irritating, corrosive and/or toxic gases.
ACUTE CLINICAL EFFECTS
- Bromotrifluoromethane has relatively low acute toxicity (Anon, 1971) and is thought to be one of the safest of the halon fire extinguishing agents (Anthony, 1971).
- Bromotrifluoromethane caused an increase in reaction time in human volunteers exposed to airborne concentrations of 4 to 7 percent, diminished performance at 10 percent, caused a decrease in psychomotor tests at 10-15 percent, and resulted in a feeling of impending unconsciousness at 15 percent (HSDB , 2000).
- An accidental release of the product caused headache, lightheadedness and disorientation, which are signs of CNS depression (Sass-Kortsak, 1985). Exposure to concentrations up to 80 percent caused convulsions in dogs and lethargy and CNS depression in monkeys (Van Stee & Back, 1969; Paulet, 1962).
- Bromotrifluoromethane, increases myocardial sensitivity to the arrhythmogenic effects of endogenous epinephrine (adrenaline), potentially leading to CARDIAC ARRHYTHMIAS, VENTRICULAR FIBRILLATION, and possible SUDDEN DEATH. In dogs, the risk of serious cardiac arrhythmias increased with inhalation to airborne concentrations greater than 7.5 percent (Anon, 1972; Mullin, 1979).
- In humans, these cardiac effects appear at concentrations greater than 10 percent (Anon, 1972), but individual sensitivities may vary. Prior myocardial infarction conferred no increased sensitivity for cardiac effects in dogs (Trochimowicz, 1976).
- A single exposure to a high level of bromotrifluoromethane cause reactive airways dysfunction syndrome (RADS) in a healthy 43-year-old man (de la Hoz, 1999). Vapors may cause SIMPLE ASPHYXIATION (HSDB , 2000). Direct skin contact with the liquid can cause FROSTBITE INJURY (HSDB , 2000).
CHRONIC CLINICAL EFFECTS
- There is some evidence that persons chronically exposed to fluorocarbons in refrigerants have an increased incidence of coronary heart disease (HSDB).
- Prolonged or repeated dermal contact can cause defatting dermatitis with dryness and cracking (HSDB). Inhalation of 500,000 ppm (50%) for 15 days had little effect in rats and guinea pigs; but the compound was much more toxic when pyrolyzed (Paulet, 1962).
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with liquefied gas, thaw frosted parts with lukewarm water. Keep victim warm and quiet. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
FIRST AID EYE EXPOSURE - If eye tissue is frozen, seek medical attention immediately; if tissue is not frozen, immediately and thoroughly flush the eyes with large amounts of water for at least 15 minutes, occasionally lifting the lower and upper eyelids. If irritation, pain, swelling, lacrimation, or photophobia persist, get medical attention as soon as possible. DERMAL EXPOSURE - If frostbite has occurred, seek medical attention immediately; do NOT rub the affected areas or flush them with water. In order to prevent further tissue damage, do NOT attempt to remove frozen clothing from frostbitten areas. If frostbite has NOT occurred, immediately and thoroughly wash contaminated skin with soap and water. INHALATION EXPOSURE - Move the exposed person to fresh air at once. If breathing has stopped, perform artificial respiration. Keep the affected person warm and at rest. Get medical attention as soon as possible. TARGET ORGANS - CNS and heart (National Institute for Occupational Safety and Health, 2007).
GENERAL - Remove victims of inhalation exposure from the toxic environment and administer 100% humidified supplemental oxygen with assisted ventilation as required. If frostbite has developed after eye or skin exposure, seek medical attention immediately and do not flush exposed areas with water. If frostbite has not developed, exposed skin and eyes should be copiously flushed with water.
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. Carefully observe patients with inhalation exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary. 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. SEIZURES: Administer a benzodiazepine; DIAZEPAM (ADULT: 5 to 10 mg IV initially; repeat every 5 to 20 minutes as needed. CHILD: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed) or LORAZEPAM (ADULT: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed, if seizures persist. CHILD: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed, if seizures continue). Consider phenobarbital or propofol if seizures recur after diazepam 30 mg (adults) or 10 mg (children greater than 5 years). Monitor for hypotension, dysrhythmias, respiratory depression, and need for endotracheal intubation. Evaluate for hypoglycemia, electrolyte disturbances, and hypoxia.
Cardiac monitoring may be advisable in cases of significant exposure. Whenever possible, the administration of epinephrine should be avoided in patients with chlorofluorohydrocarbon inhalation exposure (ILO, 1983). If epinephrine is required for the treatment of life-threatening conditions, it should be administered in the lowest possible dose, careful and continuous cardiac monitoring should be done, and resuscitation equipment and supplies should be readily available.
Airway protection and maintenance may be required.
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). If frostbite has occurred, DO NOT rub the affected areas, DO NOT flush the affected areas with water, or attempt to remove clothing. PREHOSPITAL Rewarming of a localized area should only be considered if the risk of refreezing is unlikely. Avoid rubbing the frozen area which may cause further damage to the area (Grieve et al, 2011; Hallam et al, 2010).
REWARMING Do not institute rewarming unless complete rewarming can be assured; refreezing thawed tissue increases tissue damage. Place affected area in a water bath with a temperature of 40 to 42 degrees Celsius for 15 to 30 minutes until thawing is complete. The bath should be large enough to permit complete immersion of the injured part, avoiding contact with the sides of the bath. A whirlpool bath would be ideal. Some authors suggest a mild antibacterial (ie, chlorhexidine, hexachlorophene or povidone-iodine) be added to the bath water. Tissues should be thoroughly rewarmed and pliable; the skin will appear a red-purple color (Grieve et al, 2011; Hallam et al, 2010; Murphy et al, 2000). Correct systemic hypothermia which can cause cold diuresis due to suppression of antidiuretic hormone; consider IV fluids (Grieve et al, 2011). Rewarming may be associated with increasing acute pain, requiring narcotic analgesics. For severe frostbite, clinical trials have shown that pentoxifylline, a phosphodiesterase inhibitor, can enhance tissue viability by increasing blood flow and reducing platelet activity (Hallam et al, 2010).
WOUND CARE Digits should be separated by sterile absorbent cotton; no constrictive dressings should be used. Protective dressings should be changed twice per day. Perform twice daily hydrotherapy for 30 to 45 minutes in warm water at 40 degrees Celsius. This helps debride devitalized tissue and maintain range of motion. Keep the area warm and dry between treatments (Hallam et al, 2010; Murphy et al, 2000). The injured extremities should be elevated and should not be allowed to bear weight. In patients at risk for infection of necrotic tissue, prophylactic antibiotics and tetanus toxoid have been recommended by some authors (Hallam et al, 2010; Murphy et al, 2000). Non-tense clear blisters should be left intact due to the risk of infection; tense or hemorrhagic blisters may be carefully aspirated in a setting where aseptic technique is provided (Hallam et al, 2010). Further surgical debridement should be delayed until mummification demarcation has occurred (60 to 90 days). Spontaneous amputation may occur. Analgesics may be required during the rewarming phase; however, patients with severe pain should be evaluated for vasospasm. IMAGING: Arteriography and noninvasive vascular techniques (e.g., plain radiography, laser Doppler studies, digital plethysmography, infrared thermography, isotope scanning), have been useful in evaluating the extent of vasospasm after thawing and assessing whether debridement is needed (Hallam et al, 2010). In cases of severe frostbite, Technetium 99 (triple phase scanning) and MRI angiography have been shown to be the most useful to assess injury and determine the extent or need for surgical debridement (Hallam et al, 2010). TOPICAL THERAPY: Topical aloe vera may decrease tissue destruction and should be applied every 6 hours (Murphy et al, 2000). IBUPROFEN THERAPY: Ibuprofen, a thromboxane inhibitor, may help limit inflammatory damage and reduce tissue loss (Grieve et al, 2011; Murphy et al, 2000). DOSE: 400 mg orally every 12 hours is recommended (Hallam et al, 2010). THROMBOLYTIC THERAPY: Thrombolysis (intra-arterial or intravenous thrombolytic agents) may be beneficial in those patients at risk to lose a digit or a limb, if done within the first 24 hours of exposure. The use of tissue plasminogen activator (t-PA) to clear microvascular thromboses can restore arterial blood flow, but should be accompanied by close monitoring including angiography or technetium scanning to evaluate the injury and to evaluate the effects of t-PA administration. Potential risk of the procedure includes significant tissue edema that can lead to a rise in interstitial pressures resulting in compartment syndrome (Grieve et al, 2011). CONTROVERSIAL: Adjunct pharmacological agents (ie, heparin, vasodilators, prostacyclins, prostaglandin synthetase inhibitors, dextran) are controversial and not routinely recommended. The role of hyperbaric oxygen therapy, sympathectomy remains unclear (Grieve et al, 2011). CHRONIC PAIN: Vasomotor dysfunction can produce chronic pain. Amitriptyline has been used in some patients; some patients may need a referral for pain management. Inability to tolerate the cold (in the affected area) has been observed following a single episode of frostbite (Hallam et al, 2010). MORBIDITIES: Frostbite can produce localized osteoporosis and possible bone loss following a severe case. These events may take a year or more to develop. Children may be at greater risk to develop more severe events (ie, early arthritis) (Hallam et al, 2010).
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. If contact with escaping gas may have caused frostbite of the eyes, do not flush with water; early ophthalmologic consultation should be obtained.
INGESTION EXPOSURE - Ingestion is unlikely. Oral exposure to escaping gas might cause frostbite injury to the upper gastrointestinal and respiratory tracts. Administer oxygen and maintain airway as clinically indicated. 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.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
Inhalation of chlorofluorohydrocarbons in concentrations of approximately 15 percent (150,000 ppm) has been reported caused death in one series(ILO, 1983), although human exposure to bromotrifluoromethane concentrations up to 17 percent (170,000 ppm) caused only mild anesthetic effects in another (Reinhardt & Reinke, 1972). Bromotrifluoromethane can act as an asphyxiant. Unconsciousness leading to death will occur when the atmospheric oxygen concentration is reduced to 6% to 8% or less (Kizer, 1984). Signs of asphyxia will be noted when atmospheric oxygen is displaced such that the oxygen concentration is 15% to 16% or less (Kizer, 1984).
MAXIMUM TOLERATED EXPOSURE
Human exposure to bromotrifluoromethane concentrations up to 17 percent (170,000 ppm) caused only mild anesthetic effects (Reinhardt & Reinke, 1972). A feeling of lightheadedness may occur with exposure to airborne chlorofluorohydrocarbon concentrations of 5 to 15 percent (50,000 to 150,000 ppm) (Ellenhorn & Barceloux, 1988). Bromotrifluoromethane can act as an asphyxiant. Unconsciousness leading to death will occur when the atmospheric oxygen concentration is reduced to 6% to 8% or less (Kizer, 1984). Signs of asphyxia will be noted when atmospheric oxygen is displaced such that the oxygen concentration is 15% to 16% or less (Kizer, 1984). In human volunteer experiments, exposure to bromotrifluoromethane concentrations less than 10 percent (100,000 ppm) for 0 to 5 minutes were shown to be safe (Anon, 1971).
- Carcinogenicity Ratings for CAS75-63-8 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Trifluobromomethane 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: Trifluorobromomethane 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 CAS75-63-8 (U.S. Environmental Protection Agency, 2011):
CALCULATIONS
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS75-63-8 (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 CAS75-63-8 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS75-63-8 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS75-63-8 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS75-63-8 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS75-63-8 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS75-63-8 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS75-63-8 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS75-63-8 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS75-63-8 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
Listed as: Bromotrifluoromethane (Halon 1301) Effective Date for Reporting Under 40 CFR 372.30: 7/8/90 Lower Thresholds for Chemicals of Special Concern under 40 CFR 372.28:
- DOT List of Marine Pollutants for CAS75-63-8 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS75-63-8 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1009 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1009 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS75-63-8 (NFPA, 2002):
-HANDLING AND STORAGE
SUMMARY
Violent reactions may occur when bromotrifluoromethane contacts the chemically-active metals of calcium, powdered aluminum, magnesium, or zinc. Therefore, precautions should be taken to avoid such interactions. Tightly-closed containers of bromotrifluoromethane should be stored in cool areas with adequate ventilation (Sittig, 1991; NIOSH , 2000). To avoid the formation of toxic decomposition products and to minimize the risk of inhalation, adequate ventilation should be provided. Also recommended is the use of a breathing device equipped with an independent air supply; if entering a tank or confined space, a lifeline should be worn (HSDB , 2000).
HANDLING
- HSDB (2000) recommends using a breathing device equipped with an independent air supply when working in areas where fluorocarbons may be present. If entering a tank or confined space, a lifeline should be worn.
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Violent reactions may occur when bromotrifluoromethane contacts the chemically-active metals of calcium, powdered aluminum, magnesium, or zinc (NIOSH , 2000; Sittig, 1991). Highly toxic fumes will be emitted when bromotrifluoromethane contacts acid or acid fumes (HSDB , 2000). Coatings, plastics, and rubber in certain forms will be attacked by liquid bromotrifluoromethane (Pohanish & Greene, 1997; HSDB , 2000).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (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 will only provide limited protection.
- Appropriate protective clothing, including neoprene gloves and eye protection, must be worn to ensure that frostbite does not occur while working with cold equipment, vapors, or liquid bromotrifluoromethane. Provide quick drench facilities and eyewash fountains within the immediate work area (HSDB , 2000; NIOSH , 2000)
- HSDB (2000) recommends using protective ointment since many of the fluorocarbons show solvent action on skin oil.
- To avoid the formation of toxic decomposition products and to minimize the risk of inhalation, adequate ventilation should be provided. Also recommended is the use of a breathing device equipped with an independent air supply; if entering a tank or confined space, a lifeline should be worn (HSDB , 2000).
EYE/FACE PROTECTION
- When working with liquid bromotrifluoromethane, eye protection should be worn to prevent tissue damage or deep burns that could result from frostbite (ILO, 1998; NIOSH , 2000).
RESPIRATORY PROTECTION
- Refer to "Recommendations for respirator selection" in the NIOSH Pocket Guide to Chemical Hazards on TOMES Plus(R) for respirator information.
- Wear a breathing device equipped with an independent air supply when working in areas containing bromotrifluormethane (HSDB , 2000).
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 75-63-8.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004) Some may burn, but none ignite readily. Containers may explode when heated. Ruptured cylinders may rocket.
NIOSH (2000) classifies bromotrifluoromethane as nonflammable gas.
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS75-63-8 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004)
Water spray, fog or regular foam. Move containers from fire area if you can do it without risk. Damaged cylinders should be handled only by specialists.
- TANK FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (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. Do not direct water at source of leak or safety devices; icing may occur. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire. Some of these materials, if spilled, may evaporate leaving a flammable residue.
- NFPA Extinguishing Methods for CAS75-63-8 (NFPA, 2002):
- Since bromotrifluoromethane itself does not burn, fires involving this compound should be extinguished with an agent that is suitable for the surrounding fire type. Containers exposed to the fire should be cooled with flooding quantities of water applied from a maximal distance (AAR, 1998; Sittig, 1991).
- Any individual fighting a fire involving bromotrifluoromethane should wear a self-contained breathing apparatus with a full facepiece operated in a positive-pressure mode (HSDB , 2000).
- "If material not involved in fire: Attempt to stop leak if without undue personnel hazard" (AAR, 1998).
Bromotrifluoromethane is noncombustible (AAR, 1998). Contacting flames or hot surfaces may cause bromotrifluoromethane to decompose, creating the highly-irritant vapors of hydrogen fluoride, hydrogen bromide, phosgene, and carbonyl fluoride (HSDB , 2000; ILO, 1998).
EXPLOSION HAZARD
- Containers of bromotrifluoromethane may violently rupture and rocket if exposed to heat of fire for prolonged periods of time (AAR, 1998).
DUST/VAPOR HAZARD
- Because vapors of fluorocarbons are 4 to 5 times heavier than air, high concentrations may accumulate in low-lying areas. The inhalation of such concentrated vapors may result in asphyxiation (due to displacement of air) (AAR, 1998; HSDB , 2000; Lewis, 1997).
REACTIVITY HAZARD
- Certain plastics, coatings, and rubber may be attacked by bromotrifluoromethane (Pohanish & Greene, 1997).
- The emission of toxic fumes of fluoride and bromide, as well as carbon dioxide, occurs when bromotrifluoromethane decomposes (HSDB , 2000; ILO, 1998; Lewis, 1996).
- Containers of bromotrifluoromethane may violently rupture and rocket if exposed to heat or fire for prolonged periods of time (AAR, 1998).
- Violent reactions may occur when bromotrifluoromethane contacts the chemically-reactive metals of calcium, powdered aluminum, magnesium, and zinc (HSDB , 2000; Lewis, 1996; Pohanish & Greene, 1997; Sittig, 1991).
- Highly toxic fumes will be emitted when bromotrifluoromethane contacts acid or acid fumes (HSDB , 2000).
- A powerful reducing agent, bromotrifluoromethane is reactive toward oxidants (ILO, 1998).
EVACUATION PROCEDURES
- Editor's Note: This material is not listed in the Table of Initial Isolation and Protective Action Distances.
- LARGE SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004)
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (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 126 (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 for at least 100 meters (330 feet) in all directions. Keep unauthorized personnel away. Stay upwind. Many gases are heavier than air and will spread along ground and collect in low or confined areas (sewers, basements, tanks). Keep out of low areas. Ventilate closed spaces before entering.
- AIHA ERPG Values for CAS75-63-8 (AIHA, 2006):
- DOE TEEL Values for CAS75-63-8 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Bromotrifluoromethane (Trifluorobromomethane) TEEL-0 (units = ppm): 1,000 TEEL-1 (units = ppm): 3,500 TEEL-2 (units = ppm): 25,000 TEEL-3 (units = ppm): 40,000 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 CAS75-63-8 (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 CAS75-63-8 (National Institute for Occupational Safety and Health, 2007):
IDLH: 40,000 ppm Note(s): Not Listed
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (ERG, 2004) Do not touch or walk through spilled material. Stop leak if you can do it without risk. Do not direct water at spill or source of leak. Use water spray to reduce vapors or divert vapor cloud drift. Avoid allowing water runoff to contact spilled material. If possible, turn leaking containers so that gas escapes rather than liquid. Prevent entry into waterways, sewers, basements or confined areas. Allow substance to evaporate. Ventilate the area.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 126 (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 will only provide limited protection.
Only those personnel who are wearing appropriate protective equipment should be allowed near the area of the spill or leak. If bromotrifluoromethane gas is leaking, the area should be ventilated to allow for the dispersion of gas, and, if it can be done without risk, the flow of gas stopped; if the source of the leak cannot be safely repaired, allow the container to empty in the open air. For liquid spills, an adsorbable material such as vermiculite, earth, or dry sand should be used for clean-up and then deposited in a sealed container (Sittig, 1991). The disposal method suggested by Sittig (1991) includes mixing the spill with a combustible fuel followed by incineration (ensuring that complete combustion has occurred to prevent phosgene formation). Remove the resulting fluoric and bromic acids with an acid scrubber.
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Atmospheric release of bromotrifluoromethane may occur during its use as a fire extinguisher and refrigerant. The general population is exposed primarily through the inhalation of air that has been contaminated by this compound (HSDB , 2000).
ENVIRONMENTAL FATE AND KINETICS
In the ambient atmosphere, bromotrifluoromethane will exist entirely in the vapor phase, based on a measured vapor pressure of greater than 760 mmHg for this compound. Extremely stable in the troposphere (it has a tropospheric half-life estimated at greater than 44 years for its reaction with photochemically-produced hydroxyl radicals), bromotrifluoromethane is expected to diffuse into the stratosphere, where it will undergo UV photolysis and where it has an estimated lifetime of 62 to 112 years (HSDB , 2000). When fluorocarbons undergo photodissociation in the stratosphere, chlorine, fluorine, and/or bromine atoms are produced in significant amounts, contributing to the destruction of the ozone layer (HSDB , 2000).
SURFACE WATER Based on a Henry's Law constant of 0.4994 atm-m(3)/mole, bromotrifluoromethane is expected to volatilize rapidly when released to water (at a half-life of 15 days for a model river). Neither adsorption to sediment or bioconcentration in aquatic organisms is expected to occur, as indicated by a calculated Koc of 244.8 and a calculated BCF of 15.3 (HSDB , 2000).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Bromotrifluoromethane is a noncorrosive, noncombustible, colorless gas with an odor described as absent to slightly ethereal. For shipping purposes, it is converted to a liquified gas (AAR, 1998; Lewis, 1997; Sittig, 1991).
VAPOR PRESSURE
DENSITY
- NORMAL TEMPERATURE AND PRESSURE
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
-168 degrees C (Lewis, 1996a; Lewis, 1997a) -267 degrees C (NIOSH, 2000)(NIOSH, 2000)
BOILING POINT
- -57.8 degrees C (Lewis, 1996)
- -58 degrees C (Ashford, 1994; Lewis, 1997)
- -72 degrees F (NIOSH , 2000)
- -57.86 degrees C (at 760 mmHg) (ILO, 1998; HSDB , 2000)
SOLUBILITY
OCTANOL/WATER PARTITION COEFFICIENT
- Log Kow = 1.86 (HSDB , 2000)
HENRY'S CONSTANT
- 0.4994 atm-m(3)/mol (at 25 degrees C) (HSDB , 2000)
SPECTRAL CONSTANTS
OTHER/PHYSICAL
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