BROMOCHLORODIFLUOROMETHANE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
BROMOCHLORODIFLUOROMETHANE BCF CHLORODIFLUOROBROMOMETANO (Spanish) CHLORODIFLUOROBROMOMETHANE CHLORODIFLUOROMONOBROMOMETHANE DIAFLON 12B1 DWUFLUOROCHLOROBROMOMETAN (Polish) FLUGEX 12B1 FLUOROCARBON 1211 FREON 12B1 HALON 1211 METHANE, BROMOCHLORODIFLUORO- R12B1
IDENTIFIERS
SYNONYM REFERENCE
- (Ashford, 1994; HSDB , 2000; ILO, 1998; Lewis, 1996; RTECS , 2000)
USES/FORMS/SOURCES
Bromochlorodifluoromethane is used in fire extinguishers as well as the production of other halo fluoro compounds (Ashford, 1994; HSDB , 2000). The Montreal Protocol of 1987 provides that production and consumption of this material be phased out by 2000 (HSDB , 2000).
Bromochlorodifluoromethane is made by the bromination (addition of bromine) of chlorodifluoromethane (Ashford, 1994). The Montreal Protocol of 1987 provides that production and consumption of this material be phased out by 2000 (HSDB , 2000).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Bromochlorodifluoromethane is a simple asphyxiant. It can cause dizziness, drowsiness, unconsciousness and death after inhalation. In liquid form (because of its low boiling point), it can cause frostbite of the skin and deep, severe burns of the eyes; corneal damage resulted from one exposure to bromochlorodifluoromethane from a fire extinguisher.
- Simple asphyxiants displace oxygen from the breathing atmosphere, mostly 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 result.
- Percutaneous absorption may result in systemic toxicity, with convulsions, delerium and central nervous system depression.
- Chlorofluorohydrocarbons have been involved in "sudden sniffing deaths" in aerosol propellant abusers. Exposure to thermal decomposition products can cause irritation of the eyes, nose, throat, and respiratory tract, and could lead to chemical pneumonitis or noncardiogenic pulmonary edema.
- A study in humans of exposure to bromochlorodifluoromethane during exercise concluded that exposure can increase cardiac arrhythmias in susceptible persons. Chlorofluorohydrocarbons lower the myocardial threshold to the arrhythmogenic action of injected epinephrine in experimental animals.
- One case of cardiac arrest, possibly from cardiac arrhythmias due to a lowering of the myocardial threshold to the arrhythmogenic activity of endogenous epinephrine, was reported after intentional abuse of bromochlorodifluoromethane from a fire extinguisher. Treatment with sympathomimetics is relatively contraindicated in combination with fluorocarbons.
- A case report concluded that individuals susceptible to malignant hyperthermia should avoid exposure to bromochlorodifluoromethane.
- 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
- Acute exposures to bromochlorodifluoromethane can cause CNS depression and excitation, as well as arrhythmias and other irregularities of the heart.
- Inhalation of 4 to 5% bromochlorodifluoromethane for one minute had no effect in human volunteers, but longer exposures caused dizziness, tingling in the fingers and toes, excitement, and cardiac irregularities (pp 60-66). Concentrations of 5 to 30% produced CNS stimulation (Beck, 1973).
- Two of ten volunteer firefighters exposed to 1000 ppm during exercise exhibited cardiac irregularities (complex ectopy) (Kaufman et al, 1992). Dizziness, palpitations, breathlessness, and numbness and tingling in the extremities were reported by a person exposed for approximately 20 seconds to an escaping stream of Halon gas. ECG showed occasional premature ventricular contractions. The symptoms resolved after 5 hours (Gerhardt, 1996).
- Experimental animals exposed to a 10% concentration showed tremor, convulsions, and death (pp 60-66). Monkeys exposed at airborne levels up to 80% had cardiac arrhythmias and hypotension (125:155-167).
- This compound is a CARDIAC SENSITIZER and can lower the cardiac threshold for arrhythmias and fibrillation caused by endogenous epinephrine (adrenaline). At least 3 cases of sudden death have been attributed to this effect (Smeeton & Clark, 1985; Steadman, 1984; Gerhardt, 1996).
- In a fatal case of occupational exposure to high concentrations of bromochlorodifluoromethane involving a fire, brain edema, heavy congestion, suffusion of alveoli, and 0.7% methemoglobin were present. (Lerman et al, 1991).
- Contact with the escaping gas has caused frostbite in exposed skin (Gerhardt, 1996).
CHRONIC CLINICAL EFFECTS
- Prolonged or repeated skin vapor contact may cause defatting dermatitis. One case of rhabdomyolysis from occupational exposure to bromochlorodifluoromethane has been reported (Denborough et al, 1988).
- Dogs who inhaled bromochlorodifluoromethane for 4 weeks were no more sensitive to the cardiac effects (Beck, 1973). The pyrolysis products were more toxic to rats than the parent compound in two-week exposures (Chambers, 1950). Inhalation caused fatty degeneration of the heart and liver in guinea pigs, dogs, and cats (Orlowski, 1982) and increased serum cholesterol (Orlowski, 1982).
-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.
GENERAL - Move victims of inhalation exposure from the toxic environment and administer 100% humidified supplemental oxygen with assisted ventilation as required. Because of the potential for rapid onset of CNS depression or seizures with possible aspiration of gastric contents, EMESIS SHOULD NOT BE INDUCED. Cautious gastric lavage followed by administration of activated charcoal may be of benefit if the patient is seen soon after the 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. 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. Cardiac monitoring may be advisable in cases of substantial exposure. Whenever possible, the administration of epinephrine should be avoided in patients with chlorofluorohydrocarbon inhalation exposure (ILO, 1988). 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).
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.
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; however, oral exposure might cause frostbite injury to the upper gastrointestinal and respiratory tracts. Administer oxygen and maintain airway as clinically indicated. Emesis, activated charcoal and gastric lavage are not recommended. Few oral exposures to liquid fluorinated hydrocarbons have been described. A single case of gastric perforation after ingestion of trichlorofluoromethane has been reported.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
Inhalation of chlorofluorohydrocarbons in concentrations of approximately 15 percent (150,000 ppm) has caused death (ILO, 1983). 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). Bromochlorodifluoromethane has been classified as a Group 5a life hazard by Underwriters Laboratories. This is a substance that is less toxic than a lethal gas (lethal at 2 to 2.5 percent for 2 hours), but more toxic than one that produces no injury at 20 percent for 2 hours (pp 60-66).
MAXIMUM TOLERATED EXPOSURE
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). 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).
- Carcinogenicity Ratings for CAS353-59-3 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed 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 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 CAS353-59-3 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS353-59-3 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS353-59-3 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS353-59-3 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS353-59-3 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS353-59-3 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS353-59-3 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS353-59-3 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS353-59-3 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS353-59-3 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS353-59-3 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
Listed as: Bromochlorodifluoromethane (Halon 1211) 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 CAS353-59-3 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS353-59-3 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1974 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1974 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS353-59-3 (NFPA, 2002):
-HANDLING AND STORAGE
SUMMARY
STORAGE
When heated, it is possible for containers to explode, and ruptured cylinders may rocket (DOT, 2000).
- ROOM/CABINET RECOMMENDATIONS
Rooms should have enough ventilation and sufficient exhaust so vapor concentrations remain below recommended levels (HSDB , 2000). Process materials should be enclosed and reaction vessels should be isolated to limit occupational exposure to fluorocarbons. All filling areas should be monitored (Clayton & Clayton, 1994).
Fluorocarbons, on contact with acid or acid fumes, may emit highly toxic fumes of hydrogen chloride or hydrogen fluoride (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.
RESPIRATORY PROTECTION
- 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 353-59-3.
-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.
Bromochlorodifluoromethane (Halon-1211) is noncombustible, and is a recommended fire extinguishing agent for gaseous and liquid fires, electrical fires, paper, wood, and textile fires, combustion engine fires, and fires involving hazardous solid materials (Anon, 1978). Bromochlorodifluoromethane is used to extinguish fires. Thermal decomposition during use in fires may present toxicity hazards (Clayton & Clayton, 1994). Bromochlorodifluoromethane can release toxic fumes of hydrogen bromide, hydrogen chloride and hydrogen fluoride when it is heated to decomposition (HSDB , 2000).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS353-59-3 (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 CAS353-59-3 (NFPA, 2002):
- Bromochlorodifluoromethane (Halon-1211) is noncombustible, and is a recommended fire extinguishing agent for gaseous and liquid fires, electrical fires, paper, wood, and textile fires, combustion engine fires, and fires involving hazardous solid materials (Anon, 1978).
Irritating and toxic fluoride, chloride, and bromide fumes may be released when bromochlorodifluoromethane is heated to decomposition (Lewis, 1996). Chlorofluorohydrocarbons can release hydrofluoric acid, hydrochloric acid, phosgene, and carbonyl fluoride when exposed to red-hot metal or undergoing thermal decomposition (ILO, 1983).
DUST/VAPOR HAZARD
- Irritating and toxic fluoride, chloride, and bromide fumes may be released when bromochlorodifluoromethane is heated to decomposition (Lewis, 1996).
- Chlorofluorohydrocarbons can release hydrofluoric acid, hydrochloric acid, phosgene, and carbonyl fluoride when exposed to red-hot metal or undergoing thermal decomposition (ILO, 1983).
- Bromochlorodifluoromethane gas is heavier than air, and therefore may accumulate in low ceiling spaces. This may cause oxygen deficiency (ILO, 1998).
REACTIVITY HAZARD
- Contact of various chlorofluorohydrocarbons with powdered aluminum or heated, fresh aluminum surfaces has resulted in flashing or sparking, or a vigorous reaction with liberation of heat (NFPA, 1986).
- Irritating and toxic fluoride, chloride, and bromide fumes may be released when bromochlorodifluoromethane is heated to decomposition (Lewis, 1996).
- Chlorofluorohydrocarbons can release hydrofluoric acid, hydrochloric acid, phosgene, and carbonyl fluoride when exposed to red-hot metal or undergoing thermal decomposition (ILO, 1983).
- If bromochlorodifluoromethane comes into contact with acids or acid fumes, highly toxic fumes of hydrogen fluoride or hydrogen chloride may be emitted (HSDB , 2000).
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 CAS353-59-3 (AIHA, 2006):
- DOE TEEL Values for CAS353-59-3 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Halon 1211 (Bromochlorodifluoromethane) TEEL-0 (units = ppm): 12.5 TEEL-1 (units = ppm): 40 TEEL-2 (units = ppm): 250 TEEL-3 (units = ppm): 5,000 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 CAS353-59-3 (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; 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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 CAS353-59-3 (National Institute for Occupational Safety and Health, 2007):
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.
Do not come into contact with or walk through spilled material. Spilled material should not be allowed to enter waterways, sewers, basements, or confined areas (HSDB , 2000). Leaking containers should be turned so that gas escapes, rather than liquid. Do this only if it can be done safely (HSDB , 2000). The area should be ventilated and the substance should be allowed to evaporate (HSDB , 2000).
Before disposing of any waste material in landfills, consult with applicable environmental regulatory agency for information on approved disposal practices (HSDB , 2000). Waste management activities associated with material disposition are unique to individual situations. Proper waste characterization and decisions regarding waste management should be coordinated with the appropriate local, state, or federal authorities to ensure compliance with all applicable rules and regulations.
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- The production and use of bromochlorodifluoromethane has resulted in it's release to the environment through various waste streams. This compound has been linked to depletion of ozone in the stratosphere (HSDB , 2000).
ENVIRONMENTAL FATE AND KINETICS
Bromochlorodifluoromethane exists as a gas in the ambient atmosphere, and is slowly degraded by reactions with hydroxyl radicals. This reaction is so slow, the half-life is estimated to be greater than 44 years (HSDB , 2000).
ABIOTIC DEGRADATION
- Bromochlorodifluoromethane is not expected to significantly degrade due to photolysis (HSDB , 2000).
BIODEGRADATION
- Bromochlorodifluoromethane is expected to slowly biodegrade, due to its' highly halogenated structure (HSDB , 2000).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- Bromochlorodifluoromethane has been shown to play an important role in the destruction of the earth's ozone layer. Production of this compound is expected to end by 2000, in accordance with the 1987 Montreal Protocol (HSDB , 2000).
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Bromochlorodifluoromethane is a colorless, almost odorless gas (HSDB , 2000).
VAPOR PRESSURE
- 2.07x10(3) mmHg (at 25 degrees C) (HSDB , 2000)
FREEZING/MELTING POINT
-159.5 degrees C (HSDB , 2000) -161 degrees C (ILO, 1998)
BOILING POINT
- -3.7 degrees C (HSDB , 2000)
- 1 degree C (Ashford, 1994)
SOLUBILITY
HENRY'S CONSTANT
- 0.094 atm.m(3)/mol (estimated) (HSDB , 2000)
OTHER/PHYSICAL
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