CHLOROPENTAFLUOROETHANE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
CFC-115 CHLOROPENTAFLUORETANO (Spanish) CHLOROPENTAFLUORETHANE (French) 1-CHLORO-1,1,2,2,2-PENTAFLUOROETHANE ETHANE, CHLOROPENTAFLUORO- F-115 FC-115 FLUOCARBON 115 FLUOROCARBON-115 FREON 115 GENETRON 115 HALOCARBON 115 MONOCHLOROPENTAFLUOROETHANE PROPELLANT 115 R-115 REFRIGERANT 115
IDENTIFIERS
SYNONYM REFERENCE
- (ACGIH, 1991; HSDB , 2000; RTECS , 2000; Sittig, 1991)
USES/FORMS/SOURCES
Chloropentafluoroethane is used as a refrigerant and dielectric gas (ACGIH, 1991; Lewis, 1997). In the past, chloropentafluoroethane was often used as a propellant for aerosol food (ACGIH, 1991) HSDB, 1999). However, its use was prohibited in 1979 due to its depleting effect on the stratospheric ozone. It currently is used as a propellant for only a few specialized items (HSDB , 2000).
Chloropentafluoroethane can be manufactured by fluorinating 1,1,1-trichloro-2,2,2-trichloroethane with hydrogen fluoride over aluminum fluoride catalysts at 450 degrees C (HSDB , 2000). It also can be manufactured by passing perchloroethylene, chlorine, and hydrogen fluoride over aluminum trifluoride (HSDB , 2000).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Chloropentafluoroethane may be irritating to the nose, throat, and lungs. Symptoms of exposure may include coughing, dyspnea, dizziness, incoordination, narcosis, nausea, vomiting, palpitations, cardiac arrhythmias, and asphyxia. Contact with the eyes or skin may cause frostbite.
- Inhalation of this compound has caused a decrease in the myocardial threshold to the arrhythmogenic action of injected epinephrine in experimental animals.
- Inhalation of evolved chloride and fluoride fumes in a fire situation could cause eye, nose, and throat irritation, chemical pneumonitis, or noncardiogenic pulmonary edema.
- 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.
-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 - Skin, central nervous system and cardiovascular system (National Institute for Occupational Safety and Health, 2007).
GENERAL - Move 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 area 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. 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 affected areas with water, or attempt to remove frozen 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.
ORAL EXPOSURE - Ingestion is unlikely because this substance is a gas at room temperature and pressure. 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 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).
MAXIMUM TOLERATED EXPOSURE
A feeling of lightheadedness may occur with exposure to airborne chlorofluorohydrocarbon concentrations of 5 to 15% (50,000 to 150,000 ppm) (Ellenhorn & Barceloux, 1988). Of 27 workers exposed to chloropentafluoroethane and chlorodifluoromethane far below published TLVs, 71% experienced lightheadedness and dizziness (compared to 21% of the controls). Thirty-six percent of the workers experienced palpitations (compared to none of the controls) (Hathaway, 1996). Early studies indicate that confusion, pulmonary irritation, tremors, and rarely coma may result from exposure to vapor concentrations of 20%; however, these effects generally were short-lived (HSDB , 2000).
In chronic exposure studies in rats, dogs, mice, and rabbits (90 exposures of 6 hours per day), no significant effects were noted at a chloropentafluoroethane concentration of 10 percent (100,000 ppm) (Waritz, 1966). "Inhalation studies with chloropentafluoroethane in anesthetized dogs, rats, and monkeys showed that exposure to 100,000 to 250,000 ppm, under certain conditions, caused an increase in blood pressure, accelerated heart rate, and depression of myocardial contractility and sensitized the heart to epinephrine. Compared to other chlorofluorocarbons, it is ranked among the least potent for cardiac sensitization" (Hathaway, 1996).
- Carcinogenicity Ratings for CAS76-15-3 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Chloropentafluoroethane 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: Chloropentafluoroethane 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 CAS76-15-3 (U.S. Environmental Protection Agency, 2011):
CALCULATIONS
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS76-15-3 (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 CAS76-15-3 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS76-15-3 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS76-15-3 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS76-15-3 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS76-15-3 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS76-15-3 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS76-15-3 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS76-15-3 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS76-15-3 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
Listed as: (Mono)chloropentafluoroethane (CFC-115) 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 CAS76-15-3 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS76-15-3 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1020 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1020 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS76-15-3 (NFPA, 2002):
-HANDLING AND STORAGE
SUMMARY
HANDLING
- To avoid frostbite, avoid contact with the liquid (AAR, 1998).
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Chloropentafluoroethane is incompatible with metals, including aluminum, zinc, and beryllium. Keep the compound away from open flames and temperatures exceeding 125 degrees F (Sittig, 1991). Chloropentafluoroethane is incompatible/reacts with alkalis and alkaline earth metals, including aluminum powder, potassium, sodium, and zinc (NIOSH, 1999).
-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.
- "Wear appropriate personal protective clothing to prevent the skin from becoming frozen from contact with the liquid or from contact with vessels containing the liquid" (NIOSH , 2000).
- Use of individual breathing devices along with forced air ventilation at the vapor concentration level will reduce the risk of inhalation. When entering tanks or other confined spaces, personnel should wear lifelines (HSDB , 2000).
EYE/FACE PROTECTION
- As contact with the compound can cause tissue damage from frostbite or burns, appropriate eye protection should be worn (NIOSH , 2000).
- Eyewash fountains or quick drench facilities should be available in the work area to personnel in case of exposure to liquids that quickly evaporate or that are extremely cold (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.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 76-15-3.
-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.
Chloropentafluoroethane is a nonflammable gas (Lewis, 1996; NIOSH , 2000). "Chloropentafluoroethane may burn, but does not readily ignite" (Sittig, 1991).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS76-15-3 (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 CAS76-15-3 (NFPA, 2002):
- Fight fire using dry chemical or carbon dioxide extinguishers (Sittig, 1991).
- "Extinguish fire using agent suitable for type of surrounding fire" (AAR, 1996).
Toxic vapors of chloride and fluoride are emitted when chloropentafluoroethane is heated to decomposition (Lewis, 1996). When the compound is involved in a fire, the following poisonous gases are produced: fluorides, chlorides, phosgene, and acid gases (Sittig, 1991). Thermal decomposition products of chlorofluorocarbons include hydrochloric and hydrofluoric acid and lesser amounts of carbonyl fluoride and phosgene. Carbonyl fluoride is highly unstable and, in the presence of moisture, rapidly changes to hydrofluoric acid and carbon dioxide (HSDB , 2000).
EXPLOSION HAZARD
- Prolonged exposure to heat or fire can cause containers of chloropentafluoroethane to rupture violently and rocket (AAR, 1998).
DUST/VAPOR HAZARD
- Toxic vapors of chloride and fluoride are emitted when chloropentafluoroethane is heated to decomposition (Lewis, 1996).
- When the compound is involved in a fire, the following poisonous gases are produced: fluorides, chlorides, phosgene, and acid gases (Sittig, 1991).
- Thermal decomposition products of chlorofluorocarbons include hydrochloric and hydrofluoric acid and lesser amounts of carbonyl fluoride and phosgene. Carbonyl fluoride is highly unstable and, in the presence of moisture, rapidly changes to hydrofluoric acid and carbon dioxide (HSDB , 2000).
- When inhaled, high levels of the compound can cause dizziness or fainting. Death can result following inhalation of extremely high levels (Sittig, 1991).
- Because fluorocarbon vapors are heavier than air (4 to 5 times), high concentrations of the vapors can accumulate in low-lying locations. This then can result in inhalation of concentrated fumes, which is potentially fatal (HSDB , 2000).
- Vapors are odorless, so leaks cannot be detected by smell. Avoid excessive inhalation of chloropentafluoroethane (CGA, 1999).
REACTIVITY HAZARD
- Toxic vapors of chloride and fluoride are emitted when chloropentafluoroethane is heated to decomposition (Lewis, 1996).
- When the compound is involved in a fire, the following poisonous gases are produced: fluorides, chlorides, phosgene, and acid gases (Sittig, 1991).
- Thermal decomposition products of chlorofluorocarbons include hydrochloric and hydrofluoric acid and lesser amounts of carbonyl fluoride and phosgene. Carbonyl fluoride is highly unstable and, in the presence of moisture, rapidly changes to hydrofluoric acid and carbon dioxide (HSDB , 2000).
- Chloropentafluoroethane is incompatible/reacts with alkalis and alkaline earth metals, including aluminum powder, potassium, sodium, and zinc (NIOSH , 2000).
Specifically, when the compound is in contact with alkalis or alkaline earth metals at high temperatures, thermal decomposition occurs (Pohanish & Greene, 1997).
- Prolonged exposure to heat or fire can cause containers of chloropentafluoroethane to rupture violently and rocket (AAR, 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 CAS76-15-3 (AIHA, 2006):
- DOE TEEL Values for CAS76-15-3 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Monochloropentafluoroethane (CFC-115) TEEL-0 (units = ppm): 1,000 TEEL-1 (units = ppm): 3,000 TEEL-2 (units = ppm): 5,000 TEEL-3 (units = ppm): 300,000 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 CAS76-15-3 (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, 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 CAS76-15-3 (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.
Until a spill cleanup is complete, restrict personnel not wearing protective equipment from leak area (Sittig, 1991). Stop gas flow and ventilate leak area to disperse gas. If vapors are leaking from a cylinder which cannot be repaired in place, remove the cylinder to a safe, open-air location and repair the leak or allow the cylinder to empty (Sittig, 1991). Use vermiculite, dry sand, earth, or a similar material to absorb spills. Deposit absorbed material in sealed containers (Sittig, 1991). In light of the proven role of fluorocarbons in depletion of the atmospheric ozone layer (Finkel, 1983; ILO, 1983), other disposal methods other than release to the environment should be considered.
"At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable 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
- When chloropentafluoroethane was used as a propellant for aerosol-dispensed foods and as a refrigerant, it likely was released through various waste streams to the environment (HSDB , 2000).
- The average global concentration of chloropentafluoroethane detected in the troposphere was 4.1 parts per trillion. At altitudes ranging from approximately 10 to 34 km, the compound's concentration in the atmosphere was about 1-5 parts per trillion during 1979 and 1980 (HSDB , 2000).
- Chlorofluorohydrocarbons have been shown to have a role in depletion of the stratospheric ozone layer (Finkel, 1983; ILO, 1983).
ENVIRONMENTAL FATE AND KINETICS
In the ambient atmosphere, chloropentafluoroethane is expected to exist only as a vapor. This is based on a gas/particle partitioning model of semivolatile organic compounds in air (HSDB , 2000). In the troposphere, vapor-phase chloropentafluoroethane is basically inert (HSDB , 2000). "This compound is expected to diffuse into the stratosphere above the ozone layer where it will slowly degrade due to direct photolysis from UV-C radiation and contribute to the catalytic removal of stratospheric ozone" (HSDB , 2000).
SURFACE WATER "Based on a recommended classification scheme, an estimated Koc value of 212, determined from measured water solubility of 250 mg/L at 25 degrees C, and a recommended regression derived equation, indicates that chloropentafluoroethane is not expected to adsorb to suspended solids and sediment in water" (HSDB , 2000). An estimated Henry's law constant of 5.58 atm-m(3)/mol determined from a 6860 mmHg vapor pressure at 25 degrees C and water solubility of 250 mg/L at 25 degrees C indicates that the compound is expected to volatilize quickly from water surfaces (HSDB , 2000).
TERRESTRIAL The compound is expected to be moderately mobile in soil, to volatilize from moist soil surfaces, and to rapidly volatilize from dry soil surfaces (HSDB , 2000).
BIODEGRADATION
- It is not expected that compounds that are highly chlorinated or fluorinated will quickly biodegrade (HSDB , 2000).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Chloropentafluoroethane is a nonflammable, colorless, odorless liquefied gas with good thermal stability (Ashford, 1994; Lewis, 1996; Lewis, 1997).
- It possesses a mild ether-like odor (NIOSH , 2000)
VAPOR PRESSURE
- 7.9 atm (at 70 degrees F) (NIOSH , 2000)
- 6860 mmHg (at 25 degrees C) (HSDB , 2000)
DENSITY
FREEZING/MELTING POINT
BOILING POINT
- -37.7 degrees C (Lewis, 1996)
- -39.1 degrees C (ACGIH, 1991)
- -45.6 degrees C (Ashford, 1994)
- -38 degrees F (NIOSH , 2000)
- -37.7 degrees F (Lewis, 1997)
FLASH POINT
- Not Applicable (NIOSH , 2000)
EXPLOSIVE LIMITS
SOLUBILITY
Chloropentafluoroethane is insoluble in water (Lewis, 1996; Lewis, 1997). 0.006% (at 77 degrees F) (NIOSH , 2000) 250 mg/L (at 25 degrees C) (HSDB , 2000)
HENRY'S CONSTANT
- 3 atm-cu m/mol (at 25 degrees C) (estimated)(HSDB , 2000)
SPECTRAL CONSTANTS
OTHER/PHYSICAL
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