CHLOROTRIFLUOROETHYLENE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
CHLOROTRIFLUOROETHYLENE 1-CHLORO-1,2,2-TRIFLUOROETHYLENE 2-CHLORO-1,1,2-TRIFLUOROETHYLENE CFE CHLORTRIFLUORAETHYLEN (German) CTFE DAIFLON ETHENE, CHLOROTRIFLUORO- ETHYLENE, CHLOROTRIFLUORO- ETHYLENE, TRIFLUOROCHLORO- FLUOROPLAST 3 GENETRON 1113 KEL F MONOMER MONOCHLOROTRIFLUOROETHYLENE R1113 TRIFLUORCHLORETHYLEN (Czech) 1,1,2-TRIFLUORO-2-CHLOROETHYLENE TRIFLUOROCHLORETHYLENE TRIFLUOROCHLOROETHYLENE TRIFLUOROMONOCHLOROETHYLENE TRIFLUOROVINYL CHLORIDE TRITHENE
IDENTIFIERS
1082-Trifluorochloroethylene 1082-Trifluorochloroethylene, inhibited 1082-Trifluorochloroethylene, stabilized
SYNONYM REFERENCE
- ((CHRIS, 2001); (HSDB, 2001); ILO , 1998)RTECS, 2001
USES/FORMS/SOURCES
Chlorotrifluoroethylene is used as a monomer for chlorotrifluoroethylene resins and as an chemical intermediate (Lewis, 1997). High performance lubricants, plastics and elastomers are synthesized using chlorotrifluoroethylene (HSDB, 2001). High yields of bromotrifluoroethylene are prepared via bromination of chlorotrifluoroethylene (HSDB, 2001).
Chlorotrifluoroethylene is derived from trichlorotrifluoroethane and zinc. The technical grade is 99.0% pure (Lewis, 1997). Another method of production involves dechlorination of 1,1,2-trichloro-1,2,2-trifluoroethane gas on an aluminum fluoride-nickel phosphate catalyst (HSDB, 2001).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Chlorotrifluoroethylene is a poison by ingestion and is moderately toxic when inhaled. Inhalation produces dizziness, nausea and vomiting acutely; longer exposure (hours) may injure the liver and kidneys, resulting in jaundice and kidney necrosis. Chlorotrifluoroethylene can act as an asphyxiant through the displacement of oxygen from air.
- Dermal or eye contact with the liquid may cause frostbite. Extended contact with the polymer can result in skin sensitization.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
TOXIC; may be fatal if inhaled or absorbed through skin. Contact with gas or liquefied gas may cause burns, severe injury and/or frostbite. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control may cause pollution.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. In case of contact with liquefied gas, thaw frosted parts with lukewarm water. In case of burns, immediately cool affected skin for as long as possible with cold water. Do not remove clothing if adhering to skin. Keep victim warm and quiet. Keep victim under observation. Effects of contact or inhalation may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
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.
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 clothing.
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 frostbite of the eyes has occurred, DO NOT flush with water; early ophthalmologic consultation should be obtained.
ORAL EXPOSURE - Ir oral exposure has caused 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
The minimum lethal human dose to this agent has not been delineated. Although no minimum lethal dose is found in current literature, it is reported that chlorotrifluoroethylene may be fatal if inhaled or absorbed through the skin (HSDB, 2001).
MAXIMUM TOLERATED EXPOSURE
- Carcinogenicity Ratings for CAS79-38-9 :
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 CAS79-38-9 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS79-38-9 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS79-38-9 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS79-38-9 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS79-38-9 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS79-38-9 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS79-38-9 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS79-38-9 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS79-38-9 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS79-38-9 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS79-38-9 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS79-38-9 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS79-38-9 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1082 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1082 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS79-38-9 (NFPA, 2002):
-HANDLING AND STORAGE
HANDLING
- Broken packages should not be handled unless appropriate personal protective equipment is worn. Any contact with liquid chlorotrifluoroethylene can cause frostbite (AAR, 2000; HSDB, 2001).
- Damaged containers of chlorotrifluoroethylene should only be handled by specialists (HSDB, 2001).
- When handling chlorotrifluoroethylene, all equipment used must be grounded (HSDB, 2001).
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Chlorotrifluoroethylene should be stored ambient temperatures, but at less than 150 degrees F (CHRIS, 2001). Any closed space that used to store chlorotrifluoroethylene should be ventilated before anyone is allowed to enter (HSDB, 2001).
Chlorotrifluoroethylene will react violently if mixed with bromine and oxygen or chlorine trifluoride and water (Lewis, 2000). Chlorotrifluoroethylene and chlorine perchlorate were pre-mixed at -196 degrees C, warmed to -78 degrees C, and then exposed to ambient temperatures. The mixture exploded (Urben, 1999). Chlorotrifluoroethylene is incompatible with 1,1-dichloroethylene and oxygen. When mixed with ethylene, there is the potential for an explosive polymerization reaction (Lewis, 2000).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
- Chlorotrifluoroethylene may be fatal if inhaled or absorbed through the skin. Positive pressure self-contained breathing apparatus should be worn (HSDB, 2001).
EYE/FACE PROTECTION
- Goggles and self-contained breathing apparatus should be worn (CHRIS, 2001).
RESPIRATORY PROTECTION
- Avoid breathing vapors (AAR, 2000).
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 79-38-9.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004) Flammable; may be ignited by heat, sparks or flames. May form explosive mixtures with air. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Vapors from liquefied gas are initially heavier than air and spread along ground. Vapors may travel to source of ignition and flash back. Some of these materials may react violently with water. Cylinders exposed to fire may vent and release toxic and flammable gas through pressure relief devices. Containers may explode when heated. Ruptured cylinders may rocket. Runoff may create fire or explosion hazard.
When exposed to heat, flames, sparks, or oxidizers, chlorotrifluoroethylene poses a very dangerous fire hazard (Lewis, 2000).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS79-38-9 (NFPA, 2002):
- INITIATING OR CONTRIBUTING PROPERTIES
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Water spray, fog or alcohol-resistant foam. FOR CHLOROSILANES, DO NOT USE WATER; use AFFF alcohol-resistant medium expansion 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 119 (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.
- NFPA Extinguishing Methods for CAS79-38-9 (NFPA, 2002):
- Stop the flow of gas to fight fire (Lewis, 2000). Fire should not be extinguished unless flow of material can be stopped (AAR, 2000).
- Water in flooding quantities should be used as fog. Vapors may be knocked down with water spray (AAR, 2000).
- Caution should be used when approaching fires. Water should be applied from as great a distance as possible (AAR, 2000). Unmanned hose holders or monitor nozzles should be used (HSDB, 2001).
- For small fires, dry chemical, carbon dioxide, water spray, or alcohol-resistant foam can be used. For larger fires, use water spray, fog, or alcohol-resistant foam (HSDB, 2001).
- Water should not be directed as the source of the leak or at safety devices, as icing may occur (HSDB, 2001).
EXPLOSION HAZARD
- Containers of chlorotrifluoroethylene may violently rupture and rocket if they are placed under prolonged exposure to fire or intense heat. Chlorotrifluoroethylene may also polymerize, causing the possible rupture of the container (AAR, 2000).
- Containers of chlorotrifluoroethylene may explode when heated. A fire or explosion hazard may be created by runoff (HSDB, 2001).
- Chlorotrifluoroethylene forms explosive mixture with air. Contact with ethylene may cause explosive polymerization (Pohanish & Greene, 1997).
DUST/VAPOR HAZARD
- Chlorotrifluoroethylene vapors are heavier than air. Flames can very easily flash back to the source of a liquid or vapor leak (AAR, 2000).
- Chlorotrifluoroethylene vapors can displace air and cause asphyxiation (AAR, 2000).
- Irritating, corrosive, and/or toxic gases are produced during fires (HSDB, 2001).
- Chlorotrifluoroethylene will emit toxic fumes of fluoride and chloride when it is heated to decomposition (Lewis, 2000).
REACTIVITY HAZARD
- CAUTION: This material may polymerize violently under high temperature conditions or upon contamination with other products. Polymerization will produce heat and high pressure buildup in containers which may lead to an explosion or container rupture (ERG, 2004).
- Chlorotrifluoroethylene will react violently with oxidizers. An explosive polymerization reaction may occur upon contact with ethylene (Pohanish & Greene, 1997).
- Terpenes and 1% tributylamine will inhibit polymerization (CHRIS, 2001).
EVACUATION PROCEDURES
- Initial Isolation and Protective Action Distances (ERG, 2004)
Data presented from the Emergency Response Guidebook Table of Initial Isolation and Protective Action Distances are for use when a spill has occurred and there is no fire. If there is a fire, or if a fire is involved, evacuation information presented under FIRE - PUBLIC SAFETY EVACUATION DISTANCES should be used. Generally, a small spill is one that involves a single, small package such as a drum containing up to approximately 200 liters, a small cylinder, or a small leak from a large package. A large spill is one that involves a spill from a large package, or multiple spills from many small packages. Suggested distances to protect from vapors of toxic-by-inhalation and/or water-reactive materials during the first 30 minutes following the spill. DOT ID No. 1082 - Trifluorochloroethylene SMALL SPILLS LARGE SPILLS
DOT ID No. 1082 - Trifluorochloroethylene, inhibited SMALL SPILLS LARGE SPILLS
DOT ID No. 1082 - Trifluorochloroethylene, stabilized SMALL SPILLS LARGE SPILLS
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 100 to 200 meters (330 to 660 feet) in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
If tank, rail car or tank truck is involved in a fire, ISOLATE for 1600 meters (1 mile) in all directions; also, consider initial evacuation for 1600 meters (1 mile) in all directions.
- PUBLIC SAFETY MEASURES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (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 CAS79-38-9 (AIHA, 2006):
Listed as 2-Chloro-1,1,2-Trifluoroethylene (Chlorotrifluoroethylene) ERPG-1 (units = ppm): 20 ERPG-2 (units = ppm): 100 ERPG-3 (units = ppm): 300 Under Ballot, Review, or Consideration: No Definitions: ERPG-1: The ERPG-1 is the maximum airborne concentration below which it is believed nearly all individuals could be exposed for up to one hour without experiencing more than mild, transient adverse health effects or perceiving a clearly defined objectionable odor. ERPG-2: The ERPG-2 is the maximum airborne concentration below which it is believed nearly all individuals could be exposed for up to one hour without experiencing or developing irreversible or other serious health effects or symptoms that could impair an individual's ability to take protective action. ERPG-3: The ERPG-3 is the maximum airborne concentration below which it is believed nearly all individuals could be exposed for up to one hour without experiencing or developing life-threatening health effects.
- DOE TEEL Values for CAS79-38-9 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS79-38-9 (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; 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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):
Listed as: Chlorotrifluoroethylene Proposed Value: AEGL-1 10 min exposure: ppm: 29 ppm mg/m3: 138 mg/m(3)
30 min exposure: ppm: 20 ppm mg/m3: 95 mg/m(3)
1 hr exposure: ppm: 16 ppm mg/m3: 76 mg/m(3)
4 hr exposure: ppm: 10 ppm mg/m3: 48 mg/m(3)
8 hr exposure: ppm: 10 ppm mg/m3: 48 mg/m(3)
Definitions: AEGL-1 is the airborne concentration of a substance above which it is predicted that the general population, including susceptible individuals, could experience notable discomfort, irritation, or certain asymptomatic non-sensory effects. However, the effects are not disabling, are transient, and are reversible upon cessation of exposure.
Listed as: Chlorotrifluoroethylene Proposed Value: AEGL-2 10 min exposure: ppm: 160 ppm mg/m3: 760 mg/m(3)
30 min exposure: ppm: 110 ppm mg/m3: 523 mg/m(3)
1 hr exposure: ppm: 86 ppm mg/m3: 409 mg/m(3)
4 hr exposure: ppm: 54 ppm mg/m3: 266 mg/m(3)
8 hr exposure: ppm: 54 ppm mg/m3: 266 mg/m(3)
Definitions: AEGL-2 is the airborne concentration 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.
Listed as: Chlorotrifluoroethylene Proposed Value: AEGL-3 10 min exposure: ppm: 1500 ppm mg/m3: 7100 mg/m(3)
30 min exposure: ppm: 690 ppm mg/m3: 3300 mg/m(3)
1 hr exposure: ppm: 420 ppm mg/m3: 2000 mg/m(3)
4 hr exposure: ppm: 150 ppm mg/m3: 710 mg/m(3)
8 hr exposure: ppm: 91 ppm mg/m3: 430 mg/m(3)
Definitions: AEGL-3 is the airborne concentration of a substance above which it is predicted that the general population, including susceptible individuals, could experience life-threatening health effects or death.
- NIOSH IDLH Values for CAS79-38-9 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Fully encapsulating, vapor protective clothing should be worn for spills and leaks with no fire. 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. FOR CHLOROSILANES, use AFFF alcohol-resistant medium expansion foam to reduce vapors. If possible, turn leaking containers so that gas escapes rather than liquid. Prevent entry into waterways, sewers, basements or confined areas. Isolate area until gas has dispersed.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004) Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
All sources of ignition should be eliminated if there is a leak (HSDB, 2001).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Due to chlorotrifluoroethylene's production and use as a plastic film for food packaging and as a chemical intermediate, it may be released to the environment through various waste streams (HSDB, 2001).
ENVIRONMENTAL FATE AND KINETICS
In the atmosphere, chlorotrifluoroethylene will exist in the vapor phase, where it will degrade by reacting with photochemically produced hydroxyl radicals (HSDB, 2001).
SURFACE WATER It is expected that chlorotrifluoroethylene would volatilize quickly from water surfaces, however it may decompose before volatilization is possible (HSDB, 2001). It is not expected that chlorotrifluoroethylene will adsorb to particulate matter in water (HSDB, 2001).
TERRESTRIAL Based upon estimates of Koc and Kow, it is assumed that chlorotrifluoroethylene would be moderately mobile in soil. While it is possible that chlorotrifluoroethylene will leach into the water, it is expected that it will decompose in water (HSDB, 2001). It is not expected that chlorotrifluoroethylene will adsorb to soil (HSDB, 2001).
OTHER In landfill leachate the measured half life of chlorotrifluoroethylene was approximately 42 days (HSDB, 2001). In a sulfide-containing buffer, chlorotrifluoroethylene will degrade in less than a day (HSDB, 2001). In a model river the volatilization half-life was calculated to be three hours; in a model lake it was calculated at four days (HSDB, 2001). It is expected that the half-life of chlorotrifluoroethylene in the atmosphere will be 2.2 to 2.3 days (HSDB, 2001). The reaction of chlorotrifluoroethylene with atomic oxygen has a rate constant of 2.7 x 10(-11) cm (2)/mol-sec (HSDB, 2001).
BIOACCUMULATION
Chlorotrifluoroethylene has a calculated bioconcentration factor (BCF) of 11. This is based on an estimated log Kow of 1.65. Based on this BCF, chlorotrifluoroethylene will not bioconcentrate in aquatic organisms (HSDB, 2001).
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Chlorotrifluoroethylene is a colorless gas (HSDB, 2001).
VAPOR PRESSURE
- 4.592 x 10(3) mmHg (at 25 degrees C) (calculated) (HSDB, 2001)
SPECIFIC GRAVITY
- TEMPERATURE AND/OR PRESSURE NOT LISTED
1.305 (liquid) (at 20 degrees C) (Lewis, 1997) 1.305 (ILO , 1998) 1.31 (at 5.7 atm) (NFPA, 1997)
DENSITY
FREEZING/MELTING POINT
-158.2 degrees C (HSDB, 2001) -157.5 degrees C (ILO , 1998; Lewis, 2000)
BOILING POINT
- -27.9 degrees C (HSDB, 2001; (ILO , 1998; Lewis, 1997)
- -26.2 degrees C (Lewis, 2000)
FLASH POINT
- -18 degrees F (-28 degrees C) (HSDB, 2001; (Lewis, 2000; Pohanish & Greene, 1997)
EXPLOSIVE LIMITS
SOLUBILITY
HENRY'S CONSTANT
- 0.31 atm-cu/mole (estimated) (HSDB, 2001)
SPECTRAL CONSTANTS
OTHER/PHYSICAL
- ORGANIC CARBON PARTITION COEFFICIENT
-REFERENCES
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