VINYL BROMIDE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
VINYL BROMIDE BROMOETHENE BROMOETHYLENE BROMURE DE VINYLE (French) ETHENE, BROMO- ETHYLENE, BROMO- MONOBROMOETHYLENE VINILE (BROMURO DI) (Italian) VINYLBROMID (German) VINYL BROMIDE, INHIBITED VINYLE (BROMURE DE) (French)
IDENTIFIERS
1085-Vinyl bromide, inhibited 1085-Vinyl bromide, stabilized
SYNONYM REFERENCE
- (RTECS , 1996; HSDB , 1996; NIOSH , 1996)
USES/FORMS/SOURCES
Vinyl bromide is used chiefly as a flame retardant in the polymer production industry, especially in the manufacture of modacrylic fibers for carpet-backing material, in manufacturing flame-resistant plastics or thermoplastic resins, and in flame-resistant fabrics for home furnishings and children's sleepwear (ACGIH, 1991) Hathaway, 1991; (HSDB , 1996). Other uses for vinyl bromide include the manufacture of copolymers, polymers, pharmaceuticals, fumigants, and as a chemical intermediate in organic synthesis. Granular products may be made from a copolymerization of vinyl bromide, vinyl acetate, and maleic anhydride. It is also used in leather and fabricated metal items, film preparation, impregnating or laminating fibers, and in rubber substitutes (ACGIH, 1991; HSDB , 1996).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Vinyl bromide may cause CNS depression and may be irritating to the eyes, skin, and mucous membranes.
- Exposure may result in dizziness, confusion, incoordination, nausea, and vomiting. Liver and kidney damage have been reported in experimental animals.
- IARC has determined that there is sufficient evidence for carcinogenicity in experimental animals. No data are available for humans.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (ERG, 2004)
Vapors may cause dizziness or asphyxiation without warning. Some may be toxic if inhaled at high concentrations. Contact with gas or liquefied gas may cause burns, severe injury and/or frostbite. Fire may produce irritating and/or toxic gases.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (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. 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. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
FIRST AID EYE EXPOSURE (LIQUID) - Immediately wash the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately. Contact lenses should not be worn when working with this chemical. DERMAL EXPOSURE (LIQUID) - Immediately flush the contaminated skin with water. If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water. Get medical attention promptly. 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. ORAL EXPOSURE (LIQUID) - If this chemical has been swallowed, get medical attention immediately. TARGET ORGANS - Eyes, skin, central nervous system, and liver (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. Exposed skin and eyes should be copiously flushed with water. 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. If bronchospasm and wheezing occur, consider treatment with inhaled sympathomimetic agents.
DERMAL EXPOSURE DECONTAMINATION: Remove contaminated clothing and jewelry and place them in plastic bags. Wash exposed areas with soap and water for 10 to 15 minutes with gentle sponging to avoid skin breakdown. A physician may need to examine the area if irritation or pain persists (Burgess et al, 1999). Treat dermal irritation or burns with standard topical therapy. Patients developing dermal hypersensitivity reactions may require treatment with systemic or topical corticosteroids or antihistamines.
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.
ORAL EXPOSURE Because of the potential for CNS depression, do not induce emesis. Significant esophageal or gastrointestinal tract irritation or burns may occur following ingestion. The possible benefit of early removal of some ingested material by cautious gastric lavage must be weighed against potential complications of bleeding or perforation. GASTRIC LAVAGE: Consider after ingestion of a potentially life-threatening amount of poison if it can be performed soon after ingestion (generally within 1 hour). Protect airway by placement in the head down left lateral decubitus position or by endotracheal intubation. Control any seizures first. ACTIVATED CHARCOAL: Administer charcoal as a slurry (240 mL water/30 g charcoal). Usual dose: 25 to 100 g in adults/adolescents, 25 to 50 g in children (1 to 12 years), and 1 g/kg in infants less than 1 year old.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
Rats exposed to 100,000 ppm of vinyl bromide in inhalation studies died after 15 minutes. Exposure to 50,000 ppm caused unconsciousness in rats after 25 minutes and death after 7 hours (ACGIH, 1991).
MAXIMUM TOLERATED EXPOSURE
Rats exposed to 25,000 ppm of vinyl bromide were anesthetized but recovered, even after exposure for 7 hours (ACGIH, 1991). Exposure of rats to 10,000 ppm of vinyl bromide for 7 hours per day, 5 days per week for 4 weeks resulted in significant body weight reductions after 15 days, but no other significant effects were seen (ACGIH, 1991). One study reported that the highest tolerable concentrations for mice was 7 mmol/L (1700 ppm) for a 10-minute exposure. At half that concentration, pronounced anesthesia occurred (Clayton & Clayton, 1994).
- Carcinogenicity Ratings for CAS593-60-2 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A2 ; Listed as: Vinyl bromide A2 :Suspected Human Carcinogen: Human data are accepted as adequate in quality but are conflicting or insufficient to classify the agent as a confirmed human carcinogen; OR, the agent is carcinogenic in experimental animals at dose(s), by route(s) of exposure, at site(s), of histologic type(s), or by mechanism(s) considered relevant to worker exposure. The A2 is used primarily when there is limited evidence of carcinogenicity in humans and sufficient evidence of carcinogenicity in experimental animals with relevance to humans.
EPA (U.S. Environmental Protection Agency, 2011): Not Assessed under the IRIS program. ; Listed as: Vinyl bromide 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): 2A ; Listed as: Vinyl bromide 2A : The agent (mixture) is probably carcinogenic to humans. The exposure circumstance entails exposures that are probably carcinogenic to humans. This category is used when there is limited evidence of carcinogenicity in humans and sufficient evidence of carcinogenicity in experimental animals. In some cases, an agent (mixture) may be classified in this category when there is inadequate evidence of carcinogenicity in humans and sufficient evidence of carcinogenicity in experimental animals and strong evidence that the carcinogenesis is mediated by a mechanism that also operates in humans. Exceptionally, an agent, mixture or exposure circumstance may be classified in this category solely on the basis of limited evidence of carcinogenicity in humans.
NIOSH (National Institute for Occupational Safety and Health, 2007): Ca ; Listed as: Vinyl bromide MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): R ; Listed as: Vinyl Bromide
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS593-60-2 (U.S. Environmental Protection Agency, 2011):
Oral: Inhalation: Unit Risk: RfC: 3x10(-3) mg/m3
Drinking Water:
CALCULATIONS
CONVERSION FACTORS Conversion factor at 68 degrees F and 760 mmHg (NIOSH , 1996) - Conversion factors at 25 degrees C and 760 mmHg (Clayton & Clayton, 1994) - 1 ppm = 4.4 mg/m(3) 1 mg/L = 228.7 ppm
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS593-60-2 (American Conference of Governmental Industrial Hygienists, 2010):
Editor's Note: The listed values are recommendations or guidelines developed by ACGIH(R) to assist in the control of health hazards. They should only be used, interpreted and applied by individuals trained in industrial hygiene. Before applying these values, it is imperative to read the introduction to each section in the current TLVs(R) and BEI(R) Book and become familiar with the constraints and limitations to their use. Always consult the Documentation of the TLVs(R) and BEIs(R) before applying these recommendations and guidelines.
- AIHA WEEL Values for CAS593-60-2 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS593-60-2 (National Institute for Occupational Safety and Health, 2007):
Listed as: Vinyl bromide REL: IDLH: Not Listed
- OSHA PEL Values for CAS593-60-2 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS593-60-2 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS593-60-2 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS593-60-2 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS593-60-2 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS593-60-2 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS593-60-2 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS593-60-2 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS593-60-2 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1085 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1085 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS593-60-2 (NFPA, 2002):
Listed as: Vinyl Bromide Hazard Ratings: Health Rating (Blue): 2 Flammability Rating (Red): 4 (4) Extremely flammable. Materials which will rapidly vaporize at normal pressure and temperature and will burn readily. Including: gases, cryogenic materials, any liquid or gaseous material having a flash point below 73 degrees F and a boiling point below 100 degrees F, and materials which can form explosive mixtures with air.
Instability Rating (Yellow): 1 (1) Materials which are normally stable, but which can become unstable at elevated temperatures and pressures, or which may react with water with some release of energy, but not violently.
Oxidizer/Water-Reactive Designation: Not Listed
-HANDLING AND STORAGE
HANDLING
- Vinyl bromide is often shipped as a liquefied compressed gas, with 0.1 percent phenol added as an inhibitor to prevent polymerization (NIOSH , 1996).
STORAGE
Vinyl bromide may polymerize in sunlight (Bretherick, 1995). Containers should be stored in a well-ventilated place, away from sources of ignition and static discharges (HSDB , 1996).
Vinyl bromide is incompatible with strong oxidizers such as perchlorates, peroxides, chlorates, permanganates and nitrates (NIOSH , 1996).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (ERG, 2004)
- A self-contained breathing apparatus should be worn when handling or fighting fires involving vinyl bromide (OHM/TADS , 1996).
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 593-60-2.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (ERG, 2004) EXTREMELY FLAMMABLE. Will be easily ignited by heat, sparks or flames. Will form explosive mixtures with air. Silane will ignite spontaneously in 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. Cylinders exposed to fire may vent and release flammable gas through pressure relief devices. Containers may explode when heated. Ruptured cylinders may rocket.
When exposed to heat or flame, vinyl bromide is a very dangerous fire hazard and is considered highly flammable (Lewis, 1996) AAR, 1994).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS593-60-2 (NFPA, 2002):
Listed as: Vinyl Bromide Flammability Rating: 4 (4) Extremely flammable. Materials which will rapidly vaporize at normal pressure and temperature and will burn readily. Including: gases, cryogenic materials, any liquid or gaseous material having a flash point below 73 degrees F and a boiling point below 100 degrees F, and materials which can form explosive mixtures with air.
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (ERG, 2004)
- TANK FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (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. For massive fire, use unmanned hose holders or monitor nozzles; if this is impossible, withdraw from area and let fire burn.
- NFPA Extinguishing Methods for CAS593-60-2 (NFPA, 2002):
- Fires involving vinyl bromide should not be extinguished unless flow of the material can be stopped. Water spray in flooding quantities should be used as fog and to cool containers and should be applied from as far away as possible (AAR, 1994).
EXPLOSION HAZARD
- Vinyl bromide may react violently with oxidizing materials (Lewis, 1996).
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).
- Vinyl bromide may react violently with oxidizing materials (Lewis, 1996).
Vinyl bromide is incompatible with strong oxidizers such as perchlorates, peroxides, chlorates, permanganates and nitrates (NIOSH , 1996).
- Vinyl bromide emits toxic fumes of bromides when heated to decomposition (Lewis, 1996).
- Vinyl bromide may polymerize in sunlight (Bretherick, 1995).
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 116 (ERG, 2004)
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (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 116 (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.
- If a fire involving vinyl bromide becomes uncontrollable or containers are exposed to direct flame, consider a one-half mile evacuation radius (AAR, 1994).
- If vinyl bromide is leaking but not on fire, consider evacuating in the downwind direction after considering size of spill, location, and weather conditions (AAR, 1994).
- AIHA ERPG Values for CAS593-60-2 (AIHA, 2006):
- DOE TEEL Values for CAS593-60-2 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Vinyl bromide TEEL-0 (units = ppm): 0.5 TEEL-1 (units = ppm): 3500 TEEL-2 (units = ppm): 6000 TEEL-3 (units = ppm): 6000 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 CAS593-60-2 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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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 CAS593-60-2 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (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. Stop leak if you can do it without risk. Do not touch or walk through spilled material. 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. Isolate area until gas has dispersed.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 116 (ERG, 2004) Sparks and flames should be kept away from spill area. The leak should be stopped if it can be done without endangering personnel. A water spray may be used to knock down vinyl bromide vapors (AAR, 1994).
Carbon or peat may be applied to material containing dissolved vinyl bromide. The material may also be sponged out (OHM/TADS , 1996). Spills containing vinyl bromide may be treated by first pouring the material onto vermiculite, sodium bicarbonate, or a 90 percent sand/10 percent soda ash mixture. Slaked lime should be added if fluoride is present in the material. The mixture may then be incinerated after covering with wood or paper (OHM/TADS , 1996). Material containing vinyl bromide may also be mixed with a flammable solvent and sprayed into an incinerator with afterburner and alkali scrubber equipment (OHM/TADS , 1996). 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
- Vinyl bromide may be released to the environment during its production or use. It may also form in air as a degradation product of 1,2-dibromoethane (HSDB , 1996).
ENVIRONMENTAL FATE AND KINETICS
Vinyl bromide is expected to exist almost entirely in the vapor phase in the atmosphere, based on its vapor pressure of 1033 mmHg at 25 degrees C. It will react with photochemically produced hydroxyl radicals with an estimated half-life of 2.4 days (HSDB , 1996). Photolysis is not expected to be an important fate process for vinyl bromide in the atmosphere (HSDB , 1996).
SURFACE WATER Vinyl bromide released to water will volatilize rapidly. The half-life estimated for a model river is 3 hours (HSDB , 1996). Photolysis, hydrolysis, and adsorption to suspended solids and sediments are not expected to be significant degradation processes for vinyl bromide in water (HSDB , 1996).
TERRESTRIAL Evaporation is expected to be a significant fate process for vinyl bromide in moist or dry soil (HSDB , 1996). Vinyl bromide is expected to be highly mobile in soil, with slight adsorption to suspended solids and sediments, and may leach through soil to contaminate groundwater supplies (HSDB , 1996).
ABIOTIC DEGRADATION
- The estimated half-life of the reaction of vinyl bromide with atomic oxygen is 1.6 years, and for the reaction with ozone, 47 days (HSDB , 1996).
- Hydrolysis is not expected to be an important fate process because of vinyl bromide's molecular structure. Photolysis is also not expected to be significant (HSDB , 1996).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Vinyl bromide is a colorless gas under normal atmospheric pressure, and is a colorless liquid under pressure. It has a characteristic pungent odor (ACGIH, 1991; HSDB , 1996).
VAPOR PRESSURE
- 895 mmHg (at 20 degrees C) (ACGIH, 1991)
- 1033 mmHg (at 20 degrees C) (Clayton & Clayton, 1994)
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
1.493 g/cm(3) (at 20 degrees C) (Clayton & Clayton, 1994) LIQUID: 1.4933 g/mL (at 20 degrees C) (ACGIH, 1991) 1.4738 g/mL (at 25 degrees C at saturation pressure) (HSDB , 1996)
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
BOILING POINT
- 15.8 degrees C; 60 degrees F (NFPA, 1994)
- 15.6 degrees C (Lewis, 1996)
FLASH POINT
- Not Applicable (NIOSH , 1996)
AUTOIGNITION TEMPERATURE
- 530 degrees C; 986 degrees F (NFPA, 1994)
EXPLOSIVE LIMITS
SOLUBILITY
It is soluble in ethanol, ether, acetone, benzene, and chloroform (Clayton & Clayton, 1994).
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = 1.57 (HSDB , 1996)
HENRY'S CONSTANT
- 2.56 x 10(-2) atm-m(3)/mol (at 25 degrees C) (estimated) (HSDB , 1996)
OTHER/PHYSICAL
Not Listed (Clayton & Clayton, 1994) Vinyl bromide may have inadequate warning properties to prevent excessive chronic exposure (Clayton & Clayton, 1994).
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