BROMACIL
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
3-sek.BUTYL-5-BROM-6-METHYLURACIL (German) 5-BROMO-3-sec-BUTYL-6-METHYLURACIL 5-BROMO-6-METHYL-3-(1-METHYLPROPYL)-2,4(1H,3H)-PYRIMIDINEDIONE 5-BROMO-6-METHYL-3-(1-METHYLPROPYL)URACIL BOREA BOROCIL BROMACIL BROMAX BROMAZIL CYNOGAN DU PONT HERBICIDE 976 EEREX GRANULAR WEED KILLER EEREX WATER SOLUBLE CONCENTRATE WEED KILLER HERBICIDE 976 HIBOR HYVAR HYVAR X HYVAR X BROMACIL HYVAR X WEED KILLER HYVAR X-L HYVAR-XL WEED KILLER HYVAR X-WS HYVAREX ISTEMUL KROVAR I WEED KILLER KROVAR II KROVAR II WEED KILLER NALKIL 2,4-(1H,3H)-PYRIMIDINEDIONE, 5-BROMO-6-METHYL-3-(1-METHYLPROPYL)- ROUT G-8 URAGAN URAGON UREABOR UROX B UROX B WATER SOLUBLE CONCENTRATE WEED KILLER UROX HA UROX HX GRANULAR WEED KILLER UROX-HX URACIL, 5-BROMO-3-sec-BUTYL-6-METHYL-
IDENTIFIERS
Editor's Note: This material is not listed in the Emergency Response Guidebook. Based on the material's physical and chemical properties, toxicity, or chemical group, a guide has been assigned. For additional technical information, contact one of the emergency response telephone numbers listed under Public Safety Measures.
SYNONYM REFERENCE
- (Budavari, 1996; Clayton & Clayton, 1994; HSDB , 1999; Lewis, 1996; RTECS , 1999)
USES/FORMS/SOURCES
Bromacil is used as an herbicide to control annual and perennial grasses and broadleaf weeds (Budavari, 1996a; Lewis, 1997; Sittig, 1991a) Lewis (1997) states that bromacil is a "substitute approved by EPA for some uses of 2,4,5-T."
Bromacil is commercially available in liquid formulations or as a wettable powder, soluble concentrate, or granules (HSDB , 1999a; NIOSH , 1999).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Bromacil may be irritating to the eyes, skin, and mucous membranes. Signs and symptoms following exposure may include vomiting, diarrhea, gastritis, and tongue numbness.
- In experimental animals, slight transient eye irritation, salivation, gastroenteritis, abdominal distention, liver enlargement and congestion, focal hepatocyte hypertrophy, hemorrhages in the heart, increased thyroid activity, swollen and hemorrhagic lymph nodes, muscular weakness, excitability, and CNS depression have occurred.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
ACUTE CLINICAL EFFECTS
- Bromacil is an irritant of the eyes, nose, throat, and skin (HSDB). It has relatively low acute toxicity in experimental animals (LD50s approximately 5 g/kg). A dose of 100 mg/kg caused vomiting, salivation, muscular weakness, excitability, diarrhea, and mydriasis in dogs (HSDB). It was a mild skin irritant in guinea pigs and a mild eye irritant in rabbits (HSDB).
CHRONIC CLINICAL EFFECTS
- Sheep given bromacil at a dose of 240 mg/kg had abdominal tympany and a stilted gait, and died after four days of dosing; pathological findings included gastroenteritis, liver enlargement, friable adrenal glands, myocardial hemorrhage, and swollen and hemorrhagic lymph nodes (HSDB). Rats given up to 650 mg/kg for 2 weeks had no ill effects (HSDB). At levels greater than 5000 ppm in the diet, bromacil caused signs of over-activity in the thyroid in rats fed for 90 days (HSDB).
- Bromacil was not a sensitizer in guinea pigs (HSDB). Dogs tolerated up to 1250 ppm in the diet for 2 years with no effect (HSDB). Some lesions in the TESTICLES were found in mice given 250 to 5000 ppm in the diet for 18 months.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
FIRST AID EYE EXPOSURE - 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 - Immediately wash the contaminated skin with soap and water. If this chemical penetrates the clothing, immediately remove the clothing, wash the skin with soap and water, and 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 - If this chemical has been swallowed, get medical attention immediately. TARGET ORGANS - Eyes, skin, respiratory system, and thyroid (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. Ingestion may result in significant esophageal or gastrointestinal tract irritation or burns, and 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 gastrointestinal tract irritation, 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. 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.
MAXIMUM TOLERATED EXPOSURE
- The maximum tolerated human exposure to this agent has not been delineated.
- Carcinogenicity Ratings for CAS314-40-9 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A3 ; Listed as: Bromacil A3 :Confirmed Animal Carcinogen with Unknown Relevance to Humans: The agent is carcinogenic in experimental animals at a relatively high dose, by route(s) of administration, at site(s), of histologic type(s), or by mechanism(s) that may not be relevant to worker exposure. Available epidemiologic studies do not confirm an increased risk of cancer in exposed humans. Available evidence does not suggest that the agent is likely to cause cancer in humans except under uncommon or unlikely routes or levels of exposure.
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: Bromacil 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 CAS314-40-9 (U.S. Environmental Protection Agency, 2011):
References: Budavari, 1996 HSDB, 1999 Lewis, 1996 RTECS, 1999 LC50- (INHALATION)RAT: LD- (ORAL)DOG: LD50- (ORAL)MOUSE: LD50- (SKIN)RABBIT: LD50- (ORAL)RAT: LD50- (SKIN)RAT:
CALCULATIONS
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS314-40-9 (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 CAS314-40-9 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS314-40-9 (National Institute for Occupational Safety and Health, 2007):
Listed as: Bromacil REL: IDLH: Not Listed
- OSHA PEL Values for CAS314-40-9 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS314-40-9 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS314-40-9 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS314-40-9 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS314-40-9 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS314-40-9 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS314-40-9 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
Listed as: Bromacil (5-Bromo-6-methyl-3-(1-methylpropyl)2,4-(1H,3H)-pyrimidinedione) Effective Date for Reporting Under 40 CFR 372.30: 1/1/95 Lower Thresholds for Chemicals of Special Concern under 40 CFR 372.28:
- DOT List of Marine Pollutants for CAS314-40-9 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS314-40-9 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions (49 CFR 172.101, 2005):
- ICAO International Shipping Name (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS314-40-9 (NFPA, 2002):
-HANDLING AND STORAGE
SUMMARY
HANDLING
- Keep this compound, especially the liquid formulation Hyvar-XL, away from heat and open flame (HSDB , 1999).
STORAGE
Bromacil should be stored in tightly closed containers. Some loss of water solubility may occur if water-soluble formulations are exposed to air (HSDB , 1999; Sittig, 1991). Containers should not be reused (HSDB , 1999).
- ROOM/CABINET RECOMMENDATIONS
Bromacil decomposes slowly in strong acids and is incompatible with oxidizers, heat, sparks, and open flames (NIOSH , 1999; Sittig, 1991).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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.
- Wear appropriate eye protection and protective clothing, including dust proof safety goggles and gloves, to prevent eye and skin contact when working with bromacil. All protective clothing should be clean and put on each day before work (NIOSH , 1999; Sittig, 1991).
- Any work area where there is a possibility of exposure to bromacil should include facilities for quickly drenching the body for emergency use. Immediately wash contaminated skin. Promptly remove and replace any clothing that becomes wet or contaminated (NIOSH , 1999; Sittig, 1991).
EYE/FACE PROTECTION
- Wear dust-proof goggles or full facepiece respiratory protection when working with bromacil powder or dust. Contact lenses should not be worn (NIOSH , 1999; Sittig, 1991).
- Eyewash fountains should be placed where there is any possibility of workers being exposed to this compound, regardless of whether or not eye protection is worn (NIOSH , 1999).
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 314-40-9.
-PHYSICAL HAZARDS
FIRE HAZARD
Editor's Note: This material is not listed in the Emergency Response Guidebook. Based on the material's physical and chemical properties, toxicity, or chemical group, a guide has been assigned. For additional technical information, contact one of the emergency response telephone numbers listed under Public Safety Measures. POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004) Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.
Dry formulations of bromacil are non-flammable, however the liquid formulation, Hyvar-XL, is combustible. Fires should be extinguished with an agent suitable for the type of surrounding fire (HSDB , 1999; NIOSH , 1999; Sittig, 1991).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS314-40-9 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
Water spray, fog or regular foam. Move containers from fire area if you can do it without risk. Dike fire control water for later disposal; do not scatter the material. Use water spray or fog; do not use straight streams.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Do not get water inside containers. Cool containers with flooding quantities of water until well after fire is out. 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 CAS314-40-9 (NFPA, 2002):
- Bromacil does not readily ignite, therefore fires should be extinguished with an agent suitable for the type of surrounding fire (Sittig, 1991).
DUST/VAPOR HAZARD
- Very toxic fumes of bromide and oxides of nitrogen are emitted when bromacil is heated to decomposition (Lewis, 1996).
REACTIVITY HAZARD
- Bromacil decomposes slowly in strong acids and is incompatible with oxidizers, heat, sparks, and open flames (NIOSH , 1999; Sittig, 1991).
EVACUATION PROCEDURES
- Editor's Note: This material is not listed in the Table of Initial Isolation and Protective Action Distances.
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 25 to 50 meters (80 to 160 feet) in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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 151 (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 in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas.
- AIHA ERPG Values for CAS314-40-9 (AIHA, 2006):
- DOE TEEL Values for CAS314-40-9 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS314-40-9 (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; 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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, 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 CAS314-40-9 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004) Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. Cover with plastic sheet to prevent spreading. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. DO NOT GET WATER INSIDE CONTAINERS.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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.
Only persons wearing protective equipment should be allowed in the contaminated area (Sittig, 1991). Powdered material should be collected in a safe manner and sealed in appropriate containers for reclamation or disposal. Liquids containing bromacil should be absorbed in materials such as dry sand, earth, or vermiculite and deposited in sealed containers (Sittig, 1991).
Incinerate bromacil in an 850 degree C unit supplied with off gas scrubbing equipment (HSDB , 1999; Sittig, 1991). 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
- Bromacil is released directly to the environment during its use as a non-selective herbicide to control weeds and grasses. It may drift to surrounding areas during aerial application and may be transported in runoff from rainfall following application (HSDB , 1999).
ENVIRONMENTAL FATE AND KINETICS
Bromacil can exist in the ambient atmosphere in the vapor and particulate-phases, based on a reported vapor pressure of 2.5 x 10(-7) mmHg (at 25 degrees C). A reaction with photochemically produced hydroxyl radicals results in rapid degradation when bromacil is in the vapor-phase, with an estimated half-life of approximately 7.6 hours. Dry and wet deposition are also important removal processes (HSDB , 1999).
SURFACE WATER Microbial and photo-sensitized degradation are major fate processes for bromacil in natural water. The rate of photodegradation depends on the intensity of the sunlight and the concentration of sensitizing agents. Adsorption to sediment, aquatic volatilization, and bioconcentration should not be important removal processes (HSDB , 1999).
TERRESTRIAL When bromacil is applied to soil, it is primarily degraded through microbial processes. It can be very mobile in soil, based on measured Koc values of 20 to 130. One study demonstrated over 96% displacement of applied bromacil following rainfall of 20-23 cm. Leaching of bromacil may occur as demonstrated by its detection in groundwater; however, organic-rich soils may minimize leaching. Photodecomposition and volatilization should not be important removal processes, although lab studies have demonstrated that 25-30% of applied bromacil may be lost from soil as carbon dioxide in 6 to 9 weeks (HSDB , 1999). Reported values for the half-life of bromacil in soil (HSDB , 1999): 60 days (listed in US Department of Agriculture's Pesticide Properties Database) 155 days (flooded soil) 198 days (flooded soil plus bean straw) 144-198 days (sandy loam soil; saturated soil conditions) 4-5 months (laboratory loam soil at 13.2 and 31.2 degrees C) (warmer temperatures resulted in faster degradation) 5-6 months (field plots treated with 4 pounds bromacil per acre) 5-6 months (4 pounds 2-(14)C-labeled bromacil per acre applied to Butlertown silt loam) 8 months (approximate) (applied annually for 6-7 years in an apple orchard)
ABIOTIC DEGRADATION
- Bromacil has an atmospheric half-life of approximately 7.6 hours at an atmospheric concentration of 5 x 10(5) hydroxyl radicals/cm(3). The rate constant for its vapor-phase reaction with photochemically produced hydroxyl radicals is approximately 5.07 x 10(-11) cm(3)/molecule-sec at 25 degrees C (HSDB , 1999).
- Direct photolysis is not an important fate process for bromacil. However, this compound is rapidly degraded by sunlight in the presence of sensitizers such as methylene blue and riboflavin. An increase in pH will generally increase the sensitized degradation rate even more. This effect occurs even under winter conditions when bromacil may exist in frozen, aqueous solutions (HSDB , 1999).
BIODEGRADATION
- Microbiological degradation is an important process in the removal of bromacil from soil. Only certain organisms, however, can aid in this process, some of which include soil diptheroids, pseudomonas, and penicillium species (HSDB , 1999).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- ECOTOXICITY VALUES (HSDB , 1999):
LC50 - BLUEGILL SUNFISH: 71 ppm for 48H -- conditions of bioassay not specified LC50 - SALMO GAIRDNERI (Rainbow Trout): 75 ppm for 48H -- conditions of bioassay not specified LC50 - CYPRINUS CARPIO (Carp): 164 ppm for 48H -- conditions of bioassay not specified LC50 - SALMO GAIRDNERI (Rainbow Trout): 56-60 mg active ingredient (as wp)/L for 48H -- conditions of bioassay not specified LC50 - COTURNIX JAPONICA: >5000 ppm for 5D in diet -- conditions of bioassay not specified LC50 - BLUEGILL: 80 mg active ingredient (as wp)/L for 24H -- conditions of bioassay not specified LC50 - PIMEPHALES PROMELAS (Fathead Minnow): 186 mg/L for 96H -- flow-through bioassay with measured concentrations, 25.0 degrees C, dissolved oxygen 8.2 mg/L, hardness 49.4 mg/L calcium carbonate, alkalinity 42.1 mg/L calcium carbonate, and pH 7.4 LC50 - PIMEPHALES PROMELAS (Fathead Minnow), 30 days old: 185 mg/L for 24H LC50 - PIMEPHALES PROMELAS (Fathead Minnow), 30 days old: 183 mg/L for 48H LC50 - PIMEPHALES PROMELAS (Fathead Minnow), 30 days old: 182 mg/L for 96H LC50 - PIMEPHALES PROMELAS (Fathead Minnow), 30 days old: 167 mg/L for 168H EC50 - PIMEPHALES PROMELAS (Fathead Minnow): 167 mg/L for 96H -- flow-through bioassay with measured concentrations, 25.0 degrees C, dissolved oxygen 8.2 mg/L, hardness 49.4 mg/L calcium carbonate, alkalinity 42.1 mg/L calcium carbonate, and pH 7.4; stress was characterized by swimming in a spiral motion and by floating vertically in the water
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Bromacil is an odorless, colorless to white, crystalline solid (Budavari, 1996; Lewis, 1996; NIOSH , 1999; Sittig, 1991).
VAPOR PRESSURE
- 8x10(-4) mmHg (at 100 degrees C) (Budavari, 1996)
- 2.5x10(-7) mmHg (at 25 degrees C) (HSDB , 1999)
- 0.033 mPa (at 25 degrees C) (HSDB , 1999)
SPECIFIC GRAVITY
- NORMAL TEMPERATURE AND PRESSURE
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
157.5-160 degrees C (Budavari, 1996) 158-159 degrees C (Clayton & Clayton, 1994; Sittig, 1991) 158-160 degrees C (ACGIH, 1991)
BOILING POINT
FLASH POINT
- Not Applicable (NIOSH , 1999)
- HYVAR XL: 112 degrees F (closed cup) (HSDB , 1999)
EXPLOSIVE LIMITS
SOLUBILITY
815 mg/L (at 20 degrees C) (Budavari, 1996) 815 ppm (at 25 degrees C) (Clayton & Clayton, 1994) 0.08% (at 77 degrees F) (NIOSH , 1999) Bromacil is slightly soluble in water (Lewis, 1996).
Bromacil is moderately soluble in acetone, acetonitrile, and ethanol (Budavari, 1996; Lewis, 1996). Xylene: 3.2 g/100 mL (at 25 degrees C) (Clayton & Clayton, 1994) SOLUBILITIES AT 25 DEGREES C (HSDB , 1999):
This compound is sparingly soluble in hydrocarbons, moderately soluble in strong aqueous bases, and decomposes slowly in strong acids (Budavari, 1996; Clayton & Clayton, 1994; HSDB , 1999; Lewis, 1996).
HENRY'S CONSTANT
- 5.07x10(-11) atm-m(3)/mol (estimated) (HSDB , 1999)
OTHER/PHYSICAL
-REFERENCES
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