TERT-BUTYL ACETATE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
tert-BUTYL ACETATE ACETIC ACID, tert-BUTYL ESTER ACETIC ACID, 1,1-DIMETHYLETHYL ESTER t-BUTYL ACETATE tert-BUTYL ESTER of ACETIC ACID TEXACO LEAD APPRECIATOR TLA
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
- (HSDB , 1995)NIOSH, 1995;(RTECS , 1995)
USES/FORMS/SOURCES
tert-Butyl acetate is utilized as a gasoline additive and solvent (ACGIH, 1991; Budavari, 1989; Lewis, 1993; Hathaway et al, 1991).
tert-Butyl acetate is a colorless liquid possessing a characteristic, fruity odor (ACGIH, 1991) NIOSH, 1995).
SYNONYM EXPLANATION
- Editor's Note: Most of the information in this document is specifically for tert-butyl acetate (CAS 540-88-5); however, some information on BUTYL ACETATES, as a class of compounds, no isomer indicated, is included. When this is done it is clearly marked as such.
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Tert-butyl acetate may be toxic by inhalation, ingestion, and skin or eye exposure.
Exposure may cause irritation of the eyes and upper respiratory tract, dermatitis, and narcosis. There is a report in the literature of an exposure to polyester lacquer that caused signs and symptoms of nervous system, respiratory, and cardiovascular disorders.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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 substance, immediately flush skin or eyes with running water for at least 20 minutes. Wash skin with soap and water. Keep victim warm and quiet. In case of burns, immediately cool affected skin for as long as possible with cold water. Do not remove clothing if adhering to skin. 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 - Flush the contaminated skin with water promptly. If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water promptly. If irritation persists after washing, get medical attention. 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 - Respiratory tract, eyes, skin, and central nervous system (National Institute for Occupational Safety and Health, 2007).
GENERAL - Move victims of inhalation exposure from the toxic environment and administer 100% humidified supplemental oxygen with assisted ventilation as required. 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.
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.
INGESTION EXPOSURE - Because of the potential for gastrointestinal tract irritation and narcosis, 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
MAXIMUM TOLERATED EXPOSURE
The maximum tolerated human exposure to this agent has not been delineated. In humans, exposure to an airborne concentration of 950 ppm for 30 minutes caused irritation of the eyes and nose, headache, and weakness (HSDB , 1995).
- Carcinogenicity Ratings for CAS540-88-5 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: tert-Butyl acetate 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: tert-Butyl acetate 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 CAS540-88-5 (U.S. Environmental Protection Agency, 2011):
CALCULATIONS
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS540-88-5 (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 CAS540-88-5 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS540-88-5 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS540-88-5 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS540-88-5 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS540-88-5 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS540-88-5 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS540-88-5 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS540-88-5 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS540-88-5 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS540-88-5 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS540-88-5 (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 CAS540-88-5 (NFPA, 2002):
-HANDLING AND STORAGE
HANDLING
- Broken containers/packages should not be handled except by personnel wearing appropriate protective clothing (AAR, 1994).
- According to 49 CFR 171.2: "No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by.../the hazardous materials regulations (49 CFR 171 to 177)" (HSDB , 1995)
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Keep tert-butyl acetate separated from heat, water, and food products (HSDB , 1995; OHM/TADS , 1995).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
- Appropriate protective clothing should be worn to prevent skin contact. If skin contact occurs, washing should be done quickly. Due to the flammability hazard, wet clothing should be removed immediately. There is no recommendation that workers need change their clothing after a work shift (AAR, 1994; NIOSH, 1995).
- AAR (1994) lists protective equipment materials compatible with butyl acetate: chlorinated polyethylene, polyurethane, polyvinyl alcohol, and styrene-butadiene rubber.
EYE/FACE PROTECTION
- Use appropriate eye protection to prevent contact with this substance (NIOSH, 1995).
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 540-88-5.
-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 129 (ERG, 2004) HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
tert-Butyl acetate is a flammable liquid, and a moderate fire hazard (Lewis, 1993) NIOSH, 1995). It is incompatible with strong alkalis, strong acids, nitrates, and strong oxidizers; contact may cause explosion and fire (ACGIH, 1991) NIOSH, 1995). This compound releases irritating fumes and acrid smoke (including, carbon monoxide and soot) when heated to decomposition (ACGIH, 1991; Lewis, 1992). tert-Butyl acetate is heavier than air and can flash back along a vapor trail: It will float on water (AAR, 1994; (CHRIS , 1995).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS540-88-5 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Dry chemical, CO2, water spray or alcohol-resistant foam. Do not use dry chemical extinguishers to control fires involving nitromethane or nitroethane.
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Water spray, fog or alcohol-resistant foam. Do not use straight streams. Move containers from fire area if you can do it without risk.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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. 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 CAS540-88-5 (NFPA, 2002):
- When fighting a fire involving tert-butyl acetate, use dry chemical, CO2, or alcohol resistant foam. Water may be ineffective (AAR, 1994; (CHRIS , 1995; Lewis, 1992; OHM/TADS , 1995).
Water can be used to cool exposed containers as well as to knock down vapor. Apply water from as far a distance as is possible. Avoid using solid streams of water, as this may spread the fire: Use water in a mist or fog (AAR, 1994; (CHRIS , 1995; Lewis, 1992; OHM/TADS , 1995).
- Do not attempt to extinguish a fire involving this compound, unless the leak can be stopped or confined (AAR, 1994).
EXPLOSION HAZARD
- tert-Butyl acetate is heavier than air and can flashback along a vapor trail (CHRIS , 1995).
- Vapor may explode in an enclosed area; containers can rupture during fire (CHRIS , 1995; OHM/TADS , 1995).
DUST/VAPOR HAZARD
- This compound releases irritating fumes and acrid smoke (including, carbon monoxide) when heated to decomposition (ACGIH, 1991; Lewis, 1992).
REACTIVITY HAZARD
- tert-Butyl acetate is incompatible with strong alkalis, strong acids, nitrates, and strong oxidizers; contact may cause explosion and fire (ACGIH, 1991) NIOSH, 1995).
- This compound releases irritating fumes and acrid smoke (including, carbon monoxide) when heated to decomposition (ACGIH, 1991; Lewis, 1992).
- tert-Butyl acetate may soften or dissolve plastics (HSDB , 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 129 (ERG, 2004)
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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 129 (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 50 meters (150 feet) in all directions. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate closed spaces before entering.
- For a spill involving this compound, stop the leak and shut off all ignition sources within the vicinity. Remain upwind, keep people away from the area, and avoid contact with the spill. If possible, stop the leak. Isolate and remove all discharged material. Water spray may be employed to knock down vapors. Alert the local fire department as well as health and pollution control agencies. Keep material out of sewers and water sources (AAR, 1994; (CHRIS , 1995; OHM/TADS , 1995).
- AIHA ERPG Values for CAS540-88-5 (AIHA, 2006):
- DOE TEEL Values for CAS540-88-5 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Butyl acetate, tert- TEEL-0 (units = ppm): 200 TEEL-1 (units = ppm): 600 TEEL-2 (units = ppm): 1000 TEEL-3 (units = ppm): 1500 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 CAS540-88-5 (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 CAS540-88-5 (National Institute for Occupational Safety and Health, 2007):
IDLH: 1500 ppm Note(s): [10%LEL]
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor suppressing foam may be used to reduce vapors. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. Use clean non-sparking tools to collect absorbed material.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004) In situ amelioration procedures: If possible, contain the leak and shut off or reduce the flow rate. In water spills, floating booms may be helpful. The partially dissolved material can be adsorbed to activated carbon. Vacuum systems, dredges, and bottom pumps may be employed to remove the sorbent from the bottom (or) the floating portion may be pumped out, transferred to a gravity separation tank, and then passed through a dual media filtration system and an activated carbon filter. If a large amount of unabsorbed material remains, ignition of this remaining material, by the local fire department, may be considered. In this instance, make sure all local public safety, health, water, and air authorities are notified (OHM/TADS , 1995). LAND SPILL (for butyl acetate): Dig a pit to contain the material (size of pit dependent on the size of the spill). Dike the flow with foamed concrete, sand bags, foamed polyurethane, or soil. Absorb liquid with cement powder or fly ash. Utilize the appropriate foam to lower the vapor and fire risks (AAR, 1994). WATER SPILL (for butyl acetate): Use spill control booms or/and any natural barriers to contain leak. If approved by the EPA for this agent, use a surface active agent (eg, alcohols, detergents, soaps). Employ a universal gelling agent. If material is dissolved at a concentration of 10 ppm or greater, apply activated charcoal at ten times the spilled amount. Utilize suction hoses to remove trapped material. Use mechanical dredges to remove masses of precipitates and pollutants (AAR, 1994). AIR SPILL (for butyl acetate): Apply water spray to knock down vapors (AAR, 1994).
When diluted, tert-butyl acetate can be treated biologically in a municipal sewage treatment plant (OHM/TADS , 1995). 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.
Apply a sorbent (straw, sawdust, peat) to the contained material. Remove this contaminated sorbent and place in a sealed, impervious container. Incineration of this material is best; any residue (solid, liquid, or sludge) has to be disposed in accordance with all applicable federal, state, and local regulations. If an approved chemical incinerator is not available, burial in a chemical waste landfill is acceptable (OHM/TADS , 1995).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- tert-Butyl acetate's release to the environment is expected to come primarily from its use as a solvent and gasoline additive; evaporation to the atmosphere is the major route. Small amounts of this compound may be released during manufacture, via waste streams. This compound occurs naturally in bananas and related fruit, although this is unlikely to be a major source of this compound in the environment. tert-Butyl acetate is produced in relatively small quantities, so environmental human exposure is probably not great (HSDB , 1995).
ENVIRONMENTAL FATE AND KINETICS
When released to the atmosphere, tert-butyl acetate will exist largely as vapor. Vapor-phase reaction with photochemically produced hydroxyl radicals is expected to be the most important degradation process; estimated half-life is 26 days. Physical washout, by rain, may be possible (HSDB , 1995).
SURFACE WATER Volatilization is expected to be important as a removal process; half-life is 6 hours. Hydrolysis will be significant in highly alkaline waters (a pH of 10 or higher); at lower pHs it is not expected to be important. Bioconcentration and aquatic adsorption are not thought to be important routes (HSDB , 1995).
TERRESTRIAL Volatilization of tert-butyl acetate from dry surface soil is expected to be rapid. Chemical hydrolysis is thought to be an important route in moist, alkaline soils (pH of 10 or higher); this route is not as important in soils with a pH of 9 or less. Based on its estimated Koc value of 134, leaching is expected to be significant (HSDB , 1995).
BIOACCUMULATION
Using a regression-derived equation, a BCF of 6.6 is estimated for tert-butyl acetate, indicating that bioconcentration is probably not great (HSDB , 1995).
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
- 116.16 (ACGIH, 1991; Budavari, 1989)
DESCRIPTION/PHYSICAL STATE
- tert-Butyl acetate is a colorless liquid possessing a characteristic, fruity odor (ACGIH, 1991) NIOSH, 1995).
PH
SPECIFIC GRAVITY
- NORMAL TEMPERATURE AND PRESSURE
- OTHER TEMPERATURE AND/OR PRESSURE
BOILING POINT
- 97.8 degrees C; 208 degrees F; 370.8 degrees K (Clayton & Clayton, 1994; (Budavari, 1989)
- 96 degrees C (ACGIH, 1991; Lewis, 1993)
FLASH POINT
- 72 degrees F (NIOSH, 1995)
- 16.6-22.2 degrees C (closed cup) (ACGIH, 1991)
- 31.1 degrees C (OHM/TADS, 1991)
EXPLOSIVE LIMITS
SOLUBILITY
tert-Butyl acetate is practically insoluble in water (ACGIH, 1991; Budavari, 1989; Lewis, 1993) NIOSH, 1995).
It is soluble in ether, alcohol, and many common industrial solvents (ACGIH, 1991; Budavari, 1989; Lewis, 1993).
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = 1.38 (HSDB , 1995)
HENRY'S CONSTANT
- 3.3 x 10(-4) atm m(3)/mole (at 25 degrees C) (estimated) (HSDB , 1995)
OTHER/PHYSICAL
1.3870 (at 20 degrees C) (Budavari, 1989) 1.3853 (Clayton & Clayton, 1994)
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