MONOETHYLAMINE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
IDENTIFIERS
1036-Ethylamine less than 50% but not more than 70% Ethylamine 2270-Ethylamine, aqueous solution, with not less than 50% but not more than 70% Ethylamine
SYNONYM REFERENCE
- (Budavari, 1989; RTECS , 1996; Lewis, 1994; Lewis, 1993; HSDB , 1996; NJFS , 1996; Clayton & Clayton, 1994)
USES/FORMS/SOURCES
Ethylamine is used in resin chemistry, petroleum refining, detergents, organic syntheses and the manufacturing of pharmaceuticals. It is a dye intermediate and is used to stabilize rubber latex. Other applications for ethylamine include use for solvent extraction and as an emulsifier for waxes (Budavari, 1989; Lewis, 1993; ITI, 1988).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Ethylamine is a strong irritant of the eyes, skin, and mucous membranes. If swallowed, it would be predicted to be irritating to the gastrointestinal tract. Contact with the liquid can cause frostbite.
- Inhalation of ethylamine may cause nausea, coughing, and pulmonary edema. Allergic respiratory sensitization may occur from long-term exposure. Difficulty breathing and symptoms of asthma may occur in sensitized individuals. Ethylamine can be harmful or fatal if inhaled or swallowed.
- Occupational exposure has caused eye irritation, corneal edema, and vision disturbances. Blue haze or halo vision may result from exposure to low concentrations.
- Myocardial degeneration and lung, liver, and kidney damage have been reported in experimental animals. Dermal contact in guinea pigs caused skin burns leading to extensive necrosis and scarring. Adrenal cortical gland necrosis has also been reported.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (ERG, 2004)
May cause toxic effects if inhaled. Vapors are extremely irritating. 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.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
May cause toxic effects if inhaled or ingested/swallowed. Contact with substance may cause severe burns to 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.
ACUTE CLINICAL EFFECTS
- Monoethylamine is a strong eye, respiratory tract, and skin irritant and corrosive. It can cause tissue necrosis and scarring (HSDB). It can produce corneal edema, resulting in halos around lights or foggy vision (HSDB). Other symptoms of acute exposure include headache, nausea, faintness, and anxiety (Clayton & Clayton, 1982, Tkachev, 1971). Children exposed to monoethylamine had higher incidences of respiratory infection, ear and mastoid disease, eye inflammation, rickets, allergies, and blood abnormalities (Tkachev, 1969).
CHRONIC CLINICAL EFFECTS
- Rabbits chronically exposed to an airborne concentration of 100 ppm of monoethylamine had signs of lung, liver, and kidney damage (Clayton & Clayton, 1982). CNS disturbances were produced in chronically exposed rats (Tkachev, 1971).
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (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 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.
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (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 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. 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. Primary eye protection (spectacles or goggles), as defined by the Occupational Safety and Health Administration (OSHA), should be used when working with this chemical. Face shields should only be worn over primary eye protection. 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, and respiratory system (National Institute for Occupational Safety and Health, 2007; OSHA, 2000).
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. ACUTE LUNG INJURY: Maintain ventilation and oxygenation and evaluate with frequent arterial blood gases and/or pulse oximetry monitoring. Early use of PEEP and mechanical ventilation may be needed.
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. If frostbite has occurred, DO NOT rub the affected areas, DO NOT flush affected areas with water, or attempt to remove clothing. PREHOSPITAL Rewarming of a localized area should only be considered if the risk of refreezing is unlikely. Avoid rubbing the frozen area which may cause further damage to the area (Grieve et al, 2011; Hallam et al, 2010).
REWARMING Do not institute rewarming unless complete rewarming can be assured; refreezing thawed tissue increases tissue damage. Place affected area in a water bath with a temperature of 40 to 42 degrees Celsius for 15 to 30 minutes until thawing is complete. The bath should be large enough to permit complete immersion of the injured part, avoiding contact with the sides of the bath. A whirlpool bath would be ideal. Some authors suggest a mild antibacterial (ie, chlorhexidine, hexachlorophene or povidone-iodine) be added to the bath water. Tissues should be thoroughly rewarmed and pliable; the skin will appear a red-purple color (Grieve et al, 2011; Hallam et al, 2010; Murphy et al, 2000). Correct systemic hypothermia which can cause cold diuresis due to suppression of antidiuretic hormone; consider IV fluids (Grieve et al, 2011). Rewarming may be associated with increasing acute pain, requiring narcotic analgesics. For severe frostbite, clinical trials have shown that pentoxifylline, a phosphodiesterase inhibitor, can enhance tissue viability by increasing blood flow and reducing platelet activity (Hallam et al, 2010).
WOUND CARE Digits should be separated by sterile absorbent cotton; no constrictive dressings should be used. Protective dressings should be changed twice per day. Perform twice daily hydrotherapy for 30 to 45 minutes in warm water at 40 degrees Celsius. This helps debride devitalized tissue and maintain range of motion. Keep the area warm and dry between treatments (Hallam et al, 2010; Murphy et al, 2000). The injured extremities should be elevated and should not be allowed to bear weight. In patients at risk for infection of necrotic tissue, prophylactic antibiotics and tetanus toxoid have been recommended by some authors (Hallam et al, 2010; Murphy et al, 2000). Non-tense clear blisters should be left intact due to the risk of infection; tense or hemorrhagic blisters may be carefully aspirated in a setting where aseptic technique is provided (Hallam et al, 2010). Further surgical debridement should be delayed until mummification demarcation has occurred (60 to 90 days). Spontaneous amputation may occur. Analgesics may be required during the rewarming phase; however, patients with severe pain should be evaluated for vasospasm. IMAGING: Arteriography and noninvasive vascular techniques (e.g., plain radiography, laser Doppler studies, digital plethysmography, infrared thermography, isotope scanning), have been useful in evaluating the extent of vasospasm after thawing and assessing whether debridement is needed (Hallam et al, 2010). In cases of severe frostbite, Technetium 99 (triple phase scanning) and MRI angiography have been shown to be the most useful to assess injury and determine the extent or need for surgical debridement (Hallam et al, 2010). TOPICAL THERAPY: Topical aloe vera may decrease tissue destruction and should be applied every 6 hours (Murphy et al, 2000). IBUPROFEN THERAPY: Ibuprofen, a thromboxane inhibitor, may help limit inflammatory damage and reduce tissue loss (Grieve et al, 2011; Murphy et al, 2000). DOSE: 400 mg orally every 12 hours is recommended (Hallam et al, 2010). THROMBOLYTIC THERAPY: Thrombolysis (intra-arterial or intravenous thrombolytic agents) may be beneficial in those patients at risk to lose a digit or a limb, if done within the first 24 hours of exposure. The use of tissue plasminogen activator (t-PA) to clear microvascular thromboses can restore arterial blood flow, but should be accompanied by close monitoring including angiography or technetium scanning to evaluate the injury and to evaluate the effects of t-PA administration. Potential risk of the procedure includes significant tissue edema that can lead to a rise in interstitial pressures resulting in compartment syndrome (Grieve et al, 2011). CONTROVERSIAL: Adjunct pharmacological agents (ie, heparin, vasodilators, prostacyclins, prostaglandin synthetase inhibitors, dextran) are controversial and not routinely recommended. The role of hyperbaric oxygen therapy, sympathectomy remains unclear (Grieve et al, 2011). CHRONIC PAIN: Vasomotor dysfunction can produce chronic pain. Amitriptyline has been used in some patients; some patients may need a referral for pain management. Inability to tolerate the cold (in the affected area) has been observed following a single episode of frostbite (Hallam et al, 2010). MORBIDITIES: Frostbite can produce localized osteoporosis and possible bone loss following a severe case. These events may take a year or more to develop. Children may be at greater risk to develop more severe events (ie, early arthritis) (Hallam et al, 2010).
EYE EXPOSURE - DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility. If contact with escaping gas causes frostbite of the eye, DO NOT flush with water; early ophthalmologic consultation should be obtained.
ORAL EXPOSURE - Because of the potential for gastrointestinal tract irritation, do not induce emesis. DILUTION: If no respiratory compromise is present, administer milk or water as soon as possible after ingestion. Dilution may only be helpful if performed in the first seconds to minutes after ingestion. The ideal amount is unknown; no more than 8 ounces (240 mL) in adults and 4 ounces (120 mL) in children is recommended to minimize the risk of vomiting. Oral exposure to escaping gas might cause frostbite injury to the upper gastrointestinal and respiratory tracts. Administer oxygen and maintain airway as clinically indicated.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
Ethylamine is a skin, eye, and mucous membrane irritant (Clayton & Clayton, 1994). In industry, exposure to ethylamine was reported to cause eye irritation and corneal edema (ACGIH, 1991). Ethylamine vapor was reported to decrease olfaction sensitivity and produce vision disturbances in humans (Clayton & Clayton, 1994). Ethylamine causes sever respiratory tract irritation and may cause delayed lung injury effects (Anon, 1997).
Severe damage occurred when ethylamine was tested in rabbit eyes (Clayton & Clayton, 1994) A 70 percent solution of ethylamine was tested on the skin of guinea pigs. Immediate results from exposure showed necrotic skin burns. When exposure was increased to 24 hours, the skin exhibited severe irritation with extensive necrosis and deep scarring (ACGIH, 1991). Rabbits repeatedly exposed to ethylamines exhibited pulmonary edema with hemorrhage and bronchopneumonia, nephritis, liver degeneration, and heart muscle deterioration (Clayton & Clayton, 1994).
- Carcinogenicity Ratings for CAS75-04-7 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Ethylamine 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: Ethylamine 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 CAS75-04-7 (U.S. Environmental Protection Agency, 2011):
CALCULATIONS
CONVERSION FACTORS Conversion Units - 1 mg/l (ppm) - 542 1 ppm (mg/m(3) - 1.84)
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS75-04-7 (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 CAS75-04-7 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS75-04-7 (National Institute for Occupational Safety and Health, 2007):
Listed as: Ethylamine REL: IDLH: IDLH: 600 ppm Note(s): Not Listed
- OSHA PEL Values for CAS75-04-7 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS75-04-7 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS75-04-7 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS75-04-7 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS75-04-7 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS75-04-7 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS75-04-7 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS75-04-7 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS75-04-7 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1036 (49 CFR 172.101, 2005):
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 2270 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1036 (ICAO, 2002):
- ICAO International Shipping Name for UN2270 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS75-04-7 (NFPA, 2002):
-HANDLING AND STORAGE
HANDLING
- Sources of ignition are prohibited where ethylamine is handled, used or stored (NJFS , 1996).
- Use non-sparking tools and equipment while handling containers of ethylamine. Distant ignition can occur (Anon, 1997; (NJFS , 1996).
STORAGE
Containers of ethylamine should be grounded and bonded during transfers. Drums must be equipped with self-closing valves, pressure vacuum bungs, and flame arresters (NJFS , 1996). Typical containers used for shipping ethylamine are tank cars, drums, cans, and glass bottles (NFPA, 1994).
- ROOM/CABINET RECOMMENDATIONS
Store in a cool, dry location away from oxidizing materials, acids, and sources of halogens. The storage area should be non-combustible and well-ventilated (NFPA, 1994). Store containers outdoors or in detached storage, protecting against physical damage. Use a standard flammable liquid storage room for indoor storage of anhydrous solutions. Or, place cylinders containing anhydrous ethylamine in a fireproof, well-ventilated, cool place (ITI, 1988). Keep ethylamine in a tightly closed container, in a cold place and protected from light (Budavari, 1989). If possible transfer aqueous ethylamine from drums or other storage containers to process containers (NJFS , 1996).
Ethylamine is incompatible with strong acids and oxidizers, cellulose nitrate, chlorine and hypochlorites. In the presence of moisture it is also incompatible with copper, tin, and zinc (NIOSH , 1996). Do not mix ethylamine with oxidizing agents such as hypochlorite. This mixture creates chlor-amines which are explosive. Distant ignition and flashback are possible. Combustion of the product generates harmful gases (Anon, 1997). Ethylamine corrodes copper, aluminum, lead, tin, zinc, and galvanized surfaces (Anon, 1997).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (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.
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective 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 full, appropriate protective clothing to avoid exposure. Wear impervious gloves and butyl rubber aprons with boots, chemical safety goggles and face shield. If physical contact occurs, immediately wash the exposed area with large quantities of water. Change wet or contaminated clothing (Anon, 1997; (NIOSH , 1996).
- If skin becomes wet or contaminated wash immediately. Emergency showers and eyewash should be provided (HSDB , 1996).
EYE/FACE PROTECTION
- Ethylamine is an eye irritant and may damage eyes. Wear a respirator that offers eye and face protection (NIOSH , 1996).
- Do not wear contact lenses when working with ethylamine (Anon, 1997).
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 75-04-7.
ENGINEERING CONTROLS
- Engineering controls are the most effective way of reducing exposure to this chemical. Isolating and enclosing operations while providing local exhaust ventilation for chemical release offers protection and can reduce the potential of exposure (NJFS , 1996).
-PHYSICAL HAZARDS
FIRE HAZARD
Editor's Note: Information from more than one emergency response guide is associated with this material. POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (ERG, 2004) EXTREMELY FLAMMABLE. May be ignited by heat, sparks or flames. May form explosive mixtures with air. 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 flammable gas through pressure relief devices. Containers may explode when heated. Ruptured cylinders may rocket.
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004) Flammable/combustible materials. May be 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.
Ethylamine is a flammable gas. Its vapors, which are heavier than air, may ignite and flash back. Unless diluted extensively, ethylamine's aqueous solutions are flammable (Anon, 1997; (NFPA, 1994). Ethylamine is a very dangerous fire hazard and a moderate explosion hazard when exposed to spark, heat or flame (Lewis, 1994).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS75-04-7 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (ERG, 2004)
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (ERG, 2004)
Water spray, fog or regular foam. Move containers from fire area if you can do it without risk. Damaged cylinders should be handled only by specialists.
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
Water spray, fog or alcohol-resistant 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. Do not get water inside containers.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (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.
- TANK FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (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 CAS75-04-7 (NFPA, 2002):
Listed as: Ethylamine, 70% Extinguishing Method(s): 1, 5 1: "Water may be ineffective" applies to a situation where materials with a flash point below 100 degrees F (37.8 degrees C) are burning. Water will only be effective if used by experienced fire fighters under favorable conditions. Even though water may not put the fire out, it can be used to protect equipment and structures. 5: Flammable liquid fires can be extinguished using carbon dioxide, dry chemical, foam, and vaporizing liquid extinguishers, as long as the fires are small to moderate in size and the flammable liquid reservoir is shallow. Use of foam to form a blanket over a flammable liquid is not effective when the liquid is water-soluble. Certain alcohol resistant foams are effective extinguishing agents for polar, non-polar, and water-soluble liquid fires. These foams are preferred for fighting flammable liquid fires except those that involve water reactive flammable liquids.
- Stop or confine gas flow before attempting to extinguish fire (NFPA, 1994) AAR, 1994).
- Keep fire-exposed containers of ethylamine cool by spraying with water. Dilute aqueous solutions thoroughly to avoid ignition or burn (NFPA, 1994).
- Use water, dry chemical, or alcohol resistant foam to extinguish fires involving ethylamine (NFPA, 1994). Solid streams of water may be ineffective (AAR, 1994).
When heated to decomposition, ethylamine emits nitrogen oxides and amine vapors (NFPA, 1994; Lewis, 1994).
EXPLOSION HAZARD
- Ethylamine is a moderate explosion hazard in a flammable situation (Lewis, 1994).
- Containers of ethylamine may explode in fire (NJFS , 1996).
- Ethylamine may explode in enclosed areas (NJFS , 1996).
DUST/VAPOR HAZARD
- Ethylamine vapors may travel to a source of ignition and flash back (NFPA, 1994).
- Vapors are flammable when mixed with air (ITI, 1988).
- Ethylamine vapor was reported to produce vision disturbances and decreased olfaction sensitivity in humans (Clayton & Clayton, 1994).
REACTIVITY HAZARD
- Ethylamine reacts with acids, chlorine, hypochlorite, halogenated compounds, and some metals. It also reacts with oxidizing materials and reactive organic compounds (NFPA, 1994).
- Ethylamine has a strong alkaline reaction (Budavari, 1989).
- When heated to decomposition, ethylamine emits nitrogen oxides and amine vapors (NFPA, 1994).
- Do not mix ethylamine with oxidizing agents such as hypochlorite. This mixture creates chlor-amines which are explosive. Distant ignition and flashback are possible. Combustion of the product generates harmful gases (Anon, 1997).
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 118 (ERG, 2004)
- LARGE SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least at least 50 meters (150 feet) in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (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.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (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 118 (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.
- PUBLIC SAFETY MEASURES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132(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.
- Evacuate a one-third mile radius if containers of ethylamine are directly exposed to flame or if a fire involving ethylamine becomes uncontrolled (AAR, 1994).
- For leaks involving ethylamine consider evacuation of the area downwind of the spilled material. Additional criteria for determining evacuation should be: the size of the spill, the location, and the weather conditions (AAR, 1994).
- AIHA ERPG Values for CAS75-04-7 (AIHA, 2006):
- DOE TEEL Values for CAS75-04-7 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Ethylamine (Monoethylamine, Ethylamine anhydrous) TEEL-0 (units = ppm): 7.5 TEEL-1 (units = ppm): 7.5 TEEL-2 (units = ppm): 49 TEEL-3 (units = ppm): 270 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 CAS75-04-7 (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; 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, 2007; 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, 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, 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, 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: Ethylamine (EA) Proposed Value: AEGL-1 10 min exposure: ppm: 7.5 ppm mg/m3: 14 mg/m(3)
30 min exposure: ppm: 7.5 ppm mg/m3: 14 mg/m(3)
1 hr exposure: ppm: 7.5 ppm mg/m3: 14 mg/m(3)
4 hr exposure: ppm: 7.5 ppm mg/m3: 14 mg/m(3)
8 hr exposure: ppm: 7.5 ppm mg/m3: 14 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: Ethylamine (EA) Proposed Value: AEGL-2 10 min exposure: ppm: 150 ppm mg/m3: 280 mg/m(3)
30 min exposure: ppm: 76 ppm mg/m3: 140 mg/m(3)
1 hr exposure: ppm: 49 ppm mg/m3: 90 mg/m(3)
4 hr exposure: ppm: 22 ppm mg/m3: 40 mg/m(3)
8 hr exposure: ppm: 14 ppm mg/m3: 26 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: Ethylamine (EA) Proposed Value: AEGL-3 10 min exposure: ppm: 810 ppm mg/m3: 1500 mg/m(3)
30 min exposure: ppm: 420 ppm mg/m3: 770 mg/m(3)
1 hr exposure: ppm: 270 ppm mg/m3: 500 mg/m(3)
4 hr exposure: ppm: 120 ppm mg/m3: 220 mg/m(3)
8 hr exposure: ppm: 76 ppm mg/m3: 140 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 CAS75-04-7 (National Institute for Occupational Safety and Health, 2007):
IDLH: 600 ppm Note(s): Not Listed
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (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. If possible, turn leaking containers so that gas escapes rather than liquid. Use water spray to reduce vapors or divert vapor cloud drift. Avoid allowing water runoff to contact spilled material. Do not direct water at spill or source of leak. Isolate area until gas has dispersed.
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004) Fully encapsulating, vapor protective clothing should be worn for spills and leaks with no fire. 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 with earth, sand or other non-combustible material and transfer to containers (except for Hydrazine). Use clean non-sparking tools to collect absorbed material.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 118 (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.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004) Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective 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.
Continuously spray leaks with water to keep containers cool and to protect vapors and people (Anon, 1997).
In a large evaporating dish, add ethylamine to sodium bisulfate and spray with sufficient water. After neutralization, route to a sewage plant (OHM/TADS , 1996). Incineration of ethylamine is controversial and disposal practices are subject to significant revision. Contact local environment agencies for current disposal guidelines (HSDB , 1996). Preferred method of disposal is incineration (Anon, 1997). 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
- Ethylamine has been reported to occur naturally in various species of marine algae and in tobacco leaves. It can also occur naturally as a decomposition product of amino acids and as a volatile emission product from animal waste. Ethylamine has also been detected as occurring naturally in various foods(HSDB, 2003).
- Ethylamine's production and use in resin chemistry and organic synthesis, as an intermediate for dyestuffs and medicinals, in oil refining, as a stabilizer for rubber latex, and as a component of tobacco smoke may result in its release to the environment through various waste streams (HSDB, 2003).
ENVIRONMENTAL FATE AND KINETICS
SURFACE WATER Ethylamine will biodegrade or volatilize with an approximate half-life of 4 days in shallow water (HSDB , 1996). Adsorption to humic materials and clays found in sediment may be an important aquatic fate process (HSDB , 1996).
ABIOTIC DEGRADATION
- Ethylamine is not expected to chemically hydrolyze in environmental conditions. Its main chemical loss mechanism is by reacting with the photochemically generated hydroxyl radicals in the environment (HSDB , 1996).
BIODEGRADATION
- Rapid degradation of ethylamine was observed when activated and non-activated sludge cultures were present (HSDB , 1996)
- Ethylamine can be degraded using biological sewage treatment. Appropriate acclimation must be achieved (HSDB , 1996).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Ethylamine is a colorless gas or liquid with an ammonia-like odor below 17.2 degrees C (ACGIH, 1991) Anon, 1997).
- In its liquid state its appearance is water-white (NIOSH , 1996).
- Ethylamine is volatile and flammable (Budavari, 1989; Lewis, 1993).
VAPOR PRESSURE
- 400 mmHg (at 2.9 degrees C) (Clayton & Clayton, 1994)
- 400 mmHg (at 2 degrees C) (ACGIH, 1991)
- 400 mmHg (at 20 degrees C) (Lewis, 1994)
- 1.18 mmHg (at 20 degrees C; 68 degrees F) (NJFS , 1996)
- 873 mmHg (at 20 degrees C) (HSDB , 1996)
- 116 kPa for Anhydrous and 60 kPa for 70% solution (Anon, 1997)
SPECIFIC GRAVITY
- OTHER TEMPERATURE AND/OR PRESSURE
0.662 g/mL (at 20/4 degrees C) (Lewis, 1994) 0.6836 g/mL (at 20/20 degrees C) (Clayton & Clayton, 1994) 0.689 g/mL (at 15/15 degrees C) (Budavari, 1989)
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
-80.6 degrees C (Lewis, 1994) -81.2 degrees C (Lewis, 1993) -114 degrees F (NIOSH , 1996)
BOILING POINT
- 17 degrees C; 62 degrees F (NFPA, 1994)
- 16.6 degrees C (Budavari, 1989; Clayton & Clayton, 1994; Lewis, 1994)
FLASH POINT
- -0.4 degrees F (Lewis, 1994)
- < -18 degrees C; 0 degrees F (NFPA, 1994)
- approximately -17.7 degrees C; 0 degrees F (open cup) (Lewis, 1993)
- < -17 degrees C (closed cup) (ACGIH, 1991)
AUTOIGNITION TEMPERATURE
- 385 degrees C; 725 degrees F (NFPA, 1994; Lewis, 1994)
EXPLOSIVE LIMITS
SOLUBILITY
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = -0.13 (HSDB , 1996)
HENRY'S CONSTANT
- 1.02x10(-5) atm-m(3)/mol (at 25 degrees C) (measured) (HSDB , 1996)
OTHER/PHYSICAL
pKa = 10.71 (Clayton & Clayton, 1994) pKb = 3.29 (Clayton & Clayton, 1994)
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