TRIETHYLAMINE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
TRIETHYLAMINE (DIETHYLAMINO)ETHANE N,N-DIETHYLETHANAMINE ETHANAMINE, N,N-DIETHYL- TEA TEN TRIAETHYLAMIN (German) TRIETILAMINA (Italian) TEN (TRIETHYLAMINE)
IDENTIFIERS
SYNONYM REFERENCE
- (RTECS , 1995; HSDB , 1995)
USES/FORMS/SOURCES
Triethylamine is used in the preparation of quaternary ammonium compounds (Budavari, 1989). It is also used as a catalytic solvent in chemical synthesis; as accelerator activators for rubber; for curing and hardening of polymers (eg, corebinding resins); as a corrosion inhibitor; and in propellants (Lewis, 1993). Triethylamine has also been used to extract organic contaminants from soils, sludges, and sediments (Meckes et al, 1993).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- The primary clinical effects are irritation of the eyes, skin, and lungs, as well as central nervous system stimulation.
- Ingestions have not been reported, but irritation or burns of the esophagus or gastrointestinal tract may be predicted to occur based on this agent's alkalinity and other irritant properties.
- Myocardial degeneration was reported in rabbits exposed to 100 ppm for 6 weeks. This effect has not been reported in humans. This agent produces marked irritation of the lungs. Rabbits exposed to concentrations as low as 100 ppm developed pulmonary injury within 6 weeks. By extrapolation of animal data, pulmonary edema might be expected in severe exposures.
- Triethylamine's central nervous system stimulant properties appear to be closely related to its inhibitory action on monoamine oxidase activity. Faintness and anxiety have been transient symptoms reported with agents in this class. Headache may be seen with systemic absorption.
- Nausea has been a transient symptom reported by workers. Cellular necrosis of the liver was noted in rabbits exposed to 100 ppm for 6 weeks. This effect has not been reported in humans.
- Triethylamine is irritating to the eyes and may cause corneal damage. A drop in rabbit eyes caused severe injury graded 9 on a scale of 1 to 10 after 24 hours. Chronic exposure to concentrations as low as 50 ppm has caused multiple erosions of the cornea and conjunctiva in rabbit eyes. Eye irritation and corneal edema have been reported in humans from industrial exposure.
- This agent may cause dermatitis and skin burns. It may also be a sensitizing agent.
- Experimental reproductive effects and experimental mutation data have been reported.
- 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.
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- 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. 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, cardiovascular system, liver and kidneys (National Institute for Occupational Safety and Health, 2007).
SUMMARY The alkalinity of triethylamine produces its primary toxic irritant effects. Move victims of inhalation exposure from the toxic atmosphere and administer 100 percent supplemental oxygen with assisted ventilation as required. Exposed skin and eyes should be copiously flushed with water. In ingestion exposures, inducing emesis should be avoided and gastric lavage done only with caution. Immediate dilution with milk or water might be beneficial.
ORAL/PARENTERAL EXPOSURE 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. 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. SEIZURES CNS stimulation has been reported, but to date seizures have not. SEIZURES: Administer a benzodiazepine; DIAZEPAM (ADULT: 5 to 10 mg IV initially; repeat every 5 to 20 minutes as needed. CHILD: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed) or LORAZEPAM (ADULT: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed, if seizures persist. CHILD: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed, if seizures continue). Consider phenobarbital or propofol if seizures recur after diazepam 30 mg (adults) or 10 mg (children greater than 5 years). Monitor for hypotension, dysrhythmias, respiratory depression, and need for endotracheal intubation. Evaluate for hypoglycemia, electrolyte disturbances, and hypoxia.
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. A number of chemicals produce abnormalities of the hematopoietic system, liver, and kidneys. Monitoring complete blood count, urinalysis, and liver and kidney function tests is suggested for patients with significant 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. If respiratory tract irritation or respiratory depression is evident, monitor arterial blood gases, chest x-ray, and pulmonary function tests. Respiratory tract irritation, if severe, can progress to pulmonary edema which may be delayed in onset up to 24 to 72 hours after exposure in some cases. 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.
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 severe eye irritation or corneal damage is present, prolonged initial flushing and early ophthalmologic consultation may be advisable.
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.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
Exposure of six rats to 1,000 ppm for 4 hours was lethal to one (Hathaway et al, 1991). GUINEA PIGS - All animals survived 250 to 500 ppm exposures and 2,000 ppm for 30 minutes, but 4 died when exposures were continued to 2 hours. One-third of the animals exposed to 1,000 ppm for 4 hours died (ACGIH, 1980).
MAXIMUM TOLERATED EXPOSURE
The lowest published toxic concentration via inhalation for humans is 12 mg/m(3)/11W-C. Toxic effects noted were changes to the visual field (RTECS , 1994). Two volunteers exposed to approximately 4.5 ppm for 8 hours experienced slight subjective visual disturbances (Hathaway et al, 1991). At 12 ppm for 1 hour, subjects experienced heavy hazing of the visual field, an inability to distinguish outlines of objects 100 meters or more away, and bluish halos around lights. There was a pronounced increase in corneal thickness. Effects are reversible, and it appears that even repeated bouts of edema do not cause permanent damage to the cornea (Hathaway et al, 1991).
Among 19 workers repeatedly exposed to time-weighted average levels of 3 ppm with brief excursions to higher levels, five workers reported foggy vision, blue haze, and halo phenomena on 47 occasions over an 11-week period (Hathaway et al, 1991).
Rabbits survived exposures to 100 ppm daily for 6 weeks, but showed pulmonary irritation, myocardial degeneration, and cellular necrosis of the liver and the kidneys (Hathaway et al, 1991). At 50 ppm, the effects on the lungs, liver, and kidneys were less severe, but there was also damage to the cornea.
Exposure of rats to 25 or 247 ppm, 6 hours/day, 5 days/week for up to 28 weeks, caused no statistically significant treatment related effects (Hathaway et al, 1991).
- Carcinogenicity Ratings for CAS121-44-8 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A4 ; Listed as: Triethylamine EPA (U.S. Environmental Protection Agency, 2011): Not Assessed under the IRIS program. ; Listed as: Triethylamine 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: Triethylamine 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 CAS121-44-8 (U.S. Environmental Protection Agency, 2011):
Oral: Inhalation: Unit Risk: RfC: 7x10(-3) mg/m3
Drinking Water:
References: RTECS, 1995 Lewis, 1992 ACGIH, 1991 Note: All data below are from RTECS (1995) unless otherwise noted. LC50- (INHALATION)MOUSE: 6 g/m(3) for 2H 1450 ppm for 4H (ACGIH, 1991) 460 ppm for 2H (ACGIH, 1991)
LCLo- (INHALATION)GUINEA_PIG: LCLo- (INHALATION)MOUSE: LCLo- (INHALATION)RAT: LD50- (INTRAPERITONEAL)MOUSE: LD50- (ORAL)MOUSE: LD50- (SKIN)RABBIT: 570 mg/kg 420 mg/kg (ACGIH, 1991)
LD50- (ORAL)RAT: LDLo- (INTRAPERITONEAL)RAT: TCLo- (INHALATION)HUMAN: TDLo- (ORAL)RABBIT:
CALCULATIONS
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS121-44-8 (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 CAS121-44-8 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS121-44-8 (National Institute for Occupational Safety and Health, 2007):
Listed as: Triethylamine REL: IDLH: IDLH: 200 ppm Note(s): Not Listed
- OSHA PEL Values for CAS121-44-8 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS121-44-8 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS121-44-8 (U.S. Environmental Protection Agency, 2010):
Listed as: Triethylamine Final Reportable Quantity, in pounds (kilograms): Additional Information: Listed as: Ethanamine, N,N-diethyl- Final Reportable Quantity, in pounds (kilograms): Additional Information:
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS121-44-8 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS121-44-8 (U.S. Environmental Protection Agency, 2010b):
Listed as: Ethanamine, N,N-diethyl- P or U series number: U404 Footnote: Listed as: Triethylamine P or U series number: U404 Footnote: Editor's Note: The D, F, and K series waste numbers and Appendix VIII to Part 261 -- Hazardous Constituents were not included. Please refer to 40 CFR Part 261.
- EPA SARA Title III, Extremely Hazardous Substance List for CAS121-44-8 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS121-44-8 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS121-44-8 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS121-44-8 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1296 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1296 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS121-44-8 (NFPA, 2002):
Listed as: Triethylamine Hazard Ratings: Health Rating (Blue): 3 (3) Seriously toxic material. Short term exposure could cause serious temporary or residual injury even though prompt medical treatment is given. Includes known or suspect small animal carcinogens, mutagens, or teratogens.
Flammability Rating (Red): 3 (3) Flammable. Liquids and solids that can be ignited under almost all ambient temperature conditions. Including liquids with a flash point below 73 degrees F and a boiling point above 100 degrees F, solid materials which form coarse dusts that burn rapidly without becoming explosive, materials which burn rapidly by reason of self-contained oxygen (ie, organic peroxides), and materials which ignite spontaneously when exposed to air.
Instability Rating (Yellow): 0 Oxidizer/Water-Reactive Designation: Not Listed
-HANDLING AND STORAGE
STORAGE
- ROOM/CABINET RECOMMENDATIONS
-PERSONAL PROTECTION
SUMMARY
- 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.
- Avoid breathing vapors. Keep upwind. Avoid bodily contact with the material. Wear appropriate chemical protective clothing, including goggles or face shield, and rubber gloves. Do not handle broken packages unless wearing appropriate personal protective equipment. Wash away any material which may have contacted the body with copious amounts of water or soap and water. Wear positive pressure self-contained breathing apparatus when fighting fires involving this material (AAR, 1992; CHRIS , 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 121-44-8.
-PHYSICAL HAZARDS
FIRE HAZARD
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.
Triethylamine is a very dangerous fire hazard when exposed to heat, flame, or oxidizers (Lewis, 1992). Vapors are heavier than air and may travel to a source of ignition and flash back (NFPA, 1991). Aqueous solutions are flammable unless diluted extensively (NFPA, 1991).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS121-44-8 (NFPA, 2002):
Listed as: Triethylamine Flammability Rating: 3 (3) Flammable. Liquids and solids that can be ignited under almost all ambient temperature conditions. Including liquids with a flash point below 73 degrees F and a boiling point above 100 degrees F, solid materials which form coarse dusts that burn rapidly without becoming explosive, materials which burn rapidly by reason of self-contained oxygen (ie, organic peroxides), and materials which ignite spontaneously when exposed to air.
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004)
- 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.
- NFPA Extinguishing Methods for CAS121-44-8 (NFPA, 2002):
- To fight fires, use carbon dioxide, dry chemical, or alcohol foam (Lewis, 1992; AAR, 1992).
- Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use water spray to knock down vapors (AAR, 1992).
Triethylamine may have hazardous reactions with oxidizing materials (Lewis, 1992). Triethylamine is dangerous when exposed to heat, flames, or oxidizing materials (Lewis, 1992). When heated to decomposition, triethylamine emits toxic fumes of oxides of nitrogen (Lewis, 1992). Products of decomposition include carbon monoxide, carbon dioxide, hydrocarbons, and oxides of nitrogen, as well as amine vapors (NFPA, 1991).
EXPLOSION HAZARD
- Triethylamine is explosive in the form of vapor when exposed to heat or flame (Lewis, 1992).
- The complex with dinitrogen tetraoxide explodes below 0 degrees C when undiluted with solvent (Lewis, 1992).
DUST/VAPOR HAZARD
- Triethylamine vapors are irritating to the eyes and mucous membranes (AAR, 1992).
- Vapors are heavier than air and may travel to a source of ignition and flash back (NFPA, 1991).
- Vapor may explode if ignited in an enclosed area (CHRIS , 1994).
REACTIVITY HAZARD
- Triethylamine does not react with water or common materials (CHRIS , 1995).
- Triethylamine may have hazardous reactions with oxidizing materials (Lewis, 1992).
- Triethylamine is dangerous when exposed to heat, flames, or oxidizing materials (Lewis, 1992).
- It is strongly alkaline (HSDB , 1995).
- Triethylamine may react violently when exposed to strong acid (HSDB , 1995).
- Triethylamine emits toxic fumes when heated to decomposition (HSDB , 1995).
- Triethylamine forms an exothermic reaction with maleic anhydride above 150 degrees C, producing carbon dioxide gas (Lewis, 1992; Bretherick, 1990).
- Triethylamine is incompatible with N2O4 (Lewis, 1992).
- Triethylamine may react with acids, oxidizing materials, chlorine, hypochlorite, halogenated compounds, reactive organic compounds, and some metals (NFPA, 1991).
- Products of decomposition include carbon monoxide, carbon dioxide, hydrocarbons, and oxides of nitrogen, as well as amine vapors (NFPA, 1991).
- A mixture of triethylamine and dinitrogen tetraoxide, containing more oxide than amine and free of solvent, exploded below 0 degrees C (Bretherick, 1990).
- Liquid triethylamine will attack some forms of plastics, rubber, and coatings (HSDB , 1994).
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 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 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 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.
- If fire becomes uncontrollable or container is exposed to direct flame, consider evacuation of one-third mile radius (AAR, 1992).
- If material is leaking, but is not on fire, consider evacuation from downwind area based on amount of material spilled, location, and weather conditions (AAR, 1992).
- AIHA ERPG Values for CAS121-44-8 (AIHA, 2006):
- DOE TEEL Values for CAS121-44-8 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS121-44-8 (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):
- NIOSH IDLH Values for CAS121-44-8 (National Institute for Occupational Safety and Health, 2007):
IDLH: 200 ppm Note(s): Not Listed
CONTAINMENT/WASTE TREATMENT OPTIONS
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 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.
At the time of this review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices (HSDB , 1994). Triethylamine has been used to extract organic contaminants from soils, sludges, and sediments. The technology was demonstrated as part of EPA's Superfund Innovative Technology Evaluation (SITE) program. The purpose of the SITE program is to assess the effectiveness of developing technologies in treating waste streams from uncontrolled hazardous waste sites. The demonstrated process is a separation technology. Materials are separated into three fractions: oil, water, and solids (Meckes et al, 1993).
LARGE SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004) Eliminate all ignition sources. Approach release from upwind. Use water spray to cool and disperse vapors, protect personnel, and dilute spills to form nonflammable mixtures. Absorb in noncombustible material for proper disposal. Control runoff and isolate discharged material for proper disposal. Report any release in excess of 5000 pounds (NFPA, 1991). Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Attempt to stop leak if it can be done without undue personnel hazard. Use water spray to disperse vapors and dilute standing pools of liquid (AAR, 1992). Land Spill: Dig a pit, pond, lagoon, or holding area to contain liquid or solid material (AAR, 1992). Land Spill: Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete (AAR, 1992). Land Spill: Absorb bulk liquid with fly ash, cement powder, or commercial sorbents (AAR, 1992). Land Spill: Apply "universal" gelling agent to immobilize spill (AAR, 1992). Land Spill: Neutralize with sodium bisulfate (NaHSO4) (AAR, 1992). Water Spill: Add sodium bisulfate (NaHSO4) (AAR, 1992). Water Spill: If dissolved in region of 10 ppm or greater concentration, apply activated carbon at ten times the spilled amount (AAR, 1992). Water Spill: Use mechanical dredges or lifts to remove immobilized masses of pollutants and precipitates (AAR, 1992). Air Release: Apply water spray or mist to knock down vapors (AAR, 1992). Air Release: Vapor knockdown water is corrosive or toxic and should be diked for containment (AAR, 1992).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Triethylamine is produced in large quantities. Large amounts of the chemical may be released to the environment, primarily in emissions and wastewater, during its production and use. It also occurs in some food and as a metabolic product (HSDB , 1994).
ENVIRONMENTAL FATE AND KINETICS
In the atmosphere, triethylamine will react with photochemically produced hydroxyl radicals. Degradation half-lives are not available for clean atmospheres, but in polluted atmospheres triethylamine completely degrades photochemically in 90 minutes. It will also be scavenged by rain. Triethylamine is a precursor of dimethylnitrosamine. The latter is formed in the atmosphere in the presence of nitrogen oxides (HSDB , 1994).
BIOACCUMULATION
Using a reported log octanol/water partition coefficient of 1.45, an estimated bioconcentration factor of 7.45 was calculated for triethylamine using a recommended regression equation. Triethylamine would therefore not be expected to bioconcentrate in aquatic organisms (HSDB , 1994).
ENVIRONMENTAL TOXICITY
- ECOTOXICITY VALUES (HSDB , 1994)
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Triethylamine is a colorless liquid with strong ammonia or fish-like odor (Budavari, 1989; AAR, 1992; Lewis, 1992).
- Triethylamine is lighter than water and floats on water. It produces a flammable, irritating vapor (CHRIS , 1995; AAR, 1992).
- HYDROCHLORIDE: Triethylamine hydrochloride occurs in the form of crystals from alcohol (Budavari, 1989).
PH
- Approximately 9-10 (aqueous solutions) (Grant, 1986)
VAPOR PRESSURE
- 54 mmHg (at 20 degrees C) (NFPA, 1991)
- 400 mmHg (at 31.5 degrees C) (HSDB , 1994)
SPECIFIC GRAVITY
- NORMAL TEMPERATURE AND PRESSURE
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
-115 degrees C (Budavari, 1989) HYDROCHLORIDE: 253-254 degrees C (sublimes at 245 degrees C) (Budavari, 1989)
BOILING POINT
- 89-90 degrees C (Budavari, 1989)
FLASH POINT
- -6 degrees C; 20 degrees F (closed cup) (Budavari, 1989)
- -9 degrees C; 16 degrees F (open cup) (NFPA, 1991)
AUTOIGNITION TEMPERATURE
- 249 degrees C; 480 degrees F (NFPA, 1991)
- 842 degrees F (CHRIS , 1994)
EXPLOSIVE LIMITS
SOLUBILITY
Triethylamine is slightly soluble in water above 18.7 degrees C. It is also miscible with water below 18.7 degrees C (Budavari, 1989). Triethylamine hydrochloride is soluble in 0.7 parts water (Budavari, 1989).
Triethylamine is miscible with alcohol and ether (Budavari, 1989). Triethylamine hydrochloride is soluble in alcohol and chloroform. It is very slightly soluble in benzene and practically insoluble in ether (Budavari, 1989).
OTHER/PHYSICAL
pKa: 10.75 (Clayton & Clayton, 1994) pKb: 3.25 (Clayton & Clayton, 1994)
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