DIETHYLAMINE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
DIETHYLAMINE DEN DIAETHYLAMIN (German) DIETHAMINE N,N-DIETHYLAMINE DIETILAMINA (Italian) DWUETYLOAMINA (Polish) ETHANAMINE, N-ETHYL-
IDENTIFIERS
USES/FORMS/SOURCES
DIETHYLAMINE (DEN) is a colorless, volatile, flammable liquid with a fishy, ammoniacal odor (HSDB). It is miscible with water and alcohol, and is soluble in ether (HSDB). It is a FIRE AND EXPLOSION HAZARD (HSDB). It can react with NITRITES to form diethylnitrosamine, an experimental animal carcinogen (HSDB). DEN is apparently not metabolized in humans and is excreted unchanged in the urine (HSDB). It is thought to be more toxic than ammonia (HSDB); however, no reports of industrial fatalities were found at the time of this review. With an odor threshold reported to range from 0.05 ppm (ACGIH, 1986) to 0.14 ppm (NIOSH/OSHA), odor is a good warning property. However, odor alone should never be used to determine if an environment is safe.
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- 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
- DEN is an irritant and might be corrosive in some circumstances (HSDB). It is a mild to moderate skin irritant and a severe eye irritant in experimental animals (RTECS , 1996). Exposure to the vapors can cause swelling of the cornea, resulting in foggy vision and/or halos around lights. Serious eye injury can occur with direct DEN contact (NIOSH/OSHA). Irritation or burns resulting in necrosis can occur with direct skin contact (ACGIH, 1986).
- When taken orally, DEN can cause severe pain, vomiting, diarrhea, cardiovascular collapse (HSDB), breathing difficulty, and chest pain (NIOSH/OSHA). It has caused liver and heart damage in experimental animals (ACGIH, 1986), as well as articaria and allergic rhinitis (RTECS , 1996).
CHRONIC CLINICAL EFFECTS
- The effects of long-term exposure to DEN are similar to its acute effects, including foggy vision, halos around lights (NIOSH/OSHA), and irritation of the lungs, bronchi and throat (ACGIH, 1986). Pulmonary edema has occured in exposed experimental animals (ACGIH, 1986).
- Rats exposed to DEN by the inhalation route for 24 weeks developed nasal lesions (Lynch, 1986). DEN exposed rats and humans developed subtle effects in the central nervous system (Tkachev, 1971; Tkachev, 1971).
-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.
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 - EYE EXPOSURE - DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility.
ORAL EXPOSURE -
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
Rabbits experienced corneal damage and pulmonary irritation after being repeatedly exposed to diethylamine vapor 50 ppm for 7 hours daily (Hathaway et al, 1991). Mild irritation of rabbits' skin was reported following dermal exposures to 10 mg for 24 hours (Lewis, 1992). Any solution 1% or stronger applied to rabbits' eyes resulted in corneal opacity (ACGIH, 1991). Experimental animals given lethal doses of diethylamine by inhalation have experienced lacrimation, muscle contraction or spasticity, and cyanosis before death (RTECS , 1993).
- Carcinogenicity Ratings for CAS109-89-7 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A4 ; Listed as: Diethylamine 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: Diethylamine 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 CAS109-89-7 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS109-89-7 (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 CAS109-89-7 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS109-89-7 (National Institute for Occupational Safety and Health, 2007):
Listed as: Diethylamine REL: TWA: 10 ppm (30 mg/m(3)) STEL: 25 ppm (75 mg/m(3)) Ceiling: Carcinogen Listing: (Not Listed) Not Listed Skin Designation: Not Listed Note(s):
IDLH: IDLH: 200 ppm Note(s): Not Listed
- OSHA PEL Values for CAS109-89-7 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS109-89-7 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS109-89-7 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS109-89-7 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS109-89-7 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS109-89-7 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS109-89-7 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS109-89-7 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS109-89-7 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1154 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1154 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS109-89-7 (NFPA, 2002):
Listed as: Diethylamine 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
Usual containers include glass bottles, drums, and cans: Keep them tightly covered (NFPA, 1991; OHM/TADS , 1993).
- ROOM/CABINET RECOMMENDATIONS
Store in a cool, dry, well-ventilated, non-combustible location (NFPA, 1991). Outdoor or detached storage is preferred (ITI, 1988).
Keep away from acids, sources of halogens, and oxidizing materials (NFPA, 1991). Keep away from sunlight (ITI, 1988).
-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.
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 109-89-7.
-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.
Diethylamine is a very dangerous fire hazard when it is exposed to heat, flame, or oxidizers (Lewis, 1992; Bretherick, 1990). This compound ignites on contact with large amounts of cellulose nitrate (Lewis, 1992). It explodes on contact with dicyanofurazan and reacts violently with sulfuric acid (Lewis, 1992). When heated to combustion, diethylamine emits toxic fumes of nitrogen oxides (Lewis, 1992; Bretherick, 1990). Vapors may travel to a source of ignition and flash back (NFPA, 1991).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS109-89-7 (NFPA, 2002):
Listed as: Diethylamine 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 CAS109-89-7 (NFPA, 2002):
- Diethylamine is a very dangerous fire hazard when it is exposed to heat, flame, or oxidizers (Lewis, 1992; Bretherick, 1990).
- If diethylamine is involved in a fire, do not try to extinguish unless flow can be stopped. Use large quantities of water as a fog and to cool containers of diethylamine. Use alcohol foam, CO2, or dry chemical (Lewis, 1992) AAR, 1987).
- Vapors may travel to a source of ignition and flash back (NFPA, 1991).
Diethylamine is a very dangerous hazard when it is exposed to heat, oxidizers, or flame (Lewis, 1992; OHM/TADS , 1993). When heated to combustion, diethylamine emits toxic fumes of nitrogen oxides, carbon monoxide, carbon dioxide, hydrocarbons, and toxic amine vapors (ACGIH, 1991; Lewis, 1992; NFPA, 1991).
EXPLOSION HAZARD
- Vapor forms explosive mixture with air, and may travel to a source of ignition and flash back (NFPA, 1991; OHM/TADS , 1993).
- Diethylamine explodes on contact with dicyanofurazan (Lewis, 1992; Bretherick, 1990).
- It reacts violently with sulfuric acid (Lewis, 1992).
DUST/VAPOR HAZARD
- Vapor forms explosive mixture with air, and may travel to a source of ignition and flash back (NFPA, 1991; OHM/TADS , 1993).
- Vapors are toxic and in sufficient concentrations can cause tracheitis, bronchitis, pneumonitis, and pulmonary edema as well as caustic burns to skin, eyes, and mucous membranes (NFPA, 1991).
REACTIVITY HAZARD
- Diethylamine is highly reactive with oxidizers and acids (Lewis, 1992).
- It explodes on contact with dicyanofurazan and reacts violently with sulfuric acid (Lewis, 1992; Bretherick, 1990).
- It ignites on contact with large amounts of cellulose nitrate (Lewis, 1992).
- Diethylamine also reacts with chlorine, hypochlorite, halogenated compounds, reactive organic compounds, and some metals (NFPA, 1991).
- Diethylamine is a very dangerous fire hazard when it is exposed to heat, flame, or oxidizers (Lewis, 1992; Bretherick, 1990).
- When heated to combustion, diethylamine emits toxic fumes of nitrogen oxides, carbon monoxide, carbon dioxide, hydrocarbons, and toxic amine vapors (ACGIH, 1991; Lewis, 1992; NFPA, 1991).
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.
- AIHA ERPG Values for CAS109-89-7 (AIHA, 2006):
- DOE TEEL Values for CAS109-89-7 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS109-89-7 (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):
- NIOSH IDLH Values for CAS109-89-7 (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.
Wear appropriate clothing and avoid all bodily contact with diethylamine. Keep heat, sparks, and oxidizing materials away from the material. Build dikes to contain flow if necessary; keep material out of water sources and sewers. If not too risky, attempt to stop the leak. Use water spray to disperse vapors and dilute pools of standing liquid (AAR, 1987). Use sand, peat, or carbon to absorb water and place into containers for later disposal (HSDB , 1993; OHM/TADS , 1993). Acetic acid can be used to neutralize water. Neutral or acidic solutions may be run through a cation exchanger (OHM/TADS , 1993). Diethylamine may be poured into sodium bisulfate in a large evaporating dish to neutralize (ITI, 1988; OHM/TADS , 1993). It may be dissolved in a combustible solvent, such as alcohol, and then burned in an open furnace carefully. The remainder may sprayed into the chamber of a furnace with an afterburner and scrubber (ITI, 1988; OHM/TADS , 1993). Contact the local sewage or air authority to discuss disposal (OHM/TADS , 1993).
For very small spills, remove all sources of ignition and ventilate the area. Wear protective clothing; absorb the spill onto paper towels. Evaporate the absorbed liquid in a fume hood. Burn the paper in a location away from combustible materials (HSDB , 1993).
LARGE SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 132 (ERG, 2004) Seek professional environmental engineering assistance through EPA's Environmental Response Team, 24-hour phone (201) 321-6660 (OHM/TADS , 1993). Land Spill: Dig a holding area to contain liquid material. Dike the surface flow using soil, sand bags, polyurethane, or foamed concrete. Absorb bulk liquid with cement powder, carbon, fly ash, or commercial sorbents. Neutralize with sodium bisulfate (AAR, 1987). Water Spill: Add sodium bisulfate. If dissolved concentration is greater than or equal to 10 parts per million, apply activated carbon at ten times the spilled amount. Use mechanical dredges to remove immobilized masses of pollutants and precipitates (AAR, 1987). Air Release: Apply water spray or mist to knock down vapors. Used knockdown water is corrosive and toxic and should be contained and treated as described above (AAR, 1987). Report any spill in excess of 100 pounds to the National Response Center (800) 424-8802 (HSDB , 1993; NFPA, 1991).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Air: Diethylamine, when released into normal air, rapidly reacts with photochemically produced hydroxyl radicals (exact rate has not been determined). In polluted air, diethylamine degrades within 2 hours. Rain also "washes" diethylamine from the air (HSDB , 1993).
- Water: Diethylamine may be dangerous if it enters water intakes; it may be explosive when confined in boiler feed or cooling system water (OHM/TADS , 1993).
- Water: It is harmful to aquatic life even in very low concentrations. If pollution occurs, notify local health and wildlife officials and operators of nearby water intakes (CHRIS , 1993).
- Water: TLm, freshwater creek chub: 85 mg/L per 48 hours (CHRIS , 1993). Freshwater chubs died after exposure to 100 ppm for 24 hours (OHM/TADS , 1993).
- Soil: No experimental degradation rates are available. Diethylamine would be expected to volatilize quickly and leach readily into the soil (HSDB , 1993).
ENVIRONMENTAL FATE AND KINETICS
OTHER AIR: Diethylamine, when released into normal air, rapidly reacts with photochemically produced hydroxyl radicals (exact rate has not been determined). In polluted air, diethylamine degrades within 2 hours. Rain also "washes" diethylamine from the air (HSDB , 1993). WATER: Diethylamine readily biodegrades in water. In concentrations of 10 ppm, the half-life is 0.9 days (longer for lower concentrations). Diethylamine also volatilizes out of water (half-life: 31.6 hours in a model river) (HSDB , 1993). SOIL: No experimental degradation rates are available. Diethylamine would be expected to volatilize quickly and leach readily into the soil (HSDB , 1993).
ENVIRONMENTAL TOXICITY
- AIR: Vapors are toxic to animals and humans and in sufficient concentrations can cause tracheitis, bronchitis, pneumonitis, and pulmonary edema as well as caustic burns to skin, eyes, and mucous membranes.
- WATER: When dissolved in water, diethylamine is caustic and corrosive and will be toxic to aquatic animals. It is especially dangerous in concentrations of greater than or equal to 10 ppm (AAR, 1987).
TLm, freshwater creek chub: 85 mg/L per 48 hours LD50, fathead minnow (30 days old): 855 mg/L per 96 hours at 24.7 degrees C (HSDB , 1993) There is no food chain concentration potential (CHRIS , 1993).
Diethylamine on or in the soil is caustic and toxic to animals. There is no food chain concentration potential (CHRIS , 1993).
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Diethylamine is a colorless liquid with a fishy, ammonia-like odor (Hathaway et al, 1991; Lewis, 1992).
PH
- This compound is highly alkaline (HSDB , 1993).
VAPOR PRESSURE
- 400 mmHg (at 38 degrees C) (ACGIH, 1991; OHM/TADS , 1993)
- 195 mmHg (at 20 degrees C) (ACGIH, 1991; OHM/TADS , 1993)
- 620 mmHg (at 50 degrees C) (ACGIH, 1991; OHM/TADS , 1993)
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
FREEZING/MELTING POINT
-38.9 degrees C (Lewis, 1992) -50 degrees C (NFPA, 1991)
BOILING POINT
- 55.5 degrees C (Lewis, 1992)
FLASH POINT
- -26 degrees C; -15 degrees F (closed cup) (Sax & Lewis, 1987)
- 5 degrees F (open cup) (CHRIS , 1993)
AUTOIGNITION TEMPERATURE
- 312 degrees C; 594 degrees F (ACGIH, 1991)
EXPLOSIVE LIMITS
SOLUBILITY
It is miscible with alcohol and chloroform (as well as most organic solvents); it is practically insoluble in ether (Budavari, 1989). Diethylamine is somewhat fat-soluble; it will dissolve hot paraffin and carnauba waxes (HSDB , 1993).
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