DIETHANOLAMINE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
AMINE, DIETHYL, 2,2-DIHYDROXY- BIS(2-HYDROXYETHYL)AMINE BIS(HYDROXYETHYL)AMINE DEA DELA 2,2'-DIHYDROXYDIETHYLAMINE DI(2-HYDROXYETHYL)AMINE DIAETHANOLAMIN (German) DIETHANOLAMIN (Czech) DIETHANOLAMINE DIETHYLAMINE, 2,2'DIHYDROXY- n,n-DIETHANOLAMINE DIETHYLOLAMINE DIOLAMINE ETHANOL, 2,2'-IMINOBIS- ETHANOL, 2,2'-IMINODI- 2-((2-HYDROXYETHYL)AMINO)ETHANOL 2,2'-IMINOBISETHANOL 2,2'-IMINODIETHANOL 2,2'-IMINODI-1-ETHANOL IMINODIETHANOL
IDENTIFIERS
SYNONYM REFERENCE
- ACGIH, 1996(a); Ashford, 1994; HSDB, 1998; RTECS, 1998
USES/FORMS/SOURCES
This compound may be used in manufacturing surface active agents used in textile specialties, herbicides, and petroleum demulsifiers (Budavari, 1996). Diethanolamine may also be used in liquid detergents for emulsion paints, cutting oils, shampoos, cosmetics, cleaners, and polishes; in textile and dye specialties; in organic syntheses; as an absorbent for acid gases; as a chemical intermediate for resins, plasticizers, and fatty alkanolamides for liquid detergents; for solubilizing 2,4-dichlorophenoxyacetic acid (2,4-D); as a humectant and softening agent; as an emulsifier intermediate for detergents; as an intermediate for rubber chemicals; as a corrosion inhibitor; and as a dispersing agent (Budavari, 1996) Hathaway, et al, 1996; (HSDB , 1998; Lewis, 1993; Sittig, 1991). This compound can also be used with cracking gases and coal or oil gases containing carbonyl sulfide that could react with monoethanolamine (Budavari, 1996).
Diethanolamine is derived through ammonolysis of ethylene oxide (Budavari, 1996; Lewis, 1993). Diethanolamine forms ethanolamine soaps through a reaction with long-chain fatty acids (Hathaway et al, 1996). When diethanolamine is dehydrated, it produces morpholine (HSDB , 1998).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Diethanolamine is irritating to the eyes, skin, and mucous membranes. In experimental animals, exposure has resulted in CNS depression, demyelination of the brain and spinal cord, a poorly regenerative anemia, renal tubular degeneration, hepatocellular cytological alterations and necrosis, fatty degeneration of the liver, cardiac myocyte degeneration, and alopecia. Inflammation, ulceration, hyperkeratosis, and acanthosis have occurred following topical application of diethanolamine.
- A case of diethanolamine-induced asthma has been reported in a worker handling cutting fluid containing diethanolamine. Rare cases of allergic contact dermatitis may occur.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
FIRST AID EYE EXPOSURE - Immediately wash the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately. Contact lenses should not be worn when working with this chemical. DERMAL EXPOSURE - Immediately 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 - 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).
GENERAL - Move victims of inhalation exposure from the toxic environment and administer 100% humidified supplemental oxygen with assisted ventilation as required. Exposed skin and eyes should be copiously flushed with water. Because of the potential for rapid onset of CNS depression or seizures with possible aspiration of gastric contents, EMESIS SHOULD NOT BE INDUCED. Cautious gastric lavage followed by administration of activated charcoal may be of benefit if the patient is seen soon after the exposure.
INHALATION EXPOSURE - INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm. If bronchospasm and wheezing occur, consider treatment with inhaled sympathomimetic agents.
DERMAL EXPOSURE - DECONTAMINATION: Remove contaminated clothing and jewelry and place them in plastic bags. Wash exposed areas with soap and water for 10 to 15 minutes with gentle sponging to avoid skin breakdown. A physician may need to examine the area if irritation or pain persists (Burgess et al, 1999). Treat dermal irritation or burns with standard topical therapy. Patients developing dermal hypersensitivity reactions may require treatment with systemic or topical corticosteroids or antihistamines.
EYE EXPOSURE - DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility.
ORAL EXPOSURE - Because of the potential for gastrointestinal tract irritation or CNS depression, DO NOT induce emesis. Significant esophageal or gastrointestinal tract irritation or burns may occur following ingestion. The possible benefit of early removal of some ingested material by cautious gastric lavage must be weighed against potential complications of bleeding or perforation. PREHOSPITAL ACTIVATED CHARCOAL ADMINISTRATION Consider prehospital administration of activated charcoal as an aqueous slurry in patients with a potentially toxic ingestion who are awake and able to protect their airway. Activated charcoal is most effective when administered within one hour of ingestion. Administration in the prehospital setting has the potential to significantly decrease the time from toxin ingestion to activated charcoal administration, although it has not been shown to affect outcome (Alaspaa et al, 2005; Thakore & Murphy, 2002; Spiller & Rogers, 2002). In patients who are at risk for the abrupt onset of seizures or mental status depression, activated charcoal should not be administered in the prehospital setting, due to the risk of aspiration in the event of spontaneous emesis. The addition of flavoring agents (cola drinks, chocolate milk, cherry syrup) to activated charcoal improves the palatability for children and may facilitate successful administration (Guenther Skokan et al, 2001; Dagnone et al, 2002).
ACTIVATED CHARCOAL: Administer charcoal as a slurry (240 mL water/30 g charcoal). Usual dose: 25 to 100 g in adults/adolescents, 25 to 50 g in children (1 to 12 years), and 1 g/kg in infants less than 1 year old. Observe patients with ingestion carefully for the possible development of esophageal or gastrointestinal tract irritation or burns. If signs or symptoms of esophageal irritation or burns are present, consider endoscopy to determine the extent of injury.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
- Carcinogenicity Ratings for CAS111-42-2 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A3 ; Listed as: Diethanolamine A3 :Confirmed Animal Carcinogen with Unknown Relevance to Humans: The agent is carcinogenic in experimental animals at a relatively high dose, by route(s) of administration, at site(s), of histologic type(s), or by mechanism(s) that may not be relevant to worker exposure. Available epidemiologic studies do not confirm an increased risk of cancer in exposed humans. Available evidence does not suggest that the agent is likely to cause cancer in humans except under uncommon or unlikely routes or levels of exposure.
EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): 3 ; Listed as: Diethanolamine 3 : The agent (mixture or exposure circumstance) is not classifiable as to its carcinogenicity to humans. This category is used most commonly for agents, mixtures and exposure circumstances for which the evidence of carcinogenicity is inadequate in humans and inadequate or limited in experimental animals. Exceptionally, agents (mixtures) for which the evidence of carcinogenicity is inadequate in humans but sufficient in experimental animals may be placed in this category when there is strong evidence that the mechanism of carcinogenicity in experimental animals does not operate in humans. Agents, mixtures and exposure circumstances that do not fall into any other group are also placed in this category.
NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed ; Listed as: Diethanolamine MAK (DFG, 2002): Category 3A ; Listed as: Diethanolamine 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 CAS111-42-2 (U.S. Environmental Protection Agency, 2011):
References: ACGIH, 1996(a); Budavari, 1996; CHRIS, 1998; Clayton & Clayton, 1994; Hathaway, et al, 1996; Lewis, 1996; HSDB, 1998; OHM/TADS, 1998; RTECS, 1998 LD50- (ORAL)GUINEA_PIG: LD50- (SKIN)GUINEA_PIG: LD50- (INTRAPERITONEAL)MOUSE: LD50- (ORAL)MOUSE: LD50- (SUBCUTANEOUS)MOUSE: LD50- (ORAL)RABBIT: LD50- (SKIN)RABBIT: 7640 mcL/kg 12,200 mg/kg 11.9 mL/kg
LD50- (INTRAMUSCULAR)RAT: LD50- (INTRAPERITONEAL)RAT: LD50- (INTRAVENOUS)RAT: LD50- (ORAL)RAT: 710 mg/kg 620 mcL/kg 12.76 g/kg 1.82 g/kg 1410-3460 mg/kg 1410 mg/kg 0.5-5 g/kg
LD50- (SUBCUTANEOUS)RAT:
CALCULATIONS
1 ppm = 4.30 mg/m(3) (at 68 degrees F and 760 mmHg) (NIOSH , 1998) 1 ppm = 4.29 mg/m(3) (at 25 degrees C) (ACGIH, 1996(a)) 1 mg/m(3) = 0.23 ppm (at 25 degrees C) (ACGIH, 1996(a))
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS111-42-2 (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 CAS111-42-2 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS111-42-2 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS111-42-2 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS111-42-2 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS111-42-2 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS111-42-2 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS111-42-2 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS111-42-2 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS111-42-2 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
Listed as: Diethanolamine Effective Date for Reporting Under 40 CFR 372.30: 1/1/87 Lower Thresholds for Chemicals of Special Concern under 40 CFR 372.28:
- DOT List of Marine Pollutants for CAS111-42-2 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS111-42-2 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 2491 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN2491 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS111-42-2 (NFPA, 2002):
-HANDLING AND STORAGE
STORAGE
Diethanolamine is solid at ambient temperature, but can be kept in liquid form at elevated temperatures or as an aqueous solution (OHM/TADS , 1998). Ethanolamines should be stored separate from strong oxidizers (such as chlorine and bromine) and strong acids, (such as hydrochloric, sulfuric, and nitric acids), because violent reactions may occur. These compounds should be stored in tightly closed containers in a cool, well-ventilated area away from heat. Keep sources of ignition such as smoking and open flames away from these compounds (Sittig, 1991). Typical shipping containers include tank cars, trucks, compartment cars, drums, cans, and bottles (OHM/TADS , 1998).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (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. fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
- Persons should avoid breathing vapors and wear appropriate chemical protective clothing to prevent contact with diethanolamine. Contaminated clothing and shoes should be removed and isolated before leaving the site (AAR, 1996). Workers should immediately wash any affected areas as soon as contamination occurs. Eyewash fountains and facilities for quickly drenching the body should be provided in areas where there is any possibility of exposure to this compound (NIOSH , 1998).
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 111-42-2.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004) Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
Diethanolamine is combustible when exposed to heat or flame and can react with oxidizing materials (Lewis, 1996). It does not burn, or burns with difficulty (AAR, 1996). Fires involving this compound may be fought using alcohol foam, water, or carbon dioxide dry chemical (Lewis, 1996).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS111-42-2 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Dry chemical, CO2, alcohol-resistant foam or water spray. Move containers from fire area if you can do it without risk. Dike fire control water for later disposal; do not scatter the material.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Do not get water inside containers. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire.
- NFPA Extinguishing Methods for CAS111-42-2 (NFPA, 2002):
- This compound does not burn, or burns with difficulty (AAR, 1996). When fighting fires involving diethanolamine, alcohol foam, water, or carbon dioxide dry chemical may be used (Lewis, 1996). Run-off water should be kept out of sewers and water sources (AAR, 1996). Water may be used to cool affected containers, disperse the vapors, and prevent the spread of fires (CHRIS , 1998; ITI, 1995).
- OHM/TADS (1998) indicates that alcohol foam should be used because water or foam may cause frothing.
DUST/VAPOR HAZARD
- Diethanolamine, when heated to decomposition, emits toxic fumes of oxides of nitrogen (Lewis, 1996).
REACTIVITY HAZARD
- Diethanolamine reacts with oxidizing materials, strong acids, acid anhydrides, and halides (Lewis, 1996; NIOSH , 1998). This compound may also react with nitrite or oxides of nitrogen to form n-nitrosodiethanolamine (ACGIH, 1996(a)).
- Diethanolamine reacts with carbon monoxide in the air. It is corrosive to copper, zinc, and galvanized iron (HSDB , 1998).
EVACUATION PROCEDURES
- Editor's Note: This material is not listed in the Table of Initial Isolation and Protective Action Distances.
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (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 153 (ERG, 2004)
CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number: MEXICO: SETIQ: 01-800-00-214-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5559-1588; For calls originating elsewhere, call: 011-52-555-559-1588.
CENACOM: 01-800-00-413-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5550-1496, 5550-1552, 5550-1485, or 5550-4885; For calls originating elsewhere, call: 011-52-555-550-1496, or 011-52-555-550-1552; 011-52-555-550-1485, or 011-52-555-550-4885.
ARGENTINA: CIQUIME: 0-800-222-2933 in the Republic of Argentina; For calls originating elsewhere, call: +54-11-4613-1100.
BRAZIL: PRÓ-QUÍMICA: 0-800-118270 (Toll-free in Brazil); For calls originating elsewhere, call: +55-11-232-1144 (Collect calls are accepted).
COLUMBIA: CISPROQUIM: 01-800-091-6012 in Colombia; For calls originating in Bogotá, Colombia, call: 288-6012; For calls originating elsewhere, call: 011-57-1-288-6012.
CANADA: UNITED STATES:
For additional details see the section entitled "WHO TO CALL FOR ASSISTANCE" under the ERG Instructions. As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate enclosed areas.
- AIHA ERPG Values for CAS111-42-2 (AIHA, 2006):
- DOE TEEL Values for CAS111-42-2 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Diethanolamine TEEL-0 (units = mg/m3): 1 TEEL-1 (units = mg/m3): 25 TEEL-2 (units = mg/m3): 150 TEEL-3 (units = mg/m3): 300 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 CAS111-42-2 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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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 CAS111-42-2 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. DO NOT GET WATER INSIDE CONTAINERS.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (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. fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
This compound is a threat to the environment and immediate steps should be taken to limit its spread to the environment. Diethanolamine can penetrate soil and contaminate groundwater and nearby streams. Material should be kept out of water sources and sewers. Dikes may be used to contain flow. Stop leaks, if it can be done without undue personnel hazard (AAR, 1996; (CHRIS , 1998). If diethanolamine is spilled on land, surface flow may be diked using soil, sand bags, foamed polyurethane, or foamed concrete. Bulk liquid may be absorbed with fly ash, cement powder, or commercial sorbents (AAR, 1996). If diethanolamine is spilled in water, trapped material may be removed with suction hoses (AAR, 1996). OHM/TADS (1998) reports that, for alkaline solutions, carbon or peat may be effective in clean-up. Water may be neutralized with dilute acetic acid and treated with cation exchangers.
One disposal method includes adding the contaminated amine to a layer of sodium bisulfate in a large evaporating dish, spraying with water to neutralize, and routing to a sewage plant (OHM/TADS , 1998). 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.
Diethanolamine may be dissolved in a combustible solvent and burned in an open furnace or may be sprinkled into the fire chamber of a furnace with an afterburner and scrubber (ITI, 1995; OHM/TADS , 1998).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Diethanolamine is released to the environment through emissions or effluents from its manufacture and use, from consumer product disposal, and from the application of agricultural chemicals (Howard, 1990). This compound is dangerous to aquatic life in high concentrations and may be dangerous if it enters water intakes (CHRIS , 1998).
ENVIRONMENTAL FATE AND KINETICS
Diethanolamine's vapor pressure indicates that it will primarily exist in the vapor phase in the atmosphere. The primary removal mechanism is reaction with photochemically generated hydroxyl radicals (half-life of 0.72-7.2 hours). Precipitation may also be a significant removal process, due to diethanolamine's complete solubility in water (Howard, 1991; (Howard, 1990).
SURFACE WATER Diethanolamine is expected to biodegrade in water, with half-lives of 14.4-168 hours (surface water) and 28.8-336 hours (groundwater) (Howard, 1991; (Howard, 1990). OHM/TADS (1998) reports that this compound will form a strong alkaline solution in water, due to the dissociation of amine groups and the subsequent formation of ammonium ions. This compound is not expected to bioconcentrate in aquatic organisms, adsorb to suspended solids and sediments, or volatilize (Howard, 1991; (Howard, 1990). The biological oxygen demand of diethanolamine is 10% (theoretical), 5 days (CHRIS , 1998).
TERRESTRIAL In soil, biodegradation is expected to be rapid, following acclimation (half-life 14.4-168 hours). Some residual amounts of this compound may leach into groundwater. Volatilization is not an important fate process (Howard, 1991; (Howard, 1990). The Koc value of 4 and the complete solubility in water indicate that this compound should be extremely mobile in soil and should not adsorb appreciably to suspended solids or sediments in water (Howard, 1990). However, the protonated form of this compound may adsorb to humic material in unsuspended sediments and solids (HSDB , 1998).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- References: (OHM/TADS , 1998)
TLM - FISH: 100 ppm for 24H -- 15-21 degrees C; Aerated TLM - BLUEGILL: 1850 ppm for 48H -- 15-21 degrees C; Aerated TLM - SUNFISH: 2100 ppm for 24H -- 20 degrees C; Aerated TLM - BLUEGILL: 2100 ppm for 24H -- 20 degrees C; Aerated TLM - MOSQUITO FISH: 1800 for 24H -- Turbid TLM - MOSQUITO FISH: 1550 for 48H -- Turbid TLM - MOSQUITO FISH: 1400 ppm for 96H -- Turbid TLM - BRINE SHRIMP: 2800 ppm for 24H -- Static CRITICAL - CREEK CHUB: 80-120 ppm for 24H -- 15-21 degrees C; Aerated LC50 - FATHEAD MINNOW: > 100 ppm for 96H -- Static LC50 - DAPHNIA MAGNA: 1.4 ppm for 96H -- Static INHIBITORY - SELENASTRUM CAPRICORNATUM: 100 ppm
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Diethanolamine exists as a faintly colored to colorless, viscous, hygroscopic liquid (above 82 degrees F) or deliquescent prisms with a mild ammoniacal odor (Ashford, 1994; Budavari, 1996; Lewis, 1996; NIOSH , 1998). CHIRS (1998) reports that this compound has a slight dead fish odor.
PH
- 11.0 (0.1 normal) (Budavari, 1996)
VAPOR PRESSURE
- 5 mmHg (at 138 degrees C) (Lewis, 1996)
- < 0.01 mmHg (at 20 degrees C) (ACGIH, 1996(a); (NIOSH , 1998)
- 0.00028 mmHg (at 25 degrees C) (Howard, 1990)
- 1.4x10(-4) mmHg (at 25 degrees C) (HSDB , 1998)
SPECIFIC GRAVITY
- OTHER TEMPERATURE AND/OR PRESSURE
1.0919 (at 30/20 degrees C) (Lewis, 1996) 1.092 (at 30/20 degrees C) (Lewis, 1993) 1.0881 (at 30/4 degrees C) (Budavari, 1996) 1.0693 (at 60/4 degrees C) (Budavari, 1996) 1.09664 (at 20/4 degrees C) (Clayton & Clayton, 1994)
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
1.09 kg/L (at 30 degrees C) (Ashford, 1994) 1.095 kg/L (at 15.6 degrees C) (ITI, 1995)
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
28.0 degrees C; 82 degrees F (Lewis, 1996; NFPA, 1994) 27.8 degrees C (ITI, 1995)
BOILING POINT
- 270 degrees C (decomposes) (Lewis, 1996)
- 269 degrees C (Lewis, 1993)
- 268 degrees C; 514 degrees F (NFPA, 1994)
- 268.8 degrees C (at 760 mmHg) (Budavari, 1996)
- 217 degrees C (at 150 mmHg) (Budavari, 1996)
- 20 degrees C (at 0.01 mmHg) (Budavari, 1996)
- > 270 degrees C (Ashford, 1994)
- 516 degrees F (decomposes) (NIOSH , 1998)
- 268.4 degrees C; 515.1 degrees F; 541.6 degrees K (CHRIS , 1998)
FLASH POINT
- 305 degrees F (open cup) (Lewis, 1996)
- 300 degrees F (Budavari, 1996)
- 152 degrees C; 306 degrees F (open cup) (Lewis, 1993)
- 172 degrees C; 342 degrees F (open cup) (NFPA, 1994)
- 280 degrees F (open cup) (Clayton & Clayton, 1994)
- 134 degrees C (open cup) (ITI, 1995)
- 279 degrees F (NIOSH , 1998)
- 152 degrees (closed cup) (ACGIH, 1996(a))
- 150 degrees C (OHM/TADS , 1998)
AUTOIGNITION TEMPERATURE
- 662 degrees C; 1224 degrees F (Lewis, 1996; NFPA, 1994)
EXPLOSIVE LIMITS
SOLUBILITY
Diethanolamine is very soluble in water (96.4% w/w) (Clayton & Clayton, 1994; Lewis, 1996). Miscible with water (Budavari, 1996).
Diethanolamine is very soluble in alcohol is soluble in methanol and acetone (Budavari, 1996; Lewis, 1993). It is insoluble in ether and benzene and hydrocarbon solvents (Ashford, 1994; Lewis, 1993). This compound is slightly soluble in ether (0.8% at 25 degrees C) and benzene (4.2% at 25 degrees C) and is hardly soluble in carbon tetrachloride (< 0.1% at 25 degrees C) and heptane (< 0.1% at 25 degrees C) (Budavari, 1996; ITI, 1995; HSDB , 1998).
OCTANOL/WATER PARTITION COEFFICIENT
HENRY'S CONSTANT
- 5.35x10(-14) atm-m(3)/mol (at 25 degrees C) (Howard, 1990)
- 3.9x10(-11) atm-m(3)/mol (at 25 degrees C) (estimated) (HSDB , 1998)
SPECTRAL CONSTANTS
OTHER/PHYSICAL
- NUCLEAR MAGNETIC RESONANCE
351.9 cp (at 30 degrees C) (Budavari, 1996) 53.85 cp (at 60 degrees C) (Budavari, 1996)
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