SODIUM AZIDE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
SODIUM AZIDE AZIDE AZIUM AZOTURE DE SODIUM (French) HYDRAZOIC ACID, SODIUM SALT KAZOE NATRIUMAZID (German) NATRIUUMAZIDE (Dutch) NEMAZYD SMITE SODIUM, AZOTURE DE (French) SODIUM, AZOTURO DI (Italian) U-3886 NATRIUMMAZID (DUTCH) SODIUM, ACOTURE DE (FRENCH)
IDENTIFIERS
SYNONYM REFERENCE
- (RTECS , 1991; EPA, 1985)
USES/FORMS/SOURCES
Sodium azide is used in the explosive and pharmaceutical industries (as a chemical preservative). It is a common preservative used in many in vitro diagnostic products, including some automatic blood cell counters, used in hospitals and laboratories (LaLuna et al, 1979). It is used with copper or iron oxides as a gas generant in automobile safety airbags. The gas generator may contain 350 to 600 grams of sodium azide (Anon, 1983). Sodium azide use in air bags is being phased out in favor of less toxic materials (Chang & Lamm, 2003). Automotive air-bag systems are triggered when a sensor in the car's bumper sends an electrical charge to a gas generator that contains sodium azide. The electrical charge initiates a chemical reaction in the generator (sealed steel or aluminum container) that produces nitrogen gas from the azide (Anon, 1983; Pernikoff, 1989) Pers Comm, 1990).
Sodium azide is used in organic syntheses; in the preparation of hydrazoic acid, lead azide, and pure sodium; in the differential selection of bacteria; in automatic blood counters; as a preservative for laboratory reagents; as a propellant for inflating automotive safety bags; as an agricultural nematocide; as a herbicide; and in fruit rot control (Budavari, 1996). It is also used industrially in the manufacturing processes of rubber, latex, wine, seed and Japanese beer (Chang & Lamm, 2003).
Sodium azide is available as the gas (hydrazoic acid) or sodium salt. Commercial isotonic buffering solutions may contain 0.1% (1 mg/mL) sodium azide as a preservative (Judge & Ward, 1989; Howard et al, 1990).
Sodium azide is manufactured in Japan and India by deriving sodium azide from hydrazine. Canada, the United States and Germany derive sodium azide from reacting ammonia with elemental sodium, forming sodium amide that in turn reacts with nitrous oxide (Rippen et al, 1996).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Sodium azide is poisonous by a variety of routes, including ingestion, skin contact, inhalation, intraperitoneal, intravenous and subcutaneous. Most industrial exposures are by inhalation. Most ingestions are either laboratory exposures or suicide attempts.
- Clinical effects may be nearly immediate or delayed in onset, and have required days or months to fully resolve in some cases.
- The most commonly reported health effect is hypotension, which can occur independent of route of exposure. Mild to moderate exposures can cause headache, mild hypotension, syncope, nausea, vomiting, diarrhea, abdominal pain, and a general feeling of apprehension and unwellness. More serious poisoning can cause central nervous system depression, coma, chest discomfort, hyperthermia or hypothermia, pulmonary edema, lactic acidosis, bradycardia or tachycardia, severe hypotension (sometimes preceded by hypertension), atrial and ventricular dysrhythmias, electrocardiographic changes, shortness of breath, diaphoresis, blurred vision, and seizures.
- Exposure to hydrazoic acid vapors evolved from sodium azide can cause irritation of eyes and mucous membranes of the respiratory tract with possible bronchitis or pulmonary edema as well as systemic effects such as hypotension.
- 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.
ACUTE CLINICAL EFFECTS
- Most information about toxic effects has been determined in cases of ingestion. Inhalation of fumes by humans has chiefly been associated with hypotension, headache, and pulmonary irritation.
- Sodium azide is a rapidly acting vasodilator; it can cause headaches and hypotension (Rippen et al, 1996).
- Hyperpnea may develop at low levels of exposure. Respiratory failure may occur; pulmonary edema has been noted (Albertson et al, 1986). Both hyper and hypothermia have been reported (Clayton & Clayton, 1994; Edmonds & Bourne, 1982; ACGIH, 1991; Gosselin et al, 1984). Hypotension may occur, and may be preceded by hypertension (Edmonds & Bourne, 1982; Albertson et al, 1986). Bradycardia or tachycardia may occur (Edmonds & Bourne, 1982).
- Neurologic effects may include headache, muscle weakness and flaccidity, seizures, and coma. Persistent metabolic acidosis occurred in a patient who ingested 10 to 20 grams (Albertson et al, 1986; HSDB, 2003). Ingestion has resulted in tachycardia, nausea, vomiting, diarrhea, headache, restlessness, polydipsia, EKG changes, and leukocytosis (HSDB, 2003).
- Reactive airway dysfunction syndrome can be a sequela of acute inhalation of sodium azide (Weiss, 1996).
- Acute exposure may also lead to conjunctival and mucous membrane irritation. Mydriasis and blurred vision have been reported (ACGIH, 1991; Clayton & Clayton, 1994; Gosselin et al, 1984).
- Effects in experimental animals include hematuria, cardiac irregularities, hypotension, seizures, unconsciousness, vascular congestion, apnea, cerebellar damage, ataxia, and death (Clayton & Clayton, 1994). Lesions have been found in the optic nerves and tracts in severely poisoned rats (HSDB, 1997).
- Doses of 6 or 12 mg/kg inhibited certain motor activities in mice (Lalonde et al, 1996).
- Sodium azide inhibits cytochrome oxidase (Lalonde et al, 1996). In this respect it is similar to HYDROGEN SULFIDE.
CHRONIC CLINICAL EFFECTS
- At the time of this review, no chronic exposure studies were found for sodium azide in humans.
- Repeated exposure of experimental animals caused necrosis and demyelination of the optic nerves and destruction of the caudate nucleus and putamen of the lenticular nucleus. Subchronic exposure in experimental animals produced hypotension, demyelination of the nerve fibers of the CNS, and increased liver weights (ACGIH, 1991).
- Other effects reported in experimental animals include liver and brain damage, lethargy, inactivity, labored breathing, necrosis of the cerebrum and thalamus, and pulmonary congestion, hemorrhage, and edema (Clayton & Clayton, 1994).
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
-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.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
INGESTION A 29-year-old woman developed cardiomyopathy and died 3 days after an inadvertent ingestion of 700 mL of a commercial buffering solution that contained 0.1% sodium azide (Judge & Ward, 1989; Howard et al, 1990). A man ingested 2 tablespoons of sodium azide mixed in water, developed coma, hypotension, and ventricular arrhythmias, and died within 2 hours (Klein-Schwartz et al, 1989). A 52-year-old man ingested 1.2 to 2 g of sodium azide and developed a generalized tonic clonic seizure 3 hours postresection and tachycardia and unresponsiveness at 30 hours after admission. He continued to deteriorate, becoming more hypotensive and bradycardic, despite receiving a total of 5 treatments with the cyanide antidote kit during hospitalization. He survived for a total of 40 hours after ingestion (Klein-Schwartz et al, 1989). The minimal lethal dosage is reported to be 10 mg/kg. Severe health effects including seizures, coma, death, acute lung injury, flaccidity, metabolic acidosis, arrhythmia, bradycardia and asystole have been observed at this dosage or greater (Chang & Lamm, 2003). Ingestion of "several grams" caused collapse and death within 40 minutes in an adult (Gosselin et al, 1984). An adult male ingested an estimated 10 to 20 g of sodium azide, developed coma, acidosis, hypertension followed by hypotension, hyperthermia, pulmonary edema, and atrial and ventricular arrhythmias, and died after 28 hours (Albertson et al, 1986). Ingestion of 15 to 20 g resulted in death within 5 hours of ingestion in a 30-year-old man (Abrams et al, 1987). An adult male ingested an unknown amount and died within 8 hours (Klein-Schwartz et al, 1989). A woman ingested an unknown amount and died within 12 hours after developing pulmonary edema, lactic acidosis, hypothermia, central nervous system depression, hypotension, and shock (Emmett & Ricking, 1975). A man died 4 hours after ingesting approximately 9 g (Marquet et al, 1996).
ANIMAL DATA
MAXIMUM TOLERATED EXPOSURE
The human hypotensive dose of sodium azide is between 0.2 and 4 mcg/kg (about 2 to 40 mcg for a 10 kg child, or about 14 to 280 mcg for a 70 kg adult) (Gosselin et al, 1984). In a review study, the authors (Chang & Lamm, 2003) reported the lowest dose in which adverse human health effects were seen as follows: Hypotension (0.01 mg/kg) Decreased mental status (0.04 mg/kg) Nausea, vomiting, diarrhea (0.04 mg/kg) Headache, temporary loss of vision (0.07 mg/kg) Sweating, collapse, palpitations (0.07 mg/kg)
Five patients developed nausea, vomiting, diaphoresis, headache, hypotension, syncope, lightheadedness, and a sense of impending doom shortly after drinking iced tea that contained sodium azide at a local restaurant. Symptoms improved with IV fluids, antiemetics and supportive care. Toxicology screening was negative in all patients. Although the source of the exposure was limited to a self-service tea urn that contained sodium azide, a police investigation did not reveal how it became contaminated. Persistent symptoms were not reported in any patient (Schwarz et al, 2014). A hospitalized woman inadvertently ingested 1 g of sodium azide and developed seizures, metabolic acidosis and hypotension requiring intensive supportive care including hemodialysis, intra-aortic balloon pumping for circulatory support and mechanical ventilation. The patient was discharged on day 11 with no long-term sequelae observed (Watanabe et al, 2007). An adult who ingested 150 mg of sodium azide in an aqueous solution developed breathlessness, tachycardia, nausea, vomiting, headache, diarrhea, polydipsia, leukocytosis, and electrocardiographic changes, but recovered over a 10 day period (Gosselin et al, 1984). An adult ingested between 50 and 60 mg and developed coma, severe headaches, hypotension, and tachycardia which lasted for an hour (Richardson et al, 1975). Ingestion of 5 to 10 mg by an adult caused only transient symptoms of indigestion, headache, sweating, and faintness (Richardson et al, 1975).
- LABORATORY/OCCUPATIONAL EXPOSURES
Five laboratory technicians drank tea made with distilled water treated with sodium azide (concentration about 224 mg/L in the tea). Each cup of tea was estimated to contain about 40 mg of sodium azide. One technician drank a half cup (about 20 mg) and felt "vaguely unwell," while 3 individuals who each drank one cup (about 40 mg) developed palpitations and a "fuzzy head". The fifth technician drank 2 cups (about 80 mg) and developed violent cramping chest pains, numbness and tingling in the legs, and fainted. Chest discomfort and apprehension continued for up to 2 months after ingestion (Edmonds & Bourne, 1982). Sodium azide was tested in the 1950's as an antihypertensive medication (ACGIH, 1986). Daily doses of 0.65 to 3.9 mg (0.01 to 0.02 mg/kg) were administered to 30 hypertensive patients for periods up to 2.5 years (ACGIH, 1986) (Edmonds & Bourne, 1982). Normal volunteers administered 1.3 mg of sodium azide 3 times daily (3.9 mg daily dose) had transient pounding headaches but no sustained effects on blood pressure (Edmonds & Bourne, 1982). Concentrations of hydrazoic acid vapor as low as 0.5 ppm have caused irritation in laboratory workers (ACGIH, 1986). A chemist acidifying 10 mg of sodium azide in a malfunctioning hood developed symptoms of dizziness, weakness, blurred vision, shortness of breath, a faint feeling, and moderate hypotension and bradycardia which lasted for about an hour (Clayton & Clayton, 1982). Hypotension has been noted in workers with hydrazoic acid vapor exposure during the manufacture of lead azide from sodium azide and lead nitrate (Clayton & Clayton, 1982). The hypotension progressively worsened during the working day and resolved after the workers left the plant (Clayton & Clayton, 1982). Ingestion of a small amount of a Tris buffering solution containing 4% sodium azide resulted in tachycardia, hypotension, and hyperventilation in one patient. A second patient inadvertently underwent gastric lavage with the same solution for collection of gastric cytology specimens and also developed hypotension(Roberts et al, 1974).
- Carcinogenicity Ratings for CAS26628-22-8 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A4 ; Listed as: Sodium azide, as sodium azide ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A4 ; Listed as: Sodium azide, as hydrazoic acid vapor EPA (U.S. Environmental Protection Agency, 2011): Not Assessed under the IRIS program. ; Listed as: Sodium azide 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: Sodium azide 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 CAS26628-22-8 (U.S. Environmental Protection Agency, 2011):
Oral: Slope Factor: RfD: 4x10(-3) mg/kg-day
Inhalation: Drinking Water:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS26628-22-8 (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. Adopted Value Adopted Value
- AIHA WEEL Values for CAS26628-22-8 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS26628-22-8 (National Institute for Occupational Safety and Health, 2007):
Listed as: Sodium azide REL: IDLH: Not Listed
- OSHA PEL Values for CAS26628-22-8 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS26628-22-8 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS26628-22-8 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS26628-22-8 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS26628-22-8 (U.S. Environmental Protection Agency, 2010b):
Listed as: Sodium azide P or U series number: P105 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 CAS26628-22-8 (U.S. Environmental Protection Agency, 2010):
Listed as: Sodium Azide (Na(N3)) Reportable Quantity, in pounds: 1000 Threshold Planning Quantity, in pounds: Note(s): a a: This material is a reactive solid. The TPQ does not default to 10,000 pounds for non-powder, non-molten, non-solution form.
- EPA SARA Title III, Community Right-to-Know for CAS26628-22-8 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS26628-22-8 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS26628-22-8 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1687 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1687 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS26628-22-8 (NFPA, 2002):
-HANDLING AND STORAGE
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Storage temperature: Ambient (HSDB , 1992) Stable at temperatures below 300 degrees C; unlimited shelf life; stable in water in the absence of light (HSDB , 1992).
-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.
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 26628-22-8.
-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.
Containers may explode in fire (HSDB , 1992).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS26628-22-8 (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 CAS26628-22-8 (NFPA, 2002):
EXPLOSION HAZARD
- Sodium azide is an unstable explosive sensitive to impacts (Sax & Lewis, 1989).
- Sodium azide reacts with heavy metals (eg, brass, copper, lead) to form dangerously explosive heavy metal azides (Sax & Lewis, 1989).
Sodium azide is commonly used in concentrations of 0.1 to 4.0% as a preservative in certain reagents used by hospital laboratories for red blood cell counting and hepatitis antigen screening. If these reagents are disposed of in drains, they can accumulate in traps and form explosive copper or lead azides which could be detonated during plumbing work (Gosselin et al, 1984).
- Sodium azide forms a violent reaction with the following (Sax & Lewis, 1989):
DUST/VAPOR HAZARD
- When heated to decomposition, sodium azide emits very toxic fumes of Na2O and oxides of nitrogen (Sax & Lewis, 1989).
REACTIVITY HAZARD
- Sodium azide is incompatible with the following (Sax & Lewis, 1989):
Acids Ammonium chloride + trichloroacetonitrile Cyanuric chloride 2,5-Dinitro-3-methylbenzoic acid + oleum Phosgene Trifluroacryloyl chloride
- When heated to decomposition, sodium azide emits very toxic fumes of Na2O and oxides of nitrogen (Sax & Lewis, 1989).
- Also see Explosion Hazard Section.
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.
- If fire becomes uncontrollable or container is exposed to direct flame, consider evacuation of one-half mile radius (AAR, 1987).
- AIHA ERPG Values for CAS26628-22-8 (AIHA, 2006):
- DOE TEEL Values for CAS26628-22-8 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Sodium azide TEEL-0 (units = mg/m3): 0.2 TEEL-1 (units = mg/m3): 3 TEEL-2 (units = mg/m3): 20 TEEL-3 (units = mg/m3): 25 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 CAS26628-22-8 (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; 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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 CAS26628-22-8 (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.
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 , 1992).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- AQUATIC FATE: Sodium azide is stable in water in the absence of light, but appears to be susceptible to photo-decomposition by solar radiation. Photolysis may result in metal nitrides initially, with the eventual formation of the free metal and nitrogen gas (HSDB , 1992).
ENVIRONMENTAL FATE AND KINETICS
ENVIRONMENTAL TOXICITY
- Ecotoxicity Values (HSDB , 1992):
EC50, Simocephalus, 8.4 mg/L/96 hours at 15 degrees C, first instar, technical material 98% LC50, G Fasciatus, 6.4 mg/L/96 hours at 21 degrees C, mature, technical material 98% LC50, Pteronarcys, 8.0 mg/L/96 hours at 15 degrees C, second year class, technical material 98% LC50, Rainbow trout, 0.8 to 1.6 mg/L/96 hours at 13 degrees C, weight 1.4 grams, technical material 98% LC50, Bluegill, 0.8 mg/L/96 hours at 18 degrees C, weight 0.4 grams, technical material 98% EC50, Daphnia Pulex, 4.2 mg/L/96 hours at 15 degrees C, first instar, technical material 98% LC50, G Fasciatus, 5.0 mg/L/96 hours at 21 degrees C, first instar, technical material 98% LC50, Bluegill, 0.7 mg/L/96 hours at 18 degrees C, weight 0.6 grams, technical material 98% Aquatic toxicity: TLm, Bluegill, 1.5 ppm/24 hours/fresh water Heritable translocation insects, oral mutation dose, 100 mg/L Mutagenic effect, Scenedesmus acutus, 0.05 to 0.8% sodium azide/1 to 2 hours
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- colorless, hexagonal crystals (Budavari, 1989)
- Sodium azide hydrolyzes to form hydrazoic acid, a colorless, volatile, HIGHLY EXPLOSIVE, liquid with a characteristic odor, which has been described as sickening (Clayton & Clayton, 1981; Sax & Lewis, 1987).
PH
- Hydrazoic acid is a weak acid (pKa = 4.72) (Clayton & Clayton, 1981).
DENSITY
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
BOILING POINT
- At approximately 300 degrees C this compound decomposes into sodium and nitrogen (Budavari, 1989; Sax & Lewis, 1987).
FLASH POINT
EXPLOSIVE LIMITS
SOLUBILITY
It is highly soluble in water (Budavari, 1989). 40.16% (at 10 degrees C) (Budavari, 1989) 41.7% (at 17 degrees C) (Budavari, 1989)
Slightly soluble in alcohol; insoluble in ether (Budavari, 1989). solubility in alcohol: 0.3% (at 25 degrees C) (HSDB , 1992)
OTHER/PHYSICAL
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