N-BUTYRONITRILE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
BUTANENITRILE n-BUTANENITRILE BUTANONITRILE n-BUTYL NITRILE BUTYRIC ACID NITRILE BUTYRONITRILE n-BUTYRONITRILE BUTYRYLONITRILE CYANOPROPANE 1-CYANOPROPANE NBN PROPYL CYANIDE n-PROPYL CYANIDE PROPYLKYANID (Czech)
IDENTIFIERS
SYNONYM REFERENCE
- (Ashford, 1994; CHRIS , 1997; HSDB , 1997; NFPA, 1994; NIOSH , 1997; RTECS , 1997; Urben, 1995)
USES/FORMS/SOURCES
n-Butyronitrile finds use as a solvent; as a basic material in chemical, industrial, and pharmaceutical intermediates and products; and, in poultry medicines (Ashford, 1994; Lewis, 1993).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- n-Butyronitrile is irritating to the eyes, skin, and mucous membranes.
- Symptoms of exposure may also include nausea, vomiting, abdominal pain, dyspnea, tachypnea, tachycardia, weakness, tremors, CNS depression, and terminal seizures.
- In experimental animal studies, occurrence of elevated urinary thiocyanate levels following n-butyronitrile exposure suggested that CYANIDE may be produced during metabolism. Human cyanide poisonings from this compound have not been reported.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (ERG, 2004)
TOXIC; may be fatal if inhaled, ingested or absorbed through skin. Inhalation or contact with some of these materials will irritate or burn 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.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (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. Wash skin with soap and water. Keep victim warm and quiet. In case of burns, immediately cool affected skin for as long as possible with cold water. Do not remove clothing if adhering to skin. 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 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. Based on animal experiments, CYANIDE might be released from n-butyronitrile during metabolism (human cases have not been reported). If CYANIDE POISONING is suspected following exposure, refer to the CYANIDE MEDITEXT(R) Medical Management for more information. EYE EXPOSURE - Immediately wash the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately. Contact lenses should not be worn when working with this chemical. DERMAL EXPOSURE - Immediately wash the contaminated skin with soap and water. If this chemical penetrates the clothing, immediately remove the clothing, wash the skin with soap and water, and get medical attention promptly. INHALATION EXPOSURE - Move the exposed person to fresh air at once. If breathing has stopped, perform artificial respiration. Keep the affected person warm and at rest. Get medical attention as soon as possible. ORAL EXPOSURE - If this chemical has been swallowed, get medical attention immediately. TARGET ORGANS - Eyes, skin, respiratory system, central nervous system, and cardiovascular system (National Institute for Occupational Safety and Health, 2007).
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. Carefully observe patients with inhalation exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary. SEIZURES: Administer a benzodiazepine; DIAZEPAM (ADULT: 5 to 10 mg IV initially; repeat every 5 to 20 minutes as needed. CHILD: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed) or LORAZEPAM (ADULT: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed, if seizures persist. CHILD: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed, if seizures continue). Consider phenobarbital or propofol if seizures recur after diazepam 30 mg (adults) or 10 mg (children greater than 5 years). Monitor for hypotension, dysrhythmias, respiratory depression, and need for endotracheal intubation. Evaluate for hypoglycemia, electrolyte disturbances, and hypoxia.
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. GASTRIC LAVAGE: Consider after ingestion of a potentially life-threatening amount of poison if it can be performed soon after ingestion (generally within 1 hour). Protect airway by placement in the head down left lateral decubitus position or by endotracheal intubation. Control any seizures first. ACTIVATED CHARCOAL: Administer charcoal as a slurry (240 mL water/30 g charcoal). Usual dose: 25 to 100 g in adults/adolescents, 25 to 50 g in children (1 to 12 years), and 1 g/kg in infants less than 1 year old. SEIZURES: Administer a benzodiazepine; DIAZEPAM (ADULT: 5 to 10 mg IV initially; repeat every 5 to 20 minutes as needed. CHILD: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed) or LORAZEPAM (ADULT: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed, if seizures persist. CHILD: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed, if seizures continue). Consider phenobarbital or propofol if seizures recur after diazepam 30 mg (adults) or 10 mg (children greater than 5 years). Monitor for hypotension, dysrhythmias, respiratory depression, and need for endotracheal intubation. Evaluate for hypoglycemia, electrolyte disturbances, and hypoxia.
Observe patients with ingestion carefully for the possible development of esophageal or gastrointestinal tract irritation or burns. If signs or symptoms of esophageal irritation or burns are present, consider endoscopy to determine the extent of injury.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
- The minimum lethal human dose to this agent has not been delineated.
MAXIMUM TOLERATED EXPOSURE
- The maximum tolerated human exposure to this agent has not been delineated.
- Carcinogenicity Ratings for CAS109-74-0 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed 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: n-Butyronitrile 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 CAS109-74-0 (U.S. Environmental Protection Agency, 2011):
References: Budavari, 1996 ITI, 1988 Lewis, 1996 RTECS, 1997 Note: Unless otherwise indicated all values are from RTECS. LC50- (INHALATION)MOUSE: LCLo- (INHALATION)RAT: 400 ppm (ITI, 1988) 1000 ppm for 4H
LD50- (INTRAPERITONEAL)MOUSE: LD50- (ORAL)MOUSE: LD50- (SKIN)RABBIT: 500 mcL/kg 500 mg/kg (ITI, 1988)
LD50- (INTRAPERITONEAL)RAT: LD50- (ORAL)RAT: LDLo- (ORAL)CAT: LDLo- (SKIN)GUINEA_PIG: LDLo- (SUBCUTANEOUS)GUINEA_PIG: LDLo- (INTRAVENOUS)RABBIT: LDLo- (ORAL)RABBIT: LDLo- (SUBCUTANEOUS)RABBIT: TCLo- (INHALATION)RAT:
CALCULATIONS
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS109-74-0 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS109-74-0 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS109-74-0 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS109-74-0 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS109-74-0 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS109-74-0 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS109-74-0 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS109-74-0 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS109-74-0 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS109-74-0 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS109-74-0 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS109-74-0 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 2411 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN2411 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS109-74-0 (NFPA, 2002):
Listed as: Butyronitrile 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
HANDLING
- Persons handling n-butyronitrile need to equip themselves with long gloves, a self-contained respirator, and a protective apron in conjunction with full protective clothing (ITI, 1988).
- Only persons equipped with appropriate protective clothing should handle broken packages/containers of this compound (AAR, 1994).
- n-Butyronitrile is stable during transport (CHRIS , 1997).
- According to 49 CFR 171.2: "No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by.../the hazardous materials regulations (49 CFR 171 to 177)" (HSDB , 1997)
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Store n-butyronitrile in a dry, cool, well-ventilated area. A detached or outside location is optimal (NFPA, 1994).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (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.
- Appropriate protective clothing should be worn to prevent skin contact. Wash the skin with large amounts of soap and water immediately after it becomes contaminated. Due to the flammability hazard, clothing which becomes wet should be removed as quickly as possible (AAR, 1994; (NIOSH , 1997).
EYE/FACE PROTECTION
- Use appropriate eye protection to prevent contact (NIOSH , 1997).
RESPIRATORY PROTECTION
- Refer to "Recommendations for respirator selection" in the NIOSH Pocket Guide to Chemical Hazards on TOMES Plus(R) for respirator information.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 109-74-0.
ENGINEERING CONTROLS
- A facility for quickly drenching the body, or body parts, with water needs to be provided within the immediate work area. This is intended to quickly remove n-butyronitrile from any body areas likely to be exposed. In some instances a hose connected to a sink may be permissible, in others a full deluge shower may be required (NIOSH , 1997).
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (ERG, 2004) HIGHLY FLAMMABLE: Will be easily 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 and poison 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.
n-Butyronitrile is a flammable liquid. It is considered a serious fire hazard when exposed to open flame, heat, or oxidizers (Lewis, 1996; NFPA, 1994). Poisonous oxides of nitrogen and cyanide fumes are produced during combustion and/or decomposition of n-butyronitrile (AAR, 1994; (CHRIS , 1997; Lewis, 1996). Vapors are heavier than air, so flashback along a vapor trail is possible. It is lighter than water (AAR, 1994; (CHRIS , 1997). This compound reacts exothermically with strong oxidizers and acids (NFPA, 1994). Emergency response personnel are to wear appropriate protective clothing including a positive-pressure self-contained breathing apparatus when dealing with this compound (NFPA, 1994).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS109-74-0 (NFPA, 2002):
Listed as: Butyronitrile 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 131 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (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. Use water spray or fog; do not use straight streams.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (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 CAS109-74-0 (NFPA, 2002):
- To combat a fire involving this compound use alcohol foam (Lewis, 1996).
- Utilize carbon dioxide, dry chemical, alcohol foam, or water spray to fight fire (AAR, 1994; (CHRIS , 1997; NFPA, 1994).
- Water may be utilized as a fog in flooding quantities to cool affected containers/structures. In solid streams, water may be ineffective. Apply water from as far away as is possible (AAR, 1994).
- Do not attempt to extinguish a fire involving this compound unless the flow can be controlled or stopped (AAR, 1994).
- To avoid poisonous decomposition products and hazardous vapors, approach any fire involving n-butyronitrile from upwind (NFPA, 1994).
EXPLOSION HAZARD
- In a fire, containers of this compound may explode (CHRIS , 1997).
DUST/VAPOR HAZARD
- Toxic cyanide and nitrogen oxide fumes are released when n-butyronitrile is heated to decomposition (Lewis, 1996).
REACTIVITY HAZARD
- This compound reacts exothermically with strong oxidizers and acids. The reaction with acids may produce hydrogen cyanide (NFPA, 1994).
- n-Butyronitrile is a n-cyano compound; in general, this class of compounds is unstable or reactive (Urben, 1995).
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 131 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 50 meters (150 feet) in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (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 131(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 CAS109-74-0 (AIHA, 2006):
- DOE TEEL Values for CAS109-74-0 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS109-74-0 (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, 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; 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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 CAS109-74-0 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (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.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (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.
Keep upwind to avoid breathing vapors. Remove any possible ignition source from the area. If possible, stop the leak. Water spray can be employed to protect personnel and disperse vapors, as well as to dilute runoff into nonflammable mixtures. Isolate and control all runoff for appropriate disposal; dikes may be used for this purpose. Keep this material out of sewers and water sources (AAR, 1994; (CHRIS , 1997; NFPA, 1994).
SMALL SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (ERG, 2004) Absorb with earth, sand or other non-combustible material and transfer to containers for later disposal. Use clean non-sparking tools to collect absorbed material.
Small quantities may be absorbed with paper, allowed to evaporate on an iron or glass dish within a fume hood, and then disposed of by burning the paper (ITI, 1988).
LARGE SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 131 (ERG, 2004) For larger amounts, add excessive calcium hypochlorite and sodium hydroxide solution. Transfer the mixture into a larger beaker Wash the site of the spill (ITI, 1988).
To dispose of this compound, stir it into excessive amounts of alcoholic sodium hydroxide solution. After an hour has passed, evaporate the alcohol and add sufficient calcium hypochlorite (ITI, 1988). Waste management activities associated with material disposition are unique to individual situations. Proper waste characterization and decisions regarding waste management should be coordinated with the appropriate local, state, or federal authorities to ensure compliance with all applicable rules and regulations.
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- n-Butyronitrile is released to the environment in waste streams from its commercial production as well as in wastewater effluents from shale oil processing and coal gasification (HSDB , 1997).
ENVIRONMENTAL FATE AND KINETICS
In the atmosphere, vapor phase n-butyronitrile will degrade by reaction with photochemically produced hydroxyl radicals; this process has a half-life of 21 days. Wet deposition may be possible (HSDB , 1997).
SURFACE WATER In water, biodegradation is thought to be the most important pathway for this compound. Based on evidence from similar nitrile compounds (ethanenitrile and isobutanenitrile), biodegradation will take place more rapidly with acclimated microorganisms. Extremely high levels of n-butyronitrile (500 ppm) can be toxic to the organisms involved in its biodegradation. Volatilization from water may be a significant process, although it will not occur quickly. Half-lives of 16.4 hours for a model river and 7.5 days for a model pond have been estimated. Adsorption to sediment is not thought to be significant (HSDB , 1997).
TERRESTRIAL Biodegradation is thought to be the most significant route in soil. Based on evidence from similar nitrile compounds, biodegradation will take place more rapidly with acclimated microorganisms. High concentrations of this compound can be toxic to the organisms involved in its biodegradation. Volatilization from dry soil surfaces is expected to occur. n-Butyronitrile is thought to be highly mobile in soil; it will leach (HSDB , 1997).
BIODEGRADATION
- Biodegradation is thought to be the most important environmental pathway for n-butyronitrile in soil and water. Based on evidence from similar nitrile compounds (ethanenitrile and isobutanenitrile), biodegradation will take place more rapidly with acclimated microorganisms. Extremely high concentrations of n-butyronitrile (500 ppm) can be toxic to the organisms involved in its biodegradation (HSDB , 1997).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- n-Butyronitrile is a colorless liquid which possesses a sharp, suffocating odor (Lewis, 1993; NFPA, 1994; NIOSH , 1997).
VAPOR PRESSURE
- 10 mmHg (at 15.4 degrees C) (Clayton & Clayton, 1994)
- 40 mmHg (at 38.4 degrees C) (Clayton & Clayton, 1994)
- 19.5 mmHg (at 25 degrees C) (HSDB , 1997)
SPECIFIC GRAVITY
- OTHER TEMPERATURE AND/OR PRESSURE
LIQUID: 0.80 (at 20/4 degrees C) (ITI, 1988; NFPA, 1994) LIQUID: 0.8091 (at 0/4 degrees C) (Budavari, 1996) LIQUID: 0.7954 (at 15/4 degrees C) (Budavari, 1996) LIQUID: 0.7817 (at 30/4 degrees C) (Budavari, 1996)
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
LIQUID: 0.79 kg/L (at 4 degrees C) (Ashford, 1994) LIQUID: 0.796 kg/L (at 15 degees C) (Clayton & Clayton, 1994; Lewis, 1993) LIQUID: 0.7936 kg/L (at 20 degrees C) (CHRIS , 1997)
FREEZING/MELTING POINT
-112 degrees C; -170 degrees F (Budavari, 1996; Ashford, 1994; NFPA, 1994) -113 degrees C; -171 degrees F; 160 degrees K (CHRIS , 1997)
BOILING POINT
- 115-117 degrees C (Ashford, 1994)
- 117 degrees C (Lewis, 1996)
- 116-117 degrees C (at 760 mmHg) (Clayton & Clayton, 1994; Lewis, 1993)
- 117-118 degrees C; 243-244 degrees F (NFPA, 1994)
- 118 degrees C; 244 degrees F; 391 degrees K (CHRIS , 1997; NIOSH , 1997)
- 117.5 degrees C (at 760 mmHg) (Budavari, 1996; ITI, 1988)
- 96.8 degrees C (at 400 mmHg) (Budavari, 1996)
- 76.7 degrees C (at 200 mmHg) (Budavari, 1996)
- 59.0 degrees C (at 100 mmHg) (Budavari, 1996)
- 47.3 degrees C (at 60 mmHg) (Budavari, 1996)
- 38.4 degrees C (at 40 mmHg) (Budavari, 1996)
- 25.7 degrees C (at 20 mmHg) (Budavari, 1996)
- 13.4 degrees C (at 10 mmHg) (Budavari, 1996)
- 2.1 degrees C (at 5 mmHg) (Budavari, 1996)
- -20.0 degrees C (at 1.0 mmHg) (Budavari, 1996)
FLASH POINT
- 29 degrees C; 85 degrees F (open cup) (Budavari, 1996; Clayton & Clayton, 1994)
- 26.1 degrees C: 79 degrees F (open cup) (Lewis, 1993; Lewis, 1996)
- 24-26 degrees C; 76-79 degrees F (open cup) (NFPA, 1994)
- 62 degrees F (open cup) (CHRIS , 1997; NIOSH , 1997)
AUTOIGNITION TEMPERATURE
- 501 degrees C; 935 degrees F (NFPA, 1994)
- 910 degrees F (CHRIS , 1997)
EXPLOSIVE LIMITS
SOLUBILITY
n-Butyronitrile is slightly soluble in water (Ashford, 1994; Clayton & Clayton, 1994; Lewis, 1996) 3% (at 77 degrees F) (NIOSH , 1997) 33,000 mg/L (at 25 degrees C) (HSDB , 1997)
This compound is soluble in alcohol, benzene, ether, and dimethylformamide (Budavari, 1996; HSDB , 1997; Lewis, 1993; Lewis, 1996). It is miscible with oxygenated solvents (Ashford, 1994).
HENRY'S CONSTANT
- 5.23x10(-5) atm-m(3)/mol (at 25 degrees C) (measured) (HSDB , 1997)
OTHER/PHYSICAL
1.38385 (at 20 degrees C) (Budavari, 1996; ITI, 1988) 1.3842 (at 20 degrees C/D) (HSDB , 1997) 1.3816 (at 24 degrees C) (Clayton & Clayton, 1994)
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