NITROPROPANE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
2-NITROPROPANE PROPANE, 2-NITRO- DIMETHYLNITROMETHANE ISONITROPROPANE NIPAR S-20 NIPAR S-20 SOLVENT NIPAR S-30 SOLVENT NITROISOPROPANE beta-NITROPROPANE 2-NP
IDENTIFIERS
79-46-9(2-nitropropane) 121-44-8(Nitropropane)
USES/FORMS/SOURCES
2-Nitropropane is a solvent which, in 5 to 25% concentrations is used to improve drying time, improve solvent release, provide better flow characteristics, increase wetting ability, increase electrostatic plating properties, and to assure greater pigment dispersion. It is also a solvent used in systems for coatings (vinyl, epoxy), and manufacture of nitrocellulose, chlorinated rubber, printing ink, adhesives, and as a gasoline additive in rocket propellant (Finkel, 1983). Industries Involved: Construction, maintenance, ship building, food packaging, furniture making and plastic products.
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- The primary symptoms at low exposure have been headache, nausea, vomiting, diarrhea, and pulmonary irritation.
- Fulminant hepatic failure and death occurred in a worker exposed to a 2-nitropropane-containing coating for 3 days in a poorly ventilated vault. A coworker survived the exposure with mildly elevated liver function tests for 12 months following the exposure.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may 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.
ACUTE CLINICAL EFFECTS
- Exposure to 2-nitropropane may produce symptoms of lethargy, weakness, headache, loss of appetite, nausea, vomiting, diarrhea, and shortness of breath. High doses may produce pulmonary edema and hemorrhage, liver damage, and METHEMOGLOBIN formation (Clayton & Clayton, 1982; ACGIH, 1986) HSDB; (Anon, 1977).
- Industrial fatalities have occurred from acute overexposure to 2-nitropropane. Workers died from hepatitis or liver damage (HSDB; Gaultlier et al, 1964; (Hine, 1978). 2-Nitropropane can irritate the mucous membranes (HSDB).
CHRONIC CLINICAL EFFECTS
- 2-Nitropropane can cause liver damage with occupational exposure (IARC, 1982; p 13). It can cause liver, intestinal tract, and respiratory congestion (Anon, 1977). It caused vascular damage, pulmonary edema, hemorrhage, and brain and liver damage in experimental animals (Clayton & Clayton, 1982).
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
The risk of aspiration may exceed the potential benefit of activated charcoal administration. It should be considered in the prehospital setting only after large ingestions. 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).
CHARCOAL DOSE Use a minimum of 240 milliliters of water per 30 grams charcoal (FDA, 1985). Optimum dose not established; usual dose is 25 to 100 grams in adults and adolescents; 25 to 50 grams in children aged 1 to 12 years (or 0.5 to 1 gram/kilogram body weight) ; and 0.5 to 1 gram/kilogram in infants up to 1 year old (Chyka et al, 2005). Routine use of a cathartic with activated charcoal is NOT recommended as there is no evidence that cathartics reduce drug absorption and cathartics are known to cause adverse effects such as nausea, vomiting, abdominal cramps, electrolyte imbalances and occasionally hypotension (None Listed, 2004).
ADVERSE EFFECTS/CONTRAINDICATIONS Complications: emesis, aspiration (Chyka et al, 2005). Aspiration may be complicated by acute respiratory failure, ARDS, bronchiolitis obliterans or chronic lung disease (Golej et al, 2001; Graff et al, 2002; Pollack et al, 1981; Harris & Filandrinos, 1993; Elliot et al, 1989; Rau et al, 1988; Golej et al, 2001; Graff et al, 2002). Refer to the ACTIVATED CHARCOAL/TREATMENT management for further information. Contraindications: unprotected airway (increases risk/severity of aspiration) , nonfunctioning gastrointestinal tract, uncontrolled vomiting, and ingestion of most hydrocarbons (Chyka et al, 2005).
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. 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.
SUPPORT INHALATION EXPOSURE INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm.
DERMAL EXPOSURE EYE EXPOSURE DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility.
ORAL EXPOSURE Do not induce emesis. 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.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
A 45-year-old man exposed to a 2-nitropropane containing coating for 3 days in a poorly ventilated vault died following a course of fulminant hepatic failure. Postmortem microscopic examination revealed massive hepatic necrosis. Serum from the first day of hospitalization contained 13 mg/L of 2-nitropropane by head-space analysis using flame-ionization gas chromatography (Harrison et al, 1987).
MAXIMUM TOLERATED EXPOSURE
A 44-year-old coworker of the above patient survived the 2-nitropropane exposure. Serum on admission contained 8.5 mg/L of 2-nitropropane. The patient remained asymptomatic with mildly elevated aspartate aminotransferase (1.33 mckat/L) and alanine aminotransferase (2 mckat/L) for 12 months (Harrison et al, 1987).
- Carcinogenicity Ratings for CAS79-46-9 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A3 ; Listed as: 2-Nitropropane 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 Assessed under the IRIS program. ; Listed as: 2-Nitropropane 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): 2B ; Listed as: 2-Nitropropane 2B : The agent (mixture) is possibly carcinogenic to humans. The exposure circumstance entails exposures that are possibly carcinogenic to humans. This category is used for agents, mixtures and exposure circumstances for which there is limited evidence of carcinogenicity in humans and less than sufficient evidence of carcinogenicity in experimental animals. It may also be used when there is inadequate evidence of carcinogenicity in humans but there is sufficient evidence of carcinogenicity in experimental animals. In some instances, an agent, mixture or exposure circumstance for which there is inadequate evidence of carcinogenicity in humans but limited evidence of carcinogenicity in experimental animals together with supporting evidence from other relevant data may be placed in this group.
NIOSH (National Institute for Occupational Safety and Health, 2007): Ca ; Listed as: 2-Nitropropane MAK (DFG, 2002): Category 2 ; Listed as: 2-Nitropropane NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
- Carcinogenicity Ratings for CAS121-44-8 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A4 ; Listed as: Triethylamine EPA (U.S. Environmental Protection Agency, 2011): Not Assessed under the IRIS program. ; Listed as: Triethylamine IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed ; Listed as: Triethylamine MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS79-46-9 (U.S. Environmental Protection Agency, 2011):
Oral: Inhalation: Unit Risk: RfC: 2x10(-2) mg/m3
Drinking Water:
- EPA Risk Assessment Values for CAS121-44-8 (U.S. Environmental Protection Agency, 2011):
Oral: Inhalation: Unit Risk: RfC: 7x10(-3) mg/m3
Drinking Water:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS79-46-9 (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.
- ACGIH TLV Values for CAS121-44-8 (American Conference of Governmental Industrial Hygienists, 2010):
Editor's Note: The listed values are recommendations or guidelines developed by ACGIH(R) to assist in the control of health hazards. They should only be used, interpreted and applied by individuals trained in industrial hygiene. Before applying these values, it is imperative to read the introduction to each section in the current TLVs(R) and BEI(R) Book and become familiar with the constraints and limitations to their use. Always consult the Documentation of the TLVs(R) and BEIs(R) before applying these recommendations and guidelines.
- AIHA WEEL Values for CAS79-46-9 (AIHA, 2006):
- AIHA WEEL Values for CAS121-44-8 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS79-46-9 (National Institute for Occupational Safety and Health, 2007):
- NIOSH REL and IDLH Values for CAS121-44-8 (National Institute for Occupational Safety and Health, 2007):
Listed as: Triethylamine REL: IDLH: IDLH: 200 ppm Note(s): Not Listed
- OSHA PEL Values for CAS79-46-9 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA PEL Values for CAS121-44-8 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS79-46-9 (U.S. Occupational Safety and Health Administration, 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS121-44-8 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS79-46-9 (U.S. Environmental Protection Agency, 2010):
Listed as: 2-Nitropropane Final Reportable Quantity, in pounds (kilograms): Additional Information: Listed as: Propane, 2-nitro- Final Reportable Quantity, in pounds (kilograms): Additional Information:
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS121-44-8 (U.S. Environmental Protection Agency, 2010):
Listed as: Triethylamine Final Reportable Quantity, in pounds (kilograms): Additional Information: Listed as: Ethanamine, N,N-diethyl- Final Reportable Quantity, in pounds (kilograms): Additional Information:
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS79-46-9 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS121-44-8 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS79-46-9 (U.S. Environmental Protection Agency, 2010b):
Listed as: 2-Nitropropane P or U series number: U171 Footnote: Listed as: Propane, 2-nitro- P or U series number: U171 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 RCRA Hazardous Waste Number for CAS121-44-8 (U.S. Environmental Protection Agency, 2010b):
Listed as: Ethanamine, N,N-diethyl- P or U series number: U404 Footnote: Listed as: Triethylamine P or U series number: U404 Footnote: Editor's Note: The D, F, and K series waste numbers and Appendix VIII to Part 261 -- Hazardous Constituents were not included. Please refer to 40 CFR Part 261.
- EPA SARA Title III, Extremely Hazardous Substance List for CAS79-46-9 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS121-44-8 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS79-46-9 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
Listed as: 2-Nitropropane Effective Date for Reporting Under 40 CFR 372.30: 1/1/87 Lower Thresholds for Chemicals of Special Concern under 40 CFR 372.28:
- EPA SARA Title III, Community Right-to-Know for CAS121-44-8 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS79-46-9 (49 CFR 172.101 - App. B, 2005):
- DOT List of Marine Pollutants for CAS121-44-8 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS79-46-9 (EPA, 2005):
- EPA TSCA Inventory for CAS121-44-8 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 2608 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN2608 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS79-46-9 (NFPA, 2002):
- NFPA Hazard Ratings for CAS121-44-8 (NFPA, 2002):
Listed as: Triethylamine Hazard Ratings: Health Rating (Blue): 3 (3) Seriously toxic material. Short term exposure could cause serious temporary or residual injury even though prompt medical treatment is given. Includes known or suspect small animal carcinogens, mutagens, or teratogens.
Flammability Rating (Red): 3 (3) Flammable. Liquids and solids that can be ignited under almost all ambient temperature conditions. Including liquids with a flash point below 73 degrees F and a boiling point above 100 degrees F, solid materials which form coarse dusts that burn rapidly without becoming explosive, materials which burn rapidly by reason of self-contained oxygen (ie, organic peroxides), and materials which ignite spontaneously when exposed to air.
Instability Rating (Yellow): 0 Oxidizer/Water-Reactive Designation: Not Listed
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
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 79-46-9.
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 121-44-8.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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 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.
2-Nitropropane is a very dangerous fire hazard when exposed to heat, open flame or oxidizers. It poses a moderate explosion hazard when shocked or heated (Sax & Lewis, 1989; Sax & Lewis, 1987).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS79-46-9 (NFPA, 2002):
- NFPA Flammability Rating for CAS121-44-8 (NFPA, 2002):
Listed as: Triethylamine Flammability Rating: 3 (3) Flammable. Liquids and solids that can be ignited under almost all ambient temperature conditions. Including liquids with a flash point below 73 degrees F and a boiling point above 100 degrees F, solid materials which form coarse dusts that burn rapidly without becoming explosive, materials which burn rapidly by reason of self-contained oxygen (ie, organic peroxides), and materials which ignite spontaneously when exposed to air.
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Dry chemical, CO2, water spray or alcohol-resistant foam. Do not use dry chemical extinguishers to control fires involving nitromethane or nitroethane.
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Water spray, fog or alcohol-resistant foam. Do not use straight streams. Move containers from fire area if you can do it without risk.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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 CAS79-46-9 (NFPA, 2002):
- NFPA Extinguishing Methods for CAS121-44-8 (NFPA, 2002):
EXPLOSION HAZARD
- 2-Nitropropane may explode on heating (Sax & Lewis, 1989).
DUST/VAPOR HAZARD
- When heated to decomposition, 2-nitropropane emits toxic fumes of oxides of nitrogen (Sax & Lewis, 1989).
REACTIVITY HAZARD
- 2-Nitropropane is incompatible with amines; strong acids, alkalies and oxidizers; metal oxides; and, combustible materials (NIOSH , 1990).
- 2-Nitropropane may explode on heating (Sax & Lewis, 1989).
- 2-Nitropropane forms violent reactions with chlorosulfonic acid and with oleum. It may react with amines + heavy metal oxides (e.g., mercury oxide or silver oxide) to form explosive salts. It may ignite on contact with mixtures of carbon + hopcalite which are used in some respirators. Hopcalite is a catalyst consisting of co-precipitated copper(II) oxide and manganese(IV) oxide (Sax & Lewis, 1989).
- 2-Nitropropane reacts with inorganic bases and amines to form salts which are flammable when dry (HSDB , 1991).
EVACUATION PROCEDURES
- Editor's Note: This material is not listed in the Table of Initial Isolation and Protective Action Distances.
- LARGE SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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 129 (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 CAS79-46-9 (AIHA, 2006):
- AIHA ERPG Values for CAS121-44-8 (AIHA, 2006):
- DOE TEEL Values for CAS79-46-9 (U.S. Department of Energy, Office of Emergency Management, 2010):
- DOE TEEL Values for CAS121-44-8 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS79-46-9 (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):
- AEGL Values for CAS121-44-8 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; United States Environmental Protection Agency Office of Pollution Prevention and Toxics, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS79-46-9 (National Institute for Occupational Safety and Health, 2007):
- NIOSH IDLH Values for CAS121-44-8 (National Institute for Occupational Safety and Health, 2007):
IDLH: 200 ppm Note(s): Not Listed
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor suppressing foam may be used to reduce vapors. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. Use clean non-sparking tools to collect absorbed material.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004) 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 , 1991). Oil skimming equipment and sorbent foams can be applied to water slicks of 2-nitropropane. Carbon or peat may be effective on dissolved portion (OHM/TADS , 1991).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- 2-Nitropropane enters the atmosphere in connection with its manufacture and use as a solvent. These sources are primarily of occupational concern. Other uses such as octane or cetane boosters in fuels could lead to more widespread exposure although no ambient monitoring is available to document such exposure (HSDB , 1991).
ENVIRONMENTAL FATE AND KINETICS
OTHER TERRESTRIAL FATE: If spilled on land, 2-nitropropane would be expected to volatilize rapidly and also leach into the soil where the rate of its degradation is unknown. Unless it is degraded in soil, there is a good possibility it will leach into the groundwater (HSDB , 1991). AQUATIC FATE: When spilled in water, 2-nitropropane will volatilize with a half-life of 9.5 hours for a typical river. It would not be expected to adsorb appreciably in soil. It could photolyze in surface water but no estimates of this or other degradative processes are available. 2-Nitropropane would not be expected to biologically concentrate in fish (HSDB , 1991). ATMOSPHERIC FATE: 2-Nitropropane can degrade in the atmosphere by photolysis and reaction with photochemically produced hydroxyl radicals. Although the half-life for the latter has been estimated to be 3.3 hours, it is reported to have "low reactivity" under photochemical smog conditions (HSDB , 1991).
ENVIRONMENTAL TOXICITY
- Effect of low concentrations of 2-nitropropane on aquatic life is unknown (CHRIS , 1991).
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- 2-Nitropropane is a colorless, oily liquid with a pleasant, fruity odor (HSDB , 2000).
- It will float as white slick on water surfaces and dissolves slowly (OHM/TADS , 1991).
PH
- 6.2 (for a 0.01 M aqueous solution) (HSDB , 1991)
VAPOR PRESSURE
- 10 mmHg (at 15.8 degrees C) (Sax & Lewis, 1989)
SPECIFIC GRAVITY
- NORMAL TEMPERATURE AND PRESSURE
- OTHER TEMPERATURE AND/OR PRESSURE
FREEZING/MELTING POINT
BOILING POINT
- 120.3 degrees C (at 760 mmHg) (Budavari, 1989)
- 110 degrees C (at 564 mmHg) (Budavari, 1989)
- 90 degrees C (at 300 mmHg) (Budavari, 1989)
- 60 degrees C (at 95 mmHg) (Budavari, 1989)
- 10 degrees C (at 7 mmHg) (Budavari, 1989)
FLASH POINT
- 24 degrees C; 75 degrees F (open cup) (Budavari, 1989; Sax & Lewis, 1987)
- 82 degrees F (closed cup) (Sax & Lewis, 1989)
AUTOIGNITION TEMPERATURE
- 427 degrees C; 802 degrees F (Sax & Lewis, 1989; Sax & Lewis, 1987)
EXPLOSIVE LIMITS
SOLUBILITY
2-Nitropropane is soluble in alcohol and ether (Sax & Lewis, 1989) and chloroform (HSDB , 1991). It is miscible with many organic solvents (Budavari, 1989; Sax & Lewis, 1989). This compound is miscible with most aromatic hydrocarbons, ketones, esters, and ethers (ACGIH, 1986).
HENRY'S CONSTANT
- 0.12 atm-m(3)/mol (Ehrenfeld et al, 1986)
OTHER/PHYSICAL
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