LACTONITRILE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
LACTONITRILE ACETALDEHYDE CYANOHYDRIN ACETOCYANOHYDRIN ETHYLIDENE CYANOHYDRIN alpha-HYDROXYPROPIONITRILE 2-HYDROXYPROPANENITRILE 2-HYDROXYPROPANNITRIL (Czech) 2-HYDROXYPROPIONITRILE LAKTONITRIL (Czech) PROPANOIC ACID, 2-HYDROXY-, NITRILE PROPIONITRILE, 2-HYDROXY-
IDENTIFIERS
SYNONYM REFERENCE
- (RTECS , 1990; EPA, 1985; HSDB , 1990)
USES/FORMS/SOURCES
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Lactonitrile is an cyanogenic aliphatic nitrile compound. Its toxicity is thought to be mainly due to the metabolic release of cyanide by hepatic biotransformation after absorption. However, some acute toxicity may be due to the parent compound itself. At least one human fatality has been reported from lactonitrile poisoning.
- Although the aliphatic nitrile compounds in general cause the same signs and symptoms as seen in cyanide poisoning, the onset of toxicity is likely to be delayed for up to several hours after exposure as some time is required for sufficient hepatic metabolism of the parent compound with release of sufficient amounts of cyanide.
- Chronic occupational exposure to other similar nitrile compounds such as acetonitrile has resulted in interference of iodine uptake by the thyroid and some cases of goiter, presumably by interference of thiocyanate produced during normal cyanide detoxification by the endogenous rhodanese enzyme. Whether this occurs with lactonitrile exposure has not been reported.
- HYDROGEN CYANIDE may be released from lactonitrile in the presence of alkali. Both cyanide and oxides of nitrogen fumes may be evolved during thermal decomposition.
- The remainder of this discussion relates to CYANIDE POISONING and TREATMENT. The possibility of DELAYED ONSET of SYMPTOMS, up to SEVERAL HOURS AFTER LACTONITRILE EXPOSURE must be kept in mind. PROLONGED OBSERVATION is usually required for initially asymptomatic individuals with aliphatic nitrile exposure.
Hydrogen cyanide gas exposure may produce death within minutes. Lesser exposures may produce nausea, vomiting, palpitations, confusion, hyperventilation, anxiety, and vertigo. Severe hypoxic signs in the absence of cyanosis suggest the diagnosis. Cyanide release after systemic lactonitrile absorption may take a considerable period, with SYMPTOM ONSET DELAYED for SEVERAL HOURS after exposure. Patients have survived potentially lethal cyanide exposures with supportive care only, and the absence of a rapidly deteriorating course does not exclude the diagnosis. Cyanosis is generally a late finding and does not occur until the stage of circulatory collapse and apnea. The patient's clinical state will depend on the extent and time since exposure. Initially the patient may experience flushing, tachycardia, tachypnea, headache, and dizziness. This may progress to agitation, stupor, coma, apnea, generalized convulsions, pulmonary edema, bradycardia, hypotension, and death.
- If systemic CYANIDE POISONING is suspected, IMMEDIATELY BEGIN ADMINISTERING 100% OXYGEN. OBTAIN THE CYANIDE ANTIDOTE KIT AND PREPARE IT FOR USE.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
ACUTE CLINICAL EFFECTS
- From its acute oral LD50 of 87 mg/kg in rats, lactonitrile is a moderately toxic compound. It can be absorbed through intact skin (Sax & Lewis, 1989; EPA, 1985). Application to the eyes has been lethal in experimental animals (Hartung, 1982; HSDB , 1993). At least one human fatality has been reported from lactonitrile poisoning (Nagata et al, 1968), and the compound has been classified as one of the highly toxic aliphatic nitriles (Zuzik, 1983).
- An important aspect is possible DELAYED ONSET of appearance of signs and symptoms, due to the time required to release cyanide by hepatic metabolism (Hartung, 1982).
- The fatal dose of cyanide salts is estimated to be 200 to 300 milligrams for an adult (Bonnichsen & Maely, 1966; Baselt & Cravey, 1989). As little as 180 milligrams can be rapidly fatal (CHRIS, 1993). Inhalation of 0.2 to 0.3 mg/L (200 to 300 ppm) may be rapidly fatal (ACGIH, 1986). However, individuals have survived much higher exposures to cyanide (Yacoub et al, 1974; Hall et al, 1987; Bismuth et al, 1984; Dodds & McKnight, 1985).
- Cyanide causes signs and symptoms including flushing, nausea, vomiting, palpitations, tachycardia, hyperpnea, headache, dizziness, confusion, hypertension, hypotension, cardiac arrhythmias and conduction defects, metabolic acidosis, seizures, anxiety, agitation, tremors, weakness, stupor, and coma (Hall & Rumack, 1986). Death may occur within a few minutes of acute cyanide exposure.
- Damage to the optic nerve has been produced in rats within 48 hours after a single injection of sodium cyanide; damage from a single exposure was progressive (Lessell & Kuwabara, 1974). A Parkinsonian-like syndrome has occurred up to several weeks after acute cyanide poisoning (Rosenberg et al, 1989). CNS signs and symptoms may be reversible up to a point (Wuthrich, 1954), but some may persist for many months (Pettigrew, 1977).
CHRONIC CLINICAL EFFECTS
- At the time of this review, no studies were found on chronic exposure to lactonitrile in humans.
- Chronic occupational exposure to other nitrile compounds such as ACETONITRILE has resulted in interference of iodine uptake by the thyroid and some cases of goiter, presumably due to interference by thiocyanate produced during normal cyanide detoxification by the endogenous rhodanese enzyme (Hartung, 1982). Whether this occurs with lactonitrile exposure has not been reported.
- Chronic occupational cyanide exposure has been associated with a variety of dermal and mucous membrane irritant complaints, usually attributed to exposure to highly alkaline aerosols or solutions of cyanide salts (Finkel, 1983; (Hartung, 1982; Proctor et al, 1988).
- True chronic cyanide toxicity in humans is rare (Proctor et al, 1988), although a variety of complaints including goiter, subclinical thyroid function and B12 and folate abnormalities, headaches, vertigo, chest discomfort, palpitations, eye and respiratory tract irritation, dermatitis, fatigue, poor appetite and sleeping, and epistaxis have been reported in cyanide-exposed workers (Proctor et al, 1998; (Colle, 1972; Saia et al, 1970; Ermans et al, 1972).
- Chronic exposure to cyanides has been reported to cause CNS effects such as insomnia, loss of memory, and tremors (Chaumont, 1960). Experimental animal studies have confirmed the central nervous system as a target for chronic cyanide toxicity. Rats fed cyanide for 11 months developed spinal cord damage (Philbrick, 1979). Other neurological effects include degeneration of the optic nerve, resulting in decreased visual acuity or blindness.
- In rats, cyanide metabolites may accumulate over long periods of chronic exposure (Tewe & Maner, 1981).
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
CYANIDE COMPOUNDS - Patients have survived exposure to hydrogen cyanide air concentrations of 500 mg/m(3) (Bonsall, 1984), ingestions of one gram of potassium cyanide (Yacoub et al, 1974; Hall et al, 1987), and complete immersion in solutions of cyanide salts (Bismuth et al, 1984; Dodds & McKnight, 1985).
- Carcinogenicity Ratings for CAS78-97-7 :
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 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 CAS78-97-7 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS78-97-7 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS78-97-7 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS78-97-7 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS78-97-7 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS78-97-7 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS78-97-7 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS78-97-7 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS78-97-7 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS78-97-7 (U.S. Environmental Protection Agency, 2010):
Listed as: Lactonitrile Reportable Quantity, in pounds: 1000 Threshold Planning Quantity, in pounds: Note(s): Not Listed
- EPA SARA Title III, Community Right-to-Know for CAS78-97-7 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS78-97-7 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS78-97-7 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS78-97-7 (NFPA, 2002):
-PERSONAL PROTECTION
SUMMARY
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 78-97-7.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS78-97-7 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- NFPA Extinguishing Methods for CAS78-97-7 (NFPA, 2002):
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS78-97-7 (AIHA, 2006):
- DOE TEEL Values for CAS78-97-7 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Lactonitrile TEEL-0 (units = mg/m3): 3.5 TEEL-1 (units = mg/m3): 10 TEEL-2 (units = mg/m3): 18 TEEL-3 (units = mg/m3): 150 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 CAS78-97-7 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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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; 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 CAS78-97-7 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Colorless or straw-colored liquid (Lewis, 1996).
SPECIFIC GRAVITY
- STANDARD TEMPERATURE AND PRESSURE
SOLUBILITY
-REFERENCES
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- 65 FR 77866: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
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- 67 FR 7164: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2002.
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- 69 FR 54144: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2004.
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