AMITRAZ
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
Amitraz Triatox Triatix Mitac Tacktic Ectodex Mitaban 1,5 di(2,4-dimethylphenyl)-3-methyl-1,3,5- trizapenta-1,4-diene N,N-(methyliminodimethylidyne) bis-2,4-xylidine 2-methyl-1,3-di(2,4-xylylimino)-2-azapropane BTS 27419 U-36059 BAAM BTS 27419 METHYLMETHANIMIDAMIDE
IDENTIFIERS
USES/FORMS/SOURCES
Amitraz is a formamidine pesticide with veterinary uses as an acaricide and insectide. It is used to control cattle ticks, mites, and other insects (lepidopterous species), and to treat generalized demodectic mange (Demodex canis) in dogs (Jones, 1990). It has been used on pear trees as a pesticide (Gosselin et al, 1984) Bonsall & Turnbull, 1983; IRIS, 1995).
Amitraz is a formamidine pesticide. Commercial preparations are formulated as a 20% solution (approximate concentration) in 75% xylene (Turnbull, 1983). This compound is also available in aromatic mixtures containing up to 2.5% of epichlorhydrin, or may be formulated in toluene (Grossman, 1993), xylene, propylene oxide, and a blend of alkyl benzene sulfonates and ethoxylated polyethers (Jones, 1990). Amitraz solutions are generally diluted 100 to 600-fold before applying to trees or livestock. Amitraz is also available as an emulsifiable concentrate or wetable powder.
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: Amitraz is an insecticide used on crops and topically for treatment of parasitic infections of farm animals. It is effective against mites, fleas, and other insects.
- TOXICOLOGY: Amitraz acts as a central alpha-2 adrenergic agonist causing CNS depression, hypotension, and bradycardia.
- EPIDEMIOLOGY: Exposure to amitraz is rare in the United States, but more common in other countries. Severe toxicity is uncommon, but deaths have been reported.
MILD TO MODERATE TOXICITY: Most patients will have mild to moderate gastrointestinal symptoms and mild sedation. Miosis is common; mydriasis may also occur. Hypersalivation is also common. SEVERE TOXICITY: Severe toxicity may include bradycardia, hypotension, sedation, seizures, respiratory depression, and coma. Hyperglycemia, acidosis (both respiratory and metabolic) and mild elevation of serum transaminase activity have also been reported. Aspiration pneumonitis may develop from the solvent vehicle (commonly xylene). There is a single report describing torsade de pointes.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
- Remove contaminated clothing and wash exposed skin with soap and water. Gastrointestinal decontamination is not recommended as patients often have vomiting and sedation, and the risk of aspiration outweighs potential benefits.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
Very little human data exist regarding the range of toxicity for ingested amitraz. Death has been reported in an adult who intentionally ingested an unknown concentration of amitraz (Bonsall & Turnball, 1983). CASE REPORT: A 53-year-old woman became comatose, developed persistent hypotension and torsades de pointes, and subsequently died after intentionally ingesting 500 mL of a pesticide containing 20% amitraz (Hu et al, 2010).
MAXIMUM TOLERATED EXPOSURE
ADULT A mentally handicapped 22-year-old man became comatose 1 hr after ingesting approximately 12.5 grams or less of amitraz in a solution. Gastric lavage, activated charcoal and sodium sulphate were administered. The individual recovered the next day (Ros & van Aken, 1994). A 30-year-old man survived after ingesting 100 milliliters of an amitraz/petroleum distillate mixture believed to contain 12.5 grams of amitraz (Kennel et al, 1996). Spontaneous vomiting occurred. A 74-year-old diabetic man believed to have ingested 6 grams or less of amitraz (30 milliliters of a xylene mixture) was unconscious for 24 hours (Bonsall & Turnball, 1983). A 29-year-old man survived a three minute period of immersion to the shoulders in a dilute amitraz cattle dip (Bonsall & Turnball, 1983). A 35-year-old man presented to the emergency department comatose (Glasgow Coma Scale 3) and hypothermic (34.5 degrees C) approximately 3 hours after intentionally ingesting approximately 50 to 100 milliliters of a product containing 12.5% amitraz in a xylene emulsion (6.25 to 12.5 grams total amount of amitraz ingested). The patient required mechanical ventilation after developing respiratory arrest. The patient also developed severe hypotension and bradycardia (35 bpm). Following supportive care, the patient gradually recovered and was extubated approximately 24 hours post-ingestion(Doganay et al, 2002). An 80-year-old man developed drowsiness, miosis, mild hypothermia (35.5 degrees C), respiratory distress, hyperglycemia, polyuria, and elevated liver enzyme levels after unintentionally ingesting approximately 1.8 grams amitraz. The onset of symptoms occurred approximately 1 hour post-ingestion. The patient gradually recovered following supportive care(Doganay et al, 2002). A 22-year-old woman developed hypotension, bradycardia, respiratory depression, and became comatose following intentional intravenous administration of 5 to 6 mL of a solution containing 12.5% amitraz and 57.5% xylene in water. The patient recovered following supportive therapy (Gursoy et al, 2005).
PEDIATRIC A 3-year-old girl developed coma and severe hyperglycemia after ingesting approximately 10.6 milliliters of an amitraz containing solution (Jones, 1990). A 17-year-old survived following ingestion of about 6 grams of amitraz (50 milliliters of amitraz/petroleum distillate) but was in a deep coma, was hypotensive and bradycardic (Kennel et al, 1996). A 4-month-old infant developed hypothermia, drowsiness, and bradycardia after ingesting 0.3 mL of a 5% amitraz solution (2.5 mg/kg). The infant completely recovered following supportive care (Zoelen et al, 2001). A 13-year-old boy was comatose (GCS 3) and hypotensive (70/50 mmHg) after ingesting 125 mL of a pesticide containing 12.5% amitraz. With symptomatic and supportive therapy, the patient gradually recovered without sequelae (Varma et al, 2013).
Dogs demonstrated no signs of toxicity after 0.25 milligram/kilogram orally and 16 milligrams/kilogram dermally. At parenteral doses of 20 mg/kg or greater, hypotension and bradycardia occurred (Anon, 1980). Rats sprayed twice 14 days apart with up to a 2000 parts per million concentration of amitraz solution showed no evidence of toxicity (Al-Qarawi et al, 1999).
- Carcinogenicity Ratings for CAS33089-61-1 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed EPA (U.S. Environmental Protection Agency, 2011): Not Assessed under the IRIS program. ; Listed as: Amitraz 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 CAS33089-61-1 (U.S. Environmental Protection Agency, 2011):
Oral: Inhalation: Drinking Water:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS33089-61-1 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS33089-61-1 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS33089-61-1 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS33089-61-1 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS33089-61-1 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS33089-61-1 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS33089-61-1 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS33089-61-1 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS33089-61-1 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS33089-61-1 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS33089-61-1 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS33089-61-1 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS33089-61-1 (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 33089-61-1.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS33089-61-1 (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 CAS33089-61-1 (NFPA, 2002):
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS33089-61-1 (AIHA, 2006):
- DOE TEEL Values for CAS33089-61-1 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS33089-61-1 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS33089-61-1 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- This compound exists as white or pale yellow monoclinic needles.
FREEZING/MELTING POINT
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