PIPERONYL BUTOXIDE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
PIPERONYL BUTOXIDE TOLUENE, alpha-(2-(2-BUTOXYETHOXY)ETHOXY)-4,5-(METHYLENEDIOXY)-2-PROPYL- 1,3-BENZODIOXOLE, 5-((2-(2-BUTOXYETHOXY)ETHOXY)METHYL)-6-PROPYL- BUTACIDE BUTOCIDE BUTOXIDE alpha-(2-(2-BUTOXYETHOXY)ETHOXY)-4,5-METHYLENEDIOXY-2-PROPYLTOLUENE alpha-(2-(2-n-BUTOXYETHOXY)-ETHOXY)-4,5-METHYLENEDIOXY-2-PROPYLTOLUENE 5-((2-(2-BUTOXYETHOXY)ETHOXY)METHYL)-6-PROPYL-1,3-BENZODIOXOLE BUTYL CARBITOL 6-PROPYLPIPERONYL ETHER BUTYL-CARBITYL (6-PROPYLPIPERONYL) ETHER FAC 5273 FMC 5273 3,4-METHYLENDIOXY-6-PROPYLBENZYL-n-BUTYL-DIAETHYLENGLYKOLAETHER (German) (3,4-METHYLENEDIOXY-6-PROPYLBENZYL) (BUTYL) DIETHYLENEGLICOL ETHER 3,4-METHYLENEDIOXY-6-PROPYLBENZYL n-BUTYLDIETHYLENEGLYCOL ETHER NUSYN-NOXFISH PB PRENTOX 6-(PROPYLPIPERONYL)-BUTYL CARBITYL ETHER 6-PROPYLPIPERONYL BUTYL DIETHYLENE GLYCOL ETHER 5-PROPYL-4-(2,5,8-TRIOXA-DODECYL)-1,3-BENZODIOXOL (German) PYBUTHRIN PYRENON PYRENONE 606 SYNPREN-FISH NIA 5273
IDENTIFIERS
USES/FORMS/SOURCES
TRADE NAMES Butacide(R) Prento(R) Pybuthrin(R)
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: Piperonyl butoxide is an insecticide and acaricide which is used as a synergist (by enzyme inhibition) to increase the potency of pyrethrins and rotenone. This chemical is often combined with hydrocarbons or other insecticides.
- TOXICOLOGY: Piperonyl butoxide inhibits mixed function oxidase enzymes of the liver which metabolize pyrethrins and pyrethroids, with which they are combined. Acute oral or dermal exposure is unlikely to result in significant signs and symptoms of systemic toxicity or dermal irritation.
- EPIDEMIOLOGY: Exposures to piperonyl butoxide are common but significant toxicity is rare.
MILD TO MODERATE TOXICITY: Piperonyl butoxide is minimally toxic. Skin irritation or significant percutaneous absorption is not expected following normal dermal exposure. Nausea, vomiting, anorexia, or diarrhea, eye irritation may be seen. One case of pathological laughter has been reported with human exposure. SEVERE TOXICITY: Not reported in humans. Primary sources of data are from animals which include reports of hyperexcitability, unsteadiness, anemias, liver injury, coma, seizures, and brain damage in large overdoses.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
ACUTE CLINICAL EFFECTS
USES: Piperonyl butoxide is an insecticide and acaricide which is used as a synergist (by enzyme inhibition) to increase the potency of pyrethrins and rotenone. This chemical is often combined with hydrocarbons or other insecticides. TOXICOLOGY: Piperonyl butoxide inhibits mixed function oxidase enzymes of the liver which metabolize pyrethrins and pyrethroids, with which they are combined. Acute oral or dermal exposure is unlikely to result in significant signs and symptoms of systemic toxicity or dermal irritation. EPIDEMIOLOGY: Exposures to piperonyl butoxide are common but significant toxicity is rare. MILD TO MODERATE TOXICITY: Piperonyl butoxide is minimally toxic. Skin irritation or significant percutaneous absorption is not expected following normal dermal exposure. Nausea, vomiting, anorexia, or diarrhea, eye irritation may be seen. One case of pathological laughter has been reported with human exposure. SEVERE TOXICITY: Not reported in humans. Primary sources of data are from animals which include reports of hyperexcitability, unsteadiness, anemias, liver injury, coma, seizures, and brain damage in large overdoses.
Nausea and vomiting may occur (Sax, 1984). Anorexia may be seen after a large single dose (Hayes, 1982). Diarrhea may occur (Sax, 1984).
Primary sources of data are from animals which include reports of hyperexcitability, unsteadiness, anemias, liver injury, coma, seizures, and brain damage in large overdoses (Hayes, 1982; Lehman AJ, 1952; Sarles & Vandegrift, 1952).
PB was absorbed systemically by all routes of administration in rats (Falk, 1972). It may accumulate in the fat (Kimura, 1983). It is extensively metabolized, forming as many as 26 metabolites in rats (Hayes & Laws, 1991).
CHRONIC CLINICAL EFFECTS
- At the time of this review, no chronic exposure studies were found for piperonyl butoxide in humans.
- Mice fed 0.3 or 0.9% piperonyl butoxide in the diet for 20 days had increased liver weight and other signs of liver toxicity (Fujitani et al, 1993b).
- Male rats given up to 2.4% of piperonyl butoxide in the diet for up to 12 weeks had clinical and histologic signs of liver damage; the highest dose group showed preneoplastic changes, including enlargement of hepatocyte nuclei and multinucleated cells. Kidney damage was also seen (Fujitani et al, 1993a).
- PB is not a sensitizer in rabbits (Hayes & Laws, 1991).
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
Move patient to fresh air. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with inhaled beta-2 agonist and corticosteroids.
Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia occurs, patient should be seen in a healthcare facility.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
- The minimal toxic or lethal dose in humans is not established. There have been no deaths reported following acute exposure to piperonyl butoxide alone.
MAXIMUM TOLERATED EXPOSURE
- No cases of severe irritation or toxic effects have been reported in the many exposures which occurred in development, manufacture, laboratory testing on insects, or field use.
- Male volunteers tolerated a single oral dose of 50 mg (0.71 mg/kg body weight) piperonyl butoxide with no signs of toxicity (HSDB , 2000).
- Carcinogenicity Ratings for CAS51-03-6 :
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): 3 ; Listed as: Piperonyl butoxide 3 : The agent (mixture or exposure circumstance) is not classifiable as to its carcinogenicity to humans. This category is used most commonly for agents, mixtures and exposure circumstances for which the evidence of carcinogenicity is inadequate in humans and inadequate or limited in experimental animals. Exceptionally, agents (mixtures) for which the evidence of carcinogenicity is inadequate in humans but sufficient in experimental animals may be placed in this category when there is strong evidence that the mechanism of carcinogenicity in experimental animals does not operate in humans. Agents, mixtures and exposure circumstances that do not fall into any other group are also placed in this category.
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 CAS51-03-6 (U.S. Environmental Protection Agency, 2011):
LD50- (ORAL)CAT: LD50- (ORAL)DOG: LD50- (ORAL)RABBIT: LD50- (ORAL)RAT: LD50- (SKIN)RAT:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS51-03-6 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS51-03-6 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS51-03-6 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS51-03-6 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS51-03-6 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS51-03-6 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS51-03-6 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS51-03-6 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS51-03-6 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS51-03-6 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
Listed as: Piperonyl butoxide Effective Date for Reporting Under 40 CFR 372.30: 1/1/95 Lower Thresholds for Chemicals of Special Concern under 40 CFR 372.28:
- DOT List of Marine Pollutants for CAS51-03-6 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS51-03-6 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS51-03-6 (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 51-03-6.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS51-03-6 (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 CAS51-03-6 (NFPA, 2002):
REACTIVITY HAZARD
- Stable to hydrolysis and ultraviolet light (Hartley & Kidd, 1987)
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS51-03-6 (AIHA, 2006):
- DOE TEEL Values for CAS51-03-6 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS51-03-6 (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 CAS51-03-6 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- A light brown liquid with a mild odor and bitter taste (HSDB , 2000).
- Piperonyl butoxide is a colorless to light brown or yellow liquid (HSDB , 2000).
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
BOILING POINT
- 180 degrees C (at 1 mmHg) (Sax, 1984)
FLASH POINT
- 170 degrees C; 340 degrees F (Sax, 1984)
SOLUBILITY
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