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Piperonyl butoxide

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Products Intro: Product Name:Piperonyl butoxide
CAS:51-03-6
Purity:0.99 Package:10g;100g;1kg;25kg;200kg;IBC
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CAS:51-03-6
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Products Intro: Product Name:Piperonyl butoxide
CAS:51-03-6
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Products Intro: Product Name:Piperonyl butoxide
CAS:51-03-6
Purity:97% (Min,HPLC)Density Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:Piperonyl butoxide
CAS:51-03-6
Purity:99% Package:25KG;5KG;1KG

Piperonyl butoxide manufacturers

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Piperonyl butoxide Basic information
Product Name:Piperonyl butoxide
Synonyms:PIPERONYL BUTOXIDE, TECH., 90%;PIPERONYL BUTOXIDE, 100MG,NEAT;PIPERONYL BUTOXIDE PESTANAL;Piperonylbutoxide~85%;pieronyl butoxide;α-[2-(2-Butoxyethoxy)ethoxy]-4,5-methylenedioxy-2-propyltoluene;1-(benzo[d][1,3]dioxol-5-yl)pentan-2-olate;Piperonylbutoxide,2-(2-Butoxyethoxy)ethyl (6-propylpiperonyl) ether, 4,5-Methylenedioxy-2-propylbenzyldiethyleneglycol butyl ether
CAS:51-03-6
MF:C19H30O5
MW:338.44
EINECS:200-076-7
Product Categories:stabilizer;pesticides;Intermediates & Fine Chemicals;Pharmaceuticals;Building Blocks;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Protected Alcohols/Phenols;51-03-6
Mol File:51-03-6.mol
Piperonyl butoxide Structure
Piperonyl butoxide Chemical Properties
Melting point <25 °C
Boiling point 180 °C
density 1.059 g/mL at 25 °C(lit.)
vapor pressure 0.02 hPa (60 °C)
refractive index n20/D 1.498(lit.)
Fp >230 °F
storage temp. 2-8°C
solubility water: slightly soluble0.0289g/L at 20.4°C
form Liquid
color Clear yellow
Specific Gravity1.060 (20/4℃)
Odormild odor or odorless
Water Solubility <0.1 g/100 mL at 18 ºC
Merck 14,7476
BRN 288063
Stability:Stable. Combustible. Incompatible with oxidizing agents.
InChIKeyHHZWGSFIZRNPFB-UHFFFAOYSA-N
LogP4.750
CAS DataBase Reference51-03-6(CAS DataBase Reference)
IARC3 (Vol. 30, Sup 7) 1987
NIST Chemistry ReferencePiperonyl butoxide(51-03-6)
EPA Substance Registry SystemPiperonyl butoxide (51-03-6)
Safety Information
Hazard Codes N,T
Risk Statements 50/53-51/53-24
Safety Statements 60-61-45-36/37/39-28A
RIDADR UN 3082 9/PG 3
WGK Germany 3
RTECS XS8050000
TSCA Yes
HazardClass 6.1(b)
PackingGroup III
HS Code 29329990
Hazardous Substances Data51-03-6(Hazardous Substances Data)
ToxicityLD50 orally in female, male rats: 6150, 7500 mg/kg (Gaines)
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
Piperonyl butoxide Usage And Synthesis
DescriptionPiperonyl butoxide (PBO) is a water insoluble colorless to pale yellow liquid that was developed in the 1940s to increase the effectiveness of various pesticides. It is currently registered as an active ingredient in more than 1500 products used for indoor or outdoor pesticides, including agricultural maintenance of some food crops.
Chemical PropertiesPiperonyl butoxide (PB) is a Light Yellow Liquid. It has no smell or a faint smell and a slightly bitter taste. It does not dissolve in water but can be dissolved in mineral oil and most organic solvents. It is stable to light, resistant to hydrolysis, and is not corrosive. In terms of toxicity, the LD50 (lethal dose for 50% of a test population) is 7500mg/kg in rats when administered orally.
UsesPiperonyl butoxide is used as a synergist for pyrethrins and their synthetic analogues. It is typically added to carbamate, pyrethrin, pyrethroid, and rotenone pesticides to greatly enhance their potency. PBO alone does not have pesticidal properties.
DefinitionChEBI: Piperonyl butoxide is a member of benzodioxoles. It has a role as a pesticide synergist.
PreparationFirst, safrole is obtained from allyl chloride and methylenedioxybenzene. Then, piperonyl butoxide is produced by catalytic hydrogenation, chloromethylation, and etherification reactions.
General DescriptionPale yellow to light brown liquid with a mild odor and a faint bitter taste.
Air & Water ReactionsInsoluble in water.
Reactivity ProfilePiperonyl butoxide can react with oxidizing materials.
Fire HazardPiperonyl butoxide is combustible.
Agricultural UsesInsecticide synergist: A U.S. EPA restricted Use Pesticide (RUP). Not listed for use in EU countries. Piperonyl butoxide is a synergist, i.e., not a pesticide itself, but enhances the properties of other chemicals. It is used with other pesticides such as pyrethrins, pyrethroids, rotenone and carbamates in food and non-food agricultural products, home and garden products, termite and mosquito products, and veterinary pesticide products. It inhibits the insect’s ability to break down an insecticide before it takes effect, thereby prolonging the action, and reduces the necessity for using a stronger formulation.
Trade nameTrade names have included Butoxide, Butacide, Butocide, and Pyrenone (mixture with allethrin).
Safety ProfilePoison by skin contact. Moderately toxic by ingestion and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. Many glycol ether compounds have dangerous human reproductive effects, Questionable carcinogen with experimental tumorigenic data. Mutation data reported. Combustible when exposed to heat or flame; can react with oxidizing materials. To fight fire, use foam, CO2, dry chemical. When heated to decomDosition it emits PLATINOL 0 cis-PLATlNUM(II) DIAMMINE- DICHLORIDE
Environmental FatePBO is rapidly degraded (half-life 8 h) in the environment by photolysis and is metabolized by soil microorganisms. Its estimated atmospheric half-life is approximately 3 h.
Metabolic pathwayPiperonyl butoxide is used primarily in admixture with pyrethrins and some of the pyrethroids to enhance and prolong their insecticidal action. Much of this use is in domestic and industrial situations. Metabolism studies were conducted soon after its discovery and first use in the 1950s and 1960s. The main impetus initially was to understand the mode of action as a synergist. When this was shown to be due to the inhibition of oxidative metabolism, further studies were conducted to address possible toxic interactions with other pesticides and drugs in man.
Piperonyl butoxide undergoes rapid photodegradation and microbial degradation in soil. It is also rapidly metabolised in insects and mammals by oxidative attack at the methylenedioxy carbon atom and in the side chain. A comprehensive review by Casida (1970) describes the chemistry, mode of action and metabolism of piperonyl butoxide and several related methylenedioxyphenyl compounds. Though published nearly 30 years ago, the review remains a very useful compilation of a large amount of information, supported by more than 300 references.
DegradationPiperonyl butoxide is stable to hydrolysis at pH 5,7 and 9 in sterile buffers in the dark at 25 °C. It is rapidly degraded in aqueous solution at pH 7 in sunlight with a DT50 of 8.4 hours (PM). The compound was found to be relatively stable under a variety of irradiation conditions as a thin film on glass or in organic solvent (methanol, benzene and cyclohexane). Loss of the butoxyethoxy side chain was observed to give 5-methyl-6-propyl-l,3- benzodioxole (2), butoxyethanol (3) and ethanediol (4) (Fishbein and Gaibel, 1970). These studies did not utilise radiolabelled compound. The partial pathways are shown in Scheme 1.
Toxicity evaluationPiperonyl butoxide has low to very low toxicity in birds.Researchers consider piperonyl butoxide moderately toxic to fish,although it is unlikely to accumulate.Some aquatic invertebrates may be highly sensitive to this compound.
As a synergist, PBO inhibits mixed-function oxidases, including cytochrome P450, and resistance-associated esterases that allow insects to degrade an insecticide, allowing enhanced insecticide efficacy. It does not effectively act as a synergist in mammals.
Piperonyl butoxide Preparation Products And Raw materials
Raw materialsParaformaldehyde-->Safrole-->Diethylene glycol monobutyl ether-->Sassafras oil
Tag:Piperonyl butoxide(51-03-6) Related Product Information
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