2-(2-Butoxyethoxy)ethyl-6-propylpiperonylether

Piperonyl butoxide Struktur
51-03-6
CAS-Nr.
51-03-6
Bezeichnung:
2-(2-Butoxyethoxy)ethyl-6-propylpiperonylether
Englisch Name:
Piperonyl butoxide
Synonyma:
PBO;Butoxide;5-[2-(2-BUTOXYETHOXY)ETHOXYMETHYL]-6-PROPYL-1,3-BENZODIOXOLE;BUTACIDE;Poperonyl butoxide;Piperronyl butoxide;1,3-Benzodioxole, 5-[[2-(2-butoxyethoxy)ethoxy]methyl]-6-propyl-;Vex;INCITE;Butacid
CBNumber:
CB4337573
Summenformel:
C19H30O5
Molgewicht:
338.44
MOL-Datei:
51-03-6.mol

2-(2-Butoxyethoxy)ethyl-6-propylpiperonylether Eigenschaften

Schmelzpunkt:
<25 °C
Siedepunkt:
180 °C
Dichte
1.059 g/mL at 25 °C(lit.)
Dampfdruck
0.02 hPa (60 °C)
Brechungsindex
n20/D 1.498(lit.)
Flammpunkt:
>230 °F
storage temp. 
2-8°C
Löslichkeit
water: slightly soluble0.0289g/L at 20.4°C
Aggregatzustand
Liquid
Farbe
Clear yellow
Wichte
1.060 (20/4℃)
Geruch (Odor)
mild odor or odorless
Wasserlöslichkeit
<0.1 g/100 mL at 18 ºC
Merck 
14,7476
BRN 
288063
Stabilität:
Stable. Combustible. Incompatible with oxidizing agents.
InChIKey
HHZWGSFIZRNPFB-UHFFFAOYSA-N
LogP
4.750
CAS Datenbank
51-03-6(CAS DataBase Reference)
IARC
3 (Vol. 30, Sup 7) 1987
NIST chemische Informationen
Piperonyl butoxide(51-03-6)
EPA chemische Informationen
Piperonyl butoxide (51-03-6)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher N,T
R-Sätze: 50/53-51/53-24
S-Sätze: 60-61-45-36/37/39-28A
RIDADR  UN 3082 9/PG 3
WGK Germany  3
RTECS-Nr. XS8050000
TSCA  Yes
HazardClass  6.1(b)
PackingGroup  III
HS Code  29329990
Giftige Stoffe Daten 51-03-6(Hazardous Substances Data)
Toxizität LD50 orally in female, male rats: 6150, 7500 mg/kg (Gaines)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 1 Warnung GHS hazard pictogramssrc="/GHS09.jpg" width="20" height="20" /> P273, P391, P501
Sicherheit
P273 Freisetzung in die Umwelt vermeiden.
P391 Verschüttete Mengen aufnehmen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

2-(2-Butoxyethoxy)ethyl-6-propylpiperonylether Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD

öLIGE, GELBE BIS BRAUNE FLüSSIGKEIT.

ARBEITSPLATZGRENZWERTE

TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).

AUFNAHMEWEGE

Aufnahme in den Körper durch Inhalation des Aerosols und durch Verschlucken.

INHALATIONSGEFAHREN

Nur ungenügende Angaben vorhanden über die Geschwindigkeit, mit der eine gesundheitsschädliche Konzentration in der Luft beim Verdampfen bei 20°C erreicht wird.

LECKAGE

Ausgelaufene Flüssigkeit in abdichtbaren Behältern sammeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. NICHT in die Umwelt gelangen lassen.

R-Sätze Betriebsanweisung:

R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R51/53:Giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R24:Giftig bei Berührung mit der Haut.

S-Sätze Betriebsanweisung:

S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.

Beschreibung

Piperonyl 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.

Chemische Eigenschaften

Piperonyl 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.

Verwenden

Piperonyl 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.

synthetische

First, safrole is obtained from allyl chloride and methylenedioxybenzene. Then, piperonyl butoxide is produced by catalytic hydrogenation, chloromethylation, and etherification reactions.

Allgemeine Beschreibung

Pale yellow to light brown liquid with a mild odor and a faint bitter taste.

Air & Water Reaktionen

Insoluble in water.

Reaktivität anzeigen

Piperonyl butoxide can react with oxidizing materials.

Brandgefahr

Piperonyl butoxide is combustible.

Landwirtschaftliche Anwendung

Insecticide 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.

Handelsname

Trade names have included Butoxide, Butacide, Butocide, and Pyrenone (mixture with allethrin).

Sicherheitsprofil

Poison 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 Fate

PBO 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.

Stoffwechselwegen

Piperonyl 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.

Toxicity evaluation

Piperonyl 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.

2-(2-Butoxyethoxy)ethyl-6-propylpiperonylether Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


2-(2-Butoxyethoxy)ethyl-6-propylpiperonylether Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 385)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Weifang Wehibest Supply Chain Co.,Ltd
+8613583620690
hotspotbiotech@163.com China 926 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578
sales@hbmojin.com China 12456 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177
peter@yan-xi.com China 5993 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806
sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +86-18949832763
info@tnjchem.com China 2989 55
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282
alice@crovellbio.com China 8823 58
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22968 58

51-03-6(2-(2-Butoxyethoxy)ethyl-6-propylpiperonylether)Verwandte Suche:


  • 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
  • Butacid
  • piperonyl butoxide (ban,bsi,iso,esa)
  • PIPERONALBUTOXIDE
  • 2-(2-Butoxyethoxy)ethyl (6-propylpiperonyl) ether, 4,5-Methylenedioxy-2-propylbenzyldiethyleneglycol butyl ether
  • Diperonyl butoxide
  • 5-{[2-(2-butoxyethoxy)ethoxy]Methyl}-6-propyl-2H-1,3-benzodioxole
  • Piperonyl butoxide,90%,tech.
  • FAC-S273
  • 5-((2-(2-Butoxyethoxy)ethoxy)methyl)-6-propylbenzo[d][1,3]dioxole
  • Piperonylbutoxide technical grade, 90%
  • 4,5-METHYLENEDIOXY-2-PROPYLBENZYLDIETHYLENEGLYCOL BUTYL ETHER
  • A-[2-(2-BUTOXYETHOXY)ETHOXY]-4,5-METHYLENEDIOXY-2-PROPYLTOLUENE
  • 6-(Propylpiperonyl)-butyl carbityl ether
  • 6-PROPYLPIPERONYL BUTYL DIETHYLENE GLYCOL ETHER
  • (3,4-METHYLENEDIOXY-6-PROPYLBENZYL)(BUTYL) DIETHYLENE GLYCOL ETHER
  • 3,4-METHYLENE-DIOXY-6-PROPYLBENZYL-N-BUTYL DIETHYLENE GLYCOL ETHER
  • 2-(2-BUTOXYETHOXY)ETHYL (6-PROPYLPIPERONYL) ETHER
  • INCITE
  • 'LGC' (1625)
  • (BUTYLCARBITYL)(6-PROPYL-PIPERONYL) ETHER
  • BUTOXIDE(R)
  • BUTACIDE(R)
  • PRENTOX
  • PIPERONYL BUTOXIDE
  • SANEX FLY KILLER
  • (3,4-methylenedioxy-6-propylbenzyl)(butyl)diethyleneglicolether
  • 3,4-Methylendioxy-6-propylbenzyl-n-butyl-diaethylenglykolaether
  • 3,4-methylenedioxy-6-propylbenzyl-n-butyl-diaethylenglykolaether
  • 2-(2-Butoxyethoxy)ethyl (6-propylpiperonyl) ether 4,5-Methylenedioxy-2-propylbenzyldiethyleneglycol butyl ether 5-[2-(2-Butoxyethoxy)ethoxymethyl]-6-propyl-1,3-benzodioxole PBO
  • 3-Benzodioxole,5-[[2-(2-butoxyethoxy)ethoxy]methyl]-6-propyl-1
  • 5-((2-(2-butoxyethoxy)ethoxy)methyl)-6-propyl-3-benzodioxole
  • 5-[[2-(2-butoxyethoxy)ethoxy]methyl]-6-propyl-3-benzodioxole
  • 5-propyl-4-(2,5,8-trioxa-dodecyl)-1,3-benzodioxol
  • 5-Propyl-4-(2,5,8-trioxa-dodecyl)-1,3-benzodioxole
  • Alleviate
  • alpha-(2-(2-butoxyethoxy)ethoxy)-4,5-(methylenedioxy)-2-propyl-toluen
  • alpha-(2-(2-butoxyethoxy)ethoxy)-4,5-methylenedioxy-2-propyltoluene
  • alpha(2-(2-Butoxyethoxy)ethoxy)-4,5-methylenedioxy-2-propyltoluene
  • alpha-(2-(2-n-Butoxyethoxy)-ethoxy)-4,5-methylenedioxy-2-propyltoluene
  • alpha-(2-(2-n-butoxyethoxy)-ethoxy-4,5-methylenedioxy-2-propyltoluene
  • Butocide
  • butoxide(synergist)
  • Butyl carbitol 6-propylpiperonyl ether
  • butylcarbitol6-propylpiperonylether
  • ENT 14,250
  • ent14,250
  • Ethanol butoxide
  • FAC 5273
  • FMC 5273
  • fmc5273
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