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Supelco

Piperonylbutoxide

PESTANAL®, analytical standard

Synonym(s):

2-(2-Butoxyethoxy)ethyl (6-propylpiperonyl) ether, 4,5-Methylenedioxy-2-propylbenzyldiethyleneglycol butyl ether

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About This Item

Empirical Formula (Hill Notation):
C19H30O5
CAS Number:
51-03-6
Molecular Weight:
338.44
Beilstein:
288063
EC Number:
200-076-7
MDL number:
MFCD00005842
UNSPSC Code:
41116107
PubChem Substance ID:
329756841
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.498 (lit.)

bp

155 °C/0.3 mmHg (lit.)

density

1.059 g/mL at 25 °C (lit.)

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

CCCCOCCOCCOCc1cc2OCOc2cc1CCC

InChI

1S/C19H30O5/c1-3-5-7-20-8-9-21-10-11-22-14-17-13-19-18(23-15-24-19)12-16(17)6-4-2/h12-13H,3-11,14-15H2,1-2H3

InChI key

FIPWRIJSWJWJAI-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H319 - H335 - H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

EUH066

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

339.8 °F - closed cup

Flash Point(C)

171 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD4067
BCBX0805
BCBR2593V
BCBR2593
SZBF229XV

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Petek Piner et al.
Environmental toxicology and pharmacology, 33(3), 414-420 (2012-03-06)
The aim of this study was to investigate the toxic effects of pyrethroid pesticide lambda-cyhalothrin in the presence of piperonyl butoxide as a modulator in the liver of juvenile Oreochromis niloticus. LC(50) (96h) value of lambda-cyhalothrin was determined as 2.901μg/L
Ranil Waliwitiya et al.
Journal of medical entomology, 49(3), 614-623 (2012-06-12)
The biochemical mechanisms underlying the increased toxicity of several plant essential oils (thymol, eugenol, pulegone, terpineol, and citronellal) against fourth instar of Aedes aegypti L. when exposed simultaneously with piperonyl butoxide (PBO) were examined. Whole body biotransformational enzyme activities including
Olivier J T Briët et al.
Malaria journal, 12, 77-77 (2013-02-28)
The effectiveness of insecticide-treated nets in preventing malaria is threatened by developing resistance against pyrethroids. Little is known about how strongly this affects the effectiveness of vector control programmes. Data from experimental hut studies on the effects of long-lasting, insecticidal
Rodolphe Poupardin et al.
PLoS neglected tropical diseases, 8(3), e2743-e2743 (2014-03-22)
Thailand is currently experiencing one of its worst dengue outbreaks in decades. As in most countries where this disease is endemic, dengue control in Thailand is largely reliant on the use of insecticides targeting both immature and adult stages of
Despina Philippou et al.
Pest management science, 69(4), 499-506 (2012-09-13)
It has been reported previously that piperonyl butoxide (PBO) can inhibit both P450 and esterase activity. Although the method by which PBO combines with cytochrome P450 has been identified, the way in which it acts as an esterase inhibitor has
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