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Merck
CN

45626

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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756841
EC Number:
200-076-7
Beilstein/REAXYS Number:
288063
MDL number:
MFCD00005842

Key Documents

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Product Name

Piperonylbutoxide, PESTANAL®, analytical standard

InChI key

FIPWRIJSWJWJAI-UHFFFAOYSA-N

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

SMILES string

CCCCOCCOCCOCc1cc2OCOc2cc1CCC

grade

analytical standard

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

Quality Level

100

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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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

339.8 °F - closed cup

flash_point_c

171 °C - closed cup

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5993
BCCD4067
BCBX0805
BCBR2593V
BCBR2593

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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
N Karatolos et al.
Insect molecular biology, 21(3), 327-334 (2012-03-31)
Spiromesifen is a novel insecticide and is classed as a tetronic acid derivative. It targets the insects' acetyl-coenzyme A carboxylase (ACCase) enzyme, causing a reduction in lipid biosynthesis. At the time of this publication, there are no reports of resistance
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
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
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
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