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Merck
CN

36189

Penconazol

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H15Cl2N3
CAS Number:
66246-88-6
Molecular Weight:
284.18
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755331
EC Number:
266-275-6
Beilstein/REAXYS Number:
541488
MDL number:
MFCD00078737

Key Documents

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Product Name

Penconazol, PESTANAL®, analytical standard

InChI key

WKBPZYKAUNRMKP-UHFFFAOYSA-N

InChI

1S/C13H15Cl2N3/c1-2-3-10(7-18-9-16-8-17-18)12-5-4-11(14)6-13(12)15/h4-6,8-10H,2-3,7H2,1H3

SMILES string

CCCC(Cn1cncn1)c2ccc(Cl)cc2Cl

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

Quality Level

100

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Application

Penconazol may be used as a reference standard in the determination of penconazol in grapefruit samples using gas chromatography (GC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Penconazol is a hydrophobic and systemic fungicide, which is effectively used against powdery mildew in vineyards.

Legal Information

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

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCM9928
BCCJ9085
BCBZ4909

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Nicoleta A Suciu et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 44(6), 525-532 (2010-02-26)
Sorption of three pesticides (chlorpyrifos, metalaxyl and penconazole) has been measured on a commercial clay montmorillonite and on the same mineral modified with either of two cationic-surfactant micelles. Both micelle-clay complexes, commercial names Cloisite 20A and Cloisite 30B, showed a
Jesús M Marín-Benito et al.
Journal of agricultural and food chemistry, 57(20), 9643-9650 (2010-06-22)
Mobility of fungicides penconazole and metalaxyl in unamended and amended vineyard soils with fresh and composted spent mushroom substrates (F-SMS and C-SMS) was studied. Experiments were performed in non-incubated and incubated (outdoors for 77 days) undisturbed soil cores under non-saturated
M Arias et al.
Journal of agricultural and food chemistry, 54(21), 8155-8162 (2006-10-13)
The upper horizons of old vineyard soils have substantial copper contents due to the traditional use of copper-based fungicides. Total copper levels in eight vineyard soils in the Rías Baixas area of Galicia (northwestern Spain) ranged from 60 to 560
Kevin C Gough et al.
Journal of agricultural and food chemistry, 57(20), 9393-9399 (2009-10-07)
Monoclonal antibodies were raised to haptens containing moieties common to both the triazole fungicide penconazole and its proposed primary urinary metabolite (4-(2,4-dichlorophenyl)-5-(H-1,2,4-triazol-1-yl)pentoic acid). The monoclonal antibody 2E4 was used to develop competitive ELISA assays where binding of antibody to immobilized
M S Rodríguez-Cruz et al.
Journal of hazardous materials, 160(1), 200-207 (2008-04-11)
Sorption-desorption of two different hydrophobic fungicides, penconazole and metalaxyl, by a series of clay minerals layered and non-layered (montmorillonite, illite, kaolinite, muscovite, sepiolite and palygorskite) modified with the two-chain cationic surfactant, dihexadecyldimetylammonium (DHDDMA) was studied by first time in this
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