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Merck

31222

Benalaxyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C20H23NO3
CAS Number:
Molecular Weight:
325.40
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
275-728-7
Beilstein/REAXYS Number:
3001587
MDL number:

Product Name

Benalaxyl, PESTANAL®, analytical standard

InChI

1S/C20H23NO3/c1-14-9-8-10-15(2)19(14)21(16(3)20(23)24-4)18(22)13-17-11-6-5-7-12-17/h5-12,16H,13H2,1-4H3

InChI key

CJPQIRJHIZUAQP-UHFFFAOYSA-N

SMILES string

COC(=O)C(C)N(C(=O)Cc1ccccc1)c2c(C)cccc2C

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

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Application

Benalaxyl may be used as a fungicide reference standard for the determination of the analyte:
  • In rabbit plasma by a chiral high-performance liquid chromatography method with a diode array detector (HPLC-DAD).
  • In vegetable samples by gas chromatography-tandem mass spectrometry (GC-MS-MS).

Benalaxyl may be used as a reference standard for the determination of the analyte in water and wine samples using enzyme linked immunosorbent assay (ELISA).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Benalaxyl is a phenylamide fungicide used for the control of Oomycetes, particularly fungi of the family Peronosporaceae, Phythophthora plasmopara, and Pythium spp. Benalaxyl acts by inhibiting RNA polymerization (polymerase complex I).
Benalaxyl is a systemic fungicide belonging to the acylalanine family. It is found to be active against Oomycetes belonging to Peronosporaceae family.

Legal Information

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

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Gopinath C Nallani et al.
Regulatory toxicology and pharmacology : RTP, 84, 26-34 (2016-12-21)
The in vitro comparative animal metabolism study is now a data requirement under EU Directive 1107/2009 for registration of plant protection products. This type of study helps determine the extent of metabolism of a chemical in each surrogate species and whether
Ping Zhang et al.
Chirality, 23(2), 93-98 (2010-06-15)
Benalaxyl (BX), methyl-N-phenylacetyl-N-2,6-xylyl alaninate, is a potent acylanilide fungicide and consist of a pair of enantiomers. The stereoselective metabolism of BX was investigated in rat and rabbit microsomes in vitro. The degradation kinetics and the enantiomer fraction (EF) were determined
Separation of Benalaxyl and its metabolites by high-performance liquid chromatography.
P Cabras et al.
Journal of chromatography, 391(1), 334-337 (1987-03-27)
Xu Gu et al.
Chirality, 20(2), 125-129 (2007-12-20)
The stereoselective degradation of the racemic benalaxyl in vegetables such as tomato, tobacco, sugar beet, capsicum, and the soil has been investigated. The two enantiomers of benalaxyl in the matrix were extracted by organic solvent and determined by validated chiral
Jing Qiu et al.
Chirality, 19(1), 51-55 (2006-11-08)
A chiral high-performance liquid chromatography method with diode array detector was developed and validated for stereoselective determination of benalaxyl (BX) in rabbit plasma. Good separation was achieved at 20 degrees C using cellulose tris-(3,5-dimethylphenylcarbamate) as chiral stationary phase, a mixture

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