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经验公式(希尔记法):
C20H23NO3
化学文摘社编号:
分子量:
325.40
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
275-728-7
Beilstein/REAXYS Number:
3001587
MDL number:
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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相关类别
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.
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
法规信息
农药列管产品
此项目有
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
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
Development of an enzyme-linked immunosorbent assay for benalaxyl and its application to the analysis of water and wine.
Giraudi G, et al.
Analytica Chimica Acta, 392(1), 85- 94 (1999)
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
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)
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