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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
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)
T Crisippi et al.
Journal of AOAC International, 76(3), 650-656 (1993-05-01)
A gas chromatographic method is described that is suitable for the determination of benalaxyl residues ranging from 10 to 0.1 micrograms/kg in several crops, must, wine, and water. The compound is extracted with acetone and purified either by partitioning between
Peng Xu et al.
Journal of agricultural and food chemistry, 57(18), 8545-8549 (2009-08-22)
The enantioselectivities of individual enantiomers of benalaxyl in acute toxicity and bioaccumulation in earthworm ( Eisenia fedtia ) were studied. The acute toxicity was tested by paper contact test. After 48 h of exposure, the calculated LC(50) values of the
I Rosso et al.
Journal of agricultural and food chemistry, 48(1), 33-36 (2000-01-19)
The applicability of an ELISA for detection and quantification of benalaxyl in red wine samples is described. The study of the influence of this matrix on the reliability of the assay indicates that red wine samples require a rapid and
Ledan Huang et al.
Chemosphere, 87(1), 7-11 (2011-12-16)
Enantioselectivity in ecotoxicity and biodegradation of chiral pesticide benalaxyl to freshwater algae Scenedesmus obliquus was studied. The 96 h-EC(50) values of rac-, R-(-)-, S-(+)-benalaxyl were 2.893, 3.867, and 8.441 mg L(-1), respectively. Therefore, the acute toxicities of benalaxyl enantiomers were
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