32972
乳氟禾草灵
PESTANAL®, analytical standard
别名:
2-乙氧基-1-甲基-2-氧乙基 5-(2-氯-4-三氟甲基苯氧基)-2-硝基苯甲酸酯, O-[5-(2-氯-α,α,α-三氟-对甲苯氧基)-2-硝基苯甲酰]-DL-乳酸乙酯
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关于此项目
经验公式（希尔记法）:
C19H15ClF3NO7
化学文摘社编号:
分子量:
461.77
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
InChI
1S/C19H15ClF3NO7/c1-3-29-17(25)10(2)30-18(26)13-9-12(5-6-15(13)24(27)28)31-16-7-4-11(8-14(16)20)19(21,22)23/h4-10H,3H2,1-2H3
SMILES string
CCOC(=O)C(C)OC(=O)c1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1[N+]([O-])=O
InChI key
CONWAEURSVPLRM-UHFFFAOYSA-N
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
General description
Lactofen is a broad-spectrum post-emergent herbicide. It acts by inhibiting protoporphyrinogen oxidase by causing lipid peroxidation of the cell membrane.
Application
Lactofen may be used as an analytical reference standard for the determination of the analyte in:
- Environmental samples by high performance liquid chromatography (HPLC) coupled to tandem mass spectrometric detector (MS/MS), ultraviolet (UV) detector and circular dichroism (CD) detector.
- Fruit and wheat flour matrices by on-line turbulent flow chromatography (TFC) combined with LC-MS/MS.
- Agricultural products using gas chromatography coupled to flame photometric detector (GC-FPD).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Aquatic Chronic 2
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
Coupled turbulent flow chromatography: LC-MS/MS method for the analysis of pesticide residues in grapes, baby food and wheat flour matrices.
Hollosi L, et al.
Chromatographia, 75(23-24), 1377-1393 (2012)
Irani Mukherjee et al.
Bulletin of environmental contamination and toxicology, 79(1), 49-52 (2007-06-30)
Lactofen, a member of the diphenyl ether chemical family, shows great potential for the control of broadleaf weeds associated with leguminous crops. It presents a high degree of selectivity when applied post-emergence to soybean and peanut crops. This paper presents
Serena Landini et al.
Phytochemistry, 62(6), 865-874 (2003-02-19)
Lactofen, the active ingredient of the soybean disease resistance-inducing herbicide, Cobra, induces large accumulations of isoflavone conjugates and aglycones in soybean tissues. The predominant isoflavones induced in cotyledon tissues are daidzein (and its conjugates) and formononetin and glycitein aglycones. The
Rosana N Malpassi
Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al, 30(1), 51-56 (2006-07-19)
Eleusine indica and Portulaca oleracea are two common weeds in peanut crops in southern Córdoba. Two chemicals are frequently used to control them, quizalofop for grasses and lactofen for dicots. The objective is to study the effects of quizalofop and
Bo Liang et al.
Journal of agricultural and food chemistry, 58(17), 9711-9715 (2010-08-18)
The diphenyl ether herbicide lactofen is commonly used to control broadleaf weeds. Once released into the environment, this herbicide is subject to microbial reactions. This study describes the biotransformation of lactofen by Brevundimonas sp. LY-2 isolated from enrichment cultures inoculated
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