45430
麦草畏
PESTANAL®, analytical standard
别名:
3,6-二氯-2-甲氧基苯甲酸, 3,6-二氯-o-对甲氧基苯甲酸
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关于此项目
线性分子式:
Cl2C6H2(OCH3)CO2H
化学文摘社编号:
分子量:
221.04
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
217-635-6
Beilstein/REAXYS Number:
2453039
MDL number:
InChI key
IWEDIXLBFLAXBO-UHFFFAOYSA-N
InChI
1S/C8H6Cl2O3/c1-13-7-5(10)3-2-4(9)6(7)8(11)12/h2-3H,1H3,(H,11,12)
SMILES string
COc1c(Cl)ccc(Cl)c1C(O)=O
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
112-116 °C (lit.)
application(s)
agriculture
environmental
format
neat
Quality Level
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General description
Dicamba is a polar phenoxy herbicide, used for the post-emergence control of broad-leaf weeds in grasslands and cereals.
Application
Dicamba may be used as an analytical reference standard for the quantification of the analyte in environmental samples using different chromatography techniques.
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
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1
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
Solid-phase extraction of dicamba and picloram from water and soil samples for HPLC analysis
Krzyszowska.JA and Vance.FG
Journal of Agricultural and Food Chemistry, 42(8), 1693-1696 (1994)
Analysis of dicamba from water using solid-phase extraction and ion-pair high-performance liquid chromatography
Arjmand M
Journal of Agricultural and Food Chemistry, 36(3), 492-494 (1988)
Manoj Ghaste et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-17)
Dicamba is a moderately volatile herbicide used for post-emergent control of broadleaf weeds in corn, soybean, and a number of other crops. With increased use of dicamba due to the release of dicamba-resistant cotton and soybean varieties, growing controversy over
Franciso P Peixoto et al.
Journal of plant physiology, 165(11), 1125-1133 (2008-04-26)
The effects of the herbicides 1,1'-dimethyl-4,4'-bipyridylium dichloride (paraquat), 3,6-dichloro-2-metoxybenzoic acid (dicamba) and 2,4-dichlorophenoxyacetic acid (2,4-D) on cell growth of non-green potato tuber calli are described. We attempted to relate the effects with toxicity, in particular the enzymes committed to the
M Sonia Rodríguez-Cruz et al.
Journal of environmental quality, 38(2), 719-728 (2009-02-27)
The sorption-desorption and interaction mechanisms of three non-ionic (linuron, alachlor, and metalaxyl) and two ionic (paraquat and dicamba) pesticides by three commercial lignins (hydrophobic macromolecule) and cellulose (hydrophilic macromolecule) as wood components were studied. Wood is a low-cost and environmentally
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