45430
Dicamba
PESTANAL®, analytical standard
동의어(들):
3,6-Dichloro-2-methoxybenzoic acid, 3,6-Dichloro-o-anisic acid
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
Cl2C6H2(OCH3)CO2H
CAS Number:
Molecular Weight:
221.04
Beilstein:
2453039
EC Number:
MDL number:
UNSPSC 코드:
41116107
PubChem Substance ID:
NACRES:
NA.24
추천 제품
Grade
analytical standard
Quality Level
제품 라인
PESTANAL®
유통기한
limited shelf life, expiry date on the label
기술
HPLC: suitable
gas chromatography (GC): suitable
mp
112-116 °C (lit.)
응용 분야
agriculture
environmental
형식
neat
SMILES string
COc1c(Cl)ccc(Cl)c1C(O)=O
InChI
1S/C8H6Cl2O3/c1-13-7-5(10)3-2-4(9)6(7)8(11)12/h2-3H,1H3,(H,11,12)
InChI key
IWEDIXLBFLAXBO-UHFFFAOYSA-N
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일반 설명
Dicamba is a polar phenoxy herbicide, used for the post-emergence control of broad-leaf weeds in grasslands and cereals.
애플리케이션
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.
법적 정보
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
이미 열람한 고객
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
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
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
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