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Supelco

Diclofop-Methyl

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C16H14Cl2O4
CAS-Nummer:
51338-27-3
Molekulargewicht:
341.19
Beilstein:
2224754
EG-Nummer:
257-141-8
MDL-Nummer:
MFCD00128052
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756737
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

mp (Schmelzpunkt)

42-48 °C (if solid)

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

COC(=O)C(C)Oc1ccc(Oc2ccc(Cl)cc2Cl)cc1

InChI

1S/C16H14Cl2O4/c1-10(16(19)20-2)21-12-4-6-13(7-5-12)22-15-8-3-11(17)9-14(15)18/h3-10H,1-2H3

InChIKey

BACHBFVBHLGWSL-UHFFFAOYSA-N

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Allgemeine Beschreibung

Diclofop-methyl is an early post-emergence phenoxypropanoic acid herbicide. Its mode of action involves inhibition of acetyl CoA carboxylase (ACCase) activity, which in turn decreases fatty acid synthesis in weeds and inhibits photosynthesis and the activity of meristem.

Anwendung

Diclofop-methyl may be used as a reference standard for the determination of diclofop-methyl in soil samples by gas-liquid chromatography (GLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Rechtliche Hinweise

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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Piktogramme

Exclamation markEnvironment
GHS07,GHS09

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCBZ5051
BCBT3269
SZBD156XV
SZBA130XV
SZBA130X

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Die Dokumentenbibliothek aufrufen

Jose L De Prado et al.
Journal of agricultural and food chemistry, 53(6), 2185-2191 (2005-03-17)
Three diclofop-methyl (DM) resistant biotypes of Lolium rigidum (R1, R2, and R3) were found in different winter wheat fields in Spain, continuously treated with DM, DM + chlortoluron, or DM + isoproturon. Herbicide rates that inhibited shoot growth by 50%
Vanesa Guillén-Casla et al.
Journal of agricultural and food chemistry, 56(7), 2303-2309 (2008-03-15)
Simple one- and two-dimensional high-performance liquid chromatography (HPLC) methods for the simultaneous enantiomeric determination of alkyloxyphenoxypropionic acid herbicides is presented. Compounds studied were ( R, S)-2-[4-(2,4-dichlorophenoxy)phenoxy]propionic acid (diclofop-acid) and ( R, S)-2-[4-(2,4-dichlorophenoxy)]methyl propionate (diclofop-methyl). Mobile phases necessary to separate their
Xiyun Cai et al.
Environmental toxicology and chemistry, 26(5), 970-975 (2007-05-25)
Information on the effects of pesticide degradation on aquatic organisms is needed to properly evaluate the ecotoxicity arising from the use of pesticides and for aquatic risk assessment. This work evaluated the toxicity of diclofop-methyl (DM) and its two major
Fatma Ünal et al.
Drug and chemical toxicology, 34(4), 390-395 (2011-07-01)
Diclofop-methyl (DM) is a chlorophenoxy derivative used in large quantities for the control of annual grasses in grain and vegetable crops. In this study, the genotoxic effects of DM were investigated by measuring chromosomal aberrations (CAs) in mouse bone-marrow cells
Qin Yu et al.
Planta, 230(4), 713-723 (2009-07-16)
This study investigates mechanisms of multiple resistance to glyphosate, acetyl-coenzyme A carboxylase (ACCase) and acetolactate synthase (ALS)-inhibiting herbicides in two Lolium rigidum populations from Australia. When treated with glyphosate, susceptible (S) plants accumulated 4- to 6-fold more shikimic acid than
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