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Supelco

Diclofop-methyl

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C16H14Cl2O4
Numero CAS:
51338-27-3
Peso molecolare:
341.19
Beilstein:
2224754
Numero CE:
257-141-8
Numero MDL:
MFCD00128052
Codice UNSPSC:
41116107
ID PubChem:
329756737
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

42-48 °C (if solid)

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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
BACHBFVBHLGWSL-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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.

Note legali

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

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Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H302,H317,H410

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCBZ5051
BCBT3269
SZBD156XV
SZBA130XV
SZBA130X

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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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