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45437

Supelco

Dichlorprop-methyl ester

PESTANAL®, analytical standard

Synonyme(s) :

Methyl 2-(2,4-dichlorophenoxy)propionate

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About This Item

Formule empirique (notation de Hill):
C10H10Cl2O3
Numéro CAS:
23844-57-7
Poids moléculaire :
249.09
Numéro Beilstein :
6059885
Numéro MDL:
MFCD00055254
Code UNSPSC :
41116107
ID de substance PubChem :
329756733
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

COC(=O)C(C)Oc1ccc(Cl)cc1Cl

InChI

1S/C10H10Cl2O3/c1-6(10(13)14-2)15-9-4-3-7(11)5-8(9)12/h3-6H,1-2H3

Clé InChI

SCHCPDWDIOTCMJ-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Informations légales

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

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCG4633
BCBT4611
SZBC094XV
SZB7340XV
SZE7340X

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Consulter la Bibliothèque de documents

F G Sánchez et al.
Analytical biochemistry, 239(1), 2-7 (1996-07-15)
This paper describes a fluorescence enzyme-linked immunosorbent assay (ELISA) for the quantification of (+/-)-2-(2, 4-dichlorophen-oxy)propionic methyl ester (dichlorprop methyl ester). Antibodies for dichlorprop methyl ester were produced by immunizing rabbits with a conjugate of dichlorprop methyl ester with bovine serum
Yun Ma et al.
Chirality, 21(4), 480-483 (2008-07-26)
Chiral pesticides currently constitute about 50% of all pesticides dosage used in China, and this ratio is increasing as more complex structures are introduced. Dichlorprop methyl (DCPPM) is a chiral herbicide consisting of a pair of enantiomers. In this study
Yue-Zhong Wen et al.
Journal of environmental sciences (China), 17(2), 237-240 (2005-11-22)
The effect of beta-cyclodextrins (beta-CDs) on the enzymatical hydrolysis of chiral dichlorprop methyl ester (DCPPM) was studied. Four kinds of beta-cyclodextrins (beta-cyclodextrin, Partly methylated-CD (PM-beta-CD), hydroxypropyl-cyclodextrin (HP-beta-CD) and carboxymethyl-cyclodextrin (CM-beta-CD)) were used. Compared with 100% DCPPM in the absence of
Yun Ma et al.
Huan jing ke xue= Huanjing kexue, 26(4), 152-155 (2005-10-11)
Enantioselective Degradation of 2,4-Dichlorprop methyl ester was studied by sediment bacteria. One DCPPM-degrading bacteria stain was isolated from contaminated sediments. The EF values were determined by chiral GC. The enantioselectivity of DCPPM biodegradation in aquatic phases were evaluated. Incubation with
Yuezhong Wen et al.
Journal of agricultural and food chemistry, 59(5), 1924-1930 (2011-02-15)
Up to 25% of the current pesticides are chiral, the molecules have chiral centers, but most of them are used as racemates. In most cases, enantiomers of chiral pesticides have different fates in the environment. Knowledge of the function of
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