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Key Documents

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45436

Supelco

Dichlorprop

PESTANAL®, analytical standard

Sinónimos:

2-(2,4-Dichlorophenoxy)propionic acid

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About This Item

Fórmula empírica (notación de Hill):
C9H8Cl2O3
Número de CAS:
120-36-5
Peso molecular:
235.06
Beilstein/REAXYS Number:
6568822
EC Number:
204-390-5
MDL number:
MFCD00002645
UNSPSC Code:
41116107
PubChem Substance ID:
329756732
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

quality

racemate

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

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

InChI

1S/C9H8Cl2O3/c1-5(9(12)13)14-8-3-2-6(10)4-7(8)11/h2-5H,1H3,(H,12,13)

InChI key

MZHCENGPTKEIGP-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.

Legal Information

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

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCD6681
BCBW2683
SZBF161XV
SZBC047XV
SZB7299XV

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Wenbang Li et al.
Molecules (Basel, Switzerland), 24(9) (2019-05-01)
Chlorophenoxy acid herbicides (CAHs), which are widely used on cereal crops, have become an important pollution source in grains. In this work, a highly hydrophobic poly (octadecyl methacrylate-co-trimethylolpropane trimethacrylate) [poly (OMA-co-TRIM)] monolithic column has been specially prepared for hydrophobic in-tube
Mélanie M Paulin et al.
Environmental microbiology, 13(6), 1513-1523 (2011-03-23)
We investigated the effect of (R,S)-dichlorprop herbicide addition to soil microcosms on the degrading indigenous microbial community by targeting multiple α-ketoglutarate-dependent (α-KG) dioxygenase-encoding genes (rdpA, sdpA and tfdA group I) at both gene and transcript level. The soil microbial community
Tong Wu et al.
Journal of agricultural and food chemistry, 59(8), 4315-4320 (2011-03-16)
To investigate the enantioselective oxidative damage of the pesticide dichlorprop (DCPP) to maize, young seedlings were exposed to solutions of DCPP enantiomers and racemate at different concentrations. Early root development was more influenced by (R)-DCPP than racemic (rac)- and (S)-DCPP.
Hirotatsu Murano et al.
Journal of agricultural and food chemistry, 56(4), 1350-1357 (2008-02-06)
The adsorption of 2-(2,4-dichloro-3-methylphenoxy)propanoic acid (DMPA) on the surface horizon of a humus-rich Andosol was examined. To investigate the mechanisms of adsorption, chemically treated Andosols, such as organic matter removed Andosol, organic matter and active metals removed Andosol, and clay
Mélanie M Paulin et al.
Applied and environmental microbiology, 76(9), 2873-2883 (2010-03-23)
The rdpA and sdpA genes encode two enantioselective alpha-ketoglutarate-dependent dioxygenases catalyzing the initial step of microbial degradation of the chiral herbicide (R,S)-2-(2,4-dichlorophenoxy)propionate (R,S-dichlorprop). Primers were designed to assess abundance and transcription dynamics of rdpA and sdpA genes in a natural
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