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Supelco

Dichloroprop-P

PESTANAL®, analytical standard

Synonym(s):

(R)-(+)-2-(2,4-Dichlorophenoxy)propionic acid

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About This Item

Empirical Formula (Hill Notation):
C9H8Cl2O3
CAS Number:
Molecular Weight:
235.06
Beilstein/REAXYS Number:
5265110
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

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

C[C@@H](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)/t5-/m1/s1

InChI key

MZHCENGPTKEIGP-RXMQYKEDSA-N

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General description

Dichloroprop-P is a selective, systemic and post-emergence herbicide, used for weed control management.

Application

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

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

pictograms

CorrosionExclamation mark

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Danger

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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The Pesticide Encyclopedia (2014)
Yuezhong Wen et al.
Environmental science & technology, 45(11), 4778-4784 (2011-05-07)
Reactive oxygen species (ROS) are considered to be the key players in cell toxicity. However, cross talk between the enantioselective toxicity of pesticides, heavy metals, and ROS is poorly understood. To decipher the puzzle, the effects of copper (Cu) on
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
Hui Chen et al.
Aquatic toxicology (Amsterdam, Netherlands), 120-121, 19-26 (2012-05-23)
The effect of heavy metal toxicity on the environment is usually linked to changes in the glutathione redox cycle and oxidative damage as causative events. However, it is unknown whether changes in the glutathione redox cycle are a cause or
Yuezhong Wen et al.
Environmental science & technology, 44(13), 4981-4987 (2010-06-12)
Chitosan, a natural polysaccharide, is widely regarded as a biocompatible and potential carrier for controlled-release drug formulations. However, the potential effect of chitosan on the environmental behavior of contaminants is poorly understood, especially on chiral chemicals. In this study, the

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