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Dichlorprop-P

PESTANAL®, analytical standard

Synonym(e):

(R)-(+)-2-(2,4-Dichlorphenoxy)-propionsäure

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About This Item

Empirische Formel (Hill-System):
C9H8Cl2O3
CAS-Nummer:
15165-67-0
Molekulargewicht:
235.06
Beilstein:
5265110
EG-Nummer:
403-980-1
MDL-Nummer:
MFCD00144036
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329753693
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

Anwendung(en)

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

InChIKey

MZHCENGPTKEIGP-RXMQYKEDSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

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

Anwendung

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

Empfohlene Produkte

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.

Rechtliche Hinweise

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

Piktogramme

CorrosionExclamation mark
GHS05,GHS07

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

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Analysenzertifikate (COA)

Lot/Batch Number
BCCF8377
BCBT4572
SZBC088XV
SZB7275XV
7275X

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Die Dokumentenbibliothek aufrufen

The Pesticide Encyclopedia (2014)
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.
Yuezhong Wen et al.
Journal of environmental monitoring : JEM, 13(4), 879-885 (2011-02-08)
To reduce the leaching potential, to prevent groundwater contamination and to maintain the efficacy of a pesticide, natural polysaccharides have received increasing attention due to their biocompatibility and useful biological reactivity for controlled release formulations (CRFs) of pesticides. In this
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
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