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Merck

45637

Supelco

Propachlor

PESTANAL®, analytical standard

Synonym(e):

2-Chlor-N-isopropylacetanilid

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About This Item

Empirische Formel (Hill-System):
C11H14ClNO
CAS-Nummer:
Molekulargewicht:
211.69
Beilstein:
2103903
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

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

CC(C)N(C(=O)CCl)c1ccccc1

InChI

1S/C11H14ClNO/c1-9(2)13(11(14)8-12)10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3

InChIKey

MFOUDYKPLGXPGO-UHFFFAOYSA-N

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Allgemeine Beschreibung

Propachlor is a herbicide, widely used in oil seeds and crop planting.

Anwendung

Propachlor may be used as an analytical reference standard for the quantification of the analyte in industrial wastewater samples and complex matrices using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Rechtliche Hinweise

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

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1

Lagerklassenschlüssel

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Persönliche Schutzausrüstung

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


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Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Multiresidue analysis of 240 pesticides in apple and lettuce by QuEChERS sample preparation and HPLC-MS/MS analysis
Wang.L, et al.
The Korean Journal of Pesticide Science, 46(5), 424-429 (2008)
Liquid-liquid extraction for sample preparation prior to gas chromatography and gas chromatography-mass spectrometry determination of herbicide and pesticide compounds
Mahara.MB, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 58(1), 31-38 (1998)
Ioannis K Konstantinou et al.
Water research, 36(11), 2733-2742 (2002-07-31)
The light-induced degradation of propachlor (2-chloro-N-isopropylacetanilide) under simulated solar irradiation has been investigated in aqueous solutions containing TiO2 suspensions as photocatalysts. The study focuses on the identification of possible intermediate products and the determination of inorganic ions formed during the
Katrice A Lippa et al.
Environmental toxicology and chemistry, 24(10), 2401-2409 (2005-11-05)
Second-order rate constants (kNuc) for aqueous-phase bimolecular nucleophilic substitution (SN2) reactions of a range of anionic nucleophiles with alachlor, propachlor, and two analogs of propachlor (a thioacetanilide and a beta-anilide) were fit to the Swain-Scott and Edwards models. Correlations of
C S Liu et al.
Chemosphere, 85(9), 1438-1443 (2011-09-07)
Chloroacetanilide herbicides are extensively used in the control of weeds and have widely resulted in nonpoint contamination of groundwater and soil resources. In the attempt to achieve better remediation for herbicide-contaminated resources, we investigated the reductive transformation of propachlor through

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