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Supelco

Propachlor

PESTANAL®, analytical standard

Sinônimo(s):

2-Chloro-N-isopropylacetanilide

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About This Item

Fórmula empírica (Notação de Hill):
C11H14ClNO
Número CAS:
1918-16-7
Peso molecular:
211.69
Beilstein:
2103903
Número CE:
217-638-2
Número MDL:
MFCD00078731
Código UNSPSC:
41116107
ID de substância PubChem:
329756851
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

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

chave InChI

MFOUDYKPLGXPGO-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

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.

Informações legais

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

Pictogramas

Skull and crossbonesEnvironment
GHS06,GHS09

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
BCCH2746
BCBW8046
BCBT5091
SZBD077XV
SZBA057XV

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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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)
K L Davison et al.
Xenobiotica; the fate of foreign compounds in biological systems, 24(10), 1003-1012 (1994-10-01)
1. 14C-labelled propachlor, alachlor, butachlor, metolachlor, methoxypropachlor and some of their mercapturic acid pathway metabolites (MAP) were given to rat either by gavage or by perfusion into a renal artery. MAP metabolites were isolated from bile and urine. 2. Rat
Katrice A Lippa et al.
Journal of agricultural and food chemistry, 52(10), 3010-3021 (2004-05-13)
The ease with which alpha-chloroacetanilide herbicides undergo displacement reactions with strong nucleophiles, and their recalcitrance toward weak ones, is intimately related to their herbicidal properties and environmental chemistry. In this study, we investigate the kinetics and mechanisms of nucleophilic substitution
C S Liu et al.
The Science of the total environment, 416, 507-512 (2012-01-10)
The process of in situ chemical oxidation (ISCO) by persulfate (S(2)O(8)(2-)) can be accelerated by metal ion activation, which more effectively degrades subsurface pollutants by enhancing sulfate radical (SO(4)(-)) generation. This study compared the results of propachlor degradation by Cu(2+)
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