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36175

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Napropamide

PESTANAL®, analytical standard

Synonym(s):

N,N-Diethyl-2-(1-naphthyloxy)propanamide

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About This Item

Linear Formula:
C10H7OCH(CH3)CON(CH2CH3)2
CAS Number:
Molecular Weight:
271.35
Beilstein:
6809160
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

mp

73-78 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

CCN(CC)C(=O)C(C)Oc1cccc2ccccc12

InChI

1S/C17H21NO2/c1-4-18(5-2)17(19)13(3)20-16-12-8-10-14-9-6-7-11-15(14)16/h6-13H,4-5H2,1-3H3

InChI key

WXZVAROIGSFCFJ-UHFFFAOYSA-N

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General description

Napropamide is a soil herbicide, which can be either sprayed on the surface or incorporated. It can be mainly used for weed control management.
Phenanthrene can be synthesized, via a multi-step synthesis process, using Haworth method involving naphthalene and succinic anhydride as the starting materials. It can undergo chlorination in acetic acid to form a mixture of cis- and trans-9,10-dichloro-9,10-dihydrophenanthrenes as the major products.

Application

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

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Legal Information

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Hepworth.DJ, et al.
Aromatic Chemistry, 13 (2002)
Alfonso Salinas-Castillo et al.
Pest management science, 61(8), 816-820 (2005-04-20)
A new, simple, rapid and selective phosphorimetric method for determining napropamide is proposed which demonstrates the applicability of heavy-atom-induced room-temperature phosphorescence for analyzing pesticides in real samples. The phosphorescence signals are a consequence of intermolecular protection and are found exclusively
José P Da Silva et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(1), 69-75 (2008-01-03)
The photochemical behaviour of the herbicide napropamide is studied on cellulose and silica surfaces, using steady-state and laser-flash diffuse reflectance techniques. The results are used to probe how the reaction sites of the host matrices influence the photo-reactive pathways. Napropamide
Fardin Sadegh-Zadeh et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 47(2), 144-151 (2012-01-19)
This study was carried out to determine the sorption-desorption, degradation and leaching of napropamide in selected Malaysian soils. The sorption capacities of the selected Malaysian soils for napropamide were the following in descending order: Linau > Teringkap > Gunung Berinchang
Yuan-Na Li et al.
Talanta, 85(1), 325-332 (2011-06-08)
A rapid non-separative spectrofluorometric method based on the second-order calibration of excitation-emission matrix (EEM) fluorescence was proposed for the determination of napropamide (NAP) in soil, river sediment, and wastewater as well as river water samples. With 0.10 mol L(-1) sodium

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