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Supelco

Imazaquin

PESTANAL®, analytical standard

Synonym(s):

2-(4-Isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-quinoline-3-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):
C17H17N3O3
CAS Number:
81335-37-7
Molecular Weight:
311.34
Beilstein:
5450078
MDL number:
MFCD00778521
UNSPSC Code:
41116107
PubChem Substance ID:
329755703
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

CC(C)C1(C)N=C(NC1=O)c2nc3ccccc3cc2C(O)=O

InChI

1S/C17H17N3O3/c1-9(2)17(3)16(23)19-14(20-17)13-11(15(21)22)8-10-6-4-5-7-12(10)18-13/h4-9H,1-3H3,(H,21,22)(H,19,20,23)

InChI key

CABMTIJINOIHOD-UHFFFAOYSA-N

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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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H312

Precautionary Statements

P280

Hazard Classifications

Acute Tox. 4 Dermal

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)

Lot/Batch Number
BCCJ6274
BCBX4650
SZBD324XV
SZB8325XV
SZE8325X

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Tomas Undabeytia et al.
Journal of agricultural and food chemistry, 52(14), 4493-4500 (2004-07-09)
The influence of two organic amendments consisting of an urban waste compost (SUW) and a commercial amendment from olive mill wastes (OW) was assessed on the sorption properties and leaching of the ionizable herbicide imazaquin on four soils with different
M Cade Smith et al.
Journal of environmental quality, 32(4), 1393-1404 (2003-08-23)
Nonequilibrium disc-flow techniques may better reproduce dynamic soil-pesticide interactions than traditional batch sorption studies. Batch kinetic and equilibrium experiments and dual-label thin-disc flow experiments were conducted with atrazine (6-chloro-N-ethyl-N'-isopropyl-1,3,5-triazine-2,4-diamine) and imazaquin [2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl)-3-quinolinecarboxylic acid] using a Demopolis silt loam (loamy-skeletal, carbonatic
José R Garbin et al.
Chemosphere, 66(9), 1692-1698 (2006-09-12)
The present work investigated the direct and indirect photolysis of pesticide residues (atrazine, imazaquin, iprodione), in aqueous solutions and under UV-visible radiation (280-480nm). Different kinds of humic substances (HS) were added to samples in order to evaluate their behaviour as
Jussara B Regitano et al.
Journal of agricultural and food chemistry, 53(10), 4096-4102 (2005-05-12)
The influence of soil pH on the leaching potential of the ionizable herbicide imazaquin was assessed on the profile of two highly weathered soils having a net positive charge in the B horizon, in contrast to a soil having a
Jennifer A McCourt et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(3), 569-573 (2006-01-13)
The sulfonylureas and imidazolinones are potent commercial herbicide families. They are among the most popular choices for farmers worldwide, because they are nontoxic to animals and highly selective. These herbicides inhibit branched-chain amino acid biosynthesis in plants by targeting acetohydroxyacid
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