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Documentos

37878

Supelco

Imazaquin

PESTANAL®, analytical standard

Sinónimos:

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

Fórmula empírica (notación de Hill):
C17H17N3O3
Número de CAS:
81335-37-7
Peso molecular:
311.34
Beilstein/REAXYS Number:
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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Categorías relacionadas

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

signalword

Warning

hcodes

H312

pcodes

P280

Hazard Classifications

Acute Tox. 4 Dermal

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ6274
BCBX4650
SZBD324XV
SZB8325XV
SZE8325X

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Chen Xuyan et al.
Journal of AOAC International, 90(2), 568-574 (2007-05-04)
A method has been developed for the quantitation of imazaquin residues in soil. The herbicide was extracted from soil with methanol-water (2 + 1, v/v) and cleaned up by strong anion-exchange solid-phase extraction cartridges. Analysis was performed by using high-performance
Tomas Undabeytia et al.
Water research, 42(4-5), 1211-1219 (2007-10-05)
Vesicle-clay complexes in which positively charged vesicles composed of didodecyldimethylammonium bromide (DDAB) were adsorbed on montmorillonite removed efficiently anionic (sulfentrazone, imazaquin) and neutral (alachlor, atrazine) pollutants from water. These complexes (0.5% w:w) removed 92-100% of sulfentrazone, imazaquin and alachlor and
Jerome B Weber et al.
Journal of agricultural and food chemistry, 51(19), 5752-5759 (2003-09-04)
Aqueous batch-type sorption-desorption studies and soil column leaching studies were conducted to determine the influence of soil properties, soil and suspension pH, and ionic concentration on the retention, release, and mobility of [14C]imazaquin in Cape Fear sandy clay loam, Norfolk
Ahmed Nasser et al.
Chemosphere, 75(1), 20-27 (2009-01-13)
The potential role of mechanochemical processes in enhancing degradation of imazaquin by soil components is demonstrated. The investigated components include montmorillonite saturated with Na(+), Ca(2+), Cu(2+)and Al(3+), Agsorb (a commercial clay mix), birnessite and hematite. The mechanical force applied was
Xuedong Wang et al.
Chemosphere, 67(11), 2156-2162 (2007-02-03)
A species of bacteria that is capable of utilizing imazaquin as the sole carbon source was isolated from soil with repeated imazaquin applications, and was identified as Arthrobacter crystallopoietes (designated as strain "WWX-1"). This isolate degrades imazaquin as high as
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