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36138

Supelco

Isoxaben

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C18H24N2O4
Número de CAS:
82558-50-7
Peso molecular:
332.39
EC Number:
407-190-8
MDL number:
MFCD00078687
UNSPSC Code:
41116107
PubChem Substance ID:
329755287
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
NMR: suitable
gas chromatography (GC): suitable

mp

175-179 °C

application(s)

agriculture
environmental

format

neat

SMILES string

CCC(C)(CC)c1cc(NC(=O)c2c(OC)cccc2OC)on1

InChI

1S/C18H24N2O4/c1-6-18(3,7-2)14-11-15(24-20-14)19-17(21)16-12(22-4)9-8-10-13(16)23-5/h8-11H,6-7H2,1-5H3,(H,19,21)

InChI key

PMHURSZHKKJGBM-UHFFFAOYSA-N

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General description

Isoxaben is a pre-emergence, broad leaf herbicide, which can be used on turf grass, small grains and ornamental type of plants in order to basically inhibit the synthesis of cellulose.

Application

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

Legal Information

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

hcodes

H413

Hazard Classifications

Aquatic Chronic 4

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

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
BCCH8255
BCBW6196
SZBD119XV
SZB8092XV
SZE8092X

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Guy Lahat et al.
Annals of surgery, 251(6), 1098-1106 (2010-05-21)
Angiosarcoma (AS) is a rare understudied soft tissue sarcoma exhibiting endothelial cell differentiation. We sought to evaluate AS natural history in the largest patient cohort reported to date and further unravel commonly deregulated molecular events of potential therapeutic utility. Medical
Dat L Tsang et al.
Plant physiology, 156(2), 596-604 (2011-04-22)
Cell expansion in plants requires cell wall biosynthesis and rearrangement. During periods of rapid elongation, such as during the growth of etiolated hypocotyls and primary root tips, cells respond dramatically to perturbation of either of these processes. There is growing
Iain W Manfield et al.
The Plant journal : for cell and molecular biology, 40(2), 260-275 (2004-09-28)
The herbicide isoxaben is a highly specific and potent inhibitor of cellulose synthesis in plants. Nevertheless, suspension-cultured cells can be habituated to grow in high concentrations of isoxaben, and apparently compensate for the disruption of cellulose synthesis by the modulation
Chad Brabham et al.
Plant physiology, 166(3), 1177-1185 (2014-08-01)
Cellulose biosynthesis is a common feature of land plants. Therefore, cellulose biosynthesis inhibitors (CBIs) have a potentially broad-acting herbicidal mode of action and are also useful tools in decoding fundamental aspects of cellulose biosynthesis. Here, we characterize the herbicide indaziflam
Alexander R Paredez et al.
Plant physiology, 147(4), 1723-1734 (2008-06-28)
To identify factors that influence cytoskeletal organization we screened for Arabidopsis (Arabidopsis thaliana) mutants that show hypersensitivity to the microtubule destabilizing drug oryzalin. We cloned the genes corresponding to two of the 131 mutant lines obtained. The genes encoded mutant
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