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Isoxaben

Isoxaben

PESTANAL®, analytical standard

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100 MG
CHF 53.20

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Spedizione prevista il28 maggio 2025


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100 MG
CHF 53.20

About This Item

Formula empirica (notazione di Hill):
C18H24N2O4
Numero CAS:
Peso molecolare:
332.39
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

CHF 53.20


Spedizione prevista il28 maggio 2025


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Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

Punto di fusione

175-179 °C

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
PMHURSZHKKJGBM-UHFFFAOYSA-N

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Descrizione generale

Isoxaben is a pre-emergence, broad leaf herbicide, which can be used on turf grass, small grains and ornamental type of plants[1] in order to basically inhibit the synthesis of cellulose[2].

Applicazioni

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

Note legali

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

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Aquatic Chronic 4

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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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
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
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
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

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