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Key Documents

PS410

Oryzalin

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H18N4O6S
CAS Number:
Molecular Weight:
346.36
Beilstein/REAXYS Number:
2177305
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

grade

analytical standard

packaging

ampule of 1000 mg

manufacturer/tradename

Chem Service, Inc. PS-410

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCCN(CCC)c1c(cc(cc1[N+]([O-])=O)S(N)(=O)=O)[N+]([O-])=O

InChI

1S/C12H18N4O6S/c1-3-5-14(6-4-2)12-10(15(17)18)7-9(23(13,21)22)8-11(12)16(19)20/h7-8H,3-6H2,1-2H3,(H2,13,21,22)

InChI key

UNAHYJYOSSSJHH-UHFFFAOYSA-N

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General description

Oryzalin is a pre-emergence selective herbicide, which belongs to the dinitroaniline class of herbicides.[1][2] It is commonly used for weed control management.[2] Its mode of action involves the inhibition of microtubule formation, disrupting cell division and causing microfibril disorientation.[2]

Application

Oryzalin may be used as a reference standard for the determination of oryzalin residues in soil by high pressure liquid chromatography method.[3]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Sens. 1 - STOT RE 2

target_organs

Blood,Kidney

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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The biochemical mechanism of action of the dinitroaniline herbicide oryzalin.
Strachan S D, et al.
Pesticide Biochemistry and Physiology, 20(2), 141-150 (1983)
Oryzalin, a dinitroaniline herbicide, binds to plant tubulin and inhibits microtubule polymerization in vitro.
Morejohn.C.L, et al.
Planta, 172(2), 252-264 (1987)
Determination of oryzalin and prosulfalin residues in soil by high pressure liquid chromatography.
Macy T D, et al.
Analytical Chemistry, 52(8), 1381-1383 (1980)
Rapid and reversible high-affinity binding of the dinitroaniline herbicide oryzalin to tubulin from Zea mays L
Hugdahl.DJ and Morejohn.CL
Plant Physiology, 102(3), 725-740 (1993)
Lili Zhang et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 11(2), 279-288 (2011-10-25)
It is still unclear how light and gibberellins are integrated to regulate petal size. Here, we report that light improves both the length and the width of the ray floret petals in G. hybrid, but GA(3) promotes only the petal

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