Quizalofop-p-ethyl (Synonyms: (R)-Quizalofop ethyl; Quinofop-ethyl)

Cat. No.: HY-B1950 Pureza: 99.10%: Ficha de datos
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Quizalofop-P-ethyl is a low-toxicity herbicide, a highly selective new type of post-emergence herbicide for dryland crops, with high selectivity between gramineous weeds and dicotyledonous crops, and it has good control efficacy against gramineous weeds in broadleaf crop fields.

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Quizalofop-p-ethyl Estructura química

No. CAS : 100646-51-3

Tamaño	Stock	Cantidad

Muestra gratis (0.1 - 0.2 mg)	Solicite ahora
Muestra gratis (0.1 - 0.2 mg)	Solicite ahora
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO ready for reconstitution	En stock	Estimated Time of Arrival: December 31
Solution
10 mM * 1 mL in DMSO	En stock	Estimated Time of Arrival: December 31
Solid
200 mg	En stock	Estimated Time of Arrival: December 31
500 mg	Obtener un presupuesto
1 g	Obtener un presupuesto

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This product is a controlled substance and not for sale in your territory.

Other Forms of Quizalofop-p-ethyl:

Quizalofop-p-ethyl (Standard) Obtener un presupuesto

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•Related Proteins:

Actividad biológica
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Descripciòn

In Vitro

Quizalofop-p-ethyl (0.5-5 mg/L, 6 days) inhibits the growth of Microcystis aeruginosa, inhibits chlorophyll a and protein content of M. aeruginosa^[2].
Quizalofop-p-ethyl (0.5-5 mg/L, 3-6 days) affects the photosynthesis by inhibiting the expression of photosynthesis-related genes psaB and psbD1^[2].
Quizalofop-p-ethyl (0.5-5 mg/L, 3-6 days) promotes the expression of MC-LR-related gene mcyH, stimulates the synthesis and release of microcystin (MC-LR) in M. aeruginosa, causing pollution to the water environment^[2].
Quizalofop-p-ethyl (0.5-5 mg/L, 24-48 h) upregulates the MDA content in M. aeruginosa, improves the activities of SOD and CAT, inducing oxidative stress^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Real Time qPCR^[2]

Cell Line:	Microcystis aeruginosa
Concentration:	0.5-5 mg/L
Incubation Time:	24-48 h
Result:	Increased the level of mcyH, decreased levels of psaB and psbD1.

Peso molecular

372.80

Fòrmula

C₁₉H₁₇ClN₂O₄

No. CAS

100646-51-3

Appearance

Solid

Color

Light yellow to yellow

SMILES

C[C@@H](OC1=CC=C(OC2=NC3=CC=C(Cl)C=C3N=C2)C=C1)C(OCC)=O

Envío

Room temperature in continental US; may vary elsewhere.

Almacenamiento

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	2 years
	-20°C	1 year

Solvente y solubilidad

In Vitro:

DMSO : ≥ 100 mg/mL (268.24 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H₂O : < 0.1 mg/mL (insoluble)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	2.6824 mL	13.4120 mL	26.8240 mL
5 mM	0.5365 mL	2.6824 mL	5.3648 mL
10 mM	0.2682 mL	1.3412 mL	2.6824 mL

View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Calculadora de molaridad
Calculadora de dilución

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Calculation results:

Working solution concentration: mg/mL

Pureza y Documentación

Purity: 99.10%

Select Batch:

Ficha de datos (270 KB) SDS (597 KB)

COA (244 KB) LCMS (95 KB)

Instrucciones de manejo (2659 KB)

Referencias

[1]. Mantzos N, et al. Dissipation and transport of quizalofop-p-ethyl herbicide in sunflower cultivation under field conditions. Environ Sci Pollut Res Int. 2016 Feb;23(4):3481-90. [Content Brief]

[2]. Yu X, et al. Effects of the herbicides quizalofop-p-ethyl and quizalofop-ethyl on the physiology, oxidative damage, synthesis, and release of microcystin-LR in Microcystis aeruginosa[J]. Science of The Total Environment, 2021, 776: 146036.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

DMSO	1 mM	2.6824 mL	13.4120 mL	26.8240 mL	67.0601 mL
	5 mM	0.5365 mL	2.6824 mL	5.3648 mL	13.4120 mL
	10 mM	0.2682 mL	1.3412 mL	2.6824 mL	6.7060 mL
	15 mM	0.1788 mL	0.8941 mL	1.7883 mL	4.4707 mL
	20 mM	0.1341 mL	0.6706 mL	1.3412 mL	3.3530 mL
	25 mM	0.1073 mL	0.5365 mL	1.0730 mL	2.6824 mL
	30 mM	0.0894 mL	0.4471 mL	0.8941 mL	2.2353 mL
	40 mM	0.0671 mL	0.3353 mL	0.6706 mL	1.6765 mL
	50 mM	0.0536 mL	0.2682 mL	0.5365 mL	1.3412 mL
	60 mM	0.0447 mL	0.2235 mL	0.4471 mL	1.1177 mL
	80 mM	0.0335 mL	0.1677 mL	0.3353 mL	0.8383 mL
	100 mM	0.0268 mL	0.1341 mL	0.2682 mL	0.6706 mL

Quizalofop-p-ethyl Related Classifications

Infection

Help & FAQs

Do most proteins show cross-species activity?
Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Quizalofop-p-ethyl100646-51-3(R)-Quizalofop ethyl Quinofop-ethylSODEnvironmental PollutantsHerbicideSuperoxide DismutaseEnvironmental ContaminantsInhibitorinhibitorinhibit

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