Tebuconazol CAS 107534-96-3

What are the targets of Tebuconazole prevention and treatment?

What are the characteristics of Tebuconazole?

(1) Wide spectrum of sterilization: Tebuconazole can be used to prevent and control dozens of diseases caused by fungi of the genera powdery mildew, rust fungus, conifer, nuclear cavity fungus, and conifer, such as rust, powdery mildew, Fusarium head blight, brown spot disease, sheath blight, root rot, etc., all of which have good protective, therapeutic, and eradication effects.
(2) Thoroughly cure the disease: Tebuconazole is a triazole fungicide. Mainly by inhibiting the biosynthesis of ergosterol in the pathogen, it achieves the effect of killing the pathogen and has protective, therapeutic, and eradication effects on diseases, making the treatment more thorough.
(3) Good compatibility: Tebuconazole can be compounded with most fungicides and insecticides, and has a good synergistic effect. Some formulations are also classic formulas for disease prevention and control.
(4) Flexible use: Tebuconazole has the characteristics of internal absorption and conduction, and can be used for spray, seed dressing and other use methods. Appropriate methods can be selected according to the actual situation.
(5) Regulating growth: Tebuconazole is a triazole fungicide that can be used to regulate plant growth, especially for seed dressing. It can prevent excessive growth of seedlings, make them stronger, more resistant to diseases, and promote early flower bud differentiation.
(6) Long shelf life: Tebuconazole, due to its strong permeability and good systemic absorption, rapidly penetrates into the target substance and remains in the body for a long time, achieving sustained killing of bacteria. Especially for soil treatment, the shelf life can reach over 90 days, greatly reducing the frequency of pesticide application.

Product Specification

Conclusion：Conform with specification and qualified.

 

What are the synthesis processes of Tebuconazole?

Synthesis method 1: Using pentanone 1,2,4-triazole and self-made catalyst Sodium Methoxide, Tebuconazole intermediate 2- (4-CHOLOPHENYLETHYL) -2-T-BUTYLOXIRANE was synthesized by reacting 2- (4-CHOLOPHENYLETHYL) -2-T-BUTYLOXIRANE with triazoles to obtain Tebuconazole This method has the advantages of fewer steps, simple instrument and equipment, low cost, and solvent recyclability Synthesis method 2: Tebuconazole is synthesized by four steps of reaction, including addition, reduction, and hydrogenation, starting from 4-chlorobenzaldehyde and Pinnadol.

 

How and where to buy Tebuconazole?

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