Tebuconazole is a systemic triazole fungicide belonging to the demethylation inhibitor (DMI) class of fungicides (FRAC Group 3). It is one of the most versatile and widely used fungicides in agriculture due to its broad-spectrum activity against many ascomycete, basidiomycete, and deuteromycete fungi.
Its mode of action is the inhibition of C14-demethylase, a key enzyme in the fungal ergosterol biosynthesis pathway. Without ergosterol, fungal cell membranes cannot form properly, leading to growth inhibition and eventual fungal death.
Tebuconazole has both protective and curative properties, making it valuable for integrated disease management programs.
Cereal Crops (Wheat, Barley, Oats, Rye):
Controls rusts, powdery mildew, Septoria leaf blotch, and Fusarium head blight.
Fruit Crops (Grapes, Apples, Bananas, Citrus):
Protects against powdery mildew, black spot, scab, and Sigatoka leaf spot.
Vegetables (Tomatoes, Cucurbits, Onions, Peppers):
Controls powdery mildew, leaf spots, and anthracnose.
Oilseeds (Soybean, Rapeseed, Peanut, Sunflower):
Effective against leaf spot, rust, and Sclerotinia stem rot.
Specialty Uses:
Wood treatment to protect against fungal decay.
Seed treatment formulations (in mixtures) to control seed-borne and soil-borne pathogens.
Broad-Spectrum Control: Effective against many foliar, seed, and soil-borne fungal pathogens.
Systemic Activity: Moves inside the plant through xylem, providing long-lasting protection.
Dual Action: Preventive and curative activity helps stop diseases at multiple stages.
Flexible Formulations: Available as EC (emulsifiable concentrate), SC (suspension concentrate), and seed treatment mixes.
Crop Versatility: Used across cereals, fruits, vegetables, oilseeds, turf, and ornamentals.
Compatibility: Often mixed with strobilurins (e.g., trifloxystrobin, azoxystrobin) or contact fungicides (e.g., mancozeb) for resistance management.
Parameter | Description | Typical Value |
---|---|---|
Chemical Name | (RS)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol | Tebuconazole |
Chemical Formula | Molecular composition | C₁₆H₂₂ClN₃O |
Molecular Weight | ~307.8 g/mol | |
Appearance | Physical state | White crystalline solid |
Formulation Types | EC, SC, FS (seed treatment) | Common: 250 g/L EC, 430 g/L SC |
Solubility | In water (20°C) | ~36 mg/L (low solubility) |
Stability | Stable under normal storage | Non-volatile, light-stable |
Mode of Action | Inhibits C14-demethylase (ergosterol biosynthesis) | Systemic fungicide |
Q1: What is Tebuconazole mainly used for?
A: It is used to control rusts, powdery mildew, leaf spots, anthracnose, and Fusarium diseases in cereals, fruits, vegetables, and oilseeds.
Q2: Is Tebuconazole systemic?
A: Yes, it is a systemic fungicide, absorbed into plant tissues and translocated via xylem.
Q3: Does Tebuconazole work preventively or curatively?
A: Both. It prevents fungal infections and also stops early-stage infections due to its curative activity.
Q4: Can Tebuconazole be mixed with other fungicides?
A: Yes, it is often combined with strobilurins (QoI fungicides) or contact fungicides for broader protection and resistance management.
Q5: What is the resistance risk with Tebuconazole?
A: Resistance can develop if overused. It should be rotated or mixed with other fungicides from different FRAC groups.
Q6: Does Tebuconazole have uses beyond crop protection?
A: Yes, it is used in wood preservation and in seed treatment formulations to control seed-borne pathogens.