• Fungicide P-Rice Buy Tebuconazole 97%Tc Tebuconazole Tech
  • Fungicide P-Rice Buy Tebuconazole 97%Tc Tebuconazole Tech
  • Fungicide P-Rice Buy Tebuconazole 97%Tc Tebuconazole Tech
  • Fungicide P-Rice Buy Tebuconazole 97%Tc Tebuconazole Tech
  • Fungicide P-Rice Buy Tebuconazole 97%Tc Tebuconazole Tech

Fungicide P-Rice Buy Tebuconazole 97%Tc Tebuconazole Tech

CAS No.: 80443-41-0
Formula: C16h22cln3o
EINECS: 107534-96-3
Appearance: Powder
Source: Organic Synthesis
Toxicity of High and Low: Highly Toxic and High Toxic Drugs
Customization:
Manufacturer/Factory, Trading Company
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Shanghai, China
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Basic Info.

Model NO.
Pesticide & Insecticides
Mode
Systemic Insecticide
Toxicological Effect
Nerve Poison
Transport Package
25kg Bag
Specification
FS WS
Trademark
MOLOTUS
Origin
China
HS Code
3808
Production Capacity
5000t

Product Description

Fungicide P-Rice Buy Tebuconazole 97%Tc Tebuconazole TechTebuconazole
Description: A fungicide effective against various foliar diseases in cereals and other field crops
Example pests controlled: Smut; Bunt; Stripe rust; Yellow leaf spot; Powdery mildew; Scelerotinia rot; Black spot; Net blotch
Example applications: Cereals including wheat, barley, oat, rye; Grapes; Peanuts; Vegetables including onions, peas, pepper; Bananas; Sugarcane

Chemical structure: 

Isomerism A chiral molecule. The technical material is an isomeric mixture of the (S-) and (R-) isomers. The R-form is more biologically active than the S-form. 
Chemical formula C16H22ClN3O
Canonical SMILES CC(C)(C)C(CCC1=CC=C(C=C1)Cl)(CN2C=NC=N2)O
Isomeric SMILES No data
International Chemical Identifier key (InChIKey) PXMNMQRDXWABCY-UHFFFAOYSA-N
International Chemical Identifier (InChI) InChI=1S/C16H22ClN3O/c1-15(2, 3)16(21, 10-20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7, 11-12, 21H, 8-10H2, 1-3H3


General status: 
Pesticide type Fungicide, Plant growth regulator
Substance group Triazole
Minimum active substance purity 950 g/kg
Known relevant impurities EU dossier - None declared
Substance origin Synthetic
Mode of action Systemic with protective, curative and eradicant action. Disrupts membrane function. Sterol biosynthesis inhibitor. 
CAS RN 107534-96-3
EC number 403-640-2
CIPAC number 494
US EPA chemical code 128997
PubChem CID 86102
Molecular mass (g mol-1) 307.82
PIN (Preferred Identification Name) Rac-(3R)-1-(4-chlorophenyl)-4, 4-dimethyl-3-(1H-1, 2, 4-triazol-1-ylmethyl)pentan-3-ol
IUPAC name (RS)-1-p-chlorophenyl-4, 4-dimethyl-3-(1H-1, 2, 4-triazol-1-ylmethyl)pentan-3-ol
CAS name Α-(2-(4-chlorophenyl)ethyl)-α-(1, 1-dimethylethyl)-1H-1, 2, 4-triazole-1-ethanol
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