FENBUCONAZOLE

- CAS No.
- 114369-43-6
- Chemical Name:
- FENBUCONAZOLE
- Synonyms
- INDAR;TROIKA;Indar 5;INDAR(R);ENABLE(R);GOVERN(R);FENETHANIL;FENBUCONAZOL;FENBUCONAZOLE;Fenbuconazole [iso]
- CBNumber:
- CB7405237
- Molecular Formula:
- C19H17ClN4
- Molecular Weight:
- 336.82
- MOL File:
- 114369-43-6.mol
- MSDS File:
- SDS
- Modify Date:
- 2025/1/27 9:38:02
Melting point | 125.0℃ |
---|---|
Boiling point | 507.14°C (rough estimate) |
Density | 1.1288 (rough estimate) |
vapor pressure | 5 x l0-6 Pa (20 °C) |
refractive index | 1.6110 (estimate) |
storage temp. | 0-6°C |
solubility | Chloroform (Slightly), DMSO (Slightly) |
Water Solubility | 0.2 mg l-1 (25 °C) |
pka | 2.34±0.10(Predicted) |
BRN | 8333667 |
LogP | 3.79 at 20℃ |
EPA Substance Registry System | Fenbuconazole (114369-43-6) |
FENBUCONAZOLE Chemical Properties,Uses,Production
Uses
Fenbuconazole is a conazole based fungicide used as a spray for the control of leaf spot, yellow and brown rust, powdery mildew and net blotch on wheat and barley and apple scab, pear scab and apple p owdery mildew on apples and pears.
Metabolic pathway
A number of sites in the fenbuconazole molecule are susceptible to
enzymic attack. Consequently, a large variety of metabolites may be
formed by oxidative attack on the phenolic rings or the aliphatic benzylic
carbon atom adjacent to the 4-chlorophenyl ring. In mammals, oxidation
at the benzylic carbon atom is an important pathway, which gives rise to
the corresponding alcohol or ketone. This pathway also leads to lactone
formation via hydrolysis of the nitrile group and elimination of a molecule
of water. The alcohol may also form conjugates with glucuronic or sulfuric
acid. Additional reactions in mammals involve hydroxylation of the
phenolic rings.
In plants, oxidation at the benzylic carbon is an important step to
further metabolites and cleavage of the linkage to the triazole ring generates
triazole, which is subsequently incorporated in a number of metabolic
products. Information presented in this entry is based on the PSD
Evaluation (PSD, 1995).
Degradation
Fenbuconazole is thermally stable up to 150 °C and there was no observed
degradation when fenbuconazole was incubated in the dark in aqueous
solutions at pH 5,7 and 9 for up to 30 days at 25 °C.
When an aqueous solution of fenbuconazole (concentration 1.5μg ml-1,
pH 7) was irradiated with a xenon arc lamp (filtered to remove wavelengths
below 290 nm), the overall radioactivity was 105% of the original
amount and the only compound detected was fenbuconazole.
FENBUCONAZOLE Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | Inquiry |
---|---|---|---|---|---|
CLEARSYNTH LABS LTD. | +91-22-45045900 | Hyderabad, India | 6257 | 58 | Inquiry |
career henan chemical co | +86-0371-86658258 +8613203830695 | China | 29859 | 58 | Inquiry |
Finetech Industry Limited | +86-27-87465837 +8618971612321 | China | 9642 | 58 | Inquiry |
Hefei TNJ Chemical Industry Co.,Ltd. | +86-0551-65418684 +8618949823763 | China | 25356 | 58 | Inquiry |
Hangzhou MolCore BioPharmatech Co.,Ltd. | +86-057181025280; +8617767106207 | China | 49734 | 58 | Inquiry |
SUZHOU SENFEIDA CHEMICAL CO.,LTD | +86-0512-83500002 +8615195660023 | China | 26362 | 58 | Inquiry |
LEAPCHEM CO., LTD. | +86-852-30606658 | China | 43340 | 58 | Inquiry |
Aladdin Scientific | United States | 57505 | 58 | Inquiry | |
Guangzhou CATO Research Chemicals Inc. | +86-020-81960175-617 +8615602392859 | China | 6335 | 58 | Inquiry |
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD. | +8618950047208 | China | 43416 | 58 | Inquiry |
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