72459-58-6 Usage
Description
TriaZoxide, also known as 1,2,4-benzotriazine 1-oxide, is a chemical compound belonging to the class of benzotriazines. It is characterized by the presence of a chlorine atom at position 7 and a 1H-imidazol-1-yl group at position 3. Triazoxide is a fungicide with various applications in agriculture and other industries.
Uses
Used in Agricultural Industry:
TriaZoxide is used as a fungicide for the control of seed-borne diseases in winter and spring barley. It helps protect the crops from fungal infections, ensuring a healthy growth and increased yield.
Used in Seed Dressing:
TriaZoxide is employed as a seed dressing, which is a protective coating applied to seeds before planting. This application helps control seed-borne diseases and enhances the overall health of the plants.
Used in Control of Specific Fungal Pathogens:
TriaZoxide is particularly effective against Pyrenophora graminea and Pyrenophora teres, two common fungal pathogens that affect barley crops. By targeting these specific pathogens, Triazoxide helps reduce the impact of fungal infections on barley production.
Used in Pesticide Formulations:
As a pesticide, Triazoxide is formulated and used in various products to control a range of fungal diseases in different crops. Its incorporation into pesticide formulations helps farmers protect their crops from a variety of fungal threats, ensuring a more stable and productive agricultural output.
Metabolic pathway
Triazoxide was the subject of an evaluation by the Pesticide Safety
Directorate of UK MAFF. The information presented below was obtained
from this source (PSD, 1994). The specific use of triazoxide (seed treatment)
gives rise to very low residues and therefore the metabolic pathways
in plants were not investigated. The compound is rather persistent
in soils and sediments but it is likely to be short-lived in water owing to
photolysis. Much is known about the absorption, distribution and elimination
of the compound in rat but only one metabolite, of apparently
many, was identified. The use pattern and consequent negligible residues
in plants did not warrant studies in nuninants and poultry.
Degradation
Triazoxide is very stable in water with extrapolated DT50 values of well
over 1 year at pH 4 and 7, and 23 days at pH 9. Aqueous photolysis is
expected to be more important under environmental conditions; the DT50
was 2-14 days at latitude 50" depending on the season. On a silica surface,
triazoxide was 95% degraded in 7 days when irradiated with a fluorescent
lamp. Details of the products were not reported.
Check Digit Verification of cas no
The CAS Registry Mumber 72459-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,5 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72459-58:
(7*7)+(6*2)+(5*4)+(4*5)+(3*9)+(2*5)+(1*8)=146
146 % 10 = 6
So 72459-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H6ClN5O/c11-7-1-2-8-9(5-7)16(17)14-10(13-8)15-4-3-12-6-15/h1-6H
72459-58-6Relevant articles and documents
Synergistic Combinations Of Active Ingredients
-
, (2012/02/15)
The present invention relates to novel active compound combinations comprising, firstly, at least one known compound of the formula (I) in which R1 and A have the meanings given in the description and, secondly, at least one further known active compound from groups (2) to (27) listed in the description, which combinations are highly suitable for controlling animal pests such as insects and unwanted acarids and also phytopathogenic fungi.
Pyrazolyl benzyl ether derivatives containing a fluoromethoxyimino group and use thereof as pesticides
-
, (2008/06/13)
The invention relates to novel pyrazolyl benzyl ethers, to a plurality of processes for their preparation and to their use for controlling harmful organisms.
Microbicidal benzotriazoles
-
, (2008/06/13)
Novel benzotriazoles of the formula STR1 in which R, X1, X2, X3, X4 and Y have the meanings given in the description, and their acid addition salts and metal salt complexes, a process for the preparation of these substances and their use as microbicides in crop protection and in material protection.
