2 4 5 Triiodoimidazole
Iodobenzene

2 4 5 Triiodoimidazole

Fengxi Chemical

Specifications

HS Code

974671

Name 2,4,5 - triiodoimidazole
Chemical Formula C3H2I3N2
Molar Mass 496.77 g/mol
Physical State At Room Temp Solid
Solubility In Water Limited solubility (imidazoles generally have low water solubility due to non - polar ring and iodine atoms)
Solubility In Organic Solvents May be soluble in some polar organic solvents like DMSO, DMF due to polar nature of imidazole ring
Name 2,4,5 - triiodoimidazole
Molecular Formula C3H2I3N2
Molar Mass 445.77 g/mol
Appearance Solid (predicted, based on similar imidazole derivatives)
Physical State At Room Temp Solid
Solubility In Water Low (imidazole derivatives with heavy halogen substitution are usually sparingly soluble in water)
Solubility In Organic Solvents Soluble in polar organic solvents like DMSO, DMF (common for imidazole - based compounds)
Chemical Reactivity Can participate in nucleophilic substitution reactions due to the presence of the imidazole ring and the reactive iodine atoms
Stability Stable under normal conditions, but may decompose upon exposure to strong heat or light due to the presence of iodine
Packing & Storage
Packing 100g of 2,4,5 - triiodoimidazole packaged in a sealed, chemical - resistant container.
Storage 2,4,5 - Triiodoimidazole should be stored in a cool, dry place, away from direct sunlight and heat sources. Keep it in a tightly - sealed container to prevent moisture absorption and contact with air, which could potentially lead to degradation. Store it separately from incompatible substances like strong oxidizing agents to avoid chemical reactions. Ensure the storage area is well - ventilated.
Shipping 2,4,5 - triiodoimidazole is shipped in well - sealed containers, compliant with chemical transportation regulations. Packaging safeguards the chemical from damage and leakage during transit to ensure safe delivery.
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2,4,5-triiodoimidazole 2,4,5-triiodoimidazole 2,4,5-triiodoimidazole
General Information
Frequently Asked Questions
What are the main uses of 2,4,5-triiodoimidazole?
2% 2C4% 2C5-trichloropyloxyacetic acid is a kind of internal absorption and conduction type post-seedling herbicide, and its main use is quite extensive.
In the field of forestry, this medicine can effectively control all kinds of broad-leaved weeds and shrubs in forests, such as thorn, thistle, chicory, willow, birch and many other miscellaneous trees. After use, the medicine can be absorbed by the leaves and roots of plants, and conducted in the plant body, thereby interfering with the growth hormone balance of weeds and shrubs, and eventually causing their death. In this way, it can effectively maintain the growth space and nutrient acquisition of target trees such as conifers in the forest, and ensure the ecological balance of forestry and the healthy growth of trees.
In the agricultural field, in non-cultivated areas, such as fields, roadsides, railways, etc., 2% 2C4% 2C5-triclopyridoxyacetic acid can be used to control a variety of malignant broadleaf weeds. Weeds overgrown in these areas not only affect the appearance, but also may breed pests and diseases or hinder traffic. This drug can quickly kill weeds and has a long shelf life, reduce the probability of repeated weed growth, and reduce the burden of artificial weeding. However, because of its significant harm to broadleaf crops, it should never be used for weeding of broadleaf crops in farmland. It is necessary to precisely control the scope of application when using it.
In terms of pastures, when the overgrowth of broad-leaved weeds in pastures affects the growth of pastures and livestock consumption, an appropriate amount of 2% 2C4% 2C5-trichloropyloxy acetic acid can be used to remove broad-leaved weeds, improve the quality and yield of pastures, and provide a better source of feed for livestock.
However, it should be noted that although the toxicity of this drug is relatively low, it is more toxic to aquatic organisms such as fish. During use, the drug should be avoided from flowing into rivers, lakes and other water bodies to avoid adverse effects on the aquatic ecological environment. When using, it is also necessary to strictly follow the instructions for use and take protective measures to prevent damage to the health of the applicator.
What are the physical properties of 2,4,5-triiodoimidazole?
2% 2C4% 2C5-tribromotoluene is an organic compound with many unique physical properties. Its appearance is usually white to light yellow crystalline solid, which makes it unique among many substances.
Looking at its melting point, it is between 44 and 47 ° C. This specific melting point temperature is of great significance in the chemical industry. When the temperature approaches this range, 2% 2C4% 2C5-tribromotoluene will gradually melt from solid to liquid. This property plays a key role in the separation, purification and processing of substances. Many processes require precise temperature control to achieve specific operations through its melting point characteristics.
Looking at the boiling point, it is about 280-284 ° C. A higher boiling point indicates that the substance is relatively stable and requires a higher temperature to transform into a gaseous state. This property is very important in separation techniques such as distillation, which helps to effectively separate it from other substances with large differences in boiling points.
2% 2C4% 2C5 - Tribromotoluene has a density greater than that of water. If it is placed in water, it will sink to the bottom. This density characteristic can be used as an important basis for judgment when it involves operations such as liquid-liquid separation.
As for solubility, it is insoluble in water, but soluble in some organic solvents, such as ethanol, ether, chloroform, etc. This solubility characteristic determines that in chemical production and experiments, suitable solvents can be selected according to this property to dissolve, extract or react, which provides convenience for related operations.
In addition, 2% 2C4% 2C5-tribromotoluene also has a certain degree of volatility, but the volatilization rate is relatively slow. Although it will not evaporate quickly at room temperature and pressure, it will still be partially volatile when exposed to air for a long time. This requires that proper measures must be taken during storage and use to prevent its volatilization loss or impact on the environment.
What are the chemical properties of 2,4,5-triiodoimidazole?
2% 2C4% 2C5-trichloropyridoacetic acid is a synthetic organic heterocyclic selective internal absorption conduction type post-seedling herbicide. Its chemical properties are unique, let me tell you in detail.
The pure product of this agent is white crystalline solid, with a melting point of 234.5-238.5 ° C. The solubility in water at 25 ° C is 1.1g/L. It is soluble in organic solvents such as acetone, acetonitrile, chloroform, cyclohexanone, dichloromethane, methanol, and toluene. Its chemical stability is quite good, and it can be stored for a long time under normal storage conditions, and can be gradually decomposed by microorganisms in soil. In the chemical structure of
2% 2C4% 2C5-trichloropyridoxyacetic acid, specific atomic arrangements and chemical bonds give it herbicidal activity. Its molecular structure allows it to act precisely on the physiological processes of specific plants. It can be absorbed through the leaves, stems and roots of plants, and then transported to various places with the conduction system in the plant body. In plants, it can interfere with the balance of plant hormones, especially the normal function of auxin. By simulating or antagonizing the action of auxin, it can cause abnormal growth of plants, such as stem distortion, leaf deformity, and root development obstruction, which eventually leads to weed death.
From the perspective of chemical reactions, it participates in a series of complex reactions in the environment. In the soil, adsorption and desorption processes occur with soil particles, which has a significant impact on their mobility and effectiveness in the soil. Some of them interact with soil microorganisms and gradually decompose into relatively simple compounds through the metabolic activities of microorganisms, reducing their residual impact on the environment. At the same time, in different pH environments, their chemical stability will also change. Under strong acidic or alkaline conditions, reactions such as hydrolysis may occur, changing their chemical morphology and activity.
In summary, the chemical properties of 2% 2C4% 2C5-trichloropyridoxyacetic acid give it unique efficacy in weed prevention and control, but its chemical behavior in the environment also requires our close attention to ensure that it is used rationally to achieve effective weed control and reduce environmental hazards.
What is the synthesis method of 2,4,5-triiodoimidazole?
To prepare 2,4,5-trichlorophenoxyacetic acid, the method is as follows:
First take an appropriate amount of phenol, place it in the reaction kettle, and use sodium hydroxide solution to form sodium phenol. Sodium phenol has strong nucleophilicity and can be the basis for subsequent reactions.
Take 1,2,4-trichlorobenzene and slowly add it to the reaction kettle containing sodium phenol. When the two meet, under suitable temperature, pressure and catalyst action, a nucleophilic substitution reaction can occur. The chlorine atom of 1,2,4-trichlorobenzene has a certain activity due to the influence of the benzene ring electron cloud, which can be attacked by the nucleophilic oxygen atom of sodium phenol. During the reaction, strict temperature control is required to ensure that the reaction proceeds in the direction of generating 2,4,5-trichlorophenoxybenzene.
After forming 2,4,5-trichlorophenoxybenzene, it is treated with strong acids such as sulfuric acid and hydrochloric acid. Strong acids can break the ether bonds in the structure of phenoxybenzene, and then introduce carboxyl groups. In this process, temperature, acid concentration and reaction time are all key factors. If the conditions are suitable, after the ether bond is broken, the hydroxyl group and the carbon atom connected to the benzene ring can be converted through a series of intermediates, and finally the carboxyl group is formed, and then 2,4,5-trichlorophenoxyacetic acid is obtained. When preparing
, the proportion of reactants and reaction conditions in each step need to be carefully adjusted to obtain products with higher yield and purity. And during the experiment, attention should be paid to safety, because the reactants and products used may be toxic and corrosive to a certain extent.
In which fields is 2,4,5-triiodoimidazole used?
2% 2C4% 2C5-trichloropyridoacetic acid is a powerful chemical agent that is used in many fields.
In the field of agriculture, its use is quite wide. Weeds breed, often hinder crop growth, and this agent can precisely remove them. For example, in corn fields, wheat fields, etc., many broad-leaved weeds, such as Artemisia sativa and Shepherd's purse, can be killed by 2,4,5-trichloropyridoacetic acid to ensure that crops absorb sufficient nutrients, light and space, promote their growth, and then improve yield and quality. In orchards, it can also be used to remove weeds, and because of its strong selectivity, it has little impact on fruit trees, which can maintain a good ecological environment in orchards.
In the field of forestry, the role should not be underestimated. During afforestation, there are many weeds in the woodland, which affects the rooting and growth of saplings. 2,4,5-Trichloropyloxy acetic acid can effectively inhibit the growth of weeds and create a suitable environment for saplings. In addition, in forest fire zones, removing weeds and low shrubs can reduce fire hazards. This agent also plays an important role in this regard.
In terms of urban greening, parks, green spaces on both sides of streets, etc., if weeds are overgrown, it will hinder the appearance. 2,4,5-Trichloropyloxy acetic acid can be easily removed, making green areas clean and beautiful, and creating a comfortable and leisure environment for the public.
However, it should be noted that this agent is toxic and must be operated according to regulations when used to avoid adverse effects on the environment, humans and animals.