4 Hydroxy 3 Iodobenzoic Acid
Iodobenzene

4-hydroxy-3-iodobenzoic Acid

Fengxi Chemical

Specifications

HS Code

658223

Chemical Formula C7H5IO3
Molar Mass 266.017 g/mol
Appearance Solid
Solubility In Water Slightly soluble
Melting Point 165 - 167 °C
Pka 2.82
Odor Odorless (usually)
Color White to off - white
Chemical Formula C7H5IO3
Molar Mass 266.017 g/mol
Appearance White to off - white solid
Melting Point 226 - 230 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in some organic solvents like ethanol, DMSO
Pka Value around 3.5 (approximate, for the carboxylic acid group)
Iodine Content High due to the presence of iodine atom
Reactivity Reactive towards bases due to carboxylic acid group and can participate in halogen - related reactions due to iodine
Chemical Formula C7H5IO3
Molar Mass 266.02 g/mol
Appearance Solid
Melting Point 197 - 201 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in some organic solvents like ethanol
Pka Around 3 - 4 (approximate value for carboxylic acid group)
Iodine Content Contains one iodine atom
Hydroxy Group Property Can participate in hydrogen bonding
Carboxylic Acid Group Property Can react in acid - base reactions
Chemical Formula C7H5IO3
Molar Mass 266.02 g/mol
Appearance Solid (color may vary depending on purity)
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in some organic solvents like ethanol, acetone
Melting Point Typically in a certain temperature range (needs specific data)
Acidity Pka Characteristic pKa value related to the carboxylic acid group
Iodine Content One iodine atom per molecule contributing to its mass and reactivity
Reactivity Can participate in reactions typical of benzoic acids and iodine - containing compounds
Packing & Storage
Packing 500g of 4 - hydroxy - 3 - iodobenzoic acid packaged in a sealed plastic bag.
Storage 4 - hydroxy - 3 - iodobenzoic acid should be stored in a cool, dry place, away from direct sunlight. Keep it in a well - 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. Ideal storage temperature is around 2 - 8°C if long - term stability is required.
Shipping 4 - Hydroxy - 3 - iodobenzoic acid is shipped in sealed, corrosion - resistant containers. They are carefully packaged to prevent breakage. Shipment follows strict chemical transport regulations to ensure safety during transit.
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4-hydroxy-3-iodobenzoic Acid 4-hydroxy-3-iodobenzoic Acid 4-hydroxy-3-iodobenzoic Acid
General Information
Frequently Asked Questions
What are the chemical properties of 4-hydroxy-3-iodobenzoic Acid?
4-Hydroxy-3-iodobenzoic acid, this is an organic compound with unique properties. Looking at its structure, above the benzene ring, the hydroxyl group, iodine atom and carboxyl group are on one side.
In terms of its chemical properties, the carboxyl group is acidic and can be neutralized with bases such as sodium hydroxide to produce corresponding carboxylic salts and water. And it can be esterified with alcohols catalyzed by concentrated sulfuric acid and heated to obtain esters and water.
Hydroxyl groups are active and can participate in many reactions. In case of strong oxidants, hydroxyl groups can be oxidized to cause structural changes. It can also react with active metals such as sodium metal to release hydrogen.
Although the iodine atom is relatively stable, it can also participate in the reaction under certain conditions. For example, in some nucleophilic substitution reactions, the iodine atom can be replaced by other nucleophilic reagents, thereby realizing the structural transformation of the compound.
Furthermore, the conjugate system of the benzene ring endows the compound with certain stability and can undergo electrophilic substitution reaction. The hydrogen atom on the benzene ring can be replaced by other groups, and the occurrence of this reaction is related to the localization effect of the existing substituents on the benzene ring. Hydroxy and carboxyl groups are ortho-para-sites, which have an important impact on the selection of reaction check points.
4-hydroxy-3-iodobenzoic acid has a wide range of uses in the field of organic synthesis. It can be used as an intermediate and can be converted into organic compounds with more complex structures through various reactions. It has potential application value in many fields such as medicine and materials.
What are the main applications of 4-hydroxy-3-iodobenzoic Acid?
4-Hydroxy-3-iodobenzoic acid is useful in many fields. In the field of medicine, this compound is often a key raw material for the preparation of drugs. Because of its specific chemical structure and activity, it may participate in the synthesis of drugs with antibacterial, anti-inflammatory and anti-tumor effects. Doctors make good medicines to treat the diseases of patients. This substance may help the medical system and save the people from the pain.
In the field of materials science, 4-hydroxy-3-iodobenzoic acid also has extraordinary performance. It can be used as a synthetic component of materials with special functions, such as the preparation of materials with special optical and electrical properties. Craftsmen use it to make materials with unique properties, or to use it in high-end electronic equipment to increase their efficiency and help the progress of science and technology.
Furthermore, in the field of chemical research, it is an important intermediate in organic synthesis. Chemists use its structural characteristics to perform various organic reactions to expand the types of organic compounds and explore new chemical reaction paths and mechanisms. Scholars use it as a basis to study the mysteries of chemistry and promote the development of chemistry.
Overall, 4-hydroxy-3-iodobenzoic acid plays an important role in the fields of medicine, materials science and chemical research, contributing to the development of various industries and has far-reaching impact.
What are the synthetic methods of 4-hydroxy-3-iodobenzoic Acid?
The synthesis of 4-hydroxy-3-iodobenzoic acid has different paths. This imitation of "Tiangong Kaiwu" is described in ancient terms.
First, 4-hydroxy benzoic acid can be started. First, 4-hydroxy benzoic acid is met with an appropriate amount of iodizing reagent. This iodizing reagent, such as iodine elemental substance, is compatible with an appropriate oxidizing agent. The oxidizing agent, such as hydrogen peroxide, is in a suitable solvent, such as glacial acetic acid, etc., and is controlled at an appropriate temperature and heated slowly. The control of temperature is about success or failure and cannot be careless, about tens of degrees Celsius. In this environment, the iodizing reagent interacts with 4-hydroxybenzoic acid, and the iodine atom gradually enters the benzene ring and falls at position 3, thus forming 4-hydroxy-3-iodobenzoic acid. After the reaction is completed, the pure product can be obtained by ordinary separation and purification methods, such as recrystallization.
Second, 3-iodine-4-methoxybenzoic acid can also be used as the starting material. First, 3-iodine-4-methoxybenzoic acid is placed in a suitable reaction vessel and heated with a strong acid, such as hydroiodic acid. The power of strong acid can break the connection between the methoxy group and the benzene ring, so that the methoxylation is iodomethane to escape, while the hydroxyl group is left in the benzene ring, so it becomes 4-hydroxy-3-iodobenzoic acid. Thereafter, the impurities are removed by recrystallization and other methods to obtain the refined product.
In addition, it can also be formed by the corresponding halogenated aromatic hydrocarbon through multi-step reaction. First, a suitable halogenated aromatic hydrocarbon is used to interact with the phenolic salt of the alkali metal to introduce a hydroxyl group, and then the iodization step is carried out, which is similar to the previous method. After iodization, separation and purification, 4-hydroxy-3-iodobenzoic acid is finally obtained.
All these synthesis methods have their own strengths and weaknesses, depending on the availability of raw materials, the amount of cost, and the difficulty of reaction.
4-hydroxy-3-iodobenzoic the market price of Acid
The market price of 4-hydroxy-3-iodobenzoic acid is difficult to determine. Its price often varies due to many factors, such as the abundance of supply, the difficulty of preparation, the amount of market demand, the quality of the process, and even the current situation. It is all related to the management of merchants.
If the supply is wide and easy to prepare, the process is exquisite and the cost is low, and the market needs to be flat, its price is low; however, if the supply is thin, the preparation is complex and the process is clumsy, the cost is high, and the market needs to be prosperous, the price will be high.
Looking at the chemical raw material market in the past, the prices of various materials fluctuated. In the event of turbulence, logistics obstruction, or sudden changes in supply and demand, the price will also change sharply. Although there is no exact past market for 4-hydroxy-3-iodobenzoic acid, it is deduced from the general practice of chemical substances that its price should be in such variables. Or at some point, due to a breakthrough in preparation, the supply of goods increases and the price drops; or due to the scarcity of raw materials, the preparation is difficult, and the price soars.
To know the exact market price, you need to ask merchants specializing in chemical materials, brokers entering and leaving the chemical market, or scrutinize the real-time market of chemical trading platforms to get a near-real price.
4-hydroxy-3-iodobenzoic Acid to pay attention to when storing and transporting
4-Hydroxy-3-iodobenzoic acid is a chemical substance, and more attention should be paid when storing and transporting it.
The first word of storage, because of its nature, should be found in a cool, dry and well ventilated place. If it is in a humid place, it is easy to be damp and deteriorate, causing its chemical properties to become easy, affecting future use. And it is advisable to keep away from fire and heat sources, because the substance may be flammable, in case of open flame or hot topic, it is dangerous to cause fire.
Furthermore, it should be stored separately from oxidizing agents, reducing agents, alkalis, etc. Contact with them, or cause violent chemical reactions, causing danger. In the storage area, suitable materials should be prepared to contain leaks in case of leakage, which can be dealt with in time to prevent their spread and cause greater harm.
As for transportation, it is necessary to ensure that the packaging is complete and the loading is secure. During transportation, the driving should be stable to avoid bumps and vibrations, and prevent material leakage caused by package damage. Transportation vehicles should also be equipped with corresponding fire equipment and leakage emergency treatment equipment. If there is a leak on the way, it can be dealt with immediately. During transportation, follow the prescribed route and do not stop near densely populated areas and important places to prevent leakage from causing serious impact on the people and the environment. Escort personnel must also be familiar with the characteristics of the substance and emergency response methods, and carefully guard the whole process to ensure the safety of transportation.