Hmit 3 Hydroxy 5 Mercapto 4 Isothiazolecarboxylic Acid Trisodium Salt
quinoline thiophene imidazole thiazole

HMIT:3-HYDROXY-5-MERCAPTO-4-ISOTHIAZOLECARBOXYLIC ACID TRISODIUM SALT

    Specifications

    HS Code

    376705

    Chemical Name 3-Hydroxy-5-mercapto-4-isothiazolecarboxylic acid trisodium salt
    Abbreviation HMIT
    Chemical Formula C3H2NNa3O3S2
    Molecular Weight 235.15 g/mol
    Appearance Typically appears as a solid (color may vary, often white to off - white)
    Solubility Soluble in water
    Ph Aqueous solutions have a characteristic pH depending on concentration
    Stability Stable under normal storage conditions but may react with strong oxidizing agents
    Use Used in some industrial applications, potentially in biocidal or corrosion - inhibiting formulations

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    General Information
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    Frequently Asked Questions

    As a leading HMIT:3-HYDROXY-5-MERCAPTO-4-ISOTHIAZOLECARBOXYLIC ACID TRISODIUM SALT supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    HMIT: What is 3-HYDROXY-5-MERCAPTO-4-ISOTHIAZOLECARBOXYLIC ACID TRISODIA SALT?
    This is called "3-hydroxy-5-mercapto-4-isothiazole carboxylic acid trisodium salt". Looking at its name, we know that this is one of the chemical substances. This substance is used in the field of chemistry, or has specific properties and uses.
    Its chemical structure contains hydroxyl groups, mercapto groups, isothiazole rings and sodium carboxylate salt parts. Hydroxyl groups often have active chemical properties and can participate in a variety of chemical reactions, such as esterification, etherification, etc., or affect the solubility and acidity of the substance. Mercapto groups are also active and can form stable complexes with a variety of metal ions, playing an important role in some biochemical reactions and industrial applications. The isothiazole ring endows the substance with unique chemical stability and biological activity, or has applications in the fields of medicine, pesticides, preservatives, etc. The sodium carboxylate part makes the substance water-soluble to a certain extent, and affects its ionic properties and chemical reactivity.
    In industrial production, or as an intermediate for the synthesis of more complex compounds. In pharmaceutical research, because of its unique chemical structure, or potential pharmacological activities, such as antibacterial, antiviral, anti-tumor, etc., it still needs to be further studied and verified. In the field of materials science, or because of its chemical activity, it is used for surface modification of materials to improve the properties of materials.
    Although it is difficult for us to fully understand its secrets, we can gain insight into its significance in chemistry and related fields only from its chemical structure and naming, and may demonstrate its unique value in more fields in the future.
    HMIT: What are the main uses of 3-HYDROXY-5-MERCAPTO-4-ISOTHIAZOLECARBOXYLIC ACID TRISODIA SALT?
    HMIT, that is, 3-hydroxy-5-mercapto-4-isothiazole carboxylic acid trisodium salt, has a wide range of uses. In the field of medicine, it can be used as a raw material for drug synthesis. Due to its specific chemical structure and activity, it can be converted into pharmaceutical ingredients with antibacterial and antiviral functions through chemical reactions. Physicians can use this to make good medicines for specific diseases and treat diseases for patients.
    In the field of materials, it can be used to prepare special functional materials. For example, adding this compound to the synthesis of some polymer materials can change the stability, corrosion resistance and other properties of the material. So that the material can still maintain good characteristics in harsh environments, prolong the service life, and is used in construction, chemical equipment, etc.
    In industrial production, it can be used as a metal corrosion inhibitor. Metals are prone to corrosion during use, and this substance can form a protective film on the metal surface, effectively slowing down the metal corrosion rate, reducing metal loss, saving resources and costs, and is of great significance in petrochemical, electric power and many other industries that rely on metal equipment.
    In agriculture, it can be developed as a new type of pesticide auxiliary agent. Added to pesticides, it can enhance the adhesion and permeability of pesticides, improve the efficacy of pesticides, reduce the amount of pesticides, reduce environmental pollution, and help the green and sustainable development of agriculture.
    In scientific research and exploration, as a chemical reagent, it provides a powerful tool for scientists to study chemical reaction mechanisms and develop new synthesis methods. Scientists can use its unique chemical properties to explore new reaction paths and promote the continuous development of chemical science.
    HMIT: What are the precautions 3-HYDROXY-5-MERCAPTO-4-ISOTHIAZOLECARBOXYLIC ACID TRISODIA SALT during use?
    3-Hydroxy-5-mercapto-4-isothiazolecarboxylate trisodium salt During use, many matters should be paid attention to.
    First, safety protection must be taken seriously. The nature of this substance may be special, and appropriate protective equipment should be worn during operation, such as gloves, goggles and protective clothing. Because it may cause irritation or even damage to the skin, eyes and respiratory tract, protection is in place to avoid the risk caused by direct contact.
    Second, strictly control environmental conditions. The stability of this substance may be affected by environmental factors, so it should be stored in a dry, cool and well-ventilated place, away from fire, heat and strong oxidants. Violent changes in humidity and temperature may cause it to deteriorate, thus affecting the use effect.
    Third, accurately grasp the dosage. Before use, the dosage should be accurately calculated and controlled according to the specific application and reaction requirements. If the dose is too small, or the desired effect cannot be achieved; if the dose is too large, it may cause side reactions or cause waste.
    Fourth, the operation process must be standardized. Whether it is dissolving, mixing or participating in the reaction, the established operating procedures must be followed. When dissolving, a suitable solvent should be selected and fully dissolved; when mixing, attention should be paid to the order of addition and stirring speed to ensure that the reaction proceeds evenly.
    Fifth, waste treatment cannot be ignored. After use, the remaining substances and related waste should be properly disposed of in accordance with regulations and must not be discarded at will. Because it may cause pollution to the environment, it is necessary to follow environmental protection requirements and choose appropriate treatment methods to reduce the harm to the environment. Only by paying attention to the above things can 3-hydroxy-5-mercapto-4-isothiazole carboxylate trisodium salt be used safely and effectively.
    HMIT: What are the physicochemical properties of 3-HYDROXY-5-MERCAPTO-4-ISOTHIAZOLECARBOXYLIC ACID TRISODIA SALT?
    3-Hydroxy-5-mercapto-4-isothiazolecarboxylic acid trisodium salt, this product has strange properties and is of great interest to explore. On the surface, it is often white to white powder, fine in texture, and pure in appearance.
    When it comes to solubility, it shows good solubility in water solvents. Just like ice and snow meet warm sun, it quickly merges into water to form a uniform solution. This solubility lays an important foundation for its application in many liquid phase systems.
    In terms of stability, it is still stable under conventional temperature and humidity environments. However, if you are exposed to extreme temperatures, or high humidity and hot topics, or severe cold, or encounter strong oxidants and reducing agents, its chemical structure may change. Just like a fragile boat sailing in a rough sea, the stability is challenged.
    Furthermore, its acidity and alkalinity are also unique. Due to the form of sodium salts, in aqueous solutions, it can moderately affect the pH of the solution, showing a weak alkaline characteristic. This alkaline characteristic can play a subtle and crucial role in a specific chemical reaction or formula system, like a delicate wedge, embedded in a complex chemical structure, affecting the balance of the whole.
    As for its smell, it is usually weak and almost tasteless. In practical application scenarios, the characteristics of this weak odor rarely introduce additional bad odor interference into the application system, providing convenience and possibility for many application fields sensitive to odor.
    In short, the physical and chemical properties of 3-hydroxy-5-mercapto-4-isothiazole trisodium carboxylate are intertwined to build its unique chemical "identity", which shows potential application value and research significance in many fields such as chemical industry and medicine.
    HMIT: What is the production method of 3-HYDROXY-5-MERCAPTO-4-ISOTHIAZOLECARBOXYLIC ACID TRISODIA SALT?
    To prepare 3-hydroxy-5-mercapto-4-isothiazole carboxylate trisodium salt (HMIT: 3 - HYDROXY - 5 - MERCAPTO - 4 - ISOTHIAZOLECARBOXYLIC ACID TRISODIUM SALT), the method is as follows:
    First take an appropriate amount of starting material, which contains mostly isothiazole-related compounds, and has groups that can be converted into target functional groups. In the reactor, add an appropriate amount of solvent, commonly used as polar organic solvents, such as dimethyl sulfoxide (DMSO) or N, N - dimethylformamide (DMF), which can effectively dissolve the raw material and promote the reaction. < Br >
    Then, a specific reagent is added to introduce the hydroxyl group. Suitable hydroxylating reagents, such as alkali metal hydroxides, can be selected. At the right temperature and reaction time, the hydroxylating reagent reacts with the corresponding group in the raw material and introduces the hydroxyl group at a specific position in the isothiazole ring. This process requires strict control of temperature. If the temperature is too high, it is easy to initiate side reactions. If it is too low, the reaction rate will be too slow. Generally, the temperature control is in a moderate range, such as 40-60 degrees Celsius. The reaction time ranges from a few hours to more than ten hours, depending on the reaction process.
    After the hydroxyl group is introduced, the introduction step of the mercapto group is carried out. Select a suitable sulfur-containing reagent, such as sodium hydride, and react with the hydroxylated product under specific conditions. This reaction needs to be carried out in an alkaline environment to facilitate the nucleophilic attack of the sulfur-containing reagent, and promote the substitution of the thiol group in the corresponding position to successfully introduce the thiol group.
    Furthermore, the carboxyl group is introduced. The product can be carried out by reacting with carbon dioxide in the presence of a specific catalyst, or using a specific carboxylation reagent, such as halocarboxylate, etc., through a series of reactions.
    Finally, the obtained isothiazole compound containing carboxyl, hydroxy and mercapto groups is reacted with sodium hydroxide, so that the hydrogen on the carboxyl, hydroxy and mercapto groups is replaced by sodium to obtain 3-hydroxy-5-mercapto-4-isothiazole carboxylic acid trisodium salt. After the reaction is completed, the pure target product can be obtained through separation and purification, such as crystallization, column chromatography and other methods.