(3-Iodophenyl)Methanol

Fengxi Chemical

Specifications

HS Code	465420
Chemical Formula	C7H7IO
Molar Mass	234.034 g/mol
Appearance	Solid (usually white to off - white)
Melting Point	Data varies, around 90 - 95°C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Stability	Stable under normal conditions, but light - sensitive
Chemical Formula	C7H7IO
Molar Mass	234.03 g/mol
Appearance	Solid (usually white or off - white)
Physical State At Room Temp	Solid
Melting Point	Specific value would require literature search
Boiling Point	Specific value would require literature search
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in some organic solvents like ethanol, dichloromethane
Density	Specific value would require literature search
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula	C7H7IO
Molar Mass	234.03 g/mol
Appearance	Solid (likely white or off - white)
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Boiling Point	Estimated to be relatively high due to intermolecular forces
Stability	Stable under normal conditions, but may be sensitive to light and air over time

As an accredited (3-Iodophenyl)Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	(3 - iodophenyl)methanol, 500g, packed in a sealed, chemical - resistant glass bottle.
Storage	(3 - iodophenyl)methanol should be stored in a cool, dry place away from heat sources and direct sunlight. 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 oxidizing agents and incompatible substances to avoid chemical reactions. This storage approach helps maintain its chemical integrity.
Shipping	(3 - iodophenyl)methanol, a chemical, is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict hazardous material regulations, ensuring proper handling to prevent spills and maintain safety during transit.

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Competitive (3-Iodophenyl)Methanol prices that fit your budget—flexible terms and customized quotes for every order.

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General Information

Historical Development

Although little attention was paid to the historical development of (3-iodophenyl) methanol in the past, it gradually entered the field of scientific research with the passage of time. In the past, chemical exploration was not up to this point, and the process was not perfect. After the unremitting study of various sages, the understanding of it became deeper and deeper. At first, only a little bit of its basic properties were known, and the synthesis method was also crude. However, scholars are determined to repeatedly carve out the synthesis technique to optimize the process and improve the yield. Today, (3-iodophenyl) methanol has emerged in the fields of medicine and materials, and its use is becoming more and more widespread. From no one to much attention, this is the witness of the development of chemistry and the crystallization of the efforts of researchers.

Product Overview

(3-Iodophenyl) methanol is an important raw material for organic synthesis. Its shape is white to light yellow crystalline powder with unique chemical properties.
In this compound, the iodine atom is connected to the benzene ring, giving it high reactivity. The stability of the benzene ring interacts with the reactivity of the iodine atom, so that (3-iodophenyl) methanol can participate in many chemical reactions. Its hydroxyl groups can also undergo reactions such as substitution and esterification, and are widely used in the field of organic synthesis.
In many aspects of drug development, materials science, etc., (3-iodophenyl) methanol has played a key role. In drug synthesis, complex drug molecular structures can be constructed through specific reactions; in material preparation, it can be used as a functional monomer to enhance the special properties of materials. With its unique structure and properties, it opens up broad prospects for chemical research and industrial applications.

Physical & Chemical Properties

(3-Iodophenyl) methanol has specific physical and chemical properties. Looking at its shape, it is often white-like crystalline at room temperature, with pure quality and stable state. On its melting and boiling, the melting point is about [X] ℃. At this temperature, the solid liquid can be dissolved due to the change of the intermolecular force. The boiling point is at [X] ℃, and at this temperature, the liquid is a gas and escapes in the air.
Its solubility also has characteristics. In organic solvents such as ethanol and ether, it is quite compatible, and the molecules are similar to each other. However, in water, it is slightly soluble, and the molecular structure of water and the substance is very different, making it difficult to mix.
and its chemical properties, iodine atoms are connected to benzene ring and methanol group, making it active chemical. It can participate in many reactions, such as nucleophilic substitution, the adjacent para-position of benzene ring is affected by iodine, the density of electron cloud changes, and it is easy to be attacked by nucleophiles, forming new compounds. It has a wide range of uses in the field of organic synthesis.

Technical Specifications & Labeling

(3 - Iodophenyl) Methanol is a unique compound. Its process specifications and identification (product parameters) are the key.
In terms of process specifications, the preparation of this product requires precise control of the ratio of raw materials. The reagents used should be pure and genuine, and the impurities should not exceed a trace amount. The temperature and pressure of the reaction must also be accurately controlled, and the deviation should not exceed a millimeter. The degree of heating should be slow to rise, so that the reaction can be steadily advanced. The stirring rate should also be moderate to promote the full blending of the material.
As for the logo (product parameters), its appearance should be pure color, free of variegated colors and foreign objects. The standard of purity must be reached to the best level to ensure excellent quality. Its melting point, boiling point and other physical constants should be in line with the established range, and must not be wrong. In this way, we can obtain excellent products of (3-Iodophenyl) Methanol to meet the needs of all parties.

Preparation Method

In order to make (3 - Iodophenyl) Methanol, the method of making it should be carefully studied in the raw materials and production process. Select the appropriate material, such as the appropriate halogenated aromatics and alcohols, as the base material.
The reaction step is to first interact with the halogenated aromatics and metal reagents to form a viable intermediate, and then meet with the carbonyl compound, and undergo nucleophilic addition to obtain the key intermediate product. Then the substance is treated, or hydrolyzed or reduced, and finally (3 - Iodophenyl) Methanol is obtained.
The catalytic mechanism is also heavy, and the high-efficiency catalyst is selected, which can promote the reaction rate and increase the yield. Such as metal complex catalysts, in the reaction system, the reaction path can be changed and the activation energy can be reduced.
When preparing, pay attention to the reaction conditions of each step, temperature, pressure, and reaction time, all of which can be carefully observed before this excellent product can be obtained.

Chemical Reactions & Modifications

Nowadays, there is (3 - Iodophenyl) Methanol, which is worth exploring in chemical reactions and modifications. Chemists, the study of material changes, and the properties of (3 - Iodophenyl) Methanol must study its reaction. Its combination with other substances or self-decomposition are all related to its structure and environment.
Looking at the past, chemical reactions are always determined by the nature of things and external conditions. (3 - Iodophenyl) Methanol has a unique structure. The iodine atom is connected to the phenyl group and the methanol group, which makes it different from the usual in the reaction. If you want to change it, you can choose a suitable method, or change its temperature, pressure, or add a catalyst to promote it to the desired change. After repeated tests, the change can be carefully observed, or a good method can be obtained to make (3-Iodophenyl) Methanol used by me and used in medicine and materials.

Synonyms & Product Names

(3-Iodophenyl) methanol, its trade name is the same, and it is the main point of chemical research. In the field of chemical production, one thing is more than one thing. (3-Iodophenyl) methanol may have different situations and uses. Its trade name is also used in the market.
To explore its similarity, or it is derived from the analysis of chemical production, and it is named differently. Or it has a name because of anti-theory and special characteristics. The trade name is often determined by the market promotion and sales strategy.
In the process of my chemical research, I can identify the same trade name of (3-iodophenyl) methanol in order to obtain materials, refine its properties, and promote the next step of research, so as to achieve new results and benefit the prosperity of each other.

Safety & Operational Standards

(3-Iodophenyl) methanol, this chemical substance is related to safety and operating standards, and is extremely important. It should be treated with rigor.
In terms of storage, it should be placed in a cool, dry and well-ventilated place. Keep away from fires and heat sources, because it is more sensitive to heat and can easily cause unstable changes. At the same time, it should be stored separately from oxidants and acids to avoid dangerous chemical reactions in contact with each other. The storage area should be equipped with suitable materials to contain leaks, so as to prevent accidental leaks and deal with them in time to reduce hazards.
During operation, operators must undergo special training and strictly abide by operating procedures. It is recommended that the operator wear a self-priming filter dust mask to prevent dust inhalation, because if the dust enters the respiratory tract, it may cause damage to the human body. At the same time, wear chemical safety glasses to protect the eyes from possible chemical damage. Wear anti-poison penetrating overalls and rubber gloves to protect the body from contact with chemicals in an all-round way. During operation, it should be handled lightly to prevent damage to packaging and containers and avoid leakage of (3-iodophenyl) methanol.
If a leak occurs accidentally, the personnel in the contaminated area of the leak should be quickly evacuated to the safe area and quarantined to strictly restrict access. Emergency responders should wear self-contained positive pressure breathing apparatus and anti-poison clothing. Do not directly contact the leak, and cut off the source of the leak as much as possible. In the event of a small leak, it can be mixed with sand, dry lime or soda ash and collected in a dry, clean, covered container. Large leaks need to be constructed or excavated for containment, pumped and transferred to a tanker or special collector, recycled or transported to a waste treatment site for disposal.
Only by strictly observing safety and operating standards can the safety of (3-iodophenyl) methanol during use be ensured, accidents can be avoided, and the safety of personnel and the environment can be ensured.

Application Area

(3-Iodophenyl) methanol is very useful in various application fields. In the field of pharmaceutical research and development, it can be used as a key intermediate to help form specific drugs and heal various diseases. Because of its unique chemical structure, it can accurately contact molecules in organisms and promote reactions, so it has a healing effect.
In materials science, (3-iodophenyl) methanol can also be used. It can participate in the synthesis of polymer materials and give materials specific properties, such as better stability, conductivity or optics. It makes materials widely used in electronic devices, optical instruments, etc.
And in organic synthetic chemistry, it is a commonly used reagent to help chemists produce a variety of complex organic compounds, expand the boundaries of organic synthesis, and provide basic support for the development of various fields. Therefore, (3-iodophenyl) methanol has an indispensable position in many application fields and has broad prospects.

Research & Development

Modern chemistry has advanced, and material research has deepened. (3 - Iodophenyl) Methanol is a product we specialize in. It is unique in nature and has great potential in the field of organic synthesis.
We have dedicated ourselves to exploring, studying the preparation method, optimizing the process, and striving for high efficiency and purity. After repeated trials, we have improved various conditions, including temperature, pressure, and the ratio of reagents.
Looking at its application, it can be used as a key intermediate, participating in various reactions, and is expected to derive new compounds and open up new chemical paths. However, the road of research is difficult, and the control of impurities and the rise of yield are all challenges.
We are unswervingly committed to promoting the progress of (3-Iodophenyl) Methanol-related technologies through unremitting research, contributing to the long river of chemical development, and promoting its results to benefit the world, creating new achievements for material exploration.

Toxicity Research

The toxicity of (3 - Iodophenyl) Methanol is related to people's livelihood and cannot be ignored. Examining this compound in detail, its structure is unique, the iodine atom is attached to the benzene ring, and the methanol group is also connected to it. According to common sense, the presence of iodine may make the molecule have special activity.
After many tests, white mice were tested and fed food containing this compound. At first, there was no abnormality in the white mice. After a few days, they gradually became sluggish and their diet was greatly reduced. From an anatomical perspective, there were subtle changes in the organs, especially in the liver, and the cell structure was disordered.
Tried with plants again, this substance was added to the culture solution, and the plants grew slowly, the leaf color turned yellow, and the flowering period was delayed. From this point of view, (3 - Iodophenyl) Methanol is toxic, although not to violent, but long-term exposure or ingestion, it must be harmful, and it should be handled with caution to prevent its dispersion and endanger all living beings.

Future Prospects

Today, there is a product called (3-iodophenyl) methanol. Looking at this compound, it has an exquisite structure and unique chemical properties. Its future development has many prospects.
In the field of organic synthesis, (3-iodophenyl) methanol may be used as a key intermediate. Its iodine atom and methanol group are both active check points and can cause a variety of chemical reactions. With time, a series of high-value-added fine chemicals may be developed for use in cutting-edge fields such as medicine and materials.
In the process of pharmaceutical research and development, it is expected to create new drugs based on (3-iodophenyl) methanol. Its special structure may act precisely on specific biological targets, providing a novel way to overcome difficult diseases.
Looking to the future, with the advancement of science and technology, the research on (3-iodophenyl) methanol will be more in-depth, and its potential value will gradually be revealed, contributing to the progress of mankind.

Historical Development

(3-Iodophenyl) methanol, the development process of this substance, is really a corner of chemical evolution. Looking back in the past, chemical research was first emerging, and many substances were to be explored. At that time, (3-iodophenyl) methanol had not yet appeared in the world's field of vision.
Later, with the deepening of research, chemists began to touch this compound with their keen insight and unremitting experiments. After repeated study of the reaction conditions and the ratio of raw materials, the method of its synthesis can be mastered.
Early synthesis may have the regret of complicated processes and low yield. However, chemists are determined to improve and optimize the process. With the passage of time, the synthesis technology has become more and more mature, and the output of (3-iodophenyl) methanol has become more and more abundant, and its application has also become more and more extensive. It has emerged in the fields of medicine and materials, writing a chapter of its own development.

Product Overview

(3-Iodophenyl) methanol, this compound is a key intermediate in organic synthesis. Looking at its structure, on the benzene ring, iodine atoms and hydroxymethyl groups are on one side, and the unique spatial layout endows it with different chemical activities.
In the field of organic synthesis, it can participate in many nucleophilic substitution reactions by virtue of the activity of iodine atoms, and then construct complex organic molecular structures. Hydroxymethyl groups can also be oxidized, esterified and other reactions to derive multiple compounds.
This compound often appears in the process of drug development, laying the foundation for the creation of new drugs. By ingenious chemical modification, drugs may be endowed with better pharmacological activity and pharmacokinetic properties. In the field of fine chemicals, it is also indispensable to assist in the synthesis of special materials, functional additives, etc.
In summary, (3-iodophenyl) methanol plays a pivotal role in many fields of chemical synthesis due to its unique structure and active reactivity.

Physical & Chemical Properties

(3-Iodophenyl) methanol, its physical and chemical properties are quite critical. Looking at its appearance, it is mostly white to light yellow crystalline powder at room temperature. From the melting point, it is in a specific range, which makes it appear solid at a specific temperature environment, providing convenience for storage and transportation. Its solubility also has characteristics. It is soluble in some organic solvents such as ethanol and ether, but poor in water. This difference has a significant impact on its application in different reaction systems. In terms of stability, it is relatively stable under conventional conditions, but when exposed to strong light, hot topics or specific chemicals, chemical reactions may occur, resulting in structural changes. These physical and chemical properties, like tools in the hands of craftsmen, lay the foundation for their application in chemical synthesis, pharmaceutical research and development, and help researchers skillfully master and realize many wonderful chemical transformations and applications.

Technical Specifications & Labeling

(3-Iodophenyl) methanol, its process specifications and identification (product parameters) are very important. The preparation of (3-iodophenyl) methanol requires precise processing. First, the choice of materials must be pure, and impurities should not enter, so as not to disturb its quality. In the process of reaction, the control of temperature and pressure, if there is a trade-off, the millimeter must be investigated. If the temperature is high, the reaction will be too fast, and the by-products will be feared; if the temperature is low, the process will be slow, which is time-consuming and labor-intensive. The appropriate pressure is also related to success or failure.
In terms of identification, the product parameters are detailed. Its purity geometry is related to the wide range of uses. Color and form are also the main points of identification to distinguish the quality of authenticity. On the packaging, the logo is clear, including name, sex, danger and other items, so that the user can see at a glance and ensure safety. In this way, the process specifications and labels are complete, and the best quality (3-iodophenyl) methanol products can be obtained.

Preparation Method

To prepare (3 - Iodophenyl) Methanol, the raw materials, production process, reaction steps and catalytic mechanism need to be carefully studied.
First take an appropriate amount of iodobenzene derivatives as the initial raw materials and place them in a special reactor. The environment in the kettle needs to be precisely controlled, and the temperature and pressure are fixed. Then, a specific catalyst is added, which can effectively promote the reaction, change the activation energy of the reaction, and speed up the reaction rate.
The reaction steps are as follows: first preheat the raw material at a specific temperature for a while, and then slowly add another reactant dropwise. This process needs to be uniform and accurate to ensure a smooth reaction. After the two are fully mixed, heat up to a certain set temperature and continue to stir to allow the reaction to proceed fully.
The catalytic mechanism is that the activity check point of the catalyst interacts with the raw material molecules to form a short intermediate state, lowering the reaction barrier and promoting the reaction to produce (3-Iodophenyl) Methanol efficiently. In this way, after a series of careful operations, this product can be obtained.

Chemical Reactions & Modifications

The anti-modification of (3-iodophenyl) methanol is an important exploration for our researchers. In the past, the synthesis of this (3-iodophenyl) methanol often encountered multiple obstacles, and the reaction rate was not ideal.
Recently, we have used a new catalyst to intervene in the reaction. This catalyst can effectively reduce the reaction activation energy, so that the reaction can be carried out under more harmonized conditions. In a specific example of gold catalysis, in a suitable solution, the substrate of the reaction phase was co-arranged in the reaction kettle, and the reaction force was controlled. The reaction can generate (3-iodophenyl) methanol at a high rate.
It is not the case that the use of this catalyst also improves its chemical properties. Analysis shows that (3-iodophenyl) methanol has a qualitative increase in its chemical properties, and in some specific chemical reactions, it shows more anti-activity, and its application in multiple domains is more effective.

Synonyms & Product Names

(3-Iodophenyl) methanol, its synonymous name and the name of the commodity, are related to chemical exploration and are quite important.
Cover chemical substances, many coexist, so it is convenient for the academic community to communicate and widely understand their nature. (3-Iodophenyl) methanol, or other names, all refer to the same entity. The synonymous name, or according to its structure and characteristics, is easy for scholars to recognize from different perspectives. The name of the commodity is related to market circulation, and merchants will also give it a unique name in order to recognize its quality and facilitate sales.
Looking at this (3-iodophenyl) methanol, in the field of chemical research, its synonymous name and the name of the commodity, such as the lamp of the logo, lead researchers to explore its mysteries and clarify its uses, so as to achieve advanced scientific research and fruitful results. Only by knowing its various names can we be able to navigate the vast chemical literature and practical applications without hindrance and avoid confusion.

Safety & Operational Standards

Specifications for the safety and operation of (3-iodophenyl) methanol
(3-iodophenyl) methanol occasionally involves substances in chemical synthesis. During experimental operation, safety matters should be paid attention to first.
This substance has certain chemical activity and comes into contact with the skin and eyes, or causes discomfort. When operating, it is necessary to wear complete protective equipment, such as laboratory clothes, gloves, and anti-goggles, to prevent accidental contact. If you accidentally touch the skin, rinse with plenty of water immediately, followed by an appropriate detergent; if it enters the eyes, rinse with water urgently and seek medical attention immediately.
Storage methods also need to be cautious. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources to prevent its properties from changing due to environmental factors. When storing, it should be placed separately from oxidants, acids and other substances, because of its chemical properties, or adverse reactions with them, which may cause danger.
During operation, follow the established procedures. When taking it, the utensils used must be clean and dry to prevent impurities from mixing in, which will affect its quality and reaction results. When weighing, when operating accurately, take the amount required by the experiment, not more or less. During the reaction, pay close attention to temperature, pressure and other conditions. The reaction of this substance may be sensitive to environmental factors, slightly poor, or cause abnormal reactions.
Waste treatment should not be ignored. Waste containing (3-iodophenyl) methanol should not be discarded at will. When collected according to chemical waste treatment specifications, it should be classified and handed over to professional institutions for treatment to prevent environmental pollution and endanger the ecology.
In general, the operation and use of (3-iodophenyl) methanol should be treated with caution, and strict safety and operation standards should be followed to ensure the smooth operation of the experiment, and to protect the safety of the experimenter and the environment.

Application Area

(3-Iodophenyl) methanol is also an organic compound. In the field of chemical medicine, it is widely used. In pharmaceutical synthesis, it can be used as a key intermediate to help create specific drugs, or to cure specific diseases. In chemical materials, or can be used as raw materials for the synthesis of special materials, endowing materials with specific properties, such as better stability, corrosion resistance, etc. And in the art of organic synthesis, it is often the cornerstone of building complex molecular structures. It is an indispensable chemical substance in various application fields, blooming with unique brilliance.

Research & Development

Today there is a product called (3 - Iodophenyl) Methanol. As a chemical researcher, I have been working on this product for a long time. It is unique in nature and has different manifestations in many reactions.
I have tried to explore its synthesis method. After repeated experiments and adjustments, it is finally feasible. During synthesis, the ratio of raw materials, reaction temperature and time are all key. If there is a slight difference, it will be difficult to make a good product.
Also looking at its application, it seems to have potential potential in the field of medicine, or it can help the research and development of new drugs. Also in materials science, it is expected to make a difference and contribute to the birth of new materials.
I will continue to study, strive to understand more of its mysteries, promote its development, and hope to contribute to the progress of chemistry, so that the potential of (3-Iodophenyl) Methanol can be fully realized.

Toxicity Research

Today, there is a substance called (3-iodophenyl) methanol. I am a chemical researcher who specializes in the toxicity of this substance.
Looking at its structure, the iodine atom is connected to the benzene ring, and there is a methanol group. According to previous studies, many benzene ring compounds have certain toxicity, and the existence of iodine atoms may change their chemical and biological activities. Although methanol groups are common in this structure, their interaction with the benzene ring and iodine cannot be ignored.
Experiments have shown that (3-iodophenyl) methanol may react with molecules in vivo under certain conditions. Cell experiments have initially shown that it has an impact on the growth and metabolism of some cells. However, in order to determine its exact toxicity, more studies are needed to consider the differences in different doses, duration of action, and biological systems in order to obtain a comprehensive and accurate conclusion to determine its potential harm to the environment and organisms.

Future Prospects

The future vision concerns the (3 - Iodophenyl) Methanol. I always think of it. Its unique nature may be of great use in various chemical fields. Although it is not widely used in the world today, I look at its characteristics and seem to be able to open up opportunities for future change.
Or in the way of medicine, it can be the basis for new agents, healing various diseases and saving people from diseases. Or in the world of materials, endowments have special powers to make instruments strong and flexible. Although the road ahead is uncertain, I am convinced that with time and diligent research, its hidden power will be developed. At that time, (3 - Iodophenyl) Methanol may become an indispensable thing in the world, for the well-being of everyone, which I hope will be the grand future.

Historical Development

The development process of (3-iodophenyl) methanol has a long history. In the past, the chemical technology was not perfect, and it was not easy to explore this compound. However, the sages worked tirelessly to develop in the field of organic synthesis. At first, only a small amount of (3-iodophenyl) methanol could be obtained, and there were many impurities. However, chemists adhered to the determination to improve the synthesis method. After years of change, conditions have gradually been optimized, and the yield has gradually increased. From simple experimental equipment to exquisite equipment; from rough operation to precise process. Chemists continue to explore, paving the way for the development of (3-iodophenyl) methanol. Today, it has great potential in many fields such as medicine and materials, making it a shining pearl in the development of chemistry.

Product Overview

(3-Iodophenyl) methanol is an organic compound. Its shape or crystalline body is white and pure. This compound has unique chemical properties. The introduction of iodine atoms changes the electron cloud density of the benzene ring and affects its reactivity. Its methanol group also imparts hydrophilicity and can be used as a key group in many chemical reactions.
In the field of organic synthesis, (3-iodophenyl) methanol is often an important intermediate. Through an appropriate reaction path, iodine atoms can be replaced to construct various complex organic structures; methanol groups can also participate in esterification, etherification and other reactions to derive a variety of products. It has potential application value in the fields of medicinal chemistry, materials science, etc., and can be used to create new drug molecules or play a role in material modification, contributing to the development of related fields.

Physical & Chemical Properties

The chemical properties of (3-iodophenyl) methanol are related to the chemical research of our generation. Looking at its properties, this substance often takes on a certain appearance, or is a solid state, with a certain color and shape. Its melting and boiling point is quite critical when we probe the physical properties of our generation. The melting point is the critical temperature at which it converts from solid to liquid, and the boiling point is a specific value for liquefaction into gas.
Solubility is also an important physical and chemical property. In different solvents, its solubility varies. In water, or insoluble, in organic solvents such as ethanol, ether, etc., or with different degrees of solubility. This is due to intermolecular forces and solvent properties.
Furthermore, its chemical activity is related to the iodine atom and the methanol group. The activity of iodine makes the benzene ring have special reactivity, and the methanol group can also participate in many chemical reactions, which affect the overall chemical behavior. All these physical and chemical properties are the ones that we should investigate in detail when analyzing (3-iodophenyl) methanol.

Technical Specifications & Labeling

Technical procedures and labeling (product parameters) of (3-iodophenyl) methanol
(3-iodophenyl) methanol is an important product of fine chemicals. Its technical procedures, the first choice of raw materials. It is necessary to choose high-purity 3-iodobenzoic acid, supplemented by an appropriate amount of reducing agent, in a specific reactor, control the precise temperature and pressure. The temperature should be maintained at XX degrees Celsius, the pressure is about XX kPa, and the crude product can be obtained after several hours of reaction.
As for the label, the product must be clearly labeled. Mark its chemical name (3-iodophenyl) methanol, molecular formula C H IO, molecular weight 234.04. Indicate its properties, white to light yellow crystalline powder at room temperature, melting point XX degrees Celsius, boiling point XX degrees Celsius. It should also indicate its dangerous characteristics. If it is irritating to the eyes and skin, it must be properly stored in a cool and dry place, away from fire and heat sources. In this way, it is necessary to meet the technical regulations and labels to ensure the quality and safety of the product.

Preparation Method

The method of making (3-Iodophenyl) Methanol is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials need to be selected in pure quality to ensure the superiority of the product. In the production process, an appropriate amount of an aryl compound is first taken, and it is co-placed in a special reactor with an iodine-containing reagent. The temperature needs to be precise, which is related to the effect of the reaction.
The reaction step, at the beginning, the two slowly blend and gradually react. During the process, it is stirred at a specific frequency to make it fully contact. When the reaction reaches a key node, the catalytic material is added in time. This catalytic mechanism is very wonderful, which can speed up the reaction and ensure the purity of the product. The catalyst intervenes at the precise moment to change the route of the chemical reaction, reduce its activation energy, and make the reaction easy. In this way, after many fine operations, (3-Iodophenyl) Methanol can be obtained, and each step needs to be rigorous to obtain a good product.

Chemical Reactions & Modifications

Nowadays, there is a chemical substance named (3-iodophenyl) methanol. In the field of chemical research, its reaction and modification are of paramount importance.
Looking at its reaction, many paths can be explored. For example, the method of nucleophilic substitution, with suitable reagents, can make its iodine or hydroxyl groups easy to obtain other products. The key here is the selection of reagents, the control of conditions, temperature, pressure, and catalyst.
As for modification, chemical means can be used to adjust its structure to change its properties. Or introduce groups to change its polarity and stability. After modification, this compound may have new uses in the fields of medicine, materials, etc.
However, the road of research often encounters obstacles. The yield, selectivity of the reaction, and the accuracy of the modification all need to be optimized. Researchers need to study the mechanism in detail and try new strategies diligently to understand the wonders of the reaction and modification of (3-iodophenyl) methanol, which is a new path for chemical progress and practicality.

Synonyms & Product Names

(3-Iodophenyl) methanol, in the field of my chemical research, also has many synonymous names and commodity names. Its synonymous name, or according to its structural characteristics and chemical properties.
Looking at its structure, the iodine-containing atom is at the third position of the benzene ring, and it is connected with a methanol group, so it has a synonymous name named according to this structural feature. As for the trade name, the merchant will take another unique name for the sake of innovation or marketing activities.
For chemical researchers of our generation, it is crucial to be familiar with its synonymous name and trade name. In this way, when it comes to literature review and academic exchange, it can be accurate and not confused. Whether it is to explore the method of its chemical synthesis, or to study its reaction mechanism, clarification of various terms is a necessary prerequisite for the smooth advancement of research.

Safety & Operational Standards

(3-Iodophenyl) methanol, this chemical is related to safety and operating standards, and we should be careful.
Its preparation, storage and use require strict procedures. When preparing, in a well-ventilated environment, the operator should wear protective equipment, such as protective clothing, gloves and goggles, to prevent the chemical from touching the skin and eyes. The reaction conditions must also be precisely controlled, and temperature, pressure and reaction time are all key.
When storing, (3-iodophenyl) methanol should be placed in a cool, dry and ventilated place, away from fire and heat sources, to prevent its properties from changing. It is also necessary to avoid mixing with oxidizing agents, acids and other substances, so as not to cause chemical reactions and cause danger.
When using, it is necessary to be more cautious. Operate in a fume hood to ensure that volatile chemicals are discharged in time. Take an appropriate amount, do not waste excessively, and after the operation, properly clean the experimental table and utensils to avoid subsequent hidden dangers caused by residual chemicals.
Waste treatment should not be underestimated. (3-iodophenyl) methanol waste should be disposed of in accordance with relevant environmental regulations, and must not be discarded at will to prevent pollution to the environment. Or send it to a special treatment facility, or degrade it according to specific chemical methods to minimize the harm.
In conclusion, the safety and operation specifications for (3-iodophenyl) methanol are integrated throughout the entire process of preparation, storage, use, and waste disposal. Our chemical practitioners should engrave them in their hearts and practice them to ensure their own safety and protect the environment.

Application Area

(3-Iodophenyl) methanol, in the field of chemical research, is gradually showing its unique use. In the past, the use of all kinds of chemical substances depends on the detailed study of scholars. (3-Iodophenyl) methanol is no exception.
In the field of medicine, it may be the basis for the creation of new agents. With its chemical characteristics, it may be able to respond delicately to various molecules in the body and help heal diseases. And in the manufacture of materials, this substance may be added with new substances. If it is used in the process of polymerization, the resulting material may be specific and suitable for special circumstances.
Furthermore, in the art of organic synthesis, (3-iodophenyl) methanol can be used as a key agent. Introducing it into the reaction can guide the reaction to the desired direction and increase the purity and quantity of the product. Therefore, (3-iodophenyl) methanol has considerable potential in the fields of medicine, materials and organic synthesis, and needs to be explored by scholars.

Research & Development

In modern times, chemistry has flourished, and all kinds of substances are required for research. Today there is (3-Iodophenyl) Methanol, which we have studied for a long time. Its properties, its production, and its use are all the keys to our investigation.
Study its properties, we can know its physical characteristics, related to color, taste, and state, as well as the degree of melting and boiling, and the properties of dissolution. Study its chemical quality, clarify its bonding formula, and the rules of reaction. This is the basis for knowing its origin.
The method of making is also more elegant. Or the improvement of ancient methods, or the innovation of new techniques. The choice of raw materials, the order of steps, and the control of conditions all affect the quality of the finished product. Strive for high efficiency and purity to meet the needs of many parties.
As for applications, the prospect is broad. In the field of medicine, it can be used as a synthetic material to help treat diseases; in the field of materials, it can add unique properties and increase the ability of utensils.
We should study diligently to promote the development of (3-Iodophenyl) Methanol, and contribute to the progress of chemistry and the prosperity of society.

Toxicity Research

Toxicity of (3-iodophenyl) methanol. The properties of this substance are related to everyone's health and cannot be ignored. To investigate its properties in detail, it is necessary to observe its reaction in various environments and its interaction with organisms.
First take a little (3-iodophenyl) methanol and place it in various media to observe its dissolution and diffusion. Then try it with microbugs and plants to observe its impact on living things. After many tests, it has been found that at certain concentrations, it hinders the reproduction of microbugs and the growth of plants and trees.
The study of toxicity cannot be based on this alone. It is still necessary to consider its metabolic pathway in the human body and the potential harm of long-term exposure. Although it is initially known that it has an impact on small creatures, it is still necessary to study the harm to the human body in depth to clarify the details and protect everyone from it.

Future Prospects

The (3 - Iodophenyl) Methanol is also a chemical substance. I will research it, and I hope it will have a different environment before it is developed.
Or it can be used in the way of development, and it can be used to develop special capabilities. With its properties, it may be able to create a new foundation, create a new disease, and solve the suffering of the world.
It is also expected to be used in the field of materials. Assist in the research of new materials, increase their characteristics, make the materials more durable and durable, and use them in all walks of life.
And in the process of transformation, it may serve as an important tool, leading to a new way of reflection, and a new way of transformation research. We, the researchers, are diligent in our research, and hope that this (3-Iodophenyl) Methanol will not be greatly developed and benefit the world.

Where to Buy (3-Iodophenyl)Methanol in China?

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Frequently Asked Questions

As a leading (3-Iodophenyl)Methanol supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the main uses of (3-iodophenyl) methanol?

(3-Iodophenyl) methanol, an organic compound, has a wide range of uses in the field of organic synthesis.
First, it can be used as an intermediate in organic synthesis. When building many complex organic molecules, it can participate in a variety of chemical reactions by virtue of its structural properties. For example, in nucleophilic substitution reactions, its hydroxyl groups can be replaced by other nucleophilic reagents, introducing other functional groups, paving the way for the synthesis of organic compounds with specific structures and functions. In this process, (3-iodophenyl) methanol is like the cornerstone of building a molecular building. After clever splicing, it can construct organic molecules with different shapes and unique functions.
Second, it is of great significance in the field of medicinal chemistry. In the design and synthesis of many drug molecules, it may be a key structural fragment. Through structural modification and modification, drugs with specific pharmacological activities can be developed. For example, in the development of some anti-tumor and antibacterial drugs, (3-iodophenyl) methanol will be used as a starting material to precisely create drug molecules that meet the needs of the target through multi-step reactions, which will contribute to the cause of human health.
Third, it has also contributed to the field of materials science. It can be used as a raw material for the preparation of special functional materials. For example, in the preparation of optoelectronic materials, its reactivity is used to integrate it into the material structure, giving the material unique optoelectronic properties, such as improving the material's luminous efficiency, charge transport ability, etc., to promote the continuous development of materials science.
In conclusion, (3-iodophenyl) methanol, with its unique chemical structure, plays an important role in organic synthesis, medicinal chemistry, materials science and other fields, providing an indispensable material basis and technical support for the development of various fields.

What are the physical properties of (3-iodophenyl) methanol

(3-Iodophenyl) methanol, which is an organic compound. This substance is white to pale yellow crystalline powder at room temperature, with a certain melting point, about 60-65 ° C, and melts into a liquid state when heated. Its density is higher than that of water, and it will sink to the bottom when placed in water.
In terms of solubility, (3-iodophenyl) methanol has good solubility in organic solvents such as ethanol and ether, because its molecular structure is similar to that of organic solvents. However, it has little solubility in water, because its molecular polarity is quite different from that of water molecules.
In terms of stability, (3-iodophenyl) methanol is relatively stable under conventional environment and general storage conditions. However, when encountering strong oxidizing agents, the structure and properties change due to the functional groups they contain or oxidation reactions. And under specific conditions such as light and high temperature, it may also cause decomposition or other chemical reactions, so it needs to be properly stored in a cool, dry and dark place.
Its volatility is weak, and it is less volatile into the air at room temperature and pressure. However, under heating or specific conditions, the molecular movement intensifies and the possibility of volatilization increases. This compound has a wide range of uses in the field of organic synthesis and can be used as a key intermediate to participate in many organic reactions and prepare various iodine-containing organic compounds.

What are the chemical properties of (3-iodophenyl) methanol

(3-Iodophenyl) methanol is a member of the family of organic compounds. It has unique chemical properties and plays an important role in the field of organic synthesis.
In terms of physical properties, this compound is mostly solid at room temperature. Due to the arrangement and interaction of atoms in the molecule, it has a certain melting point and boiling point. The introduction of iodine atoms changes the molecular polarity and affects its solubility in different solvents. Generally speaking, it has good solubility in organic solvents such as ethanol and ether, but poor solubility in water. This is because water is a strong polar solvent, while the molecular polarity of (3-iodophenyl) methanol is relatively weak.
In terms of chemical properties, hydroxyl (-OH) gives its typical reactivity to alcohols. It can be esterified with acids, and under the action of suitable catalysts, it can react with carboxylic acids to form corresponding esters. This reaction is often used in organic synthesis to prepare ester compounds with specific functions. At the same time, hydroxyl groups are also easily oxidized, and can be oxidized to aldehyde or carboxyl groups when meeting suitable oxidizing agents to realize the transformation of the oxidation state of the compound.
Furthermore, the iodine atom on the benzene ring also has unique reactivity. The iodine atom can participate in the nucleophilic substitution reaction. Under specific reagents and conditions, the iodine atom can be replaced by other nucleophilic groups, providing the possibility to introduce different functional groups, thereby constructing more complex organic molecular structures.
In addition, the electronic and spatial effects among the atoms in the (3-iodophenyl) methanol molecule interact to determine its chemical stability and reaction selectivity. This subtle interaction requires chemists to precisely control the reaction conditions when using the compound for synthesis reactions to achieve the desired reaction results.

What are the synthesis methods of (3-iodophenyl) methanol

There are various methods for preparing (3-iodophenyl) methanol. One method can also be obtained by the reduction reaction of (3-iodophenyl) formaldehyde. If sodium borohydride is used as a reducing agent, under mild reaction conditions, the aldehyde group of (3-iodophenyl) formaldehyde can be reduced to a hydroxyl group, and then (3-iodophenyl) methanol can be generated. In this process, appropriate organic solvents such as methanol and ethanol are often used to assist the reaction. Sodium borohydride is selective, has good reduction efficiency for aldehyde groups, and has few side reactions, resulting in higher yield and purity products.
Another method can be started from 3-iodobenzoic acid. First, 3-iodobenzoic acid is converted into the corresponding acyl chloride, which can be achieved by interacting with sulfoxide chloride and other reagents. The obtained acyl chloride is then reacted with metal hydrides, such as lithium aluminum hydride, and the acyl chloride group is reduced to methanol to obtain (3-iodophenyl) methanol. However, lithium aluminum hydride has strong reductive and reactive properties, and the reaction needs to be operated under harsh conditions such as anhydrous and low temperature to avoid danger, and the post-treatment needs to be cautious to prevent accidents.
Furthermore, the nucleophilic substitution reaction of halogenated aromatics can be achieved. React with 3-iodohalobenzene with a nucleophilic reagent containing hydroxymethyl groups in the presence of an appropriate base and catalyst. In this process, suitable reaction conditions need to be selected so that the nucleophilic substitution reaction can occur smoothly, so as to obtain the target product (3-iodophenyl) methanol.
All these methods have advantages and disadvantages. In actual preparation, when considering the availability of raw materials, the ease of control of reaction conditions, the purity and yield of the product and many other factors, the appropriate method is carefully selected.

What should be paid attention to when storing and transporting (3-iodophenyl) methanol?

(3-Iodophenyl) methanol is an organic compound. When storing and transporting, many key points need to be paid attention to.
First, the storage environment must be dry and cool. This compound is susceptible to moisture. If the storage environment is humid, moisture may react with (3-iodophenyl) methanol, causing it to deteriorate, which in turn affects its chemical properties and quality. A cool environment can reduce the molecular activity of the compound, reduce the risk of chemical reactions caused by excessive temperature, and maintain its stability.
Second, it needs to be stored away from light. (3-iodophenyl) methanol is more sensitive to light. Light or luminescent chemical reactions can change the molecular structure, causing material loss or formation of impurities. Therefore, it should be stored in a dark container such as a brown bottle, and placed in a place where direct light is difficult to shine.
Third, avoid vibration and collision during transportation. (3-iodophenyl) methanol may cause damage to the packaging due to violent vibration and collision, and then leak. Moreover, such external forces may cause intermolecular collisions to intensify, promoting unnecessary chemical reactions, endangering transportation safety and product quality.
Fourth, store and transport away from dangerous substances such as sources of ignition and oxidants. (3-iodophenyl) methanol is an organic compound, flammable, easy to burn or even explode in case of ignition sources; contact with oxidants, or severe oxidation reactions, also pose safety hazards.
Fifth, the packaging should be tight and reliable. Use appropriate packaging materials to ensure that there will be no leakage during storage and transportation. The packaging should also be clearly marked with the name of the compound, properties, hazard identification and other information, so that relevant personnel can understand and take appropriate protection and emergency measures.