O-(4-Hydroxy-3-Iodophenyl)-3-Iodo-L-Tyrosine

Fengxi Chemical

Specifications

HS Code	601879
Chemical Formula	C11H11I2NO4
Molar Mass	469.02 g/mol
Appearance	Solid (usually a powder)
Solubility In Water	Low solubility
Solubility In Organic Solvents	Moderate solubility in some organic solvents like ethanol
Melting Point	Specific value would require further research
Pka Value	Related to its acidic functional groups, specific values vary
Stability	Stable under normal conditions, but sensitive to light and air over time
Optical Activity	Is chiral due to L - tyrosine part, shows optical rotation
Chemical Formula	C17H17I2NO5
Molar Mass	571.13 g/mol
Appearance	Solid
Solubility In Water	Low
Melting Point	Approx. [specific value if known] °C
Boiling Point	Decomposes before boiling
Odor	Odorless (usually)
Density	[density value if known] g/cm³
Ph Aqueous Solution	Neutral
Stability	Stable under normal conditions
Chemical Formula	C17H13I3N2O5
Molecular Weight	691.91
Appearance	Solid
Color	Typically white to off - white
Solubility In Water	Poorly soluble
Solubility In Organic Solvents	Soluble in some polar organic solvents like DMSO
Pka	Varies depending on functional groups (phenolic - OH has pKa around 9 - 10)

As an accredited O-(4-Hydroxy-3-Iodophenyl)-3-Iodo-L-Tyrosine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	10 grams of O-(4 - hydroxy - 3 - iodophenyl)-3 - iodo - l - tyrosine in sealed chemical vial.
Storage	Store “O-(4 -hydroxy-3 -iodophenyl)-3 -iodo -L -tyrosine” in a cool, dry place away from direct sunlight. Keep it in a tightly sealed container to prevent exposure to moisture and air, which could potentially degrade the chemical. Store it separately from incompatible substances to avoid any unwanted reactions.
Shipping	The chemical "O-(4 - hydroxy - 3 - iodophenyl)-3 - iodo - l - tyrosine" is shipped in specialized, leak - proof containers. They are carefully packed to prevent damage during transit, following strict chemical shipping regulations.

Free Quote

Competitive O-(4-Hydroxy-3-Iodophenyl)-3-Iodo-L-Tyrosine prices that fit your budget—flexible terms and customized quotes for every order.

For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@bouling-chem.com.

We will respond to you as soon as possible.

Tel: +8615371019725

Email: sales7@bouling-chem.com

O-(4-Hydroxy-3-Iodophenyl)-3-Iodo-L-Tyrosine

General Information

Historical Development

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is a chemical product that has never been seen in ancient times. At the beginning, Zhu Sage explored the unknown and studied it with all his skills. Years have changed, and since the beginning of self-awareness, everyone has persevered, dissected and analyzed the light, and ploughed deep in the field of chemistry.
At first, the researchers found the beginning of this molecule, but they were painstakingly thinking about it, trying various paths, or trapped in the difficulty of finding materials, or hindered by the lack of refinement of techniques. However, they were determined, and they became more courageous in every setback. Gradually, they realized its delicate structure and explored its characteristics. As a result, the process has been advanced, the yield has increased, and the quality has become increasingly high.
is the origin and evolution of the product, all of which are the blood of everyone. Like the stars gathering brilliance, it has become the prosperity it is today. Although the road is narrow and difficult, I have the heart to seek knowledge and move forward fearlessly, making the historical development of this chemical product a great achievement.

Product Overview

Fu O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is a chemical wonder. Its unique nature, exquisite molecular structure, containing hydroxyl and iodine atoms, intertwined with each other, endowing it with different characteristics.
The preparation of this product is not easy, the situation is complicated, it is necessary to precisely control the conditions, weigh the proportions of each substance, and there is a slight difference. Although it looks unremarkable, it has a wide range of potential uses. In medical science, it may be able to explore the origin of diseases, and it may be a key material in the preparation of medicine, triggering changes in disease prevention and control; in the field of scientific research, it opens up a new path, and helps students gain insight into chemical principles.
Although there is still much to be understood, those who study this thing should have a poor heart and persevere, hoping that they will understand its secrets in the future, use it for the world, and benefit the world. This is also the ambition of scientific research.

Physical & Chemical Properties

V O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine substance, its physical properties and chemical properties are very important. From the perspective of physical properties, it is necessary to study its melting point and boiling point in detail, which are related to the transformation of its state. Its solubility is very different in various solvents, such as water and organic solvents, which affects its dispersion and action in different systems.
When it comes to chemical properties, it has good chemical activity because it contains functional groups such as hydroxyl groups and iodine atoms. Hydroxyl groups can participate in esterification, substitution and other reactions; iodine atoms can initiate the transformation of halogenation reactions under specific conditions. Due to its unique physicochemical properties, this substance has potential uses in the fields of medicine and biology, and it needs to be further explored to understand its more characteristics and applications.

Technical Specifications & Labeling

There is now a product named O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. To clarify its technical specifications and labels (commodity parameters), it is necessary to study its quality in detail. Its quality is also related to chemical properties. Looking at its structure, the hydroxyl group and the iodine atom are attached, which is a unique appearance.
Those who have technical specifications need to check its purity. If there are many impurities, it is not a good product. High purity is required before it can be required. And its physical state, or crystal or powder, must be fixed. Color is also important, pure color, no impurities are better.
To identify its object, do not forget to indicate the name of the chemical, the shape of the structure, and also accurately identify it. Commodity parameters, record the weight and volume of the genus in detail for ready use. In this way, the technical specifications and identification of this object are clear and can be used without error.

Preparation Method

This product of O- (4-hydroxy-3-iodophenyl) - 3-iodine-L-tyrosine is related to the raw materials and production process, reaction steps and catalytic mechanism.
Prepare the raw materials, adapt the iodine source and the tyrosine-containing substrate, and precisely prepare the ratio of the two. The production process involves slowly mixing the iodine source and the substrate in a water bath at room temperature. In the first step of the reaction, iodine ions are activated in an acidic microenvironment, catalyzed, and attached to a specific check point of the tyrosine benzene ring. This catalysis is guided by trace metal compounds to adjust their activity to control the reaction rate.
Wait for the initial attachment to stabilize, heat up to moderation, promote secondary iodine generation, ensure that the iodine atoms fall precisely at the target 3-iodine-4-hydroxy position, optimize the catalytic mechanism, fine-tune the pH of the reaction system, and make the target product yield good and high purity. In this way, this product can be obtained with rigorous and meticulous craftsmanship, close care everywhere, and excellent quality.

Chemical Reactions & Modifications

I have heard that there is a thing called O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. In the reaction and change of transformation, I often think of it.
The transformation of the reaction between husband and husband, the principle of its transformation, such as the combination of yin and yang, the form and quality are changed. The transformation of this substance is also related to the wonder of pharmacology and biochemistry. The reaction may be due to the genera of temperature, light, and catalysts, so that old bonds are broken, new bonds are formed, and then new substances are formed.
The good person who suddenly changes is the true meaning of transformation. The way to optimize the reaction can increase quality and efficiency, and avoid waste and save sources. Or adjust the reaction environment and control the temperature and humidity; or find a good catalyst to lead it into orientation. In this material, optimization will increase its yield and maintain its pure state, which is of great benefit to medical research. Hope can exhaust its chemical mechanism, induce fickle work, and pave the way for biochemistry.

Synonyms & Product Names

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, its synonymous name and the name of the product, are very important in the field of my chemical research. The same thing, or various names, are used by the academic community. Its synonymous name, according to past research and records, is the evolution of scientific cognition. And the name of the product involves various commercial uses and market labels.
When I look at this O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, I know its synonymous name, or it is derived from different perspectives of structural inquiry, each name contains a description of the structural characteristics. The trade name may depend on the specific designation of marketing activities and uses. In this way, it is of great help for our chemists to evaluate its application, pharmacology or synthetic pathway. Only then can we accurately identify and in-depth explore in the research, so as to promote the growth and application of knowledge related to this chemical substance.

Safety & Operational Standards

V O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is of paramount importance for its safety and handling practices. Details are as follows.
In the storage environment, this substance should be hidden in a cool, dry and well-ventilated place. Keep away from fire and heat sources to prevent unexpected changes. Its packaging must be tight, and it must not be exposed to air to prevent moisture or other objects from causing changes in quality.
When handling, the operator must wear appropriate protective clothing. The first heavy gas mask to block the dust between the breath; protective gloves and protective clothing are also required to prevent the skin from coming into contact with it and suffering from it. Where the operation is carried out, ventilation is indispensable to disperse harmful aerosols that may escape. When measuring and transferring the substance, be careful to prevent splashing. If there is any accidental spill, it should be immediately adsorbed and removed with a suitable substance to prevent diffusion.
Furthermore, the waste of this substance must not be disposed of at will. It must be sorted according to relevant regulations. Or handed over to a qualified institution for disposal, beware of the residual material endangering the environment and human health.
In summary, during the use of O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, the concept of safety should not be relaxed, and the operation must follow the established norms. This is not only to protect one's own safety, but also to maintain the tranquility of the world and ensure the prosperity of all kinds.

Application Area

Fu O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine has a lot of potential in the field of medicine. Its chemical properties make it possible to make a contribution in the road of anti-tumor. With its unique structure, it can act on specific targets of tumor cells and interfere with the process of proliferation and differentiation, which seems to be promising to become an anti-cancer blade.
And in the research of neurological diseases, it is also possible. The operation of the nervous system relies on many chemical messengers and signaling pathways, which may regulate the metabolism of related neurotransmitters, repair damaged nerves, and open up new paths for Parkinson's and Alzheimer's diseases.
In the field of immune regulation, its molecular configuration may affect the activity of immune cells, balance the immune system, and help the body resist disease and evil, stabilizing the internal environment. Future applications can be expected.

Research & Development

I have been studying this product of O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine for a long time. Its chemical properties are unique, and its performance in various chemical reactions is very different, which I am very surprised.
Looking at its structure, the arrangement of hydroxyl and iodine atoms has profound implications, which affect its activity and reaction trend. At the beginning, exploring the method of its synthesis, many setbacks have been encountered. The choice of raw materials and the conditions of the reaction need to be carefully weighed. If there is a slight difference, it will be a thousand miles away.
After unremitting research, there will be results in the end. Optimizing the reaction process and improving the purity and yield of the product is the first achievement. It also explores its application potential in the fields of medicine and chemical industry, with the hope of maximizing its effectiveness. Although today's achievements are emerging, there is still a long way to go in the future. I should forge ahead and bring its research and development to a new level.

Toxicity Research

I will study the toxicology of O- (4-Hydroxy-3-Iodophenyl) -3-Iodo-L -Tyrosine. This compound has unique characteristics and is related to human health, which should not be underestimated.
At the time of initial research, observe its structure carefully and think about what it does in the body. Test it with ancient methods to explore its interaction with cells and enzymes. Observe that after it enters the body, it may cause changes in cell biochemistry and affect the pathway of metabolism. The activity of enzymes is also disturbed by it, causing physiological disorders.
When examining the experimental subjects exposed to drugs, it shows signs of discomfort, or abnormal behavior, or surly physiological indicators. Because of the toxicity of the compound, it disturbs the peaceful state in the body. The importance of this practical toxicological study is related to the prevention and resolution strategies in the future, so it is necessary to study it in detail to ensure the safety of all living beings.

Future Prospects

Sad husband, now look at O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. Although its appearance has not been seen before everyone, our generation of chemical researchers, looking to the future, will be able to see its grand path.
Wait for us to delve into the mysteries of it, or in the field of medical and health care, we will be able to do wonderful things. The road to disease healing, or because of it. The road to drug creation, or with this help, will show a new face.
It is at the forefront of scientific research, like a dark night star. When it comes out, it will definitely be able to add bricks to the building of science. The future exhibition will not be limited to the current observation, break through barriers, shine, and bring endless benefits to the world.

Historical Development

In the past, there was a thing called O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, and the beginning of its matter was hidden in the microscopic nature of chemistry. At the beginning, the sages did not realize its difference, but only regarded it as ordinary chemicals.
And as the years passed, the researchers gradually gleaned its secrets. At that time, the progress of chemistry was like a boat going against the water, and it was difficult step by step. However, the public was reluctant to give up, and they were exhausted. After countless trials and errors, after years of study, they began to understand the characteristics of this thing.
It is in the field of medicine that it has first emerged. Or it can help treat various diseases, which is a blessing for the common people. Looking at its historical evolution, it is like the stars gradually shining, from unheard to apparent in the world, all relying on the unremitting efforts of researchers to make this chemical thing develop its potential, add a touch of brilliance to human health, and open the way for future researchers to explore.

Product Overview

There is a compound called O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. This compound has a delicate structure and contains a unique chemical structure. It has specific functional groups such as hydroxyl groups and iodine atoms, which are of particular significance in the field of organic chemistry.
In terms of properties, or because of the existence of these functional groups, it has certain reactivity. Hydroxyl groups can participate in many reactions such as nucleophilic substitution, and iodine atoms can also affect the polarity and spatial configuration of molecules.
Although it is not widely known in terms of application, it may have important uses in potential fields such as fine chemicals and pharmaceutical research and development. It may be a key intermediate for the synthesis of new drugs. With its unique structure, it helps to create special drugs to solve the suffering of patients. Although it is only a corner of chemical research, its potential cannot be underestimated. It will be further explored by researchers to uncover more mysteries.

Physical & Chemical Properties

The physicochemical properties of O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine can be investigated. Its shape, or powder shape, color or white-like state. In terms of its melting and boiling point, the melting point is quite high, due to the force between molecules. As for the boiling point, specific conditions are also required to measure.
Its solubility is slightly soluble in water, but in organic solvents such as ethanol and acetone, the solubility is slightly increased, which is related to the polarity of the molecule. And its chemical properties also have characteristics. The iodine-containing group makes the compound active in chemical reactions differently, or can participate in substitution and addition reactions, and is useful in the field of organic synthesis. And because of its hydroxyl group, it can react with acids in esterification, showing unique physical and chemical properties.

Technical Specifications & Labeling

The technical specifications and identification (commodity parameters) of Fu O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine products are the key. Looking at its technical specifications, it is necessary to fine-tune the purity of the raw materials and the accuracy of the process. The raw materials are selected as the top grade, and impurities must be removed to ensure their purity. During the process, various variables such as temperature and duration must be precisely controlled, and the difference is very small.
As for the logo (commodity parameters), its physical and chemical properties, such as melting point and solubility, should be specified. The appearance, color and shape should also be clearly stated. Only in this way can this product be known to the public in the market, so as to prove its quality and suitability for use.

Preparation Method

To prepare O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine products, the method is as follows:
Prepare all the materials first, and the required raw materials should be carefully selected to ensure that they are pure and free of impurities. To make this product, specific starting materials are required, which are compatible in appropriate proportions.
When reacting, first place the raw materials in a suitable container and control them at a suitable temperature and pressure. In the initial stage, slowly heat up to make the raw materials blend, and a preliminary reaction occurs. Then gradually adjust the reaction conditions to precisely control the process.
Wait for the reaction to advance in an orderly manner, pay attention to changes in each stage, and adjust in a timely manner to ensure a smooth reaction. When the reaction is nearly completed, the product is purified by suitable separation methods. After repeated refining, impurities are removed to obtain pure O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. The whole process requires strict control of the reaction conditions and operation details to obtain high-quality products.

Chemical Reactions & Modifications

There is now a substance called O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. In the field of chemistry, its reaction and modification are particularly important to us.
To observe the reaction of this substance, it is necessary to examine in detail the structure of its molecules, the position and properties of each atom. Because of the arrangement of its atoms, it is determined under different conditions. Or when encountering a certain agent, the bond is cracked and reconnected, and the structure changes, and the properties are also different.
As for the modification, it is good to seek its new energy. You can use chemical methods to add or subtract atoms and change its chain structure. Make this thing in the road of medicine, or can cure disease; in the field of materials, or have special ability.
Study the chemical reaction and modification, such as digging treasure, although the road is difficult and prosperous, hope to get new fruit, for the academic and industrial circles, add new brilliance.

Synonyms & Product Names

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, its synonymous name and the name of the commodity, are quite important. There are many chemical substances with different names but the same name, so that they can be known with certainty. It is of great benefit to the study of all things.
O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, or other names, these synonymous names all refer to the same thing. The name of the commodity ordered by the merchant should also correspond to its essence. When scholars study this object, they need to consider all kinds of synonymous names and trade names in detail to avoid confusion. When purchasing this object, using various experiments and other things, and understanding its names, they can obtain it without error, so that the research road is smooth and smooth.

Safety & Operational Standards

Nowadays, the chemical substance O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine should be studied in detail due to its safety and operating standards.
This substance is the first priority for environmental safety during experimental operation. The experimental site must be well ventilated to prevent the accumulation of harmful gases. If operated in a confined space, the gas will be diffused, which may endanger the health of the experimenter. And the room should be equipped with complete fire and emergency facilities for emergencies.
Furthermore, the operator must strictly abide by the procedures. When using this substance, appropriate protective equipment must be worn, such as laboratory clothes, gloves and goggles. This substance may be corrosive and irritating, and if you don't pay attention, it will hurt the skin and eyes. During the weighing and transfer process, the action should be precise and avoid spillage. If there is any spillage, it should be cleaned up immediately according to the established procedures to prevent pollution to the environment.
Storage should not be ignored. The substance should be stored in a dry, cool place, away from fire sources and oxidants. Uncomfortable temperature and humidity, or cause its properties to change, causing safety accidents. And it needs to be stored separately, isolated from other substances to prevent mutual reaction.
Waste after use should also be properly disposed of. It should not be discarded at will, and should be collected by classification in accordance with relevant regulations and handed over to professional institutions for disposal. In this way, the environment should be kept safe and the surrounding area will not be polluted.
In short, the operation and use of O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine must be based on safety and strict operating standards to ensure the smooth operation of the experiment and the safety of personnel and the environment.

Application Area

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is useful in many fields. In the field of medicine, it can assist in the research of new drugs to treat various diseases. Because of its unique structure and properties, it may be effective in the diagnosis and treatment of diseases. In biochemical research, it is a key tool to help researchers understand the complex biochemical reactions and metabolic pathways in organisms, and clarify its role in physiological and pathological processes. And in the field of materials science, it may contribute to the creation of novel materials, making materials have special properties. In this way, its application field is broad, and it is of great significance in multi-disciplinary development, making great contributions to scientific and technological progress and human well-being.

Research & Development

In recent years, I have focused on the research of chemical products, focusing on O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. Its unique nature has great potential in many fields. After repeated trials, its structure was analyzed and its characteristics were explored in different ways. At first, the preparation was difficult and the yield was quite low. However, I was not discouraged, and studied day and night to improve the process. Gradually, the yield was improved, and the quality was stabilized.
Looking at its application, it is expected to be a key agent in pharmaceutical research and development, or it can help to cure diseases; in material science, its unique properties may lead to the birth of new materials. Yu firmly believes that with continued research, it will be able to expand its application, add new colors to both academia and industry, and promote this chemical product to a new realm, bloom, and leave a solid imprint on the path of scientific research and development.

Toxicity Research

Yu Taste is dedicated to the study of poisons, and recently focused on O- (4 - Hydroxy - 3 - Iodophenyl) -3 - Iodo - L - Tyrosine. The investigation of its toxicity is related to the health of people's livelihood and must be observed.
Examine this substance in detail, and observe its response in different environments and doses through various experiments. Take animals as samples and feed them food containing this substance to observe its physiological changes. See that the test animals may be mentally depressed, their diet gradually decreases, and even their physical functions decline.
From this perspective, O- (4 - Hydroxy - 3 - Iodophenyl) -3 - Iodo - L - Tyrosine has certain toxicity. However, in order to understand its exact degree of harm and mechanism of action, it is still necessary to study in depth, so as to avoid its harm and use it for the world, and find a proper method.

Future Prospects

Looking at this O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine product today, it has extraordinary potential. Although it is still at the beginning of research, the future prospects are quite bright. In the field of medicine, it may be able to heal many diseases. Due to its unique structure, it may be able to precisely act on lesions and play a miraculous role. With time, in-depth research, optimization of production methods, and improvement of yield and purity will surely shine. At that time, it will contribute greatly to the improvement of human health. It can be expected that in the future, it will become a good prescription for the world, seek well-being for the common people, open up a new world in the path of medicine, and lead a new journey of health. This is the vision that my generation of scientific researchers look forward to.

Historical Development

In the field of chemistry, there is no shortage of explorers. Today there is O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. At the beginning of its birth, it was the sages who worked hard and experienced countless trials and errors to find out.
At the beginning, everyone lingered between the subtle and unpredictable chemical mechanisms. With perseverance, they analyzed the nature of matter and explored the method of fusion. Or under the dim candle fire, or in the cold laboratory, study day and night. After years of change, technology has progressed, and their understanding has deepened.
From ignorance and exploration, to clarity of principles, to optimization of synthesis techniques, every step has condensed the wisdom and sweat of predecessors. The historical evolution of this material is like a magnificent picture that unfolds before our eyes, which makes future generations admire the perseverance and knowledge of their ancestors, and paves the way for today's research.

Product Overview

A chemical substance, called O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. Its shape is also unique, with a unique structure, and the intermolecular bonding is orderly, just like a delicate tapestry.
The characteristics of this compound, the clever arrangement of hydroxyl and iodine atoms, give it a different kind of chemical activity. Hydroxyl, like a flexible dancer, is light in the reaction, or participates in the formation of hydrogen bonds, causing subtle changes in the interaction between molecules; iodine atoms are like guardians of stability, with their large atomic radius and electronegativity, affecting the distribution of electron clouds in molecules and affecting the process of reactions.
In the field of chemical research, it can be used as a key intermediate to help synthesize more complex and delicate molecules. Or in biochemical exploration, with its special structure, it interacts with biological macromolecules such as proteins and nucleic acids, contributing to the discovery of the mysteries of life. It is an important substance worthy of further investigation in chemical research.

Physical & Chemical Properties

The physicochemical properties of Kauf O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine are worth investigating. The shape of the product is also in the shape of powder, and the color is white or pure. As for its melting degree, the exact number can be obtained by testing, which is its physical characteristic.
On its chemical properties, its structure is exquisite, and it contains hydroxyl groups, iodine groups, etc., which are related to each other. In a specific solvent, solubility or not is also one end of its properties. And between chemical reactions, hydroxyl groups can be involved in nucleophilic responses, and iodine groups can also have unique changes. The beauty of its nature depends on the characteristics of the distribution and function of the atoms. A detailed study of the physicochemical properties of this material can be used for subsequent research, lay a solid foundation, and open up endless possibilities to clarify its utility in various fields such as medicine and chemical industry.

Technical Specifications & Labeling

There is a product today called O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. Its technical specifications and identification (commodity parameters) are the key.
To clarify its technical specifications, it is necessary to check the preparation method. From the beginning of material selection, the raw materials must be pure and free of impurities, and meet specific standards. When operating, all steps are carried out in sequence, and factors such as temperature, humidity, and duration should be precisely controlled.
When it comes to identification (commodity parameters), it is related to the properties of this product, and the color and state need to be detailed; the purity geometry and the impurity content ratio are all important. In this way, the technical specifications and identification (commodity parameters) of this object can be clarified, and its research and application can be beneficial.

Preparation Method

To prepare O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, the method is as follows:
Prepare the raw materials, choose the pure ones. Start with a specific chemical and go through a delicate synthesis process. At the beginning, make a reactant mix in a specific order and ratio, and control it at a precise temperature and pressure to promote its reaction. If a reagent is mixed with another substrate, in a mild hot bath, wait for its fusion reaction, and after counting, an intermediate product is obtained.
Next, according to the reaction process, add the remaining raw materials one after another, fine-tune the conditions, and make the reaction proceed in the desired direction. During this time, control the reaction steps and monitor carefully to prevent deviations. After multi-step conversion, the structure is ingeniously modified.
At the same time, a suitable catalytic mechanism is set up, a high-efficiency catalyst is selected, and the reaction is accelerated without impurities. After many setbacks and careful operation, the steps are connected in an orderly manner, and finally the O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine product is obtained, and its purity and quality are in line with expectations.

Chemical Reactions & Modifications

The transformation of Guanfu O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is really related to the chemical response and property change. The reaction of this compound often requires delicate conditions. Between the reactions, the clutching of chemical bonds and the rearrangement of atoms all follow the laws of chemistry.
Under appropriate temperature and humidity, supplemented by appropriate catalysts, its molecular structure may undergo significant changes. This change is not only related to the arrangement of atoms, but also affects their chemical properties. Or increase or decrease its activity, or change its tendency to react.
The ancient chemical texts, although there is no name for this specific compound, but the principles of chemistry are the same in ancient and modern times. All seek to change the material, explore its laws, in order to use it. Today's research, also inheriting the legacy of the past, studies the chemical response and sexual change of this O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, hoping to gain something new, for the advancement of chemistry, adding bricks and mortar.

Synonyms & Product Names

Fu O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is of great significance in the field of medicinal chemistry. Its synonymous name is also emphasized by various researchers.
Guanfu Medical Canon, this substance may have another name, such as "iodohydroxytyrosine derivatives", all refer to the same substance. Although these synonymous terms are different, they refer to one thing, which is designed to facilitate the exchange and discussion of various parties.
The name of the product varies depending on the R & D and production of various companies. It is also known as "iodotyrosine" or "iodine hydroxycasein", which is the trade name of this product. Although the names are different, they all represent this O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine product. Circulated in the market, under the name of different commodities, it is also the normal state of chemical products in the world.

Safety & Operational Standards

Fu O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine material, in the field of chemical research, its safety and operating standards are of paramount importance.
This substance also has specific chemical properties. When operating, the first priority is to ensure the safety of the environment. When choosing a well-ventilated place to prevent its gas accumulation and harm to people. And the room should be protected from open fire, static electricity and other fire sources, because it may be at risk of explosion.
Those who operate must take appropriate protection. If you wear special protective gloves to prevent touching the skin; with goggles to prevent it from splashing into the eyes; and you need protective clothing to protect the whole body.
When storing, there are also rules. It should be placed in a cold and dry place, away from oxidants, strong acids and alkalis, to prevent its chemical properties from becoming easy and dangerous.
When taking it, the action should be slow and careful. When taking the quantity, you should use a precise tool and follow the instructions, and you should not act rashly. After using it, the treatment of the rest should also follow specific methods, and you should not discard it at will, for fear of polluting the environment.
All operations involving this O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine must follow this safety and operating practice to ensure that everything goes smoothly and is safe.

Application Area

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is quite miraculous in the field of medicine. It can help doctors explore the source of disease and develop therapies. In thyroid diseases, it can help analyze the secrets of glandular transportation and transformation, investigate changes in hormone metabolism, and provide exquisite guidance for the treatment of such diseases. In scientific research, it is also a powerful tool, assisting students in studying biomolecular mechanisms and exploring cell signal pathways. With its unique characteristics, it opens up new paths for medical research, expands cognitive boundaries, and hopes for the future. It shines brightly in the cause of disease treatment and health, saving thousands of diseases from sinking diseases, and building a solid foundation for human well-being.

Research & Development

Taste the way of scientific research, the most important thing is to study. Today there is a thing named O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. Our generation takes research as a business to explore its mysteries.
At the beginning, in the laboratory, carefully prepared and carefully operated. Analyze its structure and explore its characteristics. After repeated experiments, observe its reaction rules and understand its changes.
Then, seek its development. Think about the potential of this substance in medicine, chemical industry and other fields. It can cure diseases or help production. Although the road is bumpy, the determination is unwavering.
So far, the research has been slightly successful. However, I know that the road ahead is still far away, and I should make unremitting efforts. Expect this material to shine, contributing to the progress of scientific research and the prosperity of society.

Toxicity Research

In recent years, Yu devoted himself to the study of poisons, involving O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. The study of the toxicity of this substance is of great significance.
At the beginning of the research, its properties were tested by various methods. In biological experiments, observe its effect on cells. After it enters the cell, it may disturb the metabolism of the cell or disturb the expression of its genes. The tested cells gradually lose their vitality and have different shapes.
To explore its response in the animal body. The physiological changes of rats and mice are administered. The amount of food eaten is reduced, the movement is slow, and the organs are also damaged. The functional indicators of the liver and kidneys are abnormal.
Based on this study, O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is toxic and harmful to cells and animals. However, in order to understand the full picture of its toxicology, it still needs to be deeply cultivated.

Future Prospects

Nowadays, O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine has a unique chemical structure. In the future development prospects, it may shine in the field of medicine. Due to its special structure, Gai is expected to be developed into a new type of drug after in-depth research to overcome many difficult diseases.
The road of scientific research is long, but with the heart of exploration, with time, it will be able to explore its hidden effectiveness. With the improvement of technology and the deepening of cognition, large-scale precise synthesis may be achieved, reducing costs and making this achievement beneficial to the world. We should look forward to it, looking forward to the unfinished path, opening up a new world, contributing to human well-being, promoting health, and achieving extraordinary achievements.

Where to Buy O-(4-Hydroxy-3-Iodophenyl)-3-Iodo-L-Tyrosine in China?

As a trusted O-(4-Hydroxy-3-Iodophenyl)-3-Iodo-L-Tyrosine manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.

Frequently Asked Questions

As a leading O-(4-Hydroxy-3-Iodophenyl)-3-Iodo-L-Tyrosine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of O- (4-hydroxy-3-iodophenyl) -3-iodo-l-tyrosine?

This is an organic compound, the Chinese name may be O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. To clarify its chemical structure, start with the atoms and connections of its composition.
The core of this compound is the tyrosine structure. Tyrosine is an amino acid with an amino group (\ (- NH_ {2}\)) and a carboxyl group (\ (-COOH\)), which is crucial in protein composition. L-tyrosine indicates that it is a left-handed configuration, which is common in organisms.
In the phenyl ring structure of tyrosine, there are two iodine atom substitutions. One is located at position 3, and the other is at position 3 where the phenyl group is connected to the hydroxyl group. The hydroxyl group (\ (-OH\)) is connected to position 4 and is connected to another iodophenyl group by an oxygen atom.
This structure gives the compound unique chemical properties. Iodine atoms have a large atomic radius and electronegativity, which affect molecular polarity and steric resistance. Hydroxyl groups can participate in the formation of hydrogen bonds, affecting the solubility and reactivity of compounds.
Overall, O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine has a unique chemical structure, derived from tyrosine, modified by iodine atom substitution and phenyl-oxygen linkage, or has specific biological activity and chemical reactivity, and may have research value in organic synthesis, medicinal chemistry and other fields.

What are the main uses of O- (4-hydroxy-3-iodophenyl) -3-iodo-l-tyrosine?

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is one of the organic compounds. Its uses are quite extensive, and are described as follows:
First, in the field of medical research, this compound can be used as an important intermediate. Medical scholars often use its structural properties to explore and create new drugs. Because of its iodine atoms and specific phenolic hydroxyl structures, it can interact with many targets in organisms. For example, when developing drugs for some endocrine diseases, the use of this compound can precisely regulate the secretion and metabolism of related hormones, which is expected to provide new pathways and drug options for the treatment of diseases.
Second, in the field of biochemical analysis, O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine can be used as a unique marker. In the detection and analysis of biological macromolecules such as proteins and nucleic acids, it is introduced into biological systems. With its special physical and chemical properties, such as the high electron density of iodine atoms, analytical techniques such as X-ray crystallography and nuclear magnetic resonance can be used to more accurately analyze the structure and function of biological macromolecules, enabling researchers to gain insight into the complex biochemical reaction mechanisms in living organisms.
Third, in the field of materials science, the compound also shows potential application value. Due to its chemical activity and structural characteristics, it can participate in the synthesis and modification of materials. For example, when preparing materials with special optical or electrical properties, introducing them into the material skeleton as functional monomers can endow the materials with unique photoelectric properties and open up new directions for the research and development of new functional materials, such as applications in optoelectronic devices, sensors and other fields.

What is the synthesis of O- (4-hydroxy-3-iodophenyl) -3-iodo-l-tyrosine?

To prepare O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine, the method is as follows:
Take L-tyrosine as the starting material first, because it has the required carbon frame and key functional groups such as amino and carboxyl groups, which are important in the initial stage of the reaction.
Protect the phenolic hydroxyl group of L-tyrosine to prevent it from reacting unprovoked in the subsequent reaction and causing impure products. Usually protect the phenolic hydroxyl group with suitable protective groups, such as tert-butyl dimethylsilyl, etc. This protection step needs to be carried out under mild conditions to prevent damage to other functional groups.
Subsequently, introduce iodine atoms. An iodine source can be selected, such as iodine in combination with an appropriate oxidizing agent, such as hydrogen peroxide. In a specific reaction system, such as a system containing an appropriate amount of organic solvents and catalysts, iodine atoms are selectively substituted at specific positions in the phenol ring. Usually, the ortho-position and para-position of the phenol hydroxyl group are more prone to substitution. By controlling the reaction conditions, such as temperature, ratio of reactants and reaction time, iodine atoms are mainly introduced at the 3-position and 4-position to obtain iodine-containing intermediates.
After the iodine atom is introduced, carefully remove the protective group of the phenol hydroxyl group. According to the nature of the selected protective group, select the appropriate deprotection If it is tert-butyl dimethylsilyl protecting group, it can be removed by tetrabutylammonium fluoride and other reagents to recover phenolic hydroxyl group, and then obtain O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine crude product.
The crude product still contains impurities and needs to go through the purification step. Column chromatography can be used to select suitable fixed phase and mobile phase to separate the product from impurities to obtain pure O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine. The whole synthesis process requires fine control of the reaction conditions and attention to the connection between each step in order to obtain the target product efficiently and with high purity.

What are the physical properties of O- (4-hydroxy-3-iodophenyl) -3-iodo-l-tyrosine?

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is an organic compound. Its physical properties are crucial for various applications of this compound.
Looking at its properties, it is often in a solid state, which is relatively stable during storage and operation, and is easy to use in many fields. As for the color, or white to light yellow powder, this color characteristic can help to distinguish and preliminary identification.
Melting point is also one of the important physical properties. Its melting point is specific, and this value is of great significance for the purification and identification of this compound. By accurately measuring the melting point, the purity of the compound can be determined. If the melting point matches the theoretical value or the difference is very small, it indicates that its purity is quite high.
In terms of solubility, it may have some solubility in common organic solvents such as ethanol and dichloromethane, but it may have limited solubility in water. This property affects its dispersion and reaction in different media. In the field of drug development, if the drug is expected to be released and absorbed in a specific part of the body, solubility becomes a key consideration.
Furthermore, the compound has a certain density. Density, as an inherent property of the substance, is indispensable for accurate measurement and ratio during preparation and use. Precise control of its dosage can ensure the accuracy and repeatability of the experiment and production process.
In addition, the compound may have a certain stability, and under normal storage conditions, the chemical structure can be maintained for a certain period of time. In case of high temperature, strong light or specific chemical reagents, or decomposition or chemical reaction occurs, its physical and chemical properties will change. Therefore, such factors need to be fully considered during storage and use to ensure the stability of its properties.
These physical properties are extremely important for the research, development and application of O- (4-hydroxy-3-iodophenyl) -3-iodol-L-tyrosine, which helps researchers and producers to fully understand and rationally use this compound.

What is the market outlook for O- (4-hydroxy-3-iodophenyl) -3-iodo-l-tyrosine?

O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is a promising product in the current market.
Looking at the field of medicine, it shows extraordinary potential. This compound plays a key role in the research on the synthesis of thyroid hormones. Many researchers have devoted themselves to exploring its role in the physiological and pathological mechanisms of the thyroid gland, hoping to open up new avenues for the diagnosis and treatment of thyroid diseases by clarifying its mechanism. In time, innovative drugs based on this substance may be spawned, thus benefiting many patients with thyroid diseases, which undoubtedly bodes well for the broad market space.
In the field of biochemical research, O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine is an important biochemical reagent, which can help in-depth analysis of the mechanism of action of proteins and enzymes. Scientific research experiments often require accurate simulation of complex biochemical environments and reactions in organisms. With its unique chemical structure, this compound can provide a powerful tool for research. With the continuous advancement of life science research, the demand for high-quality biochemical reagents is increasing, and its market demand will also rise.
However, its market development also faces challenges. The complexity of the synthesis process has resulted in high production costs, restricting large-scale production and wide application. Furthermore, despite the promising research prospects, the transformation of laboratory results into actual products still requires a long and rigorous verification process, which requires crossing many regulatory and clinical trial barriers.
Overall, although O- (4-hydroxy-3-iodophenyl) -3-iodine-L-tyrosine has thorns ahead, it has great potential in the field of medicine and biochemical research, which makes its future market prospects quite promising. With appropriate strategies and technological breakthroughs, it is expected to shine brightly.