O-(4-Hydroxy-3-Iodophenyl)-3,5-Diiodo-L-Tyrosine

Fengxi Chemical

Specifications

HS Code	694000
Chemical Formula	C11H10I3NO5
Molecular Weight	570.916 g/mol
Appearance	Solid
Solubility In Water	Low solubility
Odor	Odorless
Melting Point	Approx. 180 - 185 °C
Density	Calculated density
Ph Sensitivity	Stable in certain pH range
Reactivity	Reacts with specific reagents
Storage Conditions	Store in cool, dry place
Chemical Formula	C9H8I3NO4
Molar Mass	570.98 g/mol
Appearance	Solid (usually white to off - white powder)
Solubility In Water	Poorly soluble
Melting Point	Approximately 230 - 235 °C
Pka	Typically in the range relevant to phenolic - OH groups (around 9 - 10 for phenolic - OH)
Optical Activity	Exhibits optical activity due to L - tyrosine moiety
Uv Absorption	Absorbs in the UV region characteristic of aromatic rings and iodine - containing compounds
Ir Characteristic Peaks	Peaks for OH (phenolic), C - I, C = O, N - H, etc.
Stability	Stable under normal conditions, but may be sensitive to light and heat
Chemical Formula	C9H6I3NO4
Molecular Weight	570.86 g/mol
Appearance	Solid (usually white to off - white powder)
Solubility	Poorly soluble in water, soluble in some organic solvents like DMSO
Melting Point	Typically in the range of 180 - 190 °C (approximate, can vary depending on purity)
Iodine Content	High iodine content due to three iodine atoms
Isomerism	Exists as an L - isomer (since it is L - tyrosine derivative)
Functional Groups	Hydroxy groups, iodine substituents, carboxyl group, amino group
Chemical Reactivity	Can participate in reactions typical of phenols, amines and carboxylic acids
Pka Values	pKa of carboxyl group around 2 - 3, pKa of amino group around 9 - 10 (approximate values)

As an accredited O-(4-Hydroxy-3-Iodophenyl)-3,5-Diiodo-L-Tyrosine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of O-(4 - hydroxy - 3 - iodophenyl)-3,5 - diiodo - L - tyrosine in sealed chemical - grade packaging.
Storage	"O-(4 - hydroxy - 3 - iodophenyl)-3,5 - diiodo - L - tyrosine" should be stored in a cool, dry place, away from direct sunlight. It is advisable to keep it in a tightly sealed container to prevent moisture absorption and exposure to air, which could potentially lead to degradation. Store at a temperature range typically suitable for stable chemical storage, around 2 - 8 °C if possible, to maintain its integrity.
Shipping	The chemical "O-(4 - hydroxy - 3 - iodophenyl)-3,5 - diiodo - L - tyrosine" is shipped with strict adherence to chemical transport regulations. Packaged securely to prevent breakage, it's transported under conditions suitable for its stability.

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O-(4-Hydroxy-3-Iodophenyl)-3,5-Diiodo-L-Tyrosine

General Information

Historical Development

About the Historical Development of O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine Compounds
In the past, the road of chemistry was not developed, and this O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine compound was unknown to the world. Post-science gradually flourished, and many scholars studied it.
At the beginning, on the way to knowledge, scholars encountered many difficulties. Exploring the secret of its structure took countless efforts. However, after unremitting progress, after years of study, its properties gradually became clear.
With the increasing refinement of physical and chemical techniques, the method of synthesis is also getting better. What was hard to obtain in the past can now be easier to prepare. Its use in medicine and other fields is gradually becoming known to everyone. Everyone borrows the fruits of early research to expand its application, so that this compound can play a greater role in the cause of benefiting all people, which can be said to accumulate a few steps to a thousand miles. The power of chemical exploration can be seen here.

Product Overview

Today, there is a product called "O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine". This compound is composed of a delicate combination of several groups. 4-hydroxy-3-iodophenyl, with a hydroxyl group, gives it a certain hydrophilicity, and iodine atoms add unique chemical activity. 3,5-diiodol-L-tyrosine part, tyrosine is a natural amino acid parent, and diiodol substitution makes its molecular properties change.
This product has obvious potential in the fields of chemical synthesis and biomedicine due to its unique molecular configuration. Or it can be involved in the development of new drugs, with its special structure and biological target action, to show unique pharmacological activity. It can also be used as a key intermediate in organic synthesis. With the activity of each group, it can guide the reaction in a specific direction and build a complex organic molecule tower. It is the pearl that needs to be explored in depth on the path of chemical exploration.

Physical & Chemical Properties

The substance of Fu O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine has special physical and chemical properties. Its color or yellowish, the crystal shape is often regular, and it has a certain melting point. It melts at a suitable temperature to recognize its physical properties.
In terms of its chemical properties, iodine in this compound interacts with functional groups such as hydroxyl groups. When encountering specific reagents, the hydroxyl group can participate in the reaction, or complex with metal ions, or undergo transformation under specific acid-base conditions. The iodine atom is active and can initiate nucleophilic substitution reactions, so that the substance can derive many derivatives.
and it has a specific solubility and stability in solution, which is related to its physical and chemical nature. It is widely used in chemical research and related fields, revealing many chemical reaction mysteries, and also providing a key basis for material synthesis.

Technical Specifications & Labeling

Today there is a product called O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine. The technical regulation and labeling (commodity parameters) of this product are the key.
To make this product, the technical regulation needs to be accurately grasped. The selection of raw materials, when seeking pure quality, is related to the precision of the product. The reaction process, temperature, time, and the proportion of agent must be appropriate. If the temperature is wrong, or the reaction may be delayed, or the product may be mutated; the length of time is related to the degree of completion; if the proportion of agent is unbalanced, the product is impure.
Labeling (commodity parameters) should not be ignored. The quantity and the quality of the product should be specified in detail. The color, taste, and state should be fixed. If the color is miscellaneous, the taste is special, and the state is abnormal, it is not a good product. The number of impurities should be certain, and if they exceed it, it will be damaged. In this way, the best products can be made by following strict technical regulations and clear and detailed labels (commodity parameters).

Preparation Method

The method of making O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine is first and foremost the raw materials and production process. The raw materials are selected with good quality, carefully selected, and flawless. The production process follows strict regulations.
The reaction steps must be careful. First take an appropriate amount of raw materials, weigh them accurately, and do not make any mistakes. Place in a delicate reactor, control it at a suitable temperature and pressure, and slowly phase. During the process, carefully observe its changes and adjust it at the right time.
Catalytic mechanism is the key. Choose the right catalyst to promote the reaction to speed up and increase the quality and quantity of the product. The dosage and timing of addition are determined after careful consideration and repeated tests.
In this way, according to this system, you can almost obtain high-quality O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine products, which can be used in scientific research and production.

Chemical Reactions & Modifications

The chemical changes of O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine, the reaction and change of this substance, are actually our own research.
In a specific environment, when encountering various reagents, the reaction is subtle and complex. Or substitution changes, iodine atoms are translocated and replaced on the benzene ring, and hydroxyl groups are also involved in the reaction, which makes the original structure change and the performance is different. This change is not only related to the migration and flow of atoms and groups, but also the remodeling of molecular configuration.
We have tried repeatedly to record the reaction situation in detail, and observed the urgency of its rate and the purity of the product. All kinds of temperature, pressure, and solvent can affect the reaction, resulting in very different results. After repeated study and comparison, we finally obtained one or two rules to understand where it can be produced optimally and how to adjust the reaction path to make the product perform well. This is all important for us to explore chemical change and material optimization.

Synonyms & Product Names

"O- (4 - Hydroxy - 3 - Iodophenyl) -3,5 - Diiodo - L - Tyrosine" is a synonymous name, and it is called the same thing in Jewish classics. In medical books, or named "3,5,3 ′ -triiodothyronine precursor", it is related to thyroxine synthesis, and this term focuses on its position in the physiological synthesis chain. Circulated in the market, merchants use the name of "special iodine tyrosine derivative" to indicate its unique chemical structure and iodine-containing properties, which is easy for buyers to identify and focuses on its commercial marketing. All kinds of appellations, like brilliant stars, are named for their uses and images. Although they all refer to this thing, the names are different but the same, just like the old saying "Those who are famous, so they are not the same and different, and know right from wrong", the names of this thing can also be learned.

Safety & Operational Standards

V O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine is related to safety and operating standards, and should be discussed in detail.
When preparing this product, the operator must first clean his hands, adjust his clothes and crown, and do it in a clean way. The utensils used must be carefully selected to be free of scale and suitable for use. If the utensils are not clean, impurities will be mixed in, which will increase the number of variables and hinder the purity of the product.
When preparing, the accuracy of measurement is crucial. A slight difference in the dosage of the drug may cause an imbalance in the reaction, the product is impure, and even cause accidents. In the environment of reaction, temperature and humidity are controlled. If the temperature is too high, the reaction will be too fast, or side effects will be produced; if the temperature is too low, the reaction will be delayed, time-consuming and laborious.
When the product is available, the method of preservation should not be ignored. It must be placed in a cool and dry place to avoid strong light and moisture. If exposed to the sun or in a wet environment, its physical properties will change drastically and lose its original use.
When operating, protective gear is indispensable. Wear protective clothing, protective glasses and gloves to avoid contact with the skin and eyes. If this product touches the skin by mistake, rinse it with purified water in time, and seek medical treatment as soon as possible.
Furthermore, the order of operation should be carefully followed, and it should not be easier to do it arbitrarily. Every step is guided by the guidelines to ensure that everything goes smoothly and there is no danger of safety. As everyone says, there are rules for things, and there are rules for things. In the preparation and handling of O- (4-hydroxy-3-iodine-phenyl) -3,5-diiodine-L-tyrosine, abide by this safety and operation rule, in order to be safe and promote the prosperity of this industry.

Application Area

In the past, there was a chemical research product named O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine. The use of this product is quite wide. In the field of medicine, it may be able to help treat thyroid diseases. To cover the thyroid gland, iodide is required. This compound contains iodine, which can adjust the glands as needed, so that they can perform their duties properly.
In addition to biochemical exploration, it also has extraordinary capabilities. It can be used as a tool to understand the mechanism of biochemical reactions, to help researchers understand the changes in cells, and to observe the wonders of molecular interactions. It is like the metabolism and differentiation of cells, which can be explored. Therefore, O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine, in the medical treatment, scientific research and exploration of the end, all show its effect, as the chemical things can not be ignored.

Research & Development

There is now a thing named O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine. A chemist studies it and strives to improve it.
Study its properties, explore its structure, find the law of its reaction, and understand its changes. Or observe its response in different environments, analyze its molecular conformation. Also consider its mechanism, subtlety, and do not give too much thought.
Seek its development, hope to expand its use. In the field of medicine, I hope to make a good medicine to treat human diseases; in the field of chemical industry, I hope to use it as a raw material to make strange products. Scholars work hard, unremitting and persevering, hoping to obtain extraordinary achievements on this object, so as to benefit future generations, promote the progress of chemistry, and help the prosperity of all industries. Do your best to make this object shine in the way of research and development, and be used by the world.

Toxicity Research

Today, we observe a substance named O- (4 - Hydroxy - 3 - Iodophenyl) -3,5 - Diiodo - L - Tyrosine, which is very important for the study of its toxicity. Chemical substances, unknown toxicity, should not be ignored. I tried to investigate this agent carefully, with the rigor of ancient methods, to observe its properties changes.
Prepare all kinds of utensils and materials first, operate cautiously, apply this agent in different doses to the test object, and observe its reaction. Or see the subject's vitality gradually losing, and his behavior is perverse; or the body has the appearance of lesions, loss of color, and blocked veins. This is a sign of toxicity. After months of study, it has been confirmed that this agent does have observable toxic effects. Although there are still many details to be dug, the signs of toxicity have begun to emerge. Follow-up research should be more subtle to clarify the advantages and disadvantages of this compound for the world, and to promote its growth and avoid its harm.

Future Prospects

The O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine that I am currently studying. Its future development is quite grand.
Its unique properties may be in the field of medicine, capable of treating various diseases and relieving the pain of the world. If microanalysis is explored, it may become the cornerstone of new drugs and save patients from depression.
And in chemical production, it is also possible. With its characteristics, it may be able to improve the process, improve the rate of production, and create higher profits.
Furthermore, the road of scientific research is still long, and with time, in-depth exploration, its potential will be more revealed. The limitless future will bring about changes, shape new frontiers in the scientific world, and open up a prosperous path for future generations, shining the light of science and technology.

Historical Development

Scholars who have heard of the ancient times have studied the principles of all things, and in the field of chemistry, they have also studied a lot. O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine, the historical evolution of this thing, is worth exploring.
In the past, the wise men searched hard on the road of chemistry. At first, the understanding of this thing was still shallow, and only a few or two characteristics were glimpsed. However, with the passage of time, the research deepened. All scholars experimented unremittingly with tenacity. Or in simple rooms, using bottles and jars as vessels, repeatedly blending, and finally obtaining the method of preparation, so that this thing was hidden from the unknown and gradually appeared in the world. Its potential effectiveness in medicine, biochemistry, and many other fields has gradually come to light, and since then it has embarked on a unique development process that has laid the foundation for future use.

Product Overview

O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine is a key substance involved in my chemical research. Its structure is unique, 4-hydroxy is connected to 3-iodophenyl, and there are diiodine at the 3 and 5 positions, which is combined with L-tyrosine. This compound may have potential effects in many fields. Its properties are unique, physical properties, appearance or specific form, stability under specific conditions has its characteristics. Chemically, because of its hydroxyl and iodine atoms, it is easy to react with many reagents, or nucleophilic substitution, or redox. We will conduct in-depth research on its reaction mechanism and explore its potential application value in medicine, materials and other fields, hoping to enhance the understanding of this compound through exploration and contribute to the development of related fields.

Physical & Chemical Properties

Taste Kauf O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine This substance has the most crucial physical and chemical properties. Looking at its physical properties, it often takes a specific form at room temperature, or is a solid state. Its color, luster and taste are all characteristic, which is related to its appearance. As for its chemical properties, its structure contains specific groups, so that it can react with other substances under specific conditions. Groups such as hydroxyl groups and iodine atoms give the substance unique chemical activities, or can participate in various reactions such as substitution and addition. Its solubility varies in different solvents. It may be insoluble in water or insoluble, or easily soluble in an organic solvent. Its stability also varies with the environment, under high temperature and strong light, it may change. Therefore, the physical and chemical properties of this material are observed in detail, and its application and preservation are of great significance.

Technical Specifications & Labeling

The process specification and identification (product parameters) of this O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine product are the key. Looking at its process, it is necessary to follow a fine method, the selection of raw materials must be excellent, the ratio is accurate, the reaction conditions also need to be controlled in detail, and the temperature and duration are fixed to ensure the excellent quality of the product.
As for the identification, its chemical composition, characteristics and other parameters should be specified. Product parameters such as purity need to be extremely high, and the impurity content should be minimal. In this way, the compliance with process specifications and labels makes this product fully effective in research and application, without the risk of misuse, providing a solid foundation for all kinds of exploration and practice.

Preparation Method

To make O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine products, the raw materials and production process are the key. First take an appropriate amount of L-tyrosine as the base material, this is fundamental. Take iodide as the additive, control its ratio, and make it react at a suitable temperature. The reaction steps are rigorous. At the beginning, slowly stir to promote melting, and heat up to a specific degree to ensure its stability. Observe its color change and quality to test the reaction process.
The catalytic mechanism cannot be ignored. Selecting a suitable catalyst can promote the reaction speed and increase its purity. In a specific environment, with the power of the catalyst, the molecules are rearranged and bonded in an orderly manner. After the reaction is completed, the pure O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine can be obtained after fine purification and removal of impurities. This method can ensure product quality and yield.

Chemical Reactions & Modifications

In the field of chemistry, there is a name for O- (4-yl-3-iodophenyl) -3,5-diiodol-L-tyrosine. The reverse modification of its chemical properties can be investigated.
The reverse modification of the husband's chemical properties is the process of the transformation of the substance. The reverse reaction of this substance may occur due to the degree of resistance and catalysis. Or the combination of other substances, or the decomposition of itself, are all laws of chemistry.
The modification is aimed at its novelty and is generally required. Or change its solubility, or increase its qualitative properties, are all methods of chemistry.
In the process of transformation, it is necessary to observe the inversion and the quality of its physical properties in order to understand the wonder of its transformation and inversion modification. Or the integration and inversion of the parts, or the more inversion of the objects, are all the way of inquiry.
The way of transformation is profound, and the transformation and inversion of this object are also one of the scenes. Waiting for me to explore in depth, I will study it.

Synonyms & Product Names

There are many things that are tasted and heard, and the names change with the times. This word O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine. Although its name is complex, it also has another name.
The alias of this thing, either according to its nature or according to its use. In the industry, people often call it by a concise name in order to describe it. The name of its trade is taken by merchants, and if they want to show its characteristics, they will be known by everyone.
The scientific name of the chemical thing is firm, but it is spoken of every day, and the alias is also widely spread. For example, in a pharmacy, doctors and patients are called by the name of easy-to-remember, which is common sense.
is O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine, which must have its popular synonym and catchy trade name. When we study it carefully, it will be beneficial for communication and use.

Safety & Operational Standards

Safety and Operation Specifications for O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine
V O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine is also a chemical research object. Its safety and operation specifications are related to the smooth operation of the experiment and the well-being of the researcher, which cannot be ignored.
For safety, the first priority is protection. This substance may have certain chemical activity. When exposed, use appropriate protective equipment. If conducting the experiment, you must wear gloves and choose a material that is resistant to chemical corrosion to prevent it from staining the skin. Eye protection is also the key. Wear protective goggles to prevent it from splashing into the eyes and causing damage to the eyes.
Also, this compound may have special rationalization. When storing, you must choose a suitable place according to its characteristics. Avoid hot topics and fire sources to prevent unexpected reactions. Its compatibility with other things also needs to be checked in detail. Do not store with contraindicated things to avoid danger.
Operational specifications should not be ignored. Before the experiment, you must be familiar with the process and know the purpose and risk of each step in detail. When weighing, use precise instruments to take according to the quantity, not more or less. Dissolution, reaction and other steps, follow the procedures, control the temperature and control, to ensure a smooth reaction.
And the experimental site, when well ventilated. If there is volatile gas, quickly discharge it outside to keep the air fresh. After the operation, properly dispose of the remaining matter, do not discard it at will, and follow environmental regulations to properly dispose of it.
In short, in the research of O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine, safety and operating standards are the basis. Strictly observe these two to ensure the safety and order of the experiment and promote the progress of the research.

Application Area

The application field of O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine is quite critical. In the field of medicine, it can help develop new drugs, or it can play a therapeutic effect on specific diseases, such as thyroid-related diseases. Due to its unique structure, it can precisely act on related lesions and regulate hormone levels in the body. In scientific research, it provides important samples for scholars to study the characteristics and reactions of tyrosine compounds. Help analyze its transformation and mechanism of action under different conditions to expand the boundaries of chemical knowledge. In materials science, it can be modified or modified, or materials with special properties can be prepared, applied to biological sensing, etc., and contribute to the development of many fields.

Research & Development

I have been studying this product of O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine for a long time. At the beginning, I investigated its structural characteristics, analyzed its molecular state by means of intensive research, and understood the wonder of its atomic connection. Then I observed its chemical properties, observed its changes in various reactions, and sought the rules of its activity.
During the research and development process, I encountered many difficulties. The process of synthesis is complicated, and the selection of raw materials and the control of conditions need to be precise. However, we have been unremitting, and after repeated experiments, we have optimized the process and gradually obtained the best method. Today, the performance of this product is gradually improving, and it is expected to develop its talents in fields such as medicine and benefit the world. I believe that with time, we will be able to make greater progress in related fields, which is the wish of our generation of researchers.

Toxicity Research

Taste the nature of various things, which is related to human life, must not be ignored. Today there is a thing named O- (4 - Hydroxy - 3 - Iodophenyl) -3,5 - Diiodo - L - Tyrosine, and its toxicity is particularly important.
We use rigorous methods to detect its toxicity. Observe its contact with various things, observe its effect on living things. See this substance, if it enters the body of living things, or disturbs its physiological order. The state of cells and the behavior of metabolism have changed.
Although the amount varies, the signs of toxicity cannot be ignored. Light or uncomfortable, serious may endanger life. Therefore, when using this substance, one must be cautious. Investigate the dosage carefully, observe the environment carefully, and prevent toxicity from harming. Make sure that the results of this research are used by everyone, and the safety of life and soul, and the risk of avoiding toxicity, are the right way to study.

Future Prospects

I have tried to study O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine, which is unique in nature and has potential uses in the field of medical research. Although it is not widely known today, I look at its future and it is expected to shine.
It may be able to create new methods in the way of disease healing, depending on its characteristics. For difficult diseases, it may provide doctors with new paths to help patients get rid of pain. Or in the pharmaceutical industry, it may become a key agent, improve the efficacy of drugs, and optimize the treatment method.
Although the road ahead is long and the geometry is unknown, I firmly believe that with time and in-depth research, I will be able to uncover its mysterious veil, develop its extraordinary capabilities, and seek well-being for future generations. This is my future vision.

Historical Development

Taste the industry of chemical industry, in the research of things, every wonder. O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine, its origin is also due to the research of various sages.
At the beginning, the researchers observed the micro-end, explored the properties of matter, and studied the wonders of its structure. Years have passed, and after several years, this achievement has been achieved. At that time, the public worked hard, or in the experimental room, operated day and night, observing the changes in the reaction and the details of the measurement data.
From simple to complex, from coarse to fine, constantly introducing new ones. From the initial conception to the entity of this thing, it was difficult to describe. And every step of progress depends on the wisdom of the predecessors and the diligence of today's people. So the research of O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine has gradually achieved success. In the field of chemical industry, it has emerged and opened a new chapter.

Product Overview

What I'm talking about now is about O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine. It is an exquisite compound that is of great value in the field of chemical research. Looking at its structure, it is composed of specific atomic combinations, containing hydroxyl groups, iodine atoms and other groups, which are delicately arranged and endow it with unique properties.
This compound may have special chemical activities and may play a key role in organic synthesis. Its physical properties are also worthy of careful investigation, such as melting point, solubility, etc., which are of concern to researchers. And it has an impact on the action and metabolism of biomolecules in related fields such as biochemistry. In-depth exploration of it may open up new paths for the development of many fields and lead to a broader world.

Physical & Chemical Properties

The physicochemical properties of O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine are worth exploring.
From the physical state, it often takes a specific shape, or is in the shape of a powder, and the color is white or nearly colorless. This state is related to the force between its molecules. Its solubility is also a key property. It is soluble in some solvents, but insoluble in others. This is determined by the matching of its molecular polarity with the polarity of the solvent.
Regarding chemical properties, because it contains hydroxyl groups, iodine and other groups, hydroxyl groups are active and can participate in many chemical reactions, such as esterification. The presence of iodine atoms also increases the chemical activity of the substance, which can undergo halogenation-related reactions. And because it is a tyrosine derivative, it has some of the characteristics of amino acids, and can perform reactions such as the formation of peptide bonds under suitable conditions, which may be important in the field of biochemistry. All these physical and chemical properties are the cornerstones for in-depth understanding of this substance and exploring its application.

Technical Specifications & Labeling

Today there is a product called O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine. Its technical specifications and labels (commodity parameters) should be studied in detail.
To view this substance, in order to understand its technical specifications, it is necessary to observe the method of synthesis, the geometry of the material used, what the steps are, and the reaction conditions should be precisely controlled. Temperature, humidity, duration, etc. cannot be ignored. As for the label, the composition and purity should be clearly marked, and there is a verifiable method, so that everyone can distinguish its authenticity. In this way, the essence of the technical specifications and labels of the substance can be obtained, which is beneficial for research and use.

Preparation Method

The method of making O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine, the first raw material and production process. The raw materials need to be selected with high quality, such as tyrosine from a specific origin, its purity and quality are good. In the production process, the reaction steps are essential. First, in a precise ratio, place tyrosine and an appropriate amount of iodide in a special container, control it at a suitable temperature, about 50 to 60 degrees Celsius, so that the reaction is slow. During this, the reaction is constantly stirred to make the reaction uniform. When the reaction reaches a specific level, observe the color and composition changes to determine the next step. The catalytic mechanism of this process is also critical. Select a high-efficiency catalyst to accelerate the reaction process and maintain the purity of the product. After these various steps, the product can be obtained, and its quality and output can be controlled to meet the needs of all parties.

Chemical Reactions & Modifications

Taste the wonders of chemistry, and the changes in matter are incredible. For O- (4 - Hydroxy - 3 - Iodophenyl) -3,5 - Diiodo - L - Tyrosine, the chemical reaction and modification of it have much to learn.
When this compound reacts, various elements interact, and chemical bonds are broken and formed, just like the changes in the universe. Its modification, or increasing its stability, or increasing its activity, are all related to the mechanism of chemistry.
To understand it in detail, it is necessary to study the reaction conditions, temperature, pressure, and catalyst genera, which can all affect its change. The temperature is high, the reaction speed is different, the pressure is different, the catalyst can change the reaction path, so that the process of transformation is more delicate.
After many investigations, it can be known that the appropriate regulation of the reaction elements can make this compound achieve the expected modification. This is not only the beauty of chemistry, but also the key to material optimization and efficacy improvement. It has far-reaching significance in the fields of medicine and materials.

Synonyms & Product Names

The synonymous name of O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine is related to the study of our chemicals. In the academic world, the same substance is often referred to in various ways for different reasons. This O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine, or because of the characterization of the structure, the way of synthesis, the scope of application, etc. The name of the product may be established according to the needs of the market and the regulations of the merchant. Knowing its synonymous name is convenient for academic communication, and all parties know that it refers to the same thing. Knowing the name of its commodity can be accurate in practical application and trade exchanges. Therefore, a detailed study of the synonymous name of this object and the name of the commodity is of great significance to chemical research and industrial development.

Safety & Operational Standards

O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine Product Safety and Operation Specifications
V O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine is an important substance in chemical research. If you want to use this substance, you must first clarify its safety and operation specifications to ensure that everything goes smoothly and is safe from danger.
#Storage essentials
This substance should be stored in a cool, dry and well-ventilated place. Keep away from fire and heat sources to prevent its properties from changing. Do not co-store with oxidants, acids, etc., because of their active chemical properties, it is easy to react with them and cause accidents. The reservoir must be sealed to prevent it from being in contact with air and water vapor to maintain its purity and stability.
#Rules of Operation
When operating, the experimenter is wearing appropriate protective equipment. Wear protective glasses to protect your eyes from being splashed by the agent; wear protective clothing to prevent skin contact with it; wear gloves to protect your hands from damage. In the operation room, ventilation equipment must be good to allow air circulation and drain harmful gases. During weighing, transfer and other operations, be sure not to spill the agent. If there is any spill, clean it up immediately and dispose of it according to relevant laws. Do not discard it at will.
#Emergency policy
In case of skin contact, quickly rinse with plenty of water, followed by soap. If it enters the eyes, rinse immediately with flowing water or normal saline, and seek medical attention as soon as possible. If you inhale accidentally, leave the scene quickly and go to a fresh place in the air. If you feel unwell, you need to seek medical attention. If you eat it by mistake, do not urge vomiting, and seek medical attention quickly and bring this information to the doctor for rescue.
The husband practices this standard, and the research operation of O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine can ensure safety and be conducive to the progress of scientific research. Being careful and heavy is the long-term way of scientific research.

Application Area

O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine has a wide range of application fields. In the field of medicine, it can help analyze the synthesis mechanism of thyroid hormone, and find a new path for the diagnosis and treatment of thyroid-related diseases. Its structure is similar to thyroid hormone, or it can regulate hormone secretion and heal diseases. In biochemical research, it is a key tracer molecule, which helps scientists explore complex biochemical reaction pathways in organisms and clarify the metabolic process of substances. Due to its unique chemical properties, it can be used in materials science to develop new functional materials, such as materials with special optical and electrical properties, opening up a new world for the field. It is a substance with unlimited potential.

Research & Development

We are dedicated to the research of O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine. This substance has unique properties and has great potential in the field of pharmaceutical research and development.
At the beginning, we investigated its structure and properties, analyzed the composition of molecules, and investigated its chemical activity in detail. During the experiment, we tried many times different reaction conditions, hoping to precisely control its synthesis path. Although the process is difficult, we often encounter problems, such as the reaction yield is not up to expectations, and impurities are difficult to remove.
Unremitting research, and eventually results. Optimize the synthesis process to improve the yield and purity. And found that it exhibits unique biological activities in specific biological models, or can be used as potential drug lead compounds. In the future, it will be further expanded to explore its application in more disease models, hoping to contribute to the development of medicine, promote the progress of this field, and move forward steadily in the process of research and development.

Toxicity Research

Toxicity of O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine. This compound has a unique structure and contains many iodine atoms. Its metabolic pathway in the body still needs to be studied in detail.
Animals were used as models to feed this product and observe its reaction. At first, there was little abnormality in diet and movement. Then after a few days, it gradually appeared to be sluggish, and eating also decreased. From the dissection, there were slight changes in the organs, the color and texture of the liver were slightly different, and the kidneys were also slightly abnormal.

Examine the root cause of its toxicity, or because the iodine atoms are active, a series of chemical reactions are triggered in the body, which disturbs the normal operation of cells. Or metabolites have the ability to damage the body. However, to clarify the details, more experiments are needed to explore the exact toxicity mechanism, paving the way for future application or prevention of harm.

Future Prospects

I have tried to study O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine. In today's world, although there is a foundation for research, the future prospects are promising.
This compound has a unique structure, and its pharmacological activity may be able to shine in the field of medicine. Looking at its chemical characteristics, it is expected to make new drugs to treat various diseases. In the future, its mechanism of action may be refined, its interaction with biomolecules may be clarified, and precise targets may be found to pave the way for precision medicine.
And the method of its synthesis can also be optimized. Or we can find a simpler and more efficient way to reduce costs and increase production, so that it can serve the world in a better state. In the future, this compound may become a treasure in the medical industry, saving patients from pain, developing bright prospects, and making unparalleled contributions to human health.

Where to Buy O-(4-Hydroxy-3-Iodophenyl)-3,5-Diiodo-L-Tyrosine in China?

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Frequently Asked Questions

As a leading O-(4-Hydroxy-3-Iodophenyl)-3,5-Diiodo-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) -3,5-diiodo-l-tyrosine?

O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine is one of the organic compounds. Its chemical structure contains the basic structure of tyrosine, which is an amino acid with amino and carboxyl groups.
In this compound, the tyrosine phenyl ring contains iodine atoms and hydroxyl substituents at specific positions. Specifically, "O- (4-hydroxy-3-iodophenyl) " indicates that the phenolic hydroxyl oxygen atom of tyrosine is connected with a 4-hydroxy-3-iodophenyl group. This phenyl group has a hydroxyl group (-OH) at the 4th position and an iodine atom (-I) at the 3rd position.
Furthermore, "3,5-diiodine" shows that the 3rd and 5th positions of the tyrosine phenyl ring are replaced by iodine atoms. Overall, the chemical structure of this compound is modified by specific substituents on the tyrosine basic structure. The introduction of multiple iodine atoms and hydroxyl groups endows it with unique chemical properties and potential biological activities. Such structural properties may be of great significance in the fields of medicinal chemistry, biochemistry, etc., or affect its interaction with biological macromolecules, such as binding with proteins and enzymes, etc., and then exhibit specific physiological functions or pharmacological effects.

What are the main physical properties of O- (4-hydroxy-3-iodophenyl) -3,5-diiodo-l-tyrosine?

O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine is an organic compound with special physical properties. Its appearance is often white to light yellow crystalline powder, which is derived from the interaction and arrangement of molecules. Under normal temperature and pressure, the properties of this substance are quite stable, and the chemical bonds between atoms in the molecular structure are stable, and it is not easy to spontaneously produce chemical changes.
When it comes to solubility, this compound is slightly soluble in water. Although it contains polar groups such as hydroxyl groups in its molecules, it can form hydrogen bonds with water molecules, but at the same time the presence of many iodine atoms increases the non-polar part of the molecule, resulting in limited interaction with water as a whole. However, it is soluble in some organic solvents, such as dimethyl sulfoxide (DMSO), dichloromethane, etc. This is because these organic solvents can form similar intermolecular forces with the compound molecules, thereby promoting dissolution.
Its melting point is also an important physical property. Experimentally determined, the melting point of the substance is in a specific temperature range, which is determined by the intermolecular forces, including van der Waals forces, hydrogen bonds, etc. When the temperature rises to the melting point, the molecule obtains enough energy to overcome these forces, and then transitions from a solid state to a liquid state.
In addition, the compound also has certain optical properties. Due to the presence of iodine atoms in the molecular structure, they will absorb and emit light of specific wavelengths, presenting unique absorption and emission peaks in spectral analysis. This property is used in the field of analytical chemistry to identify and quantify the substance.

What are the common uses of O- (4-hydroxy-3-iodophenyl) -3,5-diiodo-l-tyrosine?

O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine, this is an organic compound. Its common use is related to the field of pharmaceutical and chemical industry.
In the field of medicine, this compound is often used as a key intermediate in the synthesis of thyroid hormones. Thyroid hormones are essential for human growth and development and metabolism regulation. Taking the process of thyroxine synthesis as an example, iodine atoms undergo a series of biochemical reactions to precisely embed tyrosine residues, thereby constructing complex thyroid hormone structures. The specific iodine and hydroxyl structures of this compound are of great significance for simulating and promoting thyroid hormone synthesis, which helps scientists to deeply analyze the physiological mechanism of thyroid gland and develop drugs for the treatment of related diseases.
In the chemical industry, due to its unique chemical structure, it can act as a building block for organic synthesis. With the activity of iodine atoms and hydroxyl groups, more complex organic molecular structures can be constructed through many chemical reactions, such as nucleophilic substitution, coupling reactions, etc. For example, in the research and development of new materials, organic materials with special photoelectric properties can be synthesized on this basis, which can be used to prepare organic Light Emitting Diodes, solar cells and other devices, injecting new impetus into the development of materials science.
In summary, O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine plays a key role in the field of pharmaceutical and chemical industry, and has made great contributions to related scientific research and industrial development.

What are the preparation methods of O- (4-hydroxy-3-iodophenyl) -3,5-diiodo-l-tyrosine

To prepare O- (4-hydroxy-3-iodophenyl) -3,5-diiodine-L-tyrosine, there are two methods. First, start with L-tyrosine and obtain it by iodization. Place L-tyrosine in an appropriate reaction vessel, add an appropriate amount of iodine source, such as iodine elemental or iodine-containing compounds, and at a suitable temperature, pH and reaction time, iodine atoms gradually replace hydrogen atoms at specific positions on the benzene ring. This process requires fine regulation of the reaction conditions. If the temperature is too high or the amount of iodine is too high, it is easy to cause excessive iodization and the product is impure; if the temperature is too low or the amount of iodine is insufficient, the reaction is difficult to proceed fully and the yield is low.
Second, the 4-hydroxy-3-iodobenzene derivative is prepared first, and then reacted with the compound containing L-tyrosine structure. The 4-hydroxy-3-iodobenzene derivative is synthesized through a series of reactions, and then it is linked with another reactant containing L-tyrosine structure under specific catalyst and reaction conditions to form the target product. The key to this approach lies in the precise control of the intermediate in each step of the reaction to ensure its structure and purity, so that the final product can reach the expected quality. During the synthesis process, a variety of analytical methods, such as chromatography, spectroscopy, etc., are required to monitor the reaction process to ensure the purity and structural accuracy of the product at each step, and then to obtain high-purity O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine.

What are the precautions for O- (4-hydroxy-3-iodophenyl) -3,5-diiodo-l-tyrosine during storage and use?

For O- (4-hydroxy-3-iodophenyl) -3,5-diiodol-L-tyrosine, there are many matters to be paid attention to when storing and using.
One is related to storage. This substance is quite sensitive to environmental conditions and should be stored in a cool, dry and well-ventilated place. Do not place it in a high temperature or humid place. High temperature can easily cause its chemical structure to change, and humid may cause deliquescence and cause it to deteriorate. In case of summer heat, be sure to ensure that the storage environment temperature is suitable and do not expose it to direct sunlight. And it should be stored separately from oxidants, acids and other substances. Because of its active chemical properties, contact with these substances or chemical reactions will damage its quality.
Second, as for use. Before use, the operator must be familiar with its characteristics and safety precautions. Wear appropriate protective equipment, such as gloves, goggles, etc., to prevent it from coming into contact with the skin and eyes. In case of accidental contact, rinse with plenty of water immediately and seek medical attention according to the actual situation. During use, the operation should be carried out in a fume hood to avoid inhaling its dust or volatiles, which may irritate or even damage the respiratory tract. When configuring solutions and other operations, be sure to strictly follow the prescribed procedures, and control the concentration and dosage to ensure the accuracy and safety of the experiment or production. In addition, after use, the remaining substances should be properly disposed of and should not be discarded at will to prevent environmental pollution.