2 Amino 4 Iodoanisole
Iodobenzene

2 Amino 4 Iodoanisole

Fengxi Chemical

Specifications

HS Code

117717

Name 2 - amino - 4 - iodoanisole
Molecular Formula C7H8INO
Molecular Weight 251.05
Appearance Solid (usually white to off - white)
Cas Number 53329 - 32 - 9
Boiling Point Approx. 304.9°C at 760 mmHg
Melting Point 117 - 121°C
Solubility Soluble in organic solvents like ethanol, slightly soluble in water
Pka No widely - reported value, but amino group can be protonated under acidic conditions
Chemical Formula C7H8INO
Molecular Weight 235.05
Appearance Solid (usually off - white to light brown powder)
Melting Point Typically in the range of 90 - 94 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Purity Can be available in purities up to 98% or higher in commercial grades
Odor Weak, characteristic aromatic odor
Chemical Formula C7H8INO
Molecular Weight 249.05
Appearance Solid (usually)
Color Off - white to light yellow
Melting Point Typically around 88 - 92 °C
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Odor Mild, characteristic odor
Purity Commercially Available Often >95% pure
Name 2 - amino - 4 - iodoanisole
Chemical Formula C7H8INO
Molar Mass 249.05 g/mol
Appearance Solid (usually a powder)
Color Off - white to light brown
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in some organic solvents like ethanol, dichloromethane
Melting Point 88 - 92 °C
Odor Faint, characteristic amine - like odor
Packing & Storage
Packing 2 - amino - 4 - iodoanisole packaged in 100 - gram bottles for chemical use.
Storage 2 - Amino - 4 - iodoanisole should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly sealed container to prevent moisture absorption and exposure to air, which could lead to degradation. Store it separately from oxidizing agents and incompatible substances. Ideal storage temperatures are typically around 2 - 8°C in a well - ventilated area to ensure its stability over time.
Shipping 2 - amino - 4 - iodoanisole should be shipped in accordance with chemical regulations. Pack it in suitable, tightly - sealed containers to prevent leakage. Ship via carriers approved for transporting such chemicals, ensuring proper labeling and documentation.
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2-amino-4-iodoanisole 2-amino-4-iodoanisole 2-amino-4-iodoanisole
General Information
Frequently Asked Questions
What are the main uses of 2-amino-4-iodoanisole?
2-% hydroxy-4-mercaptophenylacetic acid, although this substance is not detailed in Tiangong Kaiwu, it has a wide range of uses in terms of medicine and chemical industry.
In the field of medicine, it can be a key raw material for synthesizing drugs. For example, many drugs with antibacterial and anti-inflammatory effects, when preparing, 2-hydroxy-4-mercaptophenylacetic acid can be used as a starting material. After delicate organic synthesis steps, specific chemical groups are introduced to construct molecular structures with specific pharmacological activities. Its construction in drug molecules is like the initial embryo material for craftsmen to carve beautiful jade, laying the foundation for drug activity.
In the field of chemical industry, it also plays an important role in the synthesis of some special materials. For example, in the preparation of special polymer materials, it can participate in the polymerization reaction as a functional monomer. With its unique chemical structure, polymer materials are endowed with special properties such as adsorption and reactivity. In the development of fine chemical products such as coatings and adhesives, 2-hydroxy-4-mercaptophenylacetic acid can optimize the performance of products, such as enhancing the adhesion of coatings and improving the bonding strength of adhesives.
Although this product is not mentioned in "Tiangong Kaiji", in today's world, science is flourishing, and chemical and pharmaceutical technologies are becoming more and more complicated. 2-Hydroxy-4-mercaptophenylacetic acid has become an indispensable link in the chain of modern industry. With the method of organic chemistry, its properties are explored, its applications are researched, and its functions in various fields are continuously expanded, which benefits people's livelihood and promotes the prosperity of the industry.
What are the synthesis methods of 2-amino-4-iodoanisole?
To prepare ethyl 2-amino-4-chlorobenzoate, there are various methods.
First, p-chlorotoluene is used as the beginning, and 4-chloro-2-nitrotoluene is first nitrified. In this step, a mixed acid of nitric acid and sulfuric acid is used to control the temperature so that the nitro group is just in the ortho-toluene position. After iron powder or sodium sulfide is used as a reducing agent, the nitro group is converted to an amino group to obtain 4-chloro-2-aminotoluene. Then an oxidizing agent such as potassium permanganate is used to convert the methyl group to a carboxyl group to obtain 2-amino-4-chlorobenzoic acid. Then ethyl 2-amino-4-chlorobenzoate was obtained by esterification reaction with ethanol catalyzed by concentrated sulfuric acid. Although this step is complicated, the raw materials are easy to obtain, and the reactions in each step are also common.
Second, start with 2-nitro-4-chlorobenzoic acid. First, nitro is reduced to amino group with a reducing agent to obtain 2-amino-4-chlorobenzoic acid. Then esterification with ethanol catalyzed by concentrated sulfuric acid can obtain the target product. This way is simpler, but the raw materials of 2-nitro-4-chlorobenzoic acid may need to be purchased out, and the cost may be high.
Third, start with p-chloroaniline. First, it is diazotized, then reacted with carbon dioxide and copper salts to introduce carboxyl groups to obtain 4-chlorobenzoic acid. After nitration with mixed acids, the nitro group is put into the carboxyl ortho-position to obtain 2-nitro-4-chlorobenzoic acid. After that, the nitro group is reduced to an amino group and then esterified. There are many steps in this way, and the conditions are harsh. However, under specific raw materials and processes, it may have advantages.
In short, the methods for synthesizing ethyl 2-amino-4-chlorobenzoate vary, and the most suitable method should be selected according to the availability of raw materials, cost, yield and equipment.
What are the physical properties of 2-amino-4-iodoanisole?
2% hydroxy-4-chloroacetophenone is a key intermediate in organic synthesis. Its physical properties are as follows:
Looking at its properties, 2-hydroxy-4-chloroacetophenone usually appears as a white to light yellow crystalline powder. This form is easy to store and use. It has good morphological stability and is easy to measure and mix in many chemical production operations.
When it comes to melting point, it is about 94 ° C - 97 ° C. Melting point is one of the key physical properties of a substance. This specific melting point range indicates that the substance will undergo a phase transition from solid to liquid in this temperature range. In synthesis, purification, and quality control, melting point determination can be used to determine the purity of a substance. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point will be reduced and the melting range will become wider.
As for solubility, 2-hydroxy-4-chloroacetophenone is slightly soluble in water. This is because water is a highly polar solvent, and the molecular polarity of the substance is relatively limited. According to the principle of "similar miscibility", its solubility in water is poor. However, it is soluble in organic solvents such as ethanol, ether, and chloroform. Organic solvents such as ethanol, ether, and chloroform have molecular polarity or structural characteristics similar to these substances, and can interact with 2-hydroxy-4-chloroacetophenone molecules such as van der Waals forces and hydrogen bonds, thereby promoting their dissolution. This solubility characteristic is extremely important in organic synthesis reactions, and suitable reaction solvents can be selected accordingly to make the reactants fully contact and promote the smooth progress of the reaction. At the same time, when the product is separated and purified, its solubility difference can also be used to achieve effective separation.
What are the precautions for 2-amino-4-iodoanisole during storage and transportation?
2-Amino-4-chlorobenzamide requires careful attention during storage and transportation.
When storing, the first environment is dry. Because of its hygroscopicity, if stored in a humid place, it is prone to moisture and deterioration, causing its chemical properties to change, affecting quality and utility. Therefore, it should be placed in a dry, well-ventilated place, away from water sources and moisture.
Temperature control is also key. This substance is quite sensitive to temperature. Excessive temperature may cause it to decompose or accelerate chemical reactions. Excessive temperature may cause it to crystallize and solidify, affecting access. Generally speaking, it should be stored in a cool environment, the temperature is preferably 2-8 ° C. It is adjusted according to the product characteristics and instructions.
It is indispensable for storage away from light. 2-Amino-4-chlorobenzamide is prone to photochemical reactions in contact with light, resulting in structural changes and reduced activity. It should be stored in a brown bottle or opaque container to prevent direct light.
During transportation, the packaging must be stable and tight. This substance is dangerous. If the packaging is damaged, it may pose a threat to transporters and the environment after leakage. Use solid packaging materials, such as thick cardboard boxes lined with plastic film, metal drums, etc., and fill with foam, sponge and other buffer materials to prevent packaging from breaking due to transportation bumps.
At the same time, the cleanliness and suitability of the means of transportation also need to be considered. Do not mix with other chemicals such as acids, alkalis, oxidizers, etc., because of their active chemical properties, contact with these substances or cause violent reactions. Transport vehicles should be kept clean, free of residual chemicals, and have good ventilation equipment to prevent the accumulation of heat and harmful gases during transportation.
Furthermore, transport personnel should be professionally trained and familiar with the characteristics of 2-amino-4-chlorobenzamide and emergency treatment methods. Check whether the packaging is in good condition regularly during transportation. Once any abnormalities such as leaks are detected, they should be dealt with immediately according to the plan to ensure the safety of personnel and the environment is not polluted.
What is the market prospect of 2-Amino-4-iodoanisole?
What is the market prospect of 2-% hydroxy-4-pyridineformamide?

Husband 2-% hydroxy-4-pyridineformamide has shown extraordinary use in various fields, and its market prospect is quite promising.
In the field of medicine, this compound may have unique pharmacological activities. It may be a key raw material for the creation of new drugs to fight various diseases. Today, pharmaceutical research and development requires compounds with specific structures and activities. If 2-% hydroxy-4-pyridineformamide is proved to be effective in the treatment of diseases, such as anti-cancer and anti-inflammatory, it will be pursued by pharmaceutical companies, and its market demand will rise like mushrooms.
In the chemical industry, it may be a high-quality intermediate. A variety of high-value fine chemicals can be derived through a series of chemical reactions. With the increasing pursuit of high-end products in the chemical industry, the demand for intermediates such as 2-% hydroxy-4-pyridineformamide will also rise steadily. Taking dyes, fragrances and other industries as an example, there is a constant demand for raw materials with special structures, and 2-% hydroxy-4-pyriformamide may emerge in the meantime, expanding new space in the chemical market.
Furthermore, the road of scientific research and exploration is endless, and new applications may emerge inadvertently. With the advancement of research, or the potential value of it in cutting-edge fields such as new materials and biotechnology may be discovered. Once new uses are revealed, it is like opening the door to wealth, and the market size will welcome explosive growth.
However, the expansion of its market also faces challenges. The high cost of research and development and the strict supervision of regulations are all obstacles to progress. However, looking at the overall situation, if 2-% hydroxy-4-pyridineformamide is well developed and utilized, its market prospect is promising, and it must occupy a place in the tide of the market.