1 Aminoisoquinoline
Quinoline Thiophene Imidazole Thiazole
1-Aminoisoquinoline
Name 1-Aminoisoquinoline
Molecular Formula C9H8N2
Molar Mass 144.17 g/mol
Appearance Solid
Color Off - white to light yellow
Melting Point 97 - 100 °C
Boiling Point 304 - 306 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Pka ~5.2
Odor Weak, characteristic odor
Stability Stable under normal conditions
FAQ

What are the main uses of 1-aminoisoquinoline?

Boronide is a chemical substance, with original properties. Its main uses are many, and it has not been directly reported in the ancient books of "Tiangong", but its use can be proved by modern knowledge.

First, in the field of synthesis, boride is often used as the original phase. It can be used in the original phase of carbonyl compounds such as aldodes and ketones. This inverse phase is good, and the performance is good. For example, benzaldehyde can reduce benzyl alcohol under the action of boride, and other functional effects in the molecule are very small. This property makes it very important in the synthesis of refined compounds, such as synthesis of chemicals and flavors. In the synthesis of chemicals, it can be cleverly used to build specific functional and molecular properties according to the target molecule.

Second, in metallurgical engineering, boration is also a wonderful use. Some gold can be recovered from gold-containing stones or liquids containing gold, etc. It can make gold particles original gold particles, so that it precipitates. For example, in a solution containing gold particles, boration can make gold particles obtain original gold powder, so as to improve the purpose of recycling.

Third, in the chemical field, boration can be used as fuel in fuel pools. Boration water can be released and the energy of fuel pools can be recycled. This fuel pool has high energy density, such as aviation, and is expected to be widely used in the relocation of energy sources and transportation, and promote the innovation of energy fields.

What are the physical properties of 1-aminoisoquinoline?

Amino-pentene light has a specific physical property.

Its color is mostly transparent. Under normal conditions, it is a liquid with good fluidity. It is similar to water, but it is not detectable. Its smell and taste can be observed, and it is slightly special fragrance. It is not rich and fragrant, and it is very special. It is impressive.

And the density, the amine-pentene light is slightly different from water. If it is placed in water, it can float on the surface, and the water is clear. Its boiling time is also fixed. Under a specific force environment, it is vaporized at a certain degree of boiling and dissolving. This degree of boiling is one of its important physical properties, and it is essential to operate like lifting and dividing.

Furthermore, the solubility of aminopentene light is also worthy of investigation. In the case of dissolution, such as ethanol and ether, it is easy to dissolve, and the two can be fused to form a homogeneous phase. However, in water, its solubility is limited, and it can be partially dissolved in water. This property also affects its existence in different environments.

Its solubility cannot be ignored. Under normal conditions, aminopentene light has a certain direction, and its molecules are easy to escape from the surface of the liquid and disperse in the air. This property is not only affected by the temperature and temperature of the environment, but also by the force of its own molecules.

The physical properties of amines and pentenes, such as color, taste, density, boiling, solubility, and solubility, interact with each other, and together form their own physical properties, laying the foundation for their use in multiple fields.

Is 1-Aminoisoquinoline Chemically Stable?

Hydroxynitrous acid is a very unstable chemical substance. Its molecular structure is unique, containing hydroxyl groups and nitroso groups, and this special structure makes its chemical properties abnormally active.

Under normal conditions, hydroxynitrous acid is easy to decompose on its own. The decomposition process is quite complicated, and it often decomposes to produce products such as nitric oxide, nitrogen dioxide and water. This decomposition reaction is easily affected by many factors, such as temperature, light, pH, etc.

When the temperature increases, the molecular thermal motion intensifies, and the chemical bonds in the hydroxynitrous acid molecule are more likely to break, and the decomposition rate accelerates. Light can also provide energy for it, causing chemical bond breakage and accelerating decomposition. Changes in pH will affect the existence and stability of hydroxynitrous acid. In an acidic environment, its decomposition rate may be different from that in an alkaline environment.

Due to its extreme instability, it is difficult to store and prepare in the laboratory for a long time. Even if it is carefully prepared, it needs to be stored under extremely harsh conditions, such as low temperature, protection from light, and isolation of some substances that may initiate reactions. Even so, it can only be retained for a short time.

In summary, the chemical properties of hydroxynitrous acid are extremely unstable. Under natural and general experimental conditions, it is very prone to decomposition and other changes, and it is difficult to exist stably.

What are the synthesis methods of 1-aminoisoquinoline?

To make 1-hydroxyisobutyric acid, there are three methods.

First, isobutyraldehyde is used as the beginning, and the double bond and aldehyde are condensed to obtain 4-hydroxy-2-methyl-2-butylenaldehyde, followed by catalytic hydrogenation to obtain 1-hydroxy isobutyric acid. In this way, the condensation step, the aldehyde group and formaldehyde are condensed under alkali catalysis, and the hydroxy aldehyde is condensed to obtain the product of alkenaldehyde. During the hydrogenation process, the alkenaldehyde is absorbed by a suitable catalyst, such as palladium carbon, and the double bond and the aldehyde group are reduced to obtain 1-hydroxy isobutyric acid.

Second, methyl methacrylate is used as the starting point, and methacrylic acid is first hydrolyzed to methacrylic acid, and then borohydrogenated-oxidized to obtain 1-hydroxy isobutyric acid. During hydrolysis, ester bonds are broken under the catalysis of acids or bases to obtain the corresponding acid. In the step of borohydrogenation-oxidation, olefins encounter borane, and the boron group is added to the small resistance, and then oxidized by hydrogen peroxide, and the boron group is transposed to a hydroxyl group to obtain the target product.

Third, with 2-methyl-2-propanol as the starting point, the first oxidation is acetone, and the acetone and formaldehyde are condensed with hydroxyaldehyde, and then the obtained product is reduced to obtain 1-hydroxy isobutyric acid. The step of oxidation is to add alcohol to a suitable oxidant, such as potassium dichromate, to dehydrogenate into ketones. Hydroxyaldehyde is condensed with the same front to obtain an aldehyde containing double bonds, and then reduced to obtain 1-hydroxy isobutyric acid.

Each way has its advantages and disadvantages. The first raw material isobutyraldehyde is easy to obtain, and the reaction steps are relatively simple. However, specific catalysts and conditions are required for hydrogenation; the secondary raw materials are common, and the borohydrogenation-oxidation selectivity is good. Only the hydrolysis and subsequent reaction conditions need to be carefully controlled; the three raw materials are easy to obtain, but the multi-step reaction results in a longer process, and the yield of each step affects the overall benefit. When choosing the method, it depends on the availability of raw materials, the level of cost, and the difficulty of the process.

What are the precautions for 1-aminoisoquinoline in storage and transportation?

In the process of light storage, all kinds of things need to be done with care.

The quality of its existence depends on the quality of the first environment. It is appropriate to use it in a cool and transparent place, and it must not be used in a high environment. Because of high temperature, it is easy to change the quality of light objects, or make the quality of light weak, or even lose its inherent characteristics. For example, in summer heat, if it is placed in a place where light is exposed, it must be damaged.

Furthermore, the quality should not be ignored. In the tidal environment, it is easy to make the material be invaded by water vapor. The light exposure of butyric acid to water, or biochemical reaction, causes it to be damaged, affecting its effect in the process and use. Therefore, it is necessary to use the method of dryness, and the phase of the surrounding environment should be controlled to a certain extent.

Until it is too late, the package must be damaged. The container needs to be used, which can be shockproof and anti-collision, and avoid damage to the object due to bumps and collisions on the way. The packaging material used should also not be light-activated and reversed by butyric acid, so as to avoid staining.

The packaging material on the way also needs to be appropriate. The degree of resistance and the degree of resistance should be similar, and it is necessary to avoid light exposure. Light may also cause the transformation of the object to be reversed, resulting in the change of light performance.

Therefore, in the storage of ethyl butyric acid, many factors such as temperature, temperature, packaging temperature, and light are all very important. If there is a slight difference, its characteristics may be affected. Therefore, it must be treated with temperature to ensure its quality.