1,10-Anthraquinone dioxide is an organic compound. Its main uses are as follows:
First, it is a key raw material for dye synthesis. In the preparation of many anthraquinone dyes, 1,10-anthraquinone dioxide is an indispensable starting material. Because the structure of anthraquinone gives the dyes excellent light resistance and washable properties, by modifying the structure of 1,10-anthraquinone dioxide, dyes with rich color and excellent performance can be synthesized. It is widely used in the textile printing and dyeing industry to give fabrics a lasting bright color.
is an important intermediate in the field of organic synthesis. Chemists can use 1,10-anthraquinone dioxide as a basis to introduce different functional groups through various chemical reactions to synthesize organic compounds with complex structures. Such compounds may have special physiological activities and can be used in drug research and development; or have unique optoelectronic properties in the field of materials science, providing the possibility for the creation of new materials.
Furthermore, it has applications in the electronics industry. Some materials containing the structure of 1,10-anthraquinone dioxide exhibit certain electrical properties due to their own electronic structure characteristics, or can be used to manufacture organic semiconductor devices, optoelectronic devices, etc., which have potential application value in the process of miniaturization and high performance of electronic components.
In addition, in some functional materials research, 1,10-anthraquinone dioxide can be introduced into polymers or composites as structural units to endow materials with special physical and chemical properties, such as improving material thermal stability, mechanical properties, etc., to broaden the application range of materials.

1% 2C10-dioxy [4.5] decane is also an organic compound. Its physical properties are quite specific, let me talk about them one by one.
First of all, its phase and appearance, under room temperature and pressure, 1% 2C10-dioxy [4.5] decane is usually colorless and transparent liquid, just like clear water, but its properties are very different from water. Looking at it, its texture is uniform, and there are no visible impurities. Under the light, it shines shimmeringly, like a treasure hidden in the world.
When it comes to the boiling point, the boiling point of this compound is quite high, about 212-214 ° C. The high boiling point indicates that it needs to supply a large amount of heat to convert it from liquid to gaseous state. This property allows it to maintain a liquid state in high temperature environments, providing a stable liquid phase environment for many chemical reactions.
Furthermore, the melting point is -10 ° C. The lower melting point makes it easy to maintain a liquid state near room temperature, unlike many substances, it solidifies into a solid state at lower temperatures, making it difficult to move.
Its density is about 1.029 g/mL, which is slightly heavier than water. If it is placed in the same container as water, it will sink underwater, and the two are distinct.
Solubility is also an important physical property. 1% 2C10-dioxy [4.5] decane is soluble in common organic solvents, such as ethanol, ether, etc. It is like a wanderer integrating into the same group and getting along well. However, its solubility in water is not good, and when it encounters water, it is difficult to blend.
In addition, 1% 2C10-dioxy [4.5] decane also has a certain degree of volatility. In the air, it will slowly evaporate. Although it does not disappear in an instant like some highly volatile substances, it will gradually decrease over time. And its smell is unique. Although it is not pungent, it is also different from common odorless liquids. When you smell it carefully, you can feel a unique smell, adding a touch of mystery to it.

1% 2C10-dioxyanthraquinone, that is, 1,10-dihydroxyanthraquinone, is chemically stable.
1,10-dihydroxyanthraquinone contains two phenolic hydroxyl groups, which are acidic to a certain extent. Under conventional conditions, the anthraquinone parent nucleus in its structure is relatively stable, and the aromatic system gives it a certain conjugate stability, which makes it difficult for general chemical reactions to break the ring.
In an oxidizing environment, its phenolic hydroxyl group can be moderately oxidized. However, this oxidation requires specific strong oxidation conditions and suitable oxidants. For example, under specific catalysts and high temperature conditions, the phenolic hydroxyl group may be further oxidized into a quinone structure. However, this situation is relatively harsh and does not occur easily in common environments.
In a reducing environment, the structure of anthraquinone may be reduced, but it also requires specific reducing agents and conditions, and it is difficult to be easily reduced in ordinary environments.
In an acid-base environment, its phenolic hydroxyl groups can react with bases to form salts under alkaline conditions, increasing solubility. However, this reaction is reversible, and the original structure can be restored in case of acid. Therefore, the overall structure remains relatively stable in a common acid-base environment.
1,10-dihydroxyanthraquinone is chemically stable under general storage and use conditions, but under the influence of specific harsh chemical conditions, corresponding chemical changes may occur.

The preparation of 1% 2C10-dioxaspiro [4.5] decane is the key to chemical technology. Although this substance is not detailed in "Tiangong Kaiji", the chemical method is also similar in ancient and modern times.
To prepare 1,10-dioxahexane, the common method begins with the selection and preparation of related raw materials. Most of the organic compounds with specific structures are used as starting materials, such as some alcohols and ether compounds containing suitable functional groups.
One method can be achieved through condensation reaction. Compounds containing hydroxyl groups and compounds containing aldehyde groups or carbonyl groups are used as raw materials, and under specific conditions, the two condensate. This process requires a suitable catalyst to promote the reaction. The choice of catalyst depends on the reaction rate and yield, such as acidic catalysts or specific metal complex catalysts.
The reaction conditions are also crucial, and the temperature and pressure need to be precisely controlled. Generally speaking, moderate heating can make the reactant molecules have enough energy to overcome the reaction energy barrier and speed up the reaction rate. However, if the temperature is too high, it is easy to cause side reactions to occur and damage the purity of the product. The control of pressure also varies depending on the reaction system, either at normal pressure or under certain pressurization conditions.
After the reaction is completed, the product needs to be separated and purified. The target product 1,10-dioxaheptane can be separated by distillation using the difference in boiling points of each component. Or by extraction, select a suitable extractant to enrich the product in a specific phase, and then after subsequent treatment, obtain pure 1,10-dioxaheptane.
Or some are prepared by cyclization reaction. Select a linear compound with suitable chain length and functional group distribution, and under specific conditions, cyclization occurs in the molecule to construct a cyclic structure of 1,10-dioxaheptane. This process also requires careful selection of reaction conditions and catalysts to ensure the high efficiency and selectivity of cyclization.

When storing and transporting 1% 2C10 - carbon dioxide xenon krypton, pay attention to various things, as follows:
First, it is related to storage. Both are gases and need to be stored in special pressure-resistant containers to prevent leakage. 1% 2C10 - carbon dioxide xenon krypton has special properties, and its storage temperature and pressure must be precisely controlled. If the temperature is too high, the gas expands, and the pressure of the container increases sharply, which is prone to explosion; if the temperature is too low, it may cause the gas to liquefy, which will affect subsequent use. The pressure also needs to meet the regulations. If it is too high or too low, it should be monitored and regulated in real time with precision instruments. And the storage place should be well ventilated, away from fire sources, heat sources and strong oxidants, to prevent accidents.
Second, about transportation. When transporting 1% 2C10-carbon dioxide xenon krypton, the carrier needs to be adapted. Special gas tanker trucks are selected, the tank material must be corrosion-resistant and pressure-resistant, and complete safety facilities, such as safety valves, pressure gauges, etc., should be equipped to ensure safety during transportation. Transportation route planning is also key, and sensitive areas such as water source reserves and densely populated areas should be avoided to reduce the risk of accidents. Transport personnel must be professionally trained, familiar with gas characteristics and emergency response methods, and regularly inspect during transportation to check whether the container is leaking and whether the pressure is normal.
Furthermore, operating norms. Whether storage or transportation, operators should strictly follow the rules. Before operation, it is necessary to fully understand the properties and potential hazards of 1% 2C10-carbon dioxide xenon krypton, wear suitable protective equipment, such as gas masks, protective gloves, etc. During operation, move slowly to avoid violent vibration, collision with the container, and prevent leakage due to external forces. If a leak unfortunately occurs, emergency plans should be initiated quickly, evacuate surrounding personnel, strictly prohibit fireworks, and take appropriate measures to plug and deal with leaks according to gas characteristics.