What is the chemical structure of N, N '-tetramethylguanidine?
The chemical structure of N, N '-tetramethylguanidine is as follows. This is an organic base compound with unique structural characteristics.
Its core structure is guanidine, and guanidine is a group formed by connecting a central carbon atom with three amino groups. The chemical expression is\ (C (NH_2) _3 ^ +\). In N, N' -tetramethylguanidine, the four amino hydrogen atoms of guanidine are replaced by four methyl groups.
In the chemical abbreviation, it is\ (C [ (N (CH_3) _2] _3\). In its spatial structure, the central carbon atom takes the form of\ (sp ^ 2\) hybridization, coexisting with the three connected nitrogen atoms in the same plane, showing a planar triangle configuration. The bond formed by the nitrogen atom and the methyl group extends beyond the plane. The introduction of
methyl groups has an impact on both its electronic and spatial effects. From the perspective of electronic effects, methyl groups are electron-supplying groups, which can increase the electron cloud density of guanidine groups and enhance their alkalinity; from the perspective of spatial effects, methyl groups increase the steric resistance of molecules, which also affects their reactivity and physical properties.
This structural feature endows N, N '-tetramethylguanidine with many special properties, and has important applications in organic synthesis, catalysis and other fields. Because of its strong alkalinity, it can be used as a base catalyst for organic reactions; and its solubility and stability are also related to its unique chemical structure.
What are the main uses of N, N '-tetramethylguanidine?
N, N '-tetramethylpiperazine is an organic compound with a wide range of uses and key functions in many fields.
First, in the field of pharmaceutical synthesis, N, N' -tetramethylpiperazine is often used as a key intermediate. Due to its unique chemical structure, it can participate in the construction of a variety of drug molecules. For example, in the synthesis of some antihistamines, N, N '-tetramethylpiperazine can react with specific reagents to form structural units with specific pharmacological activities, which can help develop new anti-allergic drugs to relieve allergic symptoms.
Second, in the field of materials science, it also has applications. In the preparation of some functional polymer materials, N, N '-tetramethylpiperazine can be used as a comonomer to participate in the polymerization reaction. By adjusting its dosage and reaction conditions, the properties of polymer materials can be improved, such as improving the solubility and thermal stability of materials, etc., and then expand the application range of materials, and play a role in electronics, packaging and other industries.
Third, in the field of organic synthesis catalysts, N, N' -tetramethylpiperazine often exhibits catalytic activity. In some organic reactions, such as esterification reactions, condensation reactions, etc., it can accelerate the reaction process and improve the reaction yield. This is because it can interact with the reactant molecules, change the reaction path, reduce the reaction activation energy, and make the reaction easier to proceed.
Fourth, in the dye industry, N, N '-tetramethylpiperazine can be used as a raw material for synthetic dyes. Through a series of chemical reactions, it is converted into dye molecules with specific colors and properties. These dyes can be used in textile, printing and dyeing industries to give fabrics rich colors and good dyeing fastness.
What are the safety precautions for N, N '-tetramethylguanidine during use?
N, N '-tetramethylpiperazine is an organic compound. When using it, pay attention to various safety matters.
First, this substance has certain toxicity. It can invade the human body through the respiratory tract, skin and digestive tract. Therefore, when using, use appropriate protective equipment, such as gas masks, protective gloves and protective clothing, to avoid contact with the skin, eyes and respiratory tract. If accidentally touched, rinse with plenty of water immediately and seek medical treatment if necessary.
Second, it is flammable. In storage and use places, fireworks should be strictly prohibited, away from fire and heat sources to prevent the risk of fire and explosion. And explosion-proof electrical equipment and ventilation system should be selected to ensure good ventilation in the place and reduce the possibility of combustible gas accumulation.
Third, during the operation, the action should be slow and stable to avoid its leakage. If there is a leakage, irrelevant personnel should be quickly evacuated, the leakage area should be isolated, and access should be strictly restricted. Emergency personnel must wear professional protective equipment and breathing apparatus, and do not let the leakage come into contact with combustible substances. In the case of a small amount of leakage, it can be absorbed by inert materials such as sand and vermiculite; in the case of a large amount of leakage, an embankment should be built or excavated for containment, and the pump should be transferred to a special collector for recycling or transported to a waste treatment site for disposal.
Fourth, storage should also be cautious. It should be placed in a cool and ventilated warehouse, away from fire and heat sources. The storage temperature should not be higher than 30 ° C, and the container should be kept sealed. And it should be stored separately from oxidants, acids, etc., and should not be mixed. The storage area should be equipped with leakage emergency treatment equipment and suitable containment materials.
Fifth, during transportation, relevant regulations should also be followed. Before transportation, it must be reported to the relevant departments for approval. The tank (tank) car used during transportation should have a grounding chain, and holes can be set in the tank to reduce shock and generate static electricity. It is strictly forbidden to mix and transport with oxidants, acids, edible chemicals, etc. During transportation, it should be protected from exposure to the sun, rain, and high temperature. Stay away from fire, heat sources, and high temperature areas during stopovers.
What are the physical properties of N, N '-tetramethylguanidine?
N, N '-tetramethylhydrazine is an organic compound. Its physical properties are quite unique. Under normal temperature and pressure, it is a colorless and transparent liquid, like clear water, with a pure and translucent texture.
Looking at its smell, it has a pungent smell. This smell is sharp and strong, and it is easy to form a strong stimulus to the human olfactory sense.
When it comes to the boiling point, it is between 113 and 114 ° C. At this temperature node, N, N' -tetramethylhydrazine will change from liquid to gaseous, realizing the phase conversion. Its melting point is -55 ° C. When the temperature drops to this point and below, it will solidify and change from a flowing liquid to a solid state.
N, N '-tetramethylhydrazine has a certain solubility and can be miscible with many common organic solvents such as water, alcohol, ether, etc. Just like fish entering water, it can be evenly dispersed in these solvents to form a uniform and stable system. This property makes it widely used in many fields of chemical production and scientific research, such as as participating in chemical reactions as a solvent, or as a medium for separation and purification of substances.
What are the preparation methods of N, N '-tetramethylguanidine?
There are several methods for preparing N, N '-tetramethylpiperazine:
First, piperazine is used as the initial raw material to react with methylation reagents. Common methylation reagents, such as iodomethane, dimethyl sulfate, etc. Under suitable reaction conditions, the nitrogen atom of piperazine will be gradually replaced by methyl to generate N, N' -tetramethylpiperazine. This reaction usually needs to be carried out in an alkaline environment. The base can be selected from potassium carbonate, sodium hydroxide, etc. Its function is to neutralize the acid generated by the reaction and promote the reaction to the direction of product formation. For example, piperazine is dissolved in a suitable organic solvent, such as acetonitrile and acetone, potassium carbonate is added, and then iodomethane is slowly added dropwise. The reaction is stirred at a certain temperature for several times, and the target product can be obtained through subsequent separation and purification steps.
Second, the method of catalytic hydromethylation is used. Nitrogen-containing heterocyclic compounds are used as starting materials and react with hydrogen and methylation reagents in the presence of catalysts. Commonly used catalysts include supported metal catalysts, such as palladium-carbon, platinum-carbon, etc. This method has relatively mild conditions and high selectivity. For example, a specific nitrogen-containing heterocyclic precursor is reacted with methanol as a methylation reagent in a hydrogen atmosphere under the action of a palladium-carbon catalyst. Methanol not only acts as a methyl donor, but also acts as a solvent. The reaction is carried out at a certain pressure and temperature. With the help of the activity check point of the catalyst, the methylation of nitrogen atoms is realized, and finally N, N '-tetramethylpiperazine is generated. After the reaction, the catalyst is removed by filtration, and then the product is purified by distillation, extraction and other means.
Third, the piperazine ring is constructed through the organic synthesis route and methyl is introduced at the same time. A suitable bifunctional compound can be used to construct the piperazine ring structure after a multi-step reaction. During or after the reaction, the methyl group is introduced by an appropriate methylation method. For example, using dihalogenated alkanes and diamines as raw materials, the condensation reaction is first carried out to generate a piperazine ring skeleton, and then the methylation reaction is carried out with the above-mentioned methylation reagents. After multi-step reaction and meticulous separation and purification, N, N '-tetramethylpiperazine can also be obtained. Although this method is a little complicated, it is an effective way for specific needs and raw materials.