What is the chemical structure of Capso 3- (Cyclohexylamino) -2-Hydroxy-1-Propanesulfonic Acid?
Capso is 3- (cyclohexylamino) -2 -hydroxy-1 -propanesulfonic acid. The chemical structure of this substance is as follows.
Looking at its name, it can be seen that its structure contains sulfonic acid groups, hydroxyl groups and amino-related parts. In terms of molecular composition, 3- (cyclohexylamino) -2 -hydroxy-1 -propanesulfonic acid uses propane as the carbon chain skeleton. The 1-carbon of propane is connected to the sulfonic acid group (-SO 🥰 H), which gives the compound a certain acidity and water solubility. The 2-carbon is connected to a hydroxyl group (-OH), which is polar and can participate in the formation of hydrogen bonds, which affects the physical and chemical properties of molecules, such as solubility and boiling point. The 3-position carbon is connected to the cyclohexyl amino group. The cyclohexyl group is a cyclic structure, which makes the molecule have certain rigidity and steric resistance. The amino group (-NH) is connected to the cyclohexyl group, which further changes the electron cloud distribution and chemical activity of the molecule. Overall, the interaction of each group in this structure determines the chemical and physical properties of 3- (cyclohexylamino) -2-hydroxy-1-propanesulfonic acid, such as the acid-base balance in solution and the interaction with other molecules. Its unique structure also makes it have specific uses in biochemical, chemical and other fields, such as as as a buffer, using its acid-base properties to maintain the pH stability of the system.
What are the main uses of Capso 3- (Cyclohexylamino) -2-Hydroxy-1-Propanesulfonic Acid?
3- (cyclohexylamino) -2-hydroxy-1-propanesulfonic acid (Capso) has a wide range of uses and is an important substance in the field of biochemical research.
First, it is very useful in the construction of biological buffer systems. Because of its suitable pH buffer range, it can make the pH of the biochemical reaction system as stable as a rock, creating a suitable environment for many pH-sensitive biochemical reactions and enzymatic reactions. Many enzymes are best active at specific pH values, and Capso can precisely regulate and maintain this pH condition, making the enzymatic reaction smooth, just like paving the way for the efficient operation of enzymes.
Second, it is also indispensable for protein and nucleic acid research. In the experimental process of protein crystallization, separation and nucleic acid electrophoresis, Capso can effectively maintain the pH stability of the system, and maintain the integrity of the structure and function of protein and nucleic acid. Protein crystallization requires strict control of conditions. The stable acid-base environment created by Capso seems to provide a reliable guarantee for the delicate "lattice" of proteins; during nucleic acid electrophoresis, the stable pH environment ensures the accurate migration rate of nucleic acids, laying the foundation for the accurate analysis of nucleic acid fragments.
Third, it also plays a key role in the field of cell culture. Cell growth is demanding on the environment. Capso can regulate the pH value of cell culture medium to meet the needs of cell growth. It is like building a comfortable "home" for cells, helping cells grow and proliferate normally, and preventing cell physiological dysfunction due to pH fluctuations. Fourth, Capso also makes important contributions in the process of drug development and analysis. In the study of drug synthesis reactions and drug stability, by virtue of its ability to maintain the pH stability of reaction systems or drug preparations, it helps researchers to deeply explore the properties and mechanisms of action of drugs, and contributes to the creation and quality improvement of new drugs.
Capso 3- (Cyclohexylamino) -2-Hydroxy-1-Propanesulfonic Acid What are the precautions when storing
Capso is 3- (cyclohexylamino) -2 -hydroxy-1 -propanesulfonic acid. When storing, there are many precautions to be made clear.
First, pay attention to the storage temperature. This substance should be stored in a cool place. If the temperature is too high, it may cause a chemical reaction, causing its chemical structure to be damaged, thus losing its original characteristics and efficacy. Generally speaking, it is recommended to store at a temperature of 2-8 ° C, so that the environment can maintain its chemical stability.
Second, humidity control is also crucial. Capso should be stored in a dry place, away from humid environments. Due to high humidity, Capso may absorb moisture, which in turn affects its purity and quality. After moisture absorption, or agglomeration occurs, it is difficult to disperse evenly during subsequent use, affecting the effect of experiment or production.
Third, avoid contact with oxidants and other substances. Capso is relatively active chemically. If it coexists with oxidants, it is easy to trigger oxidation reactions and cause it to deteriorate. Therefore, when storing, it needs to be separated from dangerous chemicals such as oxidants to prevent interaction.
Fourth, the choice of storage containers should also be careful. It is advisable to use chemically stable containers, such as glass or specific plastic containers. Such containers will not chemically react with Capso, which can ensure its stability during storage. And the container must be well sealed to prevent the intrusion of impurities such as air and moisture.
What is the common purity of Capso 3- (Cyclohexylamino) -2-Hydroxy-1-Propanesulfonic Acid?
Capso, which is 3- (cyclohexylamino) -2-hydroxy-1-propanesulfonic acid, has a common purity of about 99%. This purity is quite common in experimental applications such as biochemistry and molecular biology. Because biochemical experiments require strict purity of reagents, high-purity Capso can reduce impurity interference and ensure accurate and reliable experimental results. For example, in some specific protein research experiments, impurities can affect protein activity and stability. Capso with a purity of about 99% can avoid such problems and ensure accurate experimental data. In addition, in the field of pharmaceutical research and development, in order to ensure the quality and safety of drugs, high-purity Capso is also required as a raw material or reagent. Capso of this purity is prepared and purified by multiple fine processes, such as high-performance liquid chromatography purification, to remove various impurities and meet experimental and production standards.
How soluble is Capso 3- (Cyclohexylamino) -2-Hydroxy-1-Propanesulfonic Acid?
Capso is 3- (cyclohexylamino) -2 -hydroxy-1 -propanesulfonic acid, and its solubility is quite characteristic. It dissolves well in water, and there are sulfonic acid groups (-SO-H) and hydroxyl groups (-OH) in the Gain molecule, both of which are hydrophilic groups. By forming hydrogen bonds with water molecules, it can greatly increase its solubility in water.
In terms of organic solvents, Capso's solubility is relatively limited. Most organic solvents have weak polarities, making it difficult to form strong interactions with Capso molecules, and cannot effectively overcome the intermolecular forces of Capso molecules, making it difficult to dissolve in such solvents. However, in some polar organic solvents, such as dimethyl sulfoxide (DMSO), Capso may have a certain solubility. Due to the strong polarity of DMSO, it can form a specific interaction with Capso molecules to promote its dissolution.
In addition, temperature also affects the solubility of Capso. Generally speaking, when the temperature increases, Capso's solubility in water increases. When the temperature increases, the thermal motion of the molecule intensifies, and the collision frequency between Capso molecules and water molecules increases and the intensity increases. It is easier to destroy the intermolecular force of Capso, making it easier to disperse in water, thereby increasing the solubility.
In short, Capso has good solubility in water due to its own structural characteristics, but poor solubility in most organic solvents, and the increase in temperature is conducive to its dissolution in water.