5 Methylthiophene 2 Carboxylic Acid
quinoline thiophene imidazole thiazole

5-Methylthiophene-2-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    647261

    Chemical Formula C6H6O2S
    Molar Mass 142.176 g/mol
    Appearance Solid (Typical appearance)
    Melting Point 116 - 120 °C
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Pka Around 3 - 4 (approximate acidic strength indication)
    Density Data may vary, no widely - reported standard value
    Odor May have a characteristic organic odor

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    General Information
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    Frequently Asked Questions

    As a leading 5-Methylthiophene-2-carboxylic acid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of 5-methylthiophene-2-carboxylic acid?
    5-Methylcytosine-2-hydroxy acid has three main uses.
    First, it is related to the expression and regulation of genes. Husband genes are the foundation of biological inheritance, and the regulation of their expression is just like the command of music, which is related to the normal or not of various physiological functions of organisms. 5-Methylcytosine-2-hydroxy acid can attach to specific regions of genes, by changing the structure of chromatin, or affecting the binding of transcription factors and DNA, thereby affecting the transcription process of genes. Or activate or inhibit, so that genes can be expressed in a timely and appropriate manner according to the needs of biological growth, development and coping with the environment to maintain the order of life activities.
    Second, it also plays a key role in cell differentiation and development. During embryonic development, cells need to go through a complex differentiation process to form various tissues and organs. 5-methylcytosine-2-hydroxy acid acts as a navigator, guiding cells to differentiate according to established procedures. In different cell lineages, its content and distribution vary, determining the direction of cell differentiation and helping organisms develop from a single fertilized egg to a complete individual with complex structure and function.
    Third, it is related to the occurrence and development of diseases. When the metabolism or function of this substance is abnormal, it can cause gene expression disorders. In tumor diseases, it is common for its related regulatory mechanisms to be abnormal, or to promote the overexpression of oncogenes, or the inhibition of tumor suppressor gene expression, which in turn promotes the occurrence, development and metastasis of tumors. In addition, neurological diseases may also be related to them, providing new targets and ideas for the diagnosis, treatment and prevention of diseases.
    From this point of view, 5-methylcytosine-2-hydroxy acid plays an important role in many fields such as gene expression, cell development and disease pathology, and is a key object of life science research.
    What are the physical properties of 5-methylthiophene-2-carboxylic acid?
    5-Methylcytosine-2-carboxylic acid is a compound of great significance in the field of biochemistry. Its physical properties are quite unique, and I would like to describe them in detail.
    Looking at its properties, under normal temperature and pressure, 5-methylcytosine-2-carboxylic acid is mostly in the state of white to quasi-white crystalline powder, which makes it easy to handle and weigh in many experimental operations and applications. The melting point of this compound is a specific value, and this physical constant is of great significance for identification and purity detection. By accurately measuring the melting point, the purity of the substance can be determined. If the melting point of the sample is consistent with the theoretical value and the melting range is narrow, it indicates that its purity is very high.
    Solubility is also one of its important physical properties. 5-methylcytosine-2-carboxylic acid has a certain solubility in water, but the solubility is not very high. Moderate heating or adjusting the pH value of the solution can increase its solubility. In organic solvents, its solubility varies depending on the type of solvent. For example, in polar organic solvents such as methanol and ethanol, its solubility is relatively higher than that of non-polar organic solvents such as n-hexane and benzene. This solubility characteristic provides a basis for the selection of solvents in the process of extraction, separation and purification.
    Furthermore, the density of 5-methylcytosine-2-carboxylic acid is also a specific value. Although the density may not be considered as frequently as melting point and solubility in general experimental operations, density data are also indispensable in some aspects involving quantitative analysis of substances and phase equilibrium studies.
    In addition, the stability of this compound to light and heat cannot be ignored. Under light conditions, long-term exposure may cause changes in its structure, which in turn affect its chemical properties and biological activities. When heated, when the temperature rises to a certain extent, decomposition reactions will occur. Therefore, during storage and use, it is necessary to properly control the temperature and light conditions to ensure its quality and stability.
    What are the synthesis methods of 5-methylthiophene-2-carboxylic acid?
    There are several methods for the synthesis of 5-methyluracil-2-carboxylic acid.
    One method can be initiated by uracil. Uracil is chemically modified by introducing a methyl group at position 5 to obtain 5-methyluracil. Subsequently, it is carboxylated. This carboxylation step often requires suitable reagents and reaction conditions. For example, in the presence of a certain type of electrophilic reagent, in the presence of a suitable solvent and catalyst, 5-methyluracil is electrophilically substituted, and a carboxyl group is introduced to obtain 5-methyluracil-2-carboxylic acid.
    The second method can start from a suitable precursor containing methyl and carboxyl groups. After cyclization, the pyrimidine ring structure is constructed to form the target product. This approach requires precise design of the structure of the precursor to ensure that the reaction proceeds in the desired direction. The preparation of precursors is also key, often involving multi-step organic synthesis reactions to achieve the desired structure and purity.
    The third method, or biosynthetic means can be used. Using the catalytic activity of certain microorganisms or enzymes, using specific substrates as raw materials, 5-methyluracil-2-carboxylic acid is synthesized by enzymatic reaction. Biosynthesis has the advantages of green and high efficiency, but it is necessary to have a deep understanding of the biological system and optimize the reaction conditions to improve the yield and selectivity.
    All synthesis methods have their own advantages and disadvantages. The conditions of chemical synthesis are relatively easy to control, but the steps may be cumbersome, and toxic and harmful reagents are often involved. Biosynthesis is green and environmentally friendly, but the biological system is complex, and industrial application may need to overcome many problems. Choosing a suitable synthesis method depends on specific needs, cost considerations, and available resources.
    What is the price of 5-methylthiophene-2-carboxylic acid in the market?
    Since modern times, what is the price of pentamethylfuranaldehyde-2-carboxylic acid among the market? This is a matter of business.
    Those who cover pentamethylfuranaldehyde-2-carboxylic acid have their uses in various industries. Or used in the production of wonderful medicines, or used in the tune of Kit Kat fragrances, and have a wide range of uses, so there are many buyers in the market.
    However, its price is not constant, but it varies from time to time and changes with the situation. If the time is smooth, all kinds of materials are easy to make, the craftsmanship is also familiar, and the supply in the market is abundant, its price may tend to be flat, stable and not impatient. Merchants are all at the price of common sense, exchanging what is available to each other, and each gains its own benefits.
    If the weather is bad, the production of raw materials decreases sharply, or the method of manufacturing encounters obstacles, resulting in little output; while the demand in the market has not decreased slightly, or instead increases due to the situation, at this time the price will rise. In case of various changes that cause the supply to be poor, the price may be so high that it is staggering. Although merchants want it, they also need to weigh their financial resources and gains and losses.
    There are other reasons, such as changes in government orders and the feelings of neighboring trade, which can disturb the trend of their prices. In order to know the price of pentamethylfuranal-2-carboxylic acid in the market, it is necessary to widely observe the feelings of the four parties, know the production of raw materials, the situation of Ming industry and manufacturing, and review the changes in the market needs. Only by synthesizing and breaking it can we obtain its outline. It is impossible to be bound by the experience of one place at a time, and make hasty conclusions.
    What are the storage conditions for 5-methylthiophene-2-carboxylic acid?
    5-Methylcytosine-2-deoxynucleotide is a key substance for genetic information transmission and gene expression regulation, and its storage conditions are quite important.
    This substance needs to be stored in a low temperature environment. Generally speaking, it should be stored in a refrigerator at -20 ° C or lower. Low temperature can effectively reduce molecular activity and slow down the rate of chemical reactions, thereby preventing the degradation or deterioration of the substance. Due to high temperature, it is easy to cause molecular structure damage, so that 5-methylcytosine-2-deoxynucleotide loses its biological activity and cannot normally participate in the transmission of genetic information and gene expression regulation.
    At the same time, in order to avoid moisture affecting the stability, it should be stored in a dry place. Water may cause reactions such as hydrolysis, destroying the structure of 5-methylcytosine-2-deoxynucleotide. It can be placed in a sealed container and then placed in the refrigerator to isolate external water vapor.
    In addition, it should also minimize its exposure to light. Light or photons containing high energy, or photochemical reactions with 5-methylcytosine-2-deoxynucleotide, changing its chemical structure and properties. Therefore, when storing, choose a container protected from light, or store in a dark environment. In conclusion, 5-methylcytosine-2-deoxynucleotide needs to be stored at low temperature, dry, and protected from light to ensure its structural integrity and biological activity, providing a reliable material basis for related biological research and applications.