2 Hydroxymethyl 3 Methyl 4 2 2 2 Trifluoroethoxy Pyridine Hcl
pyridine pyrrole pyrazine piperidine piperazine

2-Hydroxymethyl-3-Methyl-4-(2,2,2-Trifluoroethoxy)Pyridine HCL

    Specifications

    HS Code

    342765

    Chemical Name 2-Hydroxymethyl-3-Methyl-4-(2,2,2-Trifluoroethoxy)Pyridine HCL
    Molecular Formula C9H11F3NO2·HCl
    Molecular Weight 257.64 (approx, considering HCl addition)
    Appearance Typically a solid (color may vary based on purity)
    Solubility Solubility characteristics can vary, may have some solubility in polar solvents like water or alcohols
    Purity Can be available in different purity grades, e.g., 95%, 98% etc.
    Melting Point Specific melting point would depend on the purity, but generally in a defined temperature range
    Boiling Point Undergoes decomposition rather than boiling in normal conditions due to HCl presence
    Flash Point Flash point data would be relevant for flammability assessment in certain solvents
    Storage Condition Stored in a cool, dry place, away from moisture and heat

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    General Information
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    Frequently Asked Questions

    As a leading 2-Hydroxymethyl-3-Methyl-4-(2,2,2-Trifluoroethoxy)Pyridine HCL supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    2-Hydroxymethyl-3-Methyl-4- (2,2,2-Trifluoroethoxy) Pyridine HCL
    2-Hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine hydrochloride is an organic compound. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry.
    In the process of research and development of Guanfu Medicine, the construction of many drug molecules requires this as a base. Due to its special structure, it contains groups such as pyridine ring, hydroxymethyl, methyl and trifluoroethoxy, giving it unique chemical properties and reactivity. By means of chemical synthesis, it can undergo various reactions with other compounds, such as nucleophilic substitution, esterification, condensation, etc., and then construct drug molecules with complex structures and specific pharmacological activities.
    In the field of materials science, it also has its uses. Due to the presence of fluorine atoms in its structure, it can change the physical and chemical properties of compounds, such as improving the stability, corrosion resistance and hydrophobicity of materials. This compound can be used as a raw material through specific reactions and processing techniques, and can prepare new materials with excellent properties, which play an important role in the electronics, chemical and other industries.
    Furthermore, in the study of organic synthetic chemistry, as an important synthetic block, it can be used to explore novel synthetic methods and strategies. Chemists have developed more efficient and green synthetic routes through in-depth investigation of their reaction properties, promoting the development of organic synthetic chemistry.
    In summary, 2-hydroxymethyl-3-methyl-4 - (2,2,2-trifluoroethoxy) pyridine hydrochloride has important uses in many fields such as medicine, materials and organic synthesis, providing an indispensable material basis for research and development in related fields.
    2-Hydroxymethyl-3-Methyl-4- (2,2,2-Trifluoroethoxy) Pyridine HCL
    The preparation of 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine hydrochloride is an important matter in organic synthesis. There are several common synthetic routes.
    First, 3-methyl-4-hydroxypyridine can be taken as the starting material. After properly protecting the hydroxyl group, this raw material is combined with 2, 2, 2-trifluoroethyl halide, such as 2, 2, 2-trifluoroethyl bromide, under the catalysis of base, nucleophilic substitution reaction is carried out. The alkali can be selected from potassium carbonate, sodium carbonate, etc., in a suitable solvent, such as N, N-dimethylformamide (DMF), heated and stirred to cause the reaction to occur, thereby introducing 2,2,2-trifluoroethoxy. Subsequently, the hydroxyl protecting group is removed, and then the hydroxymethylation reaction is carried out under suitable conditions through reagents such as formaldehyde, and finally reacts with hydrogen chloride gas or hydrochloric acid solution to form its hydrochloride salt.
    Second, 3-methylpyridine is used as the starting material. First, 3-methylpyridine is halogenated, such as bromination, and a halogen atom is introduced at the 4th position of the pyridine ring. After that, with 2,2,2-trifluoroethanol, in the presence of strong bases such as sodium hydride, nucleophilic substitution occurs, and trifluoroethoxy is introduced. Then, by hydroxymethylation with paraformaldehyde and suitable catalysts such as Lewis acid, and finally with hydrogen chloride, the target product 2-hydroxymethyl-3-methyl-4 - (2,2,2-trifluoroethoxy) pyridine hydrochloride is obtained. During the synthesis of
    , attention should be paid to the precise control of the reaction conditions. Factors such as temperature, reaction time, and reagent dosage all have significant effects on the reaction yield and product purity. After each step of the reaction, it is often necessary to perform separation and purification operations, such as column chromatography, recrystallization, etc., to ensure the purity of the intermediate product and the final product, and then achieve the purpose of efficient and high-purity synthesis of the target product.
    What are the physicochemical properties of 2-Hydroxymethyl-3-Methyl-4- (2,2,2-Trifluoroethoxy) Pyridine HCL?
    2-Hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine hydrochloride, which is an organic compound. Its physical and chemical properties are quite critical and related to many practical applications.
    Looking at its physical properties, under normal circumstances, this compound may be a solid, because many compounds containing pyridine structures and forming salts are mostly solid. In terms of color, it may be white to white-like crystalline powder, which is common in many organic salt compounds. The melting point is of great significance for the identification and purification of this substance. Unfortunately, it is not yet known in detail. However, it can be speculated that due to its molecular structure containing a variety of polar groups and cyclic structures, the intermolecular forces are complex, and the melting point may be relatively high. In terms of solubility, due to hydrochloride salts, there should be a certain solubility in water. Polar organic solvents such as ethanol and methanol may also be soluble, but in non-polar organic solvents such as n-hexane and benzene, the solubility may be very small.
    In terms of chemical properties, the structure of its hydrochloride salt determines that it has a certain acidity, which can neutralize with bases to form corresponding pyridine bases and salts. As the core structure of the compound, the pyridine ring is aromatic and can undergo a variety of electrophilic substitution reactions, such as halogenation, nitration, sulfonation, etc. The reactivity is related to the position of the substituent. The hydroxyl group at 2-hydroxymethyl group has typical properties of alcohols, and can undergo esterification, oxidation and other reactions. For example, it can be oxidized to an ester with a carboxylic acid under acid catalysis, and can be oxidized to an aldehyde group or even a carboxyl group in case of a strong oxidant. 3-methyl group is relatively stable, but it may also react under certain conditions such as strong oxidation or high temperature. 4 - (2,2,2 -trifluoroethoxy) part, the fluorine atom of the trifluoroethyl gene has strong electron-absorbing properties, which decreases the density of the ethoxy electron cloud and affects the distribution of the pyridine ring electron cloud, which in turn affects the reactivity of the whole molecule. This part of the ether bond is relatively stable and is not easy to break under normal conditions, but under severe conditions such as strong acid or high temperature, ether bond cracking reactions may occur.
    What is the market price of 2-Hydroxymethyl-3-Methyl-4- (2,2,2-Trifluoroethoxy) Pyridine HCL
    I am inquiring about the market price of 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine hydrochloride. However, this is not an easy matter, and its price is influenced by many factors.
    The first to bear the brunt is the cost of raw materials. If the price of various raw materials required for the synthesis of this compound, such as 2-hydroxymethyl-3-methylpyridine, 2,2,2-trifluoroethanol, etc., rises, the price of the finished product will also rise. Due to the scarcity of raw materials or changes in the production process of raw materials, the cost will increase, which will be transmitted to the price of the target product.
    Furthermore, the preparation process is simple, which also affects the price. If the process is complex, requires multi-step reaction, harsh reaction conditions, such as high temperature, high pressure, special catalysts, or very high requirements for reaction equipment, the production cost will increase greatly, and the price will not be low.
    The market supply and demand relationship is also the key. If the market demand for this compound is strong, such as in the fields of medicine and pesticide research and development and manufacturing, but the supply is limited, the supply is in short supply, and the price will rise. On the contrary, if the demand is low and the supply is sufficient, the price will decline.
    In addition, the size and region of the manufacturer are also related to the price. Large-scale manufacturers, due to the scale effect, the cost may be reduced, and the price may have an advantage. In different regions, prices vary due to differences in labor costs, transportation costs, and policy environments.
    In summary, due to the many influencing factors and changing at any time, it is difficult to say the exact market price. For details, you can consult relevant chemical product suppliers, traders, or refer to professional chemical market information platforms to obtain more accurate price information.
    2-Hydroxymethyl-3-Methyl-4- (2,2,2-Trifluoroethoxy) Pyridine HCL Quality Standard
    2-Hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine hydrochloride. Quality Standards for this compound are often related to multiple elements.
    When it comes to appearance, it should usually be white to off-white crystalline powder, which is pure in appearance and has no visible impurities, so that it can meet its basic character requirements.
    Content determination is extremely critical. Generally speaking, using high performance liquid chromatography (HPLC) determination, the content should not be less than 98.0%. This value ensures that the main composition of the compound is sufficient to meet the subsequent use efficiency.
    The inspection of related substances should not be underestimated. Through HPLC detection, the single impurity should not exceed 0.5%, and the total impurity should not exceed 2.0%. Strictly control the impurity content, in order to avoid the adverse effects of impurities on the properties and applications of the compound.
    Melting point is also an important indicator. The melting point range of the compound is about 150-155 ° C. The specific melting point range can assist in judging its purity and crystal form.
    Moisture content needs to be determined by Karl-Fischer method, which should be controlled below 0.5%. Excessive moisture may affect the stability and reactivity of the compound.
    Burning residue should generally not exceed 0.1%, reflecting the residual level of inorganic impurities in the compound.
    The above Quality Standards ensure the quality and quality of 2-hydroxymethyl-3-methyl-4- (2,2,2-trifluoroethoxy) pyridine hydrochloride from multiple dimensions, so that it can be used in chemical, pharmaceutical and other fields for compliance and effective application.