6 Chloro 3 Trifluoromethyl Pyridine 2 Carboxlic Acid
pyridine pyrrole pyrazine piperidine piperazine

6-CHLORO-3(TRIFLUOROMETHYL)PYRIDINE-2-CARBOXLIC ACID

    Specifications

    HS Code

    393193

    Chemical Formula C7H3ClF3NO2
    Molar Mass 225.55 g/mol
    Physical State At Room Temp Solid (assumed)

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    General Information
    Where to Buy 6-CHLORO-3(TRIFLUOROMETHYL)PYRIDINE-2-CARBOXLIC ACID in China?
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    Frequently Asked Questions

    As a leading 6-CHLORO-3(TRIFLUOROMETHYL)PYRIDINE-2-CARBOXLIC 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 is the main use of 6-CHLORO-3 (TRIFLUOROMETHYL) PYRIDINE-2-CARBOXLIC ACID?
    6-Chloro-3 (trifluoromethyl) pyridine-2-carboxylic acid, which has a wide range of uses. In the field of medicine, it is a key intermediate for the synthesis of many specific drugs. For example, when developing targeted drugs for specific diseases, its structural characteristics can enable the drug to accurately act on diseased cells, greatly improving the therapeutic effect, while reducing the damage to normal cells, bringing good news to patients.
    In the field of pesticides, it is also an important raw material for the preparation of high-efficiency pesticides. The pesticides made on the basis of it have high selectivity and strong lethality to pests, which can not only effectively prevent and control crop diseases and pests, ensure crop yield and quality, but also reduce environmental pollution and impact on non-target organisms, which is in line with the current needs of green agriculture development.
    In the field of materials science, its unique chemical structure endows materials with novel properties. For example, it can be used to prepare functional materials with special optical and electrical properties, which can be used in electronic devices, optical instruments and other fields to promote the innovation and development of related industrial technologies.
    Furthermore, in organic synthetic chemistry, it serves as an important building block for the construction of complex organic molecular structures, helping scientists explore more novel organic compounds, expanding the research boundaries of organic chemistry, and laying the foundation for the development of new materials and new drugs in various fields. In short, 6-chloro-3 (trifluoromethyl) pyridine-2-carboxylic acids play an indispensable role in many fields and are of great significance to scientific and technological progress and industrial development.
    What are the synthesis methods of 6-CHLORO-3 (TRIFLUOROMETHYL) PYRIDINE-2-CARBOXLIC ACID
    The synthesis of 6-chloro-3 (trifluoromethyl) pyridine-2-carboxylic acids has been around for a long time, and it has been evolving over time. The details are described below, which will help.
    First, a compound containing a pyridine structure is used as the starting material. Find a suitable pyridine derivative with a substituent that can be converted into a target functional group. For example, select a pyridine with a suitable halogen, alkyl and other substituents, and introduce a chlorine atom into the 6-position of the pyridine ring through a halogenation reaction. The halogenation method is often carried out under specific reaction conditions with a suitable halogenating agent. Such as chlorine gas, thionyl chloride and other reagents, in an organic solvent, the temperature and reaction time can be controlled to precisely replace the chlorine atom.
    Then, for the 3-position of the pyridine ring, trifluoromethyl is to be introduced. This step can be done with the help of trifluoromethylation reagents, common ones are trifluoromethyl halide zinc, trifluoromethyl copper, etc. In the presence of a catalyst, it is reacted with pyridine derivatives in a suitable reaction system to achieve the introduction of trifluoromethyl. In this process, factors such as the choice of catalyst, the nature of the reaction solvent, and the reaction temperature and pressure all have a significant impact on the efficiency and selectivity of the reaction.
    Second, when the structure of 6-chloro-3 (trifluoromethyl) pyridine is completed, the carboxyl group is to be constructed at the 2-position. The commonly used method is to react with the corresponding pyridine derivatives with metal-organic reagents, such as Grignard reagent or lithium reagent, to form a metallized intermediate. Then the intermediate is reacted with carbon dioxide and subsequently acidified to obtain 6-chloro-3 (trifluoromethyl) pyridine-2-carboxylic acid. In this process, the preparation of metal-organic reagents needs to be carefully handled, the mode and amount of carbon dioxide needs to be precisely controlled, and the conditions of the acidification step also depend on the purity and yield of the product.
    Third, another method is to gradually construct the target molecule through a multi-step reaction. First, a simple compound containing a pyridine skeleton is converted into a multi-step functional group, and chlorine atoms, trifluoromethyl groups and carboxyl groups are introduced in sequence. This strategy requires careful planning of the order and conditions of each step of the reaction to ensure the smooth progress of each step of the reaction and minimize the occurrence of side reactions. For example, the pyridine ring can be properly protected first, and after the introduction of the functional group at a specific position, the protective group can be removed and the next reaction can be carried out. In this way, after many setbacks, 6-chloro-3 (trifluoromethyl) pyridine-2-carboxylic acid is finally obtained.
    The above synthesis methods have their own advantages and disadvantages. In practical application, the appropriate method should be weighed and selected according to many factors such as the availability of raw materials, the difficulty of reaction, cost considerations, and product purity requirements.
    What is the market price of 6-CHLORO-3 (TRIFLUOROMETHYL) PYRIDINE-2-CARBOXLIC ACID
    6-Chloro-3 (trifluoromethyl) pyridine-2-carboxylic acid, the price of this product in the market is difficult to determine. The price of the cover often changes for various reasons.
    First, the situation of supply and demand determines its price. If there are many people in the market who need it, but the amount of production is small, the price will increase; conversely, if the supply exceeds demand, the price will drop.
    Second, the cost of production is also related to its price. The preparation of the technology may require all kinds of materials. If the material is expensive, and the process is difficult, labor-intensive, and requires a lot of manpower, material resources, and financial resources, the cost of its production will be high, and the price will rise accordingly.
    Third, changes in the current situation also have an impact. If there is a blockage in business, inconvenient transportation, or a natural or man-made disaster, causing damage to the production area and obstruction of the production system, the price will also fluctuate.
    Furthermore, the quality is different, and the price is also different. Those with high quality will naturally have a high price; those with lower quality will have a slightly lower price.
    Looking at the market sentiment in the past, the price will fluctuate. However, if you want to know the exact price at the moment, you need to consult various suppliers, or observe the latest market conditions. For chemical products, their prices often change with the market, and they cannot be held together.
    What are the physical and chemical properties of 6-CHLORO-3 (TRIFLUOROMETHYL) PYRIDINE-2-CARBOXLIC ACID
    6-Chloro-3 (trifluoromethyl) pyridine-2-carboxylic acid, this physical property is related to all ends of chemistry and is quite important.
    Its shape, under normal conditions, or in a crystalline state, is as white as snow, pure in quality and regular in crystal shape, with a sense of transparency. Looking at it, it can be seen that its fine crystals are arranged in an orderly manner, showing a unique structure.
    It is related to the melting point, which is about a certain range of values. This is the critical temperature of the solidified conversion liquid when heated, which is of great significance for its purification and identification. After precise experimental determination, its melting point is [X] ° C. This characteristic can help to distinguish between authenticity and purity. The boiling point of
    also has a key property. Under a specific pressure environment, the temperature at which a liquid turns into a gas. The boiling point of the substance is about [X] ° C at atmospheric pressure. If the pressure changes, the boiling point will also change. This follows the laws of physical chemistry.
    In terms of solubility, in organic solvents, such as ethanol and ether, the degree of solubility varies. In ethanol, it can be dissolved in an appropriate amount to form a uniform and stable solution, while in water, the solubility is relatively small and only a little can be dissolved. This property is related to the ratio of polar groups and non-polar parts in the molecular structure.
    In terms of chemical activity, it is very active due to the presence of pyridine rings and carboxyl groups, chlorine atoms, and trifluoromethyl groups. The carboxyl group can neutralize with the base, such as meeting with sodium hydroxide, quickly forming a salt, and releasing water molecules at the same time. This reaction is often the way to prepare carboxylic salts in organic synthesis. Chlorine atoms can be replaced by nucleophiles, introducing other groups to expand the function of the molecule. The strong electron absorption of trifluoromethyl groups changes the electron cloud density of the pyridine ring, which affects the check point and activity of the electrophilic substitution reaction, making the reaction easier to occur at a specific location, creating various possibilities for organic synthesis. It has a wide range of uses in pharmaceutical chemistry, material chemistry and other fields.
    6-CHLORO-3 (TRIFLUOROMETHYL) PYRIDINE-2-CARBOXLIC ACID What are the precautions during storage and transportation
    6-Chloro-3 (trifluoromethyl) pyridine-2-carboxylic acid, this is a chemical substance. During storage and transportation, many matters need careful attention.
    First, when storing, be sure to choose a cool, dry and well-ventilated place. This substance is afraid of moisture, and moisture can easily cause it to deteriorate, which in turn affects the quality and characteristics. Therefore, the humidity in the warehouse should be precisely controlled, not too high. It should also be kept away from fires and heat sources. Because the substance is heated or exposed to open flames, it may be dangerous, such as burning or even exploding.
    Second, storage needs to be classified. Do not mix with oxidants, alkalis, etc. This is because the chemical properties of 6-chloro-3 (trifluoromethyl) pyridine-2-carboxylic acids are active, and contact with these substances may cause violent chemical reactions, endangering safety.
    Third, during transportation, the packaging must be stable. The packaging material must be able to withstand a certain external impact to prevent the package from being damaged due to bumps and collisions during transportation, resulting in material leakage. The transportation vehicle must also be clean and free of other residues that may react with it.
    Fourth, transportation and storage personnel need to be professionally trained. Familiar with the characteristics of the substance, the hazards and emergency treatment methods. In case of emergencies such as leakage, it can respond quickly and correctly to reduce the harm.
    In conclusion, the storage and transportation of 6-chloro-3 (trifluoromethyl) pyridine-2-carboxylic acids requires all-round consideration and strict operation according to regulations to ensure personnel safety and material quality.