Perhydropyrrole
pyridine pyrrole pyrazine piperidine piperazine

Perhydropyrrole

    Specifications

    HS Code

    854785

    Name Perhydropyrrole
    Synonyms Hexahydropyrrole
    Molecular Formula C5H11N
    Molar Mass 85.15 g/mol
    Appearance Colorless liquid
    Odor Ammoniacal odor
    Density 0.819 g/cm³
    Boiling Point 106 - 107 °C
    Melting Point -63 °C
    Solubility In Water Miscible
    Flash Point 12 °C
    Pka 11.27

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    General Information
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    Frequently Asked Questions

    As a leading Perhydropyrrole 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 chemical structure of Perhydropyrrole?
    The perhydropyrrole of a chemical compound is also the same. Its chemical properties are specific. This is the first and nitrogen-containing quintiles, composed of five atoms, one of which is nitrogen, and the fourth is carbon.
    The atoms in the

    The atom of perhydropyrrole is divided into carbon and nitrogen atoms, and its location also affects the integrity of the molecule.
    The atom of perhydropyrrole is composed of five elements, nitrogen-carbon atoms and other atoms. This is the basis of its chemical and physical properties, and determines its performance in the reaction and application of multiplication.
    What are the physical properties of Perhydropyrrole?
    The perhydropyrrole, also known as octopyrrole, has a physical properties. Its color liquid has a special smell. The melting temperature is low, and it is at -65 ° C. Because the molecular force is not very high, it is the melting liquid at the low temperature. The boiling temperature is 106-107 ° C, reflecting the attractive force of the molecule. It needs to be energized at this degree to make the molecule overcome the attractive force and vaporize.
    Its density is nearly 0.86 g/cm ³, and the water is low, so if the water is mixed, it can float on the water surface. In terms of solubility, it is soluble in many soluble substances, such as ethanol, ether, etc., and its molecules are soluble and have similar solubility; it also has a certain solubility in water, because the nitrogen atoms in the molecule can form water molecules.
    In addition, its solubility is low, and it is easy to disperse when it is open in the air. This is because the molecular force is not low, and the molecule is easy to obtain sufficient energy and the liquid is on the surface. And its vapor phase density is higher than that in the air. If it leaks in low air, the vapor is easy to polymerize. In addition, the physical properties of perhydropyrrole are close to the molecular force and the molecular force.
    What are the common uses of Perhydropyrrole?
    Perhydropyrrole, also known as azacyclohexane, is a crucial heterocyclic compound in the field of organic synthesis. It has a wide range of common uses and plays a key role in many fields.
    In the field of organic synthesis, perhydropyrrole often acts as a key intermediate. Due to its special structure, there are lone pair electrons on the nitrogen atom, and the ring system has a certain tension, so it is chemically active and can participate in a variety of chemical reactions. For example, nucleophilic substitution reactions, the nitrogen atom of perhydropyrrole can react with electrophilic reagents such as halogenated hydrocarbons as nucleophiles to generate a series of nitrogen-containing derivatives, which is an important step in the construction of more complex organic molecules. For another example, it can participate in the reductive amination reaction, react with aldodes or ketones in the presence of reducing agents to form new carbon-nitrogen bonds, which is of great significance in the preparation of various amine compounds. Many drug molecules and bioactive substances contain such structural fragments.
    In the field of medicinal chemistry, the perhydropyrrole structure is also quite common. Because it has a certain alkalinity, it can interact with specific targets in organisms. After many drug molecules are introduced into the perhydropyrrole structure, they can enhance their affinity with receptors and enhance drug activity. For example, some antidepressants contain a perhydropyrrole unit in their molecular structure, which regulates the transmission of neurotransmitters by binding to neurotransmitter receptors, thus exerting the effect of treating depression symptoms. For example, some antibacterial drugs, the perhydropyrrole structure helps to enhance the drug's ability to penetrate the bacterial cell wall or cell membrane, thereby enhancing antibacterial activity.
    In addition, perhydropyrrole is also used in the field of materials science. It can be used as a monomer to participate in polymerization reactions to prepare polymer materials with special properties. These polymers may have good solubility, film-forming properties, and selective recognition of certain substances, showing potential application value in the preparation of sensors, separation membranes, and other materials.
    To sum up, perhydropyrrole is an extremely important compound in the fields of organic synthesis, medicinal chemistry and materials science due to its unique chemical properties and structural characteristics, and plays an indispensable role.
    What are the preparation methods of Perhydropyrrole?
    The method of preparing perhydropyrrole has various paths in the past. First, it can be started by a suitable nitrogen-containing precursor and transformed through a specific reaction. For example, a nitrogen-containing cyclic compound is hydrogenated one by one by hydrogenating the unsaturated bonds in it, and then perhydropyrrole is formed. This process requires the selection of suitable hydrogenation reagents and reaction conditions. If a metal hydride is used as a hydrogenating agent, under appropriate temperature and pressure, the hydrosaturation of unsaturated bonds can be promoted.
    Furthermore, the ingenious strategy of organic synthesis can be used. Using a compound with a specific functional group as raw material, the structure of perhydropyrrole can be constructed through a multi-step reaction. First, the functional group conversion reaction is used to build the prototype of the pyrrole ring, and then the reduction reaction is carried out to hydrogenate the unsaturated part of the ring. In this process, the sequence of reaction steps and the precise selection of reagents are all crucial. Each step of the reaction requires strict control of conditions, such as reaction temperature, reaction time, and the proportion of reactants, to ensure the purity and yield of the product.
    Or derived from natural products. Some nitrogen-containing natural products in nature may have structures similar to perhydropyrrole. By chemically modifying them to remove unnecessary groups and hydrogenating specific sites, perhydropyrrole can also be obtained. However, this approach often requires cumbersome separation and purification steps to obtain high-purity products. To prepare perhydropyrrole, it is necessary to weigh the advantages and disadvantages of each method according to the actual situation, and choose the most suitable method.
    What are the precautions for using Perhydropyrrole?
    Perhydropyrrole, also known as octahydropyrrole, when using, many things need to be paid attention to.
    First, it is related to safety. This is a chemical substance with certain risks. It is flammable. When operating, be sure to stay away from open flames and hot topics to prevent fire. And if it touches the skin inadvertently or causes irritation, rinse quickly with plenty of water. If it splashes into the eyes, it is even more necessary to rinse immediately and seek medical attention. In addition, inhaling its volatile gas may be harmful to health, so it is appropriate to operate in a well-ventilated place. If necessary, wear appropriate protective equipment, such as gas masks.
    Second, it involves storage. It should be stored in a cool, dry and ventilated place, away from oxidants, acids and other substances, due to contact with them, or severe reactions. Storage containers must be sealed to prevent leakage.
    Third, about the use of specifications. In experiments or production, the established operating procedures must be strictly followed. Read the relevant information carefully before use to be familiar with its properties and reaction characteristics. The amount of usage should also be precisely controlled to avoid waste and ensure the effect of experiments or production.
    Fourth, waste disposal should not be underestimated. Used perhydropyrrole and related waste should not be discarded at will, and should be properly disposed of in accordance with environmental protection requirements to prevent environmental pollution.
    All of these are for those who should pay attention when using perhydropyrrole, and must not be negligent to avoid causing trouble.