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N-Methylpiperazine

Product Description

N-Methylpiperazine, CAS 109-01-3, is a heterocyclic amine belonging to the piperazine class of compounds. This colorless to light yellow liquid is an important organic building block and chemical intermediate in various industrial and laboratory applications.


Description of N-Methylpiperazine CAS 109-01-3:

N-Methylpiperazine features a piperazine ring structure, which is a six-membered heterocyclic ring with two nitrogen atoms located in adjacent positions. One of these nitrogen atoms is substituted with a methyl (-CH3) group, distinguishing it from other piperazine derivatives. Its structural formula can be represented as C5H12N2, and its systematic name is 1-methylpiperazine.


Properties of N-Methylpiperazine CAS 109-01-3:

  • Physical State: N-Methylpiperazine is typically a colorless to light yellow liquid at room temperature, with a distinctive amine odor.

  • Solubility: It is soluble in water as well as common organic solvents such as ethanol, ether, and benzene.

  • Boiling Point: Its boiling point varies slightly depending on purity and pressure conditions but generally lies around 108-110°C.

  • Melting Point: Below room temperature, it is a liquid, hence does not have a distinct melting point.


Applications of N-Methylpiperazine CAS 109-01-3:

  1. Pharmaceutical Industry: N-Methylpiperazine is used as a starting material or intermediate in the synthesis of various medicinally active compounds, including antipsychotics, antidepressants, and central nervous system (CNS) agents.

  2. Agriculture: Certain derivatives of N-Methylpiperazine find applications in the development of agrochemicals, including pesticides and plant growth regulators.

  3. Chemical Industry: As a versatile amine, it participates in a wide range of organic reactions, including condensation, substitution, and Michael additions, making it valuable in the synthesis of polymers, dyes, and surfactants.

  4. Research: In laboratories, N-Methylpiperazine serves as a model compound for studying the behavior and reactivity of piperazine-based molecules, which are often encountered in natural products and pharmaceuticals.

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