Description

1-Methylpiperidin-4-amine dihydrochloride (CAS No. 1193-03-9) is a high-purity organic compound with the molecular formula C₆H₁₆Cl₂N₂. This dihydrochloride salt form of 1-methylpiperidin-4-amine is widely utilized in pharmaceutical research, chemical synthesis, and biochemical applications due to its stability and solubility. It serves as a versatile intermediate in the development of active pharmaceutical ingredients (APIs), ligands, and specialty chemicals. With a well-defined structure and rigorous quality control, this product is ideal for researchers requiring reliable and consistent reagents for their experiments. Available in various quantities to accommodate lab-scale to industrial-scale needs, it is packaged under inert conditions to ensure long-term stability.

Properties

• CAS Number: 1193-03-9
• Complexity: 64.9
• IUPAC Name: 1-methylpiperidin-4-amine;dihydrochloride
• InChI: InChI=1S/C6H14N2.2ClH/c1-8-4-2-6(7)3-5-8;;/h6H,2-5,7H2,1H3;2*1H
• InChI Key: ILOBUZORFXDVEW-UHFFFAOYSA-N
• Exact Mass: 186.0690539
• Molecular Formula: C6H16Cl2N2
• Molecular Weight: 187.11
• SMILES: CN1CCC(CC1)N.Cl.Cl
• Topological: 29.3
• Monoisotopic Mass: 186.0690539
• Synonyms: 1-Methylpiperidin-4-amine dihydrochloride, 1193-03-9, 4-Piperidinamine, 1-methyl-, hydrochloride (1:2), 1-methylpiperidin-4-amine;dihydrochloride, 4-amino-1-methylpiperidine dihydrochloride, SCHEMBL767785, DTXSID70621403, ILOBUZORFXDVEW-UHFFFAOYSA-N, MFCD26743699, AKOS022172545, SB41430, 1-Methylpiperidin-4-aminedihydrochloride, 1-Methylpiperidin-4-amine–hydrogen chloride (1/2)

1-Methylpiperidin-4-amine dihydrochloride is primarily used as a key intermediate in pharmaceutical synthesis, particularly in the development of central nervous system (CNS) drugs and receptor modulators. Its piperidine scaffold makes it valuable for designing bioactive molecules in medicinal chemistry. The compound is also employed in catalysis and as a building block for heterocyclic compounds. Researchers utilize it in biochemical assays and structure-activity relationship (SAR) studies. Its dihydrochloride form enhances solubility, facilitating reactions in aqueous or polar solvents.

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