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Atomfair Pipecolic Acid C6H11NO2

Description Pipecolic Acid (CAS 3105-95-1) is a heterocyclic organic compound with the molecular formula C6H11NO2. Also known as piperidine-2-carboxylic acid , it is a non-proteinogenic amino acid that serves as a key intermediate in lysine metabolism. This high-purity compound is ideal for biochemical and pharmaceutical research, offering exceptional quality and consistency. Pipecolic Acid is available in various grades, including analytical and reagent standards, ensuring suitability for HPLC, LC-MS, and NMR applications. Its stable crystalline form and well-characterized structure make it a reliable choice for synthetic chemistry, enzymology studies, and metabolic pathway investigations.

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Description

Description

Pipecolic Acid (CAS 3105-95-1) is a heterocyclic organic compound with the molecular formula C6H11NO2. Also known as piperidine-2-carboxylic acid, it is a non-proteinogenic amino acid that serves as a key intermediate in lysine metabolism. This high-purity compound is ideal for biochemical and pharmaceutical research, offering exceptional quality and consistency. Pipecolic Acid is available in various grades, including analytical and reagent standards, ensuring suitability for HPLC, LC-MS, and NMR applications. Its stable crystalline form and well-characterized structure make it a reliable choice for synthetic chemistry, enzymology studies, and metabolic pathway investigations.

  • CAS No: 3105-95-1
  • Molecular Formula: C6H11NO2
  • Molecular Weight: 129.16
  • Exact Mass: 129.078978594
  • Monoisotopic Mass: 129.078978594
  • IUPAC Name: piperidine-2-carboxylic acid
  • SMILES: C1CCNC(C1)C(=O)O
  • Synonyms: piperidine-2-carboxylic acid, Pipecolic acid, 535-75-1, DL-Pipecolinic acid, 2-PIPERIDINECARBOXYLIC ACID

Application

Pipecolic Acid is widely used in biochemical research as a precursor for the synthesis of pharmaceuticals and bioactive compounds. It plays a role in studying lysine metabolism and neurological disorders. Researchers utilize it in enzymology to investigate enzyme mechanisms and substrate specificity. Additionally, it serves as a chiral building block in asymmetric synthesis and drug development.

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