18865-33-3

Usage

Uses

Used in Industrial Applications:
(1,5-diaminopentyl)phosphonic acid is used as a corrosion inhibitor to protect materials from degradation caused by chemical or electrochemical reactions. Its ability to form complexes with metal ions also makes it a valuable chelating agent in various industrial processes.
Used in Pharmaceutical Development:
Due to its potential biological activities, (1,5-diaminopentyl)phosphonic acid is being investigated for its use in pharmaceuticals. Its unique structure allows it to interact with biological systems, offering possibilities for the development of new drugs and therapies.
Used in Agrochemicals:
(1,5-diaminopentyl)phosphonic acid also holds promise in the agrochemical industry. Its potential applications include the development of new pesticides, herbicides, or fertilizers that can improve crop yields and protect plants from diseases and pests.
Overall, (1,5-diaminopentyl)phosphonic acid is a versatile compound with a wide range of applications across different industries, and its potential for further research and development is substantial.

Upstream product

• 95691-20-6 (1,5-Diamino-pentyl)-phosphinic acid 

Relevant academic research and scientific papers

1-Aminoalkylphosphonous Acids. Part 1. Isosteres of the Protein Amino Acids

The synthesis of 1-aminoalkylphosphonous acids, isosteres of the protein amino acids, by addition of hypophosphorous acid to diphenylmethylimines is described.These analogues of glycine, alanine, valine, leucine, isoleucine, phenylalanine, tyrosine, tryptophan, serine, threonine, methionine, cysteine, cystine, glutamic acid, lysine, ornithine, arginine, and proline have been prepared and the analogues of alanine, valine, leucine, phenylalanine, and methionine resolved.The alanine, valine and methionine analogues have interesting antimicrobial activity and the alanine analogue has plant growth inhibiting properties.Oxidation of the appropriate 1-aminoalkylphosphonous acids gave the 1-aminoalkylphosphonic acid analogues of (+/-)-alanine, (-)-alanine, (+/-)-valine, (-)-valine, (+/-)-serine, (+/-)-threonine, (+/-)-lysine, (-)-leucine, and (+/-)-ornithine.

Multi-organ technetium complexes production and use thereof

Chemical complexes, useful as radiopharmaceuticals, are formed by reacting technetium-99m with substituted or unsubstituted alkyl monophosphonic acids and certain ester derivatives thereof. The complexes are formed by reducing pertechnetate ion chemically or electrolytically in the presence of the phosphonic acid. By chemical modification of the phosphonic acid complexing agent, it is possible to "tailor" complexes for kidney, liver or bone imaging. The complexes are normally used in a physiologically acceptable aqueous medium.