Issue 34, 2021

Dihydronicotinamide riboside: synthesis from nicotinamide riboside chloride, purification and stability studies

Abstract

In the present work, we describe an efficient method for scalable synthesis and purification of 1,4-dihydronicotinamide riboside (NRH) from commercially available nicotinamide riboside chloride (NRCl) and in the presence of sodium dithionate as a reducing agent. NRH is industrially relevant as the most effective, synthetic NAD+ precursor. We demonstrated that solid phase synthesis cannot be used for the reduction of NRCl to NRH in high yield, whereas a reduction reaction in water at room temperature under anaerobic conditions is shown to be very effective, reaching a 55% isolation yield. For the first time, by using common column chromatography, we were able to highly purify this sensitive bio-compound with good yield. A series of identifications and analyses including HPLC, NMR, LC-MS, FTIR, and UV-vis spectroscopy were performed on the purified sample, confirming the structure of NRH as well as its purity to be 96%. Thermal analysis of NRH showed higher thermal stability compared to NRCl, and with two major weight losses, one at 218 °C and another at 805 °C. We also investigated the long term stability effects of temperature, pH, light, and oxygen (as air) on the NRH in aqueous solutions. Our results show that NRH can be oxidized in the presence of oxygen, and it hydrolyzed quickly in acidic conditions. It was also found that the degradation rate is lower under a N2 atmosphere, at lower temperatures, and under basic pH conditions.

Graphical abstract: Dihydronicotinamide riboside: synthesis from nicotinamide riboside chloride, purification and stability studies

Supplementary files

Article information

Article type
Paper
Submitted
15 Mar 2021
Accepted
07 Jun 2021
First published
14 Jun 2021
This article is Open Access
Creative Commons BY license

RSC Adv., 2021,11, 21036-21047

Dihydronicotinamide riboside: synthesis from nicotinamide riboside chloride, purification and stability studies

A. Zarei, L. Khazdooz, M. Enayati, S. Madarshahian, T. J. Wooster, G. Ufheil and A. Abbaspourrad, RSC Adv., 2021, 11, 21036 DOI: 10.1039/D1RA02062E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements