Pharmaceutical Materials

CAS No.1094-61-7

Name

beta-nicotinamide mononucleotide

Synonyms

NMN

BETA-NMN

NICOTINAMIDE RIBOTIDE

Nicotinamide mononucleotide

B-NICOTINAMIDE MONONUCLEOTIDE

β-Nicotinamide mononucleotide

beta-nicotinamide mononucleotide

BETA-NICOTINAMIDE MONONUCLEOTIDE

BETA-NICOTINAMIDE RIBOSE MONOPHOSPHATE

3-carbamoyl-1-(5-O-phosphonopentofuranosyl)pyridinium

NICOTINAMIDE-1-IUM-1-BETA-D-RIBOFURANOSIDE 5′-PHOSPHATE

3-(aminocarbonyl)-1-(5-O-phosphonato-beta-D-ribofuranosyl)pyridinium

3-(Aminocarbonyl)-1-(5-O-phosphonato-beta-D-ribofuranosyl)pyridinium

3-carbamoyl-1-[5-O-(hydroxyphosphinato)-beta-D-ribofuranosyl]pyridinium

Pyridinium, 3-(aminocarbonyl)-1-(5-O-phosphono-beta-D-ribofuranosyl)-, inner salt

 

Attribute	Details
Chemical Name	β-Nicotinamide Mononucleotide (β-NMN)
Abbreviation	NMN
CAS Number	1094-61-7
Molecular Formula	C11H15N2O8P
Molecular Weight	334.22 g/mol
Physical State	White to slightly yellow, crystalline powder
Odor	Odorless
Solubility	Highly soluble in water, insoluble in acetone
Stability	Light-sensitive, should be stored away from light and moisture (with a shelf life of 24 months)
pH Value	Weakly acidic (pH = 3~4)
Occurrence	Naturally occurring in animal tissues and present in minimal amounts in the diet; it is an intermediate in the NAD⁺ metabolism
Biological Role	Acts as a key intermediate in the synthesis of Coenzyme I (NAD⁺), which is involved in numerous biochemical reactions related to immunity and metabolism
Applications	Widely used in pharmaceuticals, cosmetics, food additives, and dietary supplements; studied for its potential to increase NAD⁺ levels in tissues, alleviate age-related physiological decline, and improve metabolic functions
Synthesis Methods	Prepared through chemical synthesis or biotechnological methods; the latter is simpler, more environmentally friendly, and cost-effective
Safety Information	Generally recognized as safe; however, handling should be done with appropriate personal protective equipment to avoid skin and eye contact

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