β-Nicotinamide Mononucleotide (NMN) - ≥95% , CAS No.1094-61-7

CAS: 1094-61-7 Cat. No.: N131850 Molecular Weight: 334.22 Beilstein Registry Number: 3570187 EC Number: 214-136-5
AVAILABLE TO ORDER
GRADE & PURITY ≥95%
Synonyms
nicotinamide ribonucleotide | NMN zwitterion | beta-Nicotinamide mononucleotide | Nicotinamide ribotide | nicotinamide D-ribonucleotide | nicotinamide mononucleotide | beta-nicotinamide D-ribonucleotide | beta-NMN | nicotinamide nucleotide | NMN
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Size
Status
Price
Qty
25mg
N131850-25mg
5
$9.90
100mg
N131850-100mg
5
$10.90
500mg
N131850-500mg
3

$11.90

$17.90
Save $6.00 (33.52%)
1g
N131850-1g
≥10

$12.90

$19.90
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5g
N131850-5g
3

$14.90

$22.90
Save $8.00 (34.93%)
25g
N131850-25g
5

$31.90

$47.90
Save $16.00 (33.40%)
100g
N131850-100g
2

$100.90

$151.90
Save $51.00 (33.57%)
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 56 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

A product of the eNAMPT reaction and a NAD+ intermediate

β-Nicotinamide mononucleotide (NMN) is used to study binding motifs within RNA aptamers and ribozyme activation processes involving β-nicotinamide mononucleotide (β-NMN)-activated RNA fragments.

β-Nicotinamide mononucleotide is a product of the extracellular Nicotinamide phosphoribosyltransferase (eNAMPT) reaction and a key NAD+ intermediate. It ameliorates glucose intolerance by restoring NAD+ levels in HFD-induced T2D mice. It also enhances hepatic insulin sensitivity and restores gene expression related to oxidative stress, inflammatory response, and circadian rhythm, partly through SIRT1 activation.

Specifications

Synonyms
nicotinamide ribonucleotide | NMN zwitterion | beta-Nicotinamide mononucleotide | Nicotinamide ribotide | nicotinamide D-ribonucleotide | nicotinamide mononucleotide | beta-nicotinamide D-ribonucleotide | beta-NMN | nicotinamide nucleotide | NMN
Specifications & Purity
≥95%
Biochemical and Physiological Mechanisms
Product of the NAMPT reaction and\xa0a key intermediate in the biosynthesis of nicotinamide adenine dinucleotide (NAD + ). Ameliorates glucose intolerance by restoring NAD + levels in high-fat diet (HFD)-induced T2D mice. Enhances hepatic insulin sensitiv
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥95%
Names and Identifiers
Pubchem Sid488181949
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181949
Canonical SmilesC1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)(O)[O-])O)O)C(=O)N
IUPAC Name[(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate
InChIKeyDAYLJWODMCOQEW-TURQNECASA-N
INCHI1S/C11H15N2O8P/c12-10(16)6-2-1-3-13(4-6)11-9(15)8(14)7(21-11)5-20-22(17,18)19/h1-4,7-9,11,14-15H,5H2,(H3-,12,16,17,18,19)/t7-,8-,9-,11-/m1/s1
Isomeric SMILES C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)[O-])O)O)C(=O)N
WGK Germany 3
Molecular Weight 334.22
Beilstein 3570187
Reaxy-Rn 40276623
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=40276623&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
ClassPyridine nucleotides
SubclassNicotinamide nucleotides
Intermediate Tree Nodes Not available
Direct ParentNicotinamide nucleotides
Alternative Parents Pentose phosphates  Glycosylamines  Monosaccharide phosphates  Nicotinamides  Alkyl phosphates  Pyridinium derivatives  Vinylogous amides  Tetrahydrofurans  Heteroaromatic compounds  Primary carboxylic acid amides  Secondary alcohols  1,2-diols  Azacyclic compounds  Oxacyclic compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  Organonitrogen compounds  Organopnictogen compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Nicotinamide-nucleotide - Pentose-5-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Monosaccharide phosphate - Nicotinamide - Pyridine carboxylic acid or derivatives - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Pyridinium - Pyridine - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - 1,2-diol - Carboxamide group - Secondary alcohol - Primary carboxylic acid amide - Azacycle - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organic zwitterion - Alcohol - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nicotinamide nucleotides. These are pyridine nucleotides, in which the pyridine base is nicotinamide or a derivative thereof.
External Descriptors nicotinamide mononucleotide
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
LDHB Tchem L-lactate dehydrogenase B chain (463 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDH1 Tchem Malate dehydrogenase cytoplasmic (119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GAPDH Tchem Glyceraldehyde-3-phosphate dehydrogenase liver (1284 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
GLUD1 Glutamate dehydrogenase (27 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
panE Ketopantoate reductase (28 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

41 results found

Lot NumberCertificate TypeDateItem
H2231896Certificate of AnalysisMar 11, 2026 N131850
H2231705Certificate of AnalysisMar 11, 2026 N131850
I2510639Certificate of AnalysisAug 20, 2025 N131850
A2620141Certificate of AnalysisAug 20, 2025 N131850
I2510644Certificate of AnalysisAug 20, 2025 N131850
I2510645Certificate of AnalysisAug 20, 2025 N131850
I2510646Certificate of AnalysisAug 20, 2025 N131850
G2321285Certificate of AnalysisMay 09, 2025 N131850
G2321649Certificate of AnalysisMay 09, 2025 N131850
G2321642Certificate of AnalysisMay 09, 2025 N131850
G2321634Certificate of AnalysisMay 09, 2025 N131850
G2321628Certificate of AnalysisMay 09, 2025 N131850
G2321302Certificate of AnalysisMay 09, 2025 N131850
B2328606Certificate of AnalysisDec 17, 2024 N131850
B2328601Certificate of AnalysisDec 17, 2024 N131850
K2421499Certificate of AnalysisNov 08, 2024 N131850
K2421504Certificate of AnalysisNov 08, 2024 N131850
K2421508Certificate of AnalysisNov 08, 2024 N131850
K2421511Certificate of AnalysisNov 08, 2024 N131850
H2231626Certificate of AnalysisJun 19, 2024 N131850
H2507505Certificate of AnalysisApr 23, 2024 N131850
J2425643Certificate of AnalysisApr 23, 2024 N131850
J2425769Certificate of AnalysisApr 23, 2024 N131850
J2425770Certificate of AnalysisApr 23, 2024 N131850
L2107071Certificate of AnalysisSep 19, 2023 N131850
L2106693Certificate of AnalysisSep 19, 2023 N131850
L2106810Certificate of AnalysisSep 19, 2023 N131850
I2405021Certificate of AnalysisJun 13, 2023 N131850
G2109284Certificate of AnalysisApr 18, 2023 N131850
G2109283Certificate of AnalysisApr 18, 2023 N131850
G2109282Certificate of AnalysisApr 18, 2023 N131850
B2328936Certificate of AnalysisFeb 16, 2023 N131850
B2328608Certificate of AnalysisFeb 16, 2023 N131850
B2328607Certificate of AnalysisFeb 16, 2023 N131850
B2328602Certificate of AnalysisFeb 16, 2023 N131850
H2231700Certificate of AnalysisJun 18, 2022 N131850
H2231625Certificate of AnalysisJun 18, 2022 N131850
H2231624Certificate of AnalysisJun 18, 2022 N131850
C2226321Certificate of AnalysisFeb 17, 2022 N131850
C2226312Certificate of AnalysisFeb 17, 2022 N131850
C2226284Certificate of AnalysisFeb 17, 2022 N131850

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Chemical and Physical Properties
SolubilitySoluble in PBS (10 mg/ml).
Sensitivityheat sensitive
Specific Rotation[α]-24° (C=2,H2O)
Melt Point(°C)166 °C
Molecular Weight334.220 g/mol
XLogP3-3.500
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count8
Rotatable Bond Count5
Exact Mass334.057 Da
Monoisotopic Mass334.057 Da
Topological Polar Surface Area166.000 Ų
Heavy Atom Count22
Formal Charge0
Complexity455.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Jiyan Xu, Xinlu Chen, Shuai Liu, Ziqi Wei, Minhui Xu, Linhao Jiang, Xue Han, Liangyu Peng, Xiaoping Gu, Tianjiao Xia.  (2023)  Nicotinamide mononucleotide pretreatment improves long-term isoflurane anesthesia-induced cognitive impairment in mice.  BEHAVIOURAL BRAIN RESEARCH,      [PMID:37931707] [10.1016/j.bbr.2023.114738]
2. Qi Shen, Shi-Jia Zhang, Bin-Hui Xu, Zhi-Yu Chen, Feng Peng, Neng Xiong, Ya-Ping Xue, Yu-Guo Zheng.  (2023)  Semirational engineering of Cytophaga hutchinsonii polyphosphate kinase for developing a cost-effective, robust, and efficient adenosine 5′-triphosphate regeneration system.  APPLIED AND ENVIRONMENTAL MICROBIOLOGY,      [PMID:37902313] [10.1128/aem.01106-23]
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