Nicotinamide riboside chloride( NR-CL) - ≥99.5% , CAS No.23111-00-4

CAS: 23111-00-4 Cat. No.: N1492503 Molecular Weight: 290.7 EC Number: 807-820-5
AVAILABLE TO ORDER
GRADE & PURITY ≥99.5%
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
N1492503-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$13.90
25g
N1492503-25g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$45.90
100g
N1492503-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$99.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥99.5% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Nicotinamide riboside is involved in nicotinate and nicotinamide metabolism. Nicotinamide riboside was originally identified as a nutrient in milk and later discovered to be a NAD(+) precursor.

Specifications

Specifications & Purity
≥99.5%
Storage
Protected from light, Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥99.5%
Names and Identifiers
Canonical SmilesC1=CC(=C[N+](=C1)C2C(C(C(O2)CO)O)O)C(=O)N.[Cl-]
IUPAC Name1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyridin-1-ium-3-carboxamide;chloride
InChIKeyYABIFCKURFRPPO-IVOJBTPCSA-N
INCHI1S/C11H14N2O5.ClH/c12-10(17)6-2-1-3-13(4-6)11-9(16)8(15)7(5-14)18-11;/h1-4,7-9,11,14-16H,5H2,(H-,12,17);1H/t7-,8-,9-,11-;/m1./s1
Isomeric SMILES C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)C(=O)N.[Cl-]
Molecular Weight 290.7
Reaxy-Rn 48663754
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=48663754&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
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Glycosyl compounds
Direct ParentGlycosylamines
Alternative Parents Pentoses  Nicotinamides  Pyridinium derivatives  Vinylogous amides  Heteroaromatic compounds  Oxolanes  Secondary alcohols  Primary carboxylic acid amides  Azacyclic compounds  Oxacyclic compounds  Organic oxides  Organic chloride salts  Primary alcohols  Hydrocarbon derivatives  Organic zwitterions  Organonitrogen compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents N-glycosyl compound - Pentose monosaccharide - Nicotinamide - Pyridine carboxylic acid or derivatives - Monosaccharide - Pyridine - Pyridinium - Vinylogous amide - Heteroaromatic compound - Oxolane - Secondary alcohol - Carboxamide group - Primary carboxylic acid amide - Organoheterocyclic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Organic salt - Hydrocarbon derivative - Primary alcohol - Organonitrogen compound - Organic oxide - Alcohol - Organic nitrogen compound - Organic chloride salt - Organic zwitterion - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

3 results found

Lot NumberCertificate TypeDateItem
K2505508Certificate of AnalysisOct 11, 2025 N1492503
K2505509Certificate of AnalysisOct 11, 2025 N1492503
K2505510Certificate of AnalysisOct 11, 2025 N1492503
Chemical and Physical Properties
SensitivityMoisture sensitive;Heat sensitive;light sensitive
Molecular Weight290.700 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass290.067 Da
Monoisotopic Mass290.067 Da
Topological Polar Surface Area117.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity314.000
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 Count2
Documents & Articles
Citations of This Product
References
1. Seongsu Kang, Jiwon Park, Eunbyul Cho, Dohyun Kim, Sanghyun Ye, Eui Taek Jeong, Seung-Hyun Jun, Nae-Gyu Kang.  (2025)  Distinctive Gene Expression Profiles and Biological Responses of Skin Fibroblasts to Nicotinamide Mononucleotide: Implications for Longevity Effects on Skin.  Biomedicines,  13  (10): (2395).  [PMID:41153679] [10.3390/biomedicines13102395]
2. Yi Zhang, Ying Guo, Wenxi He, Yaping Zhao, Zhaode Feng, Mengjiao Shi, Xinyan Li, Liangwen Yan, Jiayi Xu, Kailing Hu, Rongrong Liu, Yinggang Zhang, Gang Wang, Hao Li, Pengfei Liu.  (2025)  Deciphering the rules of disulfidptosis: a genome-wide signature for identifying disulfidptosis-related genes and analyzing hepatocellular carcinoma chemotherapy sensitivities.  FREE RADICAL BIOLOGY AND MEDICINE,      [PMID:41138962] [10.1016/j.freeradbiomed.2025.10.278]
Solution Calculators
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