Nicotinamide N-Oxide - ≥98% , CAS No.1986-81-8

CAS: 1986-81-8 Cat. No.: N123035 Peso molecular: 138.12 Número EC: 217-859-4
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
3-Pyridinecarboxamide, 1-oxide | Nicotinamide N-oxide | InChI=1/C6H6N2O2/c7-6(9)5-2-1-3-8(10)4-5/h1-4H,(H2,7,9) | Nicotinamide N1-oxide | 1-oxido-pyridin-1-ium-3-carboxamide | 1-oxide-nicotinamide | J-512155 | AKOS000282814 | nicotinamide-n-oxide | USSFUV
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
N123035-5g
4

17,90US$

26,90US$
Guardar 9,00 US$ (33.46%)
25g
N123035-25g
2

47,90US$

71,90US$
Guardar 24,00 US$ (33.38%)
100g
N123035-100g
3

131,90US$

197,90US$
Guardar 66,00 US$ (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Nicotinamide N-oxide is a niacin-related compound used in studies of mechanisms of niacin-related granulocyte differentiation of cells such as human promyelocytic leukemia cells (HL-60). Nicotinamide N-oxide reduced expression of c-myc in HL-60 cell line.

Specifications

Sinónimos
3-Pyridinecarboxamide, 1-oxide | Nicotinamide N-oxide | InChI=1/C6H6N2O2/c7-6(9)5-2-1-3-8(10)4-5/h1-4H, (H2, 7, 9) | Nicotinamide N1-oxide | 1-oxido-pyridin-1-ium-3-carboxamide | 1-oxide-nicotinamide | J-512155 | AKOS000282814 | nicotinamide-n-oxide | USSFUV
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504754660
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504754660
Sonrisas canónicasC1=CC(=C[N+](=C1)[O-])C(=O)N
IUPAC Name1-oxidopyridin-1-ium-3-carboxamide
InChIKeyUSSFUVKEHXDAPM-UHFFFAOYSA-N
INCHI1S/C6H6N2O2/c7-6(9)5-2-1-3-8(10)4-5/h1-4H,(H2,7,9)
Isómeros SMILES C1=CC(=C[N+](=C1)[O-])C(=O)N
WGK Alemania 3
Peso molecular 138.12
Reaxy-Rn 115925
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=115925&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
SuperclassOrganoheterocyclic compounds
ClasePyridines and derivatives
SubclassPyridinecarboxylic acids and derivatives
Intermediate Tree Nodes Pyridinecarboxamides
Direct ParentNicotinamides
Alternative Parents Heteroaromatic compounds  Carboximidic acids  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Nicotinamide - Heteroaromatic compound - Azacycle - Carboximidic acid derivative - Carboximidic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as nicotinamides. These are heterocyclic aromatic compounds containing a pyridine ring substituted at position 3 by a carboxamide group.
External Descriptors a small molecule
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
MTARC1 Tbio Mitochondrial amidoxime-reducing component 1 (51 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

5 results found

Lot NumberCertificate TypeFechaArticulo
F2622047Certificate of AnalysisJun 29, 2026 N123035
B2219289Certificate of AnalysisDec 10, 2025 N123035
B2219319Certificate of AnalysisDec 10, 2025 N123035
B2219357Certificate of AnalysisDec 10, 2025 N123035
K1318020Certificate of AnalysisJul 09, 2025 N123035
Propiedades químicas y físicas
SensibilidadHygroscopic
Punto de fusión (°C)291-293°C
Peso molecular138.120 g/mol
XLogP3-1.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass138.043 Da
Monoisotopic Mass138.043 Da
Topological Polar Surface Area68.600 Ų
Heavy Atom Count10
Formal Charge0
Complexity138.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Haitao Yang, Xinyu Zhou, Baihao Zhang, Yuzhen Shan, Yichen Jin, Enzhuang Pan, Dong Xu, Liwen Fan, Panpan Zhao, Yong Sun, Jingquan Dong.  (2025)  HSP90α facilitates the dephosphorylation of DRP1 at the Ser637 residue, thereby promoting NLRP3 inflammasome activation and exacerbating brain injury in sepsis.  FREE RADICAL BIOLOGY AND MEDICINE,      [PMID:41314440] [10.1016/j.freeradbiomed.2025.11.056]
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