nl
Winkelwagen
JBSNF-000088 is supplied by Rexar as a research-grade chemical reference material for analytical chemistry, compound identification and laboratory comparison workflows. Also known as 6-Methoxynicotinamide, this substituted pyridine carboxamide incorporates methoxy, pyridine and carboxamide structural features and is provided exclusively for controlled research environments requiring verified chemical identity, consistent structural documentation and reproducible analytical comparison.
Research-grade material distributed by Rexar within the European Union.
JBSNF-000088 (CAS 7150-23-4) is supplied in sealed laboratory packaging to support traceability, storage integrity and laboratory handling procedures.
Rexar Technical Compound Datasheet (PDF)
Molecular structure data and selected physicochemical properties can be consulted via: JBSNF-000088 (6-Methoxynicotinamide) on PubChem
JBSNF-000088 is a synthetic heteroaromatic compound with the molecular formula C7H8N2O2. Its molecular architecture combines a substituted pyridine ring, a methoxy group and a carboxamide functionality within a compact nitrogen- and oxygen-containing aromatic framework.
The structure contains two nitrogen atoms and two oxygen atoms distributed across chemically distinct functional environments. This relatively small but analytically differentiated molecular framework is suitable for chromatographic, mass-spectrometric and spectroscopic characterisation.
A defining structural element of JBSNF-000088 is its substituted pyridine ring. This six-membered aromatic heterocycle contains one nitrogen atom incorporated directly into the aromatic ring system.
The pyridine nitrogen contributes a characteristic heteroaromatic electronic environment and provides analytical features relevant to chromatography, mass spectrometry, NMR spectroscopy and comparative compound identification.
JBSNF-000088 contains a carboxamide functionality directly associated with the substituted pyridine framework. The carboxamide group contains both carbonyl and nitrogen-containing structural environments.
This functionality contributes significantly to molecular polarity and hydrogen-bonding behaviour and may produce characteristic carbonyl and N-H-associated features during infrared and NMR analysis.
The molecular formula C7H8N2O2 reflects a structure containing carbon, hydrogen, nitrogen and oxygen distributed across several chemically distinct functional groups.
The combination of heteroaromatic, ether-like and amide structural elements provides several analytical markers for comparative compound identification.
The carboxamide group of JBSNF-000088 contains a carbonyl carbon bonded to an amide nitrogen. This structural region contributes both hydrogen-bond donor and acceptor characteristics.
The amide carbonyl may provide a characteristic infrared absorption feature and a distinguishable carbon environment during carbon NMR analysis.
JBSNF-000088 contains a methoxy substituent attached to the pyridine ring. The methoxy group consists of an oxygen atom connected to a methyl group and the aromatic heterocyclic framework.
This substituent introduces a chemically distinct oxygen-containing environment and may influence electronic distribution, chromatographic retention and spectroscopic characteristics.
The pyridine portion of JBSNF-000088 contains one ring nitrogen atom incorporated directly into the aromatic system.
This nitrogen-containing environment contributes to molecular polarity and may influence protonation behaviour, chromatographic retention and mass-spectrometric response under different analytical conditions.
A second nitrogen atom is present within the carboxamide functionality. This nitrogen environment differs chemically from the aromatic pyridine nitrogen.
The presence of two chemically distinct nitrogen environments can provide useful differentiation during spectroscopic and analytical comparison.
The two oxygen atoms in JBSNF-000088 occupy different structural environments: one within the methoxy group and one within the carboxamide carbonyl.
These chemically distinct oxygen-containing functionalities influence molecular polarity, hydrogen bonding and chromatographic behaviour and may provide characteristic features during infrared and NMR analysis.
JBSNF-000088 contains hydrogen-bond donor and acceptor sites arising primarily from the carboxamide functionality, pyridine nitrogen and methoxy oxygen atom.
The distribution of these sites may influence solvation, crystal packing, chromatographic behaviour and interactions with polar analytical stationary phases.
The molecule combines an aromatic pyridine framework with a polar carboxamide group and an oxygen-containing methoxy substituent. This creates several localised polar regions within a relatively compact molecular structure.
This structural character is relevant when evaluating solvent selection, mobile-phase composition and sample preparation for analytical workflows.
The aromatic pyridine ring provides a relatively rigid structural core, while rotation around bonds associated with the methoxy and carboxamide substituents may introduce limited conformational flexibility.
No defined stereogenic centre is present in the standard molecular representation, and the compound is represented without specified stereochemistry.
Under liquid chromatographic conditions, retention may be influenced by the pyridine ring, methoxy group, carboxamide functionality, heteroatom distribution and overall molecular polarity.
Retention time and peak shape may vary according to mobile-phase composition, pH, stationary-phase chemistry, temperature and sample concentration.
LC-based methods may be used for qualitative identity comparison, purity profiling and retention-time verification of JBSNF-000088 reference material.
The combination of a heteroaromatic ring, methoxy substituent and polar carboxamide functionality may require optimisation of mobile-phase composition and stationary-phase chemistry to obtain suitable retention and peak symmetry.
With a molecular weight of approximately 152.15 g/mol, JBSNF-000088 falls within a mass range suitable for routine LC-MS analysis. Appropriate ionisation techniques may support detection of protonated, deprotonated or adducted molecular species depending on solvent composition, mobile-phase conditions and instrument parameters.
Fragmentation may involve the methoxy group, carboxamide functionality or substituted pyridine framework and can support structural confirmation when compared with authenticated reference data.
Proton NMR analysis may show characteristic resonances associated with pyridine-ring proton environments, the methoxy methyl group and the amide proton environment under suitable analytical conditions.
Carbon NMR analysis may provide distinguishable signals corresponding to heteroaromatic carbons, the methoxy carbon and the carboxamide carbonyl carbon.
Infrared analysis may reveal characteristic absorption features associated with the amide carbonyl, N-H functionality, aromatic C-H environments and the methoxy group.
The carboxamide functionality may provide prominent absorption characteristics that can assist structural comparison when evaluated against an authenticated reference spectrum.
The aromatic pyridine region of JBSNF-000088 may support ultraviolet-based chromatographic detection. Suitable detection wavelengths should be selected according to measured absorbance characteristics and validated laboratory methods.
Substitution by methoxy and carboxamide groups may influence the precise electronic absorption profile of the compound.
JBSNF-000088 contains two nitrogen atoms and two oxygen atoms distributed across pyridine, carboxamide and methoxy structural environments.
This arrangement provides chemically distinct heteroatom-associated features that may be useful during mass-spectrometric, chromatographic and spectroscopic characterisation.
JBSNF-000088 is supplied as a laboratory powder. Solid-state characteristics such as crystallinity, particle morphology, residual moisture and residual solvent content may depend on manufacturing and purification procedures.
Analytical laboratories may use melting behaviour, powder analysis or spectroscopic comparison as supplementary identity indicators where appropriate.
JBSNF-000088 may serve as a qualitative reference compound in structural verification and comparative analytical workflows involving LC-MS, HPLC, NMR and infrared spectroscopy. Laboratory procedures may include retention-time comparison, molecular-weight confirmation and comparative spectral profiling.
JBSNF-000088 can be structurally described as a substituted pyridine carboxamide containing methoxy, heteroaromatic nitrogen and amide functionalities.
Its compact molecular architecture provides several distinct structural markers, including a pyridine nitrogen, a methoxy substituent and a carboxamide functionality, which can support comparative analytical identification.
The substituted pyridine core contains a six-membered aromatic heterocycle incorporating one nitrogen atom. Methoxy and carboxamide substituents occupy distinct positions on the heteroaromatic framework.
This pyridine core provides characteristic nitrogen- and carbon-associated environments that may assist analytical identification.
JBSNF-000088 contains a methoxy group attached directly to the pyridine framework. This oxygen-containing substituent introduces a methyl environment distinct from the heteroaromatic carbon framework.
The methoxy group may provide useful differentiation during proton and carbon NMR analysis and may influence chromatographic behaviour through its contribution to molecular polarity.
The carboxamide functionality is directly associated with the substituted pyridine framework and contains both a carbonyl group and an amide nitrogen.
This arrangement provides chemically distinctive carbonyl and nitrogen environments that may support infrared, NMR and mass-spectrometric identification.
JBSNF-000088 contains one carbonyl group within the carboxamide functionality. This carbonyl environment contributes significantly to molecular polarity.
The amide carbonyl may provide a distinct carbon NMR signal and a prominent infrared absorption feature useful for comparative analytical identification.
The pyridine nitrogen and carboxamide functionality of JBSNF-000088 may influence protonation and ionisation behaviour under different analytical conditions.
Mobile-phase pH, solvent composition and ionisation parameters can therefore affect chromatographic retention and mass-spectrometric response.
The molecular formula C7H8N2O2 contains two nitrogen atoms distributed across pyridine and amide environments and two oxygen atoms distributed across methoxy and carbonyl functionalities.
Theoretical elemental composition may support identity verification when combined with mass spectrometry and spectroscopic analysis.
As a chemical reference material, JBSNF-000088 may be used for qualitative structural comparison, method development and analytical identity verification in laboratories examining substituted pyridines, nicotinamide-related structures or methoxy-substituted heteroaromatic reference materials.
Analytical reproducibility depends on consistent sample preparation, validated instrument parameters, suitable reference documentation and controlled storage conditions.
Each unit is supplied in sealed laboratory packaging designed to support material integrity during storage and transport. Batch identification labelling supports traceability and internal documentation within controlled research environments.
Packaging should remain closed when the material is not in use and should be protected from moisture, excessive heat and direct light.
What is the CAS number of JBSNF-000088?
The CAS number is 7150-23-4.
What is the PubChem CID of JBSNF-000088?
The PubChem compound identifier is 250810.
What is the molecular formula of JBSNF-000088?
The molecular formula is C7H8N2O2.
What is the molecular weight of JBSNF-000088?
The molecular weight is approximately 152.15 g/mol.
What is another name for JBSNF-000088?
JBSNF-000088 is also known as 6-Methoxynicotinamide.
What type of chemical structure does JBSNF-000088 contain?
JBSNF-000088 contains a substituted pyridine framework with methoxy and carboxamide structural regions.
Does JBSNF-000088 contain a methoxy group?
Yes. The molecular structure contains one methoxy substituent attached to the pyridine framework.
Does JBSNF-000088 contain an amide group?
Yes. The structure contains one carboxamide functionality.
In which form is JBSNF-000088 supplied?
It is supplied as a laboratory powder in sealed packaging.
Is this product intended for human or animal use?
No. This material is supplied exclusively as a laboratory reference compound.
Disclaimer:
This product is supplied exclusively as a chemical reference material for laboratory and analytical purposes. Not for human or animal consumption. Not intended for food, supplement, cosmetic, medical, diagnostic or therapeutic use.
| Intended use: | Laboratory research and analytical reference purposes only |
| Application area: | Analytical chemistry, reference comparison and method development |
| End user: | Professional users in controlled research environments |
| Regulatory classification: | Chemical reference material |
