Picolinamide - 10mM in DMSO , CAS No.1452-77-3

CAS: 1452-77-3 Cat. No.: P421668 Summenformel: C6H6N2O Molekulargewicht: 122.12 Beilstein Registry Number: 22(3/4)311 EG-Nummer: 215-921-5 PubChem CID: 15070
Zu bestellen verfügbar
GRADE & PURITY 10mM in DMSO
Synonyms
C01950 | NSC 524473 | alpha-Picolinamide | PICOLINAMIDE [INCI] | 2-Carbamoylpyridine | Picolinamide; 2-Pyridinecarboxamide | pyridine amide | s4710 | .alpha.-Pyridinecarboxamide | J-008082 | 2-Pyridinecarboxamide | 2-pyridine-carboxamide | alpha - picolin
Storage
Protected from light,Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Deutschland (EU)
USA*
Price
Qty
1ml
P421668-1ml
—
1 Auf Lager
25,95€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -80°C Ships Dry ice packs + Cold packs 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 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Picolinamide is potential inhibitor of poly (ADP-ribose) synthetase of nuclei from rat pancreatic islet cells. It acts as bidentate ligand and forms complexes with lanthanide nitrates, thiocyanates and perchlorates. Picolinamide can be used as template in preparation of molecular imprinting polymer. Picolinamide can be used in a study to evaluate kinetics and mechanism of liberation of picolinamide from chromium(III)-picolinamide complexes in perchloric acid.
Picolinamide was used as template in preparation of molecular imprinting polymer1. Picolinamide was used in a study to evaluate kinetics and mechanism of liberation of picolinamide from chromium(III)-picolinamide complexes in HClO42.

Specifications

Synonyme
C01950 | NSC 524473 | alpha-Picolinamide | PICOLINAMIDE [INCI] | 2-Carbamoylpyridine | Picolinamide; 2-Pyridinecarboxamide | pyridine amide | s4710 | .alpha.-Pyridinecarboxamide | J-008082 | 2-Pyridinecarboxamide | 2-pyridine-carboxamide | alpha - picolin
Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
Pyridylamide is a potential inhibitor of ADP ribose synthetase. Pyridinamides act as bidentate ligands and form complexes with lanthanide nitrates, thiocyanates and perchlorates.
Storage
Protected from light,Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
C1=CC=NC(=C1)C(=O)N
IUPAC Name
pyridine-2-carboxamide
InChIKey
IBBMAWULFFBRKK-UHFFFAOYSA-N
INCHI
1S/C6H6N2O/c7-6(9)5-3-1-2-4-8-5/h1-4H,(H2,7,9)
Isomere SMILES
C1=CC=NC(=C1)C(=O)N
WGK Deutschland
3
PubChem CID
15070
Molekulargewicht
122.12
Beilstein
22(3/4)311
Reaxy-Rn
109617

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
KlassePyridines and derivatives
SubclassPyridinecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentPyridinecarboxamides
Alternative Parents 2-heteroaryl carboxamides  Heteroaromatic compounds  Primary carboxylic acid amides  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyridinecarboxamide - 2-heteroaryl carboxamide - Heteroaromatic compound - Primary carboxylic acid amide - Carboxamide group - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as pyridinecarboxamides. These are compounds containing a pyridine ring bearing a carboxamide.
External Descriptors pyridinecarboxamide
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Siedepunkt (°C)143 °C/20 mmHg
Schmelzpunkt (°C)105 °C
Molekulargewicht122.120 g/mol
XLogP30.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass122.048 Da
Monoisotopic Mass122.048 Da
Topological Polar Surface Area56.000 Ų
Heavy Atom Count9
Formal Charge0
Complexity114.000
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
FAQs und Artikel
Citations of This Product
Lösungsrechner
Bewertungen

Kundenbewertungen

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.