Packings
500 ml
500 ml

Product Information

Basic information about this product

Article No. 006303
Grade AR
Purity 99.5%
CAS No. 110-86-1
Molecular Formula C5H5N
Molecular Weight 79.10
H.S. Code 29333100
Shelf Life 60 Months

Hazard Information

Safety and hazard classification

GHS02 GHS02
GHS07 GHS07
Hazard Symbols
GHS02, GHS07

Safety Information

Important safety instructions and precautions

Signal Word: Danger
UN No.: 1282
IMCO Class No.: 3
Packing Group: II
Hazardous Statement: H225-H302-H312-H332
Precaution Statement: P210-P280

Product Description

Detailed information about the product

Product Overview

Pyridine 99.5% Dried AR (CAS No. 110-86-1) is a nitrogen-containing aromatic heterocycle in which the pyridine ring provides a basic ring nitrogen with a lone pair available for protonation, nucleophilic interactions and coordination to metal centres. This combination of basicity, polarity and organic-solvent compatibility gives pyridine a distinctive role in laboratory chemistry as both a reaction medium and a functional reagent. It readily participates in acid-base chemistry and can form pyridinium salts, while its nitrogen donor character also enables coordination with suitable metal species.

The Dried AR grade is intended for analytical and general laboratory procedures in which the presence of uncontrolled moisture could influence a reaction, reagent system or analytical result. Its reduced-moisture character is particularly relevant to moisture-sensitive preparation, acid-base and derivatisation chemistry, and procedures where pyridine functions simultaneously as solvent and base. Pyridine is well established in acylation and dehydrohalogenation chemistry, condensation reactions, organic synthesis and coordination applications, while pyridine-based analytical reagent systems also occur in established laboratory methods.

Typical Applications

  • Solvent and base in acylation reactions, including reactions involving alcohols and related nucleophiles.
  • Dehydrohalogenation and other base-mediated organic transformations.
  • Solvent– base medium for condensation reactions such as Knoevenagel-type chemistry.
  • Preparation of pyridinium salts and other pyridine-derived intermediates in organic synthesis.
  • Ligand or coordinating solvent in metal-complex and coordination-chemistry studies.
  • Preparation of analytical reagents and reaction systems where controlled moisture is important.
  • Laboratory research involving moisture-sensitive organic transformations and reagent preparation.

Common Synonyms

  • Azabenzene
  • Azine
  • Pyridin
  • Py

Storage Conditions

Keep tightly closed and protected from atmospheric moisture to preserve the product's dried character, particularly after opening, and minimise unnecessary exposure during dispensing or transfer. Store in a cool, well-ventilated area away from excessive heat and incompatible materials, with the container promptly reclosed after use to limit evaporation and moisture uptake.