P57506
Pyridine
ReagentPlus®, ≥99%
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About This Item
Empirical Formula (Hill Notation):
C5H5N
CAS Number:
Molecular Weight:
79.10
UNSPSC Code:
12352005
NACRES:
NA.21
PubChem Substance ID:
EC Number:
203-809-9
Beilstein/REAXYS Number:
103233
MDL number:
Assay:
≥99%
Bp:
115 °C (lit.)
Vapor pressure:
10 mmHg ( 13.2 °C), 20 mmHg ( 25 °C)
vapor density
2.72 (vs air)
Quality Level
vapor pressure
10 mmHg ( 13.2 °C), 20 mmHg ( 25 °C)
product line
ReagentPlus®
assay
≥99%
form
liquid
autoignition temp.
899 °F
expl. lim.
12.4 %
dilution
(for general lab use)
impurities
≤0.1% water (Karl Fischer)
refractive index
n20/D 1.509 (lit.)
pH
8.5 (25 °C, 15.82 g/L)
bp
115 °C (lit.)
mp
−42 °C (lit.)
density
0.978 g/mL at 25 °C (lit.)
SMILES string
C1=CN=CC=C1
InChI
1S/C5H5N/c1-2-4-6-5-3-1/h1-5H
InChI key
JUJWROOIHBZHMG-UHFFFAOYSA-N
General description
Pyridine (Pyr) is a nitrogen-containing six-membered heterocyclic compound that is commonly used as a solvent in organic synthesis. It also has wide applications as a base, catalyst, and intermediate for synthesis.
Application
Pyridine can be used as a solvent:
- To synthesize glycophospholipids and phosphate diesters or phosphonate monoesters in the presence of trichloroacetonitrile as an activating reagent.
- In Knoevenagel condensation reactions.
- In the TEMPO-mediated radical polymerization of 3-vinylpyridine.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
68.0 °F - closed cup
flash_point_c
20 °C - closed cup
Regulatory Information
危险化学品
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Ye Wei et al.
Journal of the American Chemical Society, 135(10), 3756-3759 (2013-02-27)
We describe here a [3+3]-type condensation reaction of O-acetyl ketoximes and α,β-unsaturated aldehydes that is synergistically catalyzed by a copper(I) salt and a secondary ammonium salt (or amine). This redox-neutral reaction allows modular synthesis of a variety of substituted pyridines
Wen Zhou et al.
Inorganic chemistry, 52(5), 2271-2273 (2013-02-20)
The reaction of 2,2'-bipyridine (bpy) with monomeric chromium(II) precursors was used to prepare the S = 1 complexes Cr(tBu-acac)2(bpy) (1) and (η(5)-Cp)(η(1)-Cp)Cr(bpy) (3), as well as the S = 2 compound Cr[N(SiMe3)2]2(bpy) (4). The crystallographically determined bond lengths indicate that
Maria Milina et al.
Angewandte Chemie (International ed. in English), 54(5), 1591-1594 (2014-11-08)
Without techniques sensitive to complex pore architectures, synthetic efforts to enhance molecular transport in zeolite and other porous materials through hierarchical structuring lack descriptors for their rational design. The power of positron annihilation lifetime spectroscopy (PALS) to characterize the pore
Global Trade Item Number
| SKU | GTIN |
|---|---|
| P57506-500ML | 04061834392354 |
| P57506-1L | 04061837230400 |
| P57506-4L | 04061834392347 |