Sigma-Aldrich
Pyridine R. G. ACS Reagent, . 99.5%, 500 ml
- Part Number:
- MIL-33553-500ML
- Lead Time:
- 2-4 weeks
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- Quantity:
- each
- Size:
- 500 ml / 16 ounce
- Style:
- chemical
- DOT Rated:
- HazMat Transport Fee Required
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Description
Pyridine R. G. ACS Reagent Ph.Eur. ≥99.5% 500mL
- CAS Number 110-86-1
- Empirical Formula (Hill Notation) C5H5N
- Molecular Weight 79.10
- Beilstein/REAXYS Number 103233
- EC Number 203-809-9
- MDL number MFCD00011732
- PubChem Substance ID 329754576
- NACRES NA.21
Grade | ACS reagent, Reagent. Ph. Eur. |
Vapor Density | 2.72 (vs air) |
Vapor Pressure | 10 mmHg (13.2°C) |
Grade | puriss. p.a. |
Assay | ≥99.5% (GC) |
Autoignition Temperature | 899°F |
Expl. Lim. | 12.4 % |
Impurities | ≤0.0005% KMnO4 Red. matter (as O) |
Refractive Index | n20/D 1.509 (lit.) |
bp | 115°C (lit.) |
mp | −42°C (lit.) |
solubility | H2O: in accordance |
Density | 0.978 g/mL at 25°C (lit.) |
anion traces | chloride (Cl-): ≤5 Mg/kg |
cation traces | Al: ≤0.5 Mg/kg |
General description
Pyridine is a basic N-heterocyclic compound. It acts as a nitrogen donor ligand and forms many metal-pyridine complexes. Its complexes having tetrahedral and octahedral geometries can be differentiated by infrared spectral investigations.
Application
Pyridine (py) may be used in the preparation of vanadium oxide nanoparticles and iron benzenedicarboxylates, Fe(OH)(BDC)(py)0.85 (BDC = 1,4-benzenedicarboxylate, py = pyridine). It may be employed as a catalyst in Knoevenagel condensation reaction.
Safety Information
Signal word Danger
Hazard statements H225-H302 + H312 + H332-H315-H319
Precautionary statements P210-P280-P305 + P351 + P338
RIDADR UN1282 - class 3 - PG 2 - Pyridine
WGK Germany 2
RTECS UR8400000
Flash Point(F) 62.6°F
Flash Point(C) 17°C
Documents
Warnings
Note: These chemicals are for research & laboratory use only. Your order will not be processed if you do not work for, and ship to, a registered laboratory or research facility. Not for topical applications. An official Declaration of Use form may be required.
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General description Cyclohexane undergoes oxidation in the presence of various oxidants such as hydrogen peroxide, tert-butyl hydroperoxide and molecular oxygen.[2]
Application Cyclohexane has been used to prepare a 1.3M solution of sec-butyllithium.[3] It may be used as a starting Reagent for the synthesis of adipic acid[1] and ε-caprolactam.[1]