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Not to be confused with Pyrimidine.
Full structural formula of pyridine
Skeletal formula of pyridine, showing the numbering convention
Ball-and-stick diagram of pyridine
Space-filling model of pyridine
Pyridine sample.jpg
Preferred IUPAC name
Other names
110-86-1 YesY
3D model (Jmol) Interactive image
ChEMBL ChEMBL266158 YesY
ChemSpider 1020 YesY
ECHA InfoCard 100.003.464
EC Number 203-809-9
KEGG C00747 YesY
PubChem 1049
Molar mass 79.10 g·mol−1
Appearance colorless to yellow liquid[2]
Odor nauseating, fish-like[2]
Density 0.9819 g/mL[3]
Melting point −41.6 °C (−42.9 °F; 231.6 K)
Boiling point 115.2 °C (239.4 °F; 388.3 K)
Vapor pressure 16 mmHg (20 °C)[2]
Acidity (pKa) 5.25 (for the conjugate acid)[4][5]
Viscosity 0.88 cP
2.2 D[6]
Safety data sheet See: data page
Flammable (F)
Harmful (Xn)
R-phrases R20 R21 R22 R34 R36 R38
NFPA 704
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g., gasoline) Health code 3: Short exposure could cause serious temporary or residual injury. E.g., chlorine gas Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point 21 °C (70 °F; 294 K)
Explosive limits 1.8%–12.4%[2]
5 ppm (TWA)
Lethal dose or concentration (LD, LC):
891 mg/kg (rat, oral)
1500 mg/kg (mouse, oral)
1580 mg/kg (rat, oral)[7]
9000 ppm (rat, 1 hr)[7]
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 5 ppm (15 mg/m3)[2]
REL (Recommended)
TWA 5 ppm (15 mg/m3)[2]
IDLH (Immediate danger)
1000 ppm[2]
Related compounds
Related amines
Related compounds
Supplementary data page
Refractive index (n),
Dielectric constantr), etc.
Phase behaviour
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. The pyridine ring occurs in many important compounds, including azines and the vitamins niacin and pyridoxine.

Pyridine was discovered in 1849 by the Scottish chemist Thomas Anderson as one of the constituents of bone oil. Two years later, Anderson isolated pure pyridine through fractional distillation of the oil. It is a colorless, highly flammable, weakly alkaline, water-soluble liquid with a distinctive, unpleasant fish-like smell.

Pyridine is used as a precursor to agrochemicals and pharmaceuticals and is also an important solvent and reagent. Pyridine is added to ethanol to make it unsuitable for drinking (see denatured alcohol). It is used in the in vitro synthesis of DNA,[9] in the synthesis of sulfapyridine (a drug against bacterial and viral infections), antihistaminic drugs tripelennamine and mepyramine, as well as water repellents, bactericides, and herbicides. Some chemical compounds, although not synthesized from pyridine, contain its ring structure. They include B vitamins niacin and pyridoxal, the anti-tuberculosis drug isoniazid, nicotine and other nitrogen-containing plant products.[10] Historically, pyridine was produced from coal tar and as a byproduct of coal gasification. However, increased demand for pyridine resulted in the development of more economical methods of synthesis from acetaldehyde and ammonia, and more than 20,000 tonnes per year are manufactured worldwide.


Physical properties[edit]

Crystal structure of pyridine

Pyridine is a colorless liquid that boils at 115.2 °C and freezes at −41.6 °C. Its density, 0.9819 g/cm3, is close to that of water, and its refractive index is 1.5093 at a wavelength of 589 nm and a temperature of 20 °C.[11] Addition of up to 40 mol% of water to pyridine gradually lowers its melting point from −41.6 °C to −65.0 °C.[12] The molecular electric dipole moment is 2.2 debyes.[6] Pyridine is diamagnetic and has a diamagnetic susceptibility of −48.7 × 10−6 cm3·mol−1.[13] The standard enthalpy of formation is 100.2 kJ·mol−1 in the liquid phase[14] and 140.4 kJ·mol−1 in the gas phase. At 25 °C pyridine has a viscosity[15] of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1.[16][17] The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.[18] The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point.[19]

Pyridine crystallizes in an orthorhombic crystal system with space group Pna21 and lattice parameters a = 1752 pm, b = 897 pm, c = 1135 pm, and 16 formula units per unit cell (measured at 153 K). For comparison, crystalline benzene is also orthorhombic, with space group Pbca, a = 729.2 pm, b = 947.1 pm, c = 674.2 pm (at 78 K), but the number of molecules per cell is only 4.[20] This difference is partly related to the lower symmetry of the individual pyridine molecule (C2v vs. D6h for benzene). A trihydrate (pyridine·3H2O) is known; it also crystallizes in an orthorhombic system in the space group Pbca, lattice parameters a = 1244 pm, b = 1783 pm, c = 679 pm and eight formula units per unit cell (measured at 223 K).[12]

The critical parameters of pyridine are pressure 6.70 MPa, temperature 620 K and volume 229 cm3·mol−1.[21] In the temperature range 340–426 °C its vapor pressure p can be described with the Antoine equation

where T is temperature, A = 4.16272, B = 1371.358 K and C = −58.496 K.[22]

The optical absorption spectrum of pyridine in hexane contains three bands at the wavelengths of 195 nm (π → π* transition, molar absorptivity ε = 7500 L·mol−1·cm−1), 251 nm (π → π* transition, ε = 2000 L·mol−1·cm−1) and 270 nm (n → π* transition, ε = 450 L·mol−1·cm−1).[23] The 1H nuclear magnetic resonance (NMR) spectrum of pyridine contains three signals with the integral intensity ratio of 2:1:2 that correspond to the three chemically different protons in the molecule. These signals originate from the α-protons (positions 2 and 6, chemical shift 8.5 ppm), γ-proton (position 4, 7.5 ppm) and β-protons (positions 3 and 5, 7.1 ppm). The carbon analog of pyridine, benzene, has only one proton signal at 7.27 ppm. The larger chemical shifts of the α- and γ-protons in comparison to benzene result from the lower electron density in the α- and γ-positions, which can be derived from the resonance structures. The situation is rather similar for the 13C NMR spectra of pyridine and benzene: pyridine shows a triplet at δ(α-C) = 150 ppm, δ(β-C) = 124 ppm and δ(γ-C) = 136 ppm, whereas benzene has a single line at 129 ppm. All shifts are quoted for the solvent-free substances.[24] Pyridine is conventionally detected by the gas chromatography and mass spectrometry methods.[25]

Chemical properties[edit]

Pyridine is miscible with water and virtually all organic solvents.[11] It is weakly basic, and with hydrochloric acid it forms a crystalline hydrochloride salt that melts at 145–147 °C.[26] Most chemical properties of pyridine are typical of a heteroaromatic compound. In organic reactions, pyridine behaves both as a tertiary amine, undergoing protonation, alkylation, acylation, and N-oxidation at the nitrogen atom, and as an aromatic compound, undergoing nucleophilic substitutions.

Because of the electronegative nitrogen in the pyridine ring, the molecule is relatively electron deficient. It, therefore, enters less readily electrophilic aromatic substitution reactions, which are characteristic of benzene derivatives. However, unlike benzene and its derivatives, pyridine is more prone to nucleophilic substitution and metalation of the ring by strong organometallic bases.[27][28] The reactivity of pyridine can be distinguished for three chemical groups. With electrophiles, electrophilic substitution takes place where pyridine expresses aromatic properties. With nucleophiles, pyridine reacts at positions 2 and 4 and thus behaves similar to imines and carbonyls. The reaction with many Lewis acids results in the addition to the nitrogen atom of pyridine, which is similar to the reactivity of tertiary amines. The ability of pyridine and its derivatives to oxidize, forming amine oxides (N-oxides), is also a feature of tertiary amines.[29]

The nitrogen center of pyridine features a basic lone pair of electrons. Because this lone pair is not part of the aromatic ring, pyridine is a base, having chemical properties similar to those of tertiary amines. The pKa of the conjugate acid (the pyridinium cation) is 5.25. Pyridine is protonated by reaction with acids and forms a positively charged aromatic polyatomic ion called pyridinium. The bond lengths and bond angles in pyridine and pyridinium are almost identical.[30] The pyridinium cation is isoelectronic with benzene. Pyridinium p-toluenesulfonate (PPTS) is an illustrative pyridinium salt; it is produced by treating pyridine with p-toluenesulfonic acid.

Pyridine can act as Lewis base, donating its pair of electrons to a Lewis acid as in the sulfur trioxide pyridine complex.

Pyridine itself is a relatively weak ligand in forming complexes with transition metal ions. For example, it forms a 1:1 complexes with nickel(II), Ni2+, and copper(II), Cu2+, with log K1 values of around 1.9 and 2.6, respectively.[31] The infrared spectra of pyridine complexes have been discussed in detail.[32][33] Picolinic acid, which is a substituted derivative of pyridine, forms strong complexes due to the chelate effect; 2,2′-bipyridine and 1,10-phenanthroline, which can also be viewed as substituted derivatives of pyridine, also form strong complexes, such as in ferroin, which can be used as an redox indicator in the quantitative analysis of iron.[34]

The η6 coordination mode, as occurs in η6 benzene complexes, is observed only in sterically encumbered derivatives that block the nitrogen center.[35]

Molecular properties[edit]

Pyridine with its free electron pair

Pyridine has a conjugated system of six π electrons that are delocalized over the ring. The molecule is planar and, thus, follows the Hückel criteria for aromatic systems. In contrast to benzene, the electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. For this reason, pyridine has a dipole moment and a weaker resonant stabilization than benzene (resonance energy 117 kJ·mol−1 in pyridine vs. 150 kJ·mol−1 in benzene).[36] The electron localization in pyridine is also reflected in the shorter C–N ring bond (137 pm for the C–N bond in pyridine vs. 139 pm for C–C bond in benzene),[35] whereas the carbon–carbon bonds in the pyridine ring have the same 139 pm length as in benzene. These bond lengths lie between the values for the single and double bonds and are typical of aromatic compounds.

All the ring atoms in the pyridine molecule are sp2-hybridized. The nitrogen is involved in the π-bonding aromatic system using its unhybridized p orbital. The lone pair is in an sp2 orbital, projecting outward from the ring in the same plane as the σ bonds. As a result, the lone pair does not contribute to the aromatic system but importantly influences the chemical properties of pyridine, as it easily supports bond formation via an electrophilic attack. However, because of the separation of the lone pair from the aromatic system of the ring affects, the nitrogen atom cannot exhibit a positive mesomeric effect.

Many analogues of pyridine are known where N is replaced by other heteroatoms (see figure below). Substitution of one C–H in pyridine with a second N gives rise to the diazine heterocycles (C4H4N2), with the names pyridazine, pyrimidine, and pyrazine.

Bond lengths and angles of benzene, pyridine, phosphorine, arsabenzene, stibabenzene, and bismabenzene
Electron orbitals in pyridine
Resonance structures of pyridine
Electron orbitals in protonated pyridine


Impure pyridine was undoubtedly prepared by early alchemists by heating animal bones and other organic matter,[37] but the earliest documented reference is attributed to the Scottish scientist Thomas Anderson.[38][39] In 1849, Anderson examined the contents of the oil obtained through high-temperature heating of animal bones.[39] Among other substances, he separated from the oil a colorless liquid with unpleasant odor, from which he isolated pure pyridine two years later. He described it as highly soluble in water, readily soluble in concentrated acids and salts upon heating, and only slightly soluble in oils.

Owing to its flammability, Anderson named the new substance pyridine, after Greek: πῦρ (pyr) meaning fire. The suffix idine was added in compliance with the chemical nomenclature, as in toluidine, to indicate a carbon cycle containing a nitrogen atom.[40]

The chemical structure of pyridine was determined decades after its discovery. Wilhelm Körner (1869)[41] and James Dewar (1871)[42][43] suggested that, in analogy between quinoline and naphthalene, the structure of pyridine is derived from benzene by substituting one C–H unit with a nitrogen atom.[44][45] The suggestion by Körner and Dewar was later confirmed in an experiment where pyridine was reduced to piperidine with sodium in ethanol. In 1876, William Ramsay combined acetylene and hydrogen cyanide into pyridine in a red-hot iron-tube furnace. This was the first synthesis of a heteroaromatic compound.[25][46]

The contemporary methods of pyridine production had a low yield, and the increasing demand for the new compound urged to search for more efficient routes. A breakthrough came in 1924 when the Russian chemist Aleksei Chichibabin invented a pyridine synthesis reaction, which was based on inexpensive reagents.[47] This method is still used for the industrial production of pyridine.[48]


Pyridine is not abundant in nature, except for the leaves and roots of belladonna (Atropa belladonna)[49] and in marshmallow (Althaea officinalis).[50] Pyridine derivatives, however, are often part of biomolecules such as the eponymous pyridine nucleotides and alkaloids.

In daily life, trace amounts of pyridine are components of the volatile organic compounds that are produced in roasting and canning processes, e.g. in fried chicken,[51] sukiyaki,[52] roasted coffee,[53] potato chips,[54] and fried bacon.[55] Traces of pyridine can be found in Beaufort cheese,[56] vaginal secretions,[57] black tea,[58] saliva of those suffering from gingivitis,[59] and sunflower honey.[60] The smoke of tobacco[61][62] and cannabis[25] also contain small amounts of pyridine.


The systematic name of pyridine, within the Hantzsch–Widman nomenclature recommended by the IUPAC, is azine. However, systematic names for simple compounds are used very rarely; instead, heterocyclic nomenclature follows historically established common names. IUPAC discourages the use of azine in favor of pyridine.[63] The numbering of the ring atoms in pyridine starts at the nitrogen (see infobox). An allocation of positions by letter of the Greek alphabet (α-γ) and the substitution pattern nomenclature common for homoaromatic systems (ortho, meta, para) are used sometimes. Here α (ortho), β (meta), and γ (para) refer to the 2, 3, and 4 position, respectively. The systematic name for the pyridine derivatives is pyridinyl, wherein the position of the substituted atom is preceded by a number. However, here again the historical name pyridyl is encouraged by the IUPAC and used instead of the systematic name.[64] The cationic derivative formed by the addition of an electrophile to the nitrogen atom is called pyridinium.


Historically, pyridine was extracted from coal tar or obtained as a byproduct of coal gasification. The process was labor-consuming and inefficient: coal tar contains only about 0.1% pyridine,[65] and therefore a multi-stage purification was required, which further reduced the output. Nowadays, most pyridine is produced synthetically using various name reactions, and the major ones are discussed below.[48]

Chichibabin synthesis[edit]

The Chichibabin pyridine synthesis was reported in 1924 and is still in use in industry.[47] In its general form, the reaction can be described as a condensation reaction of aldehydes, ketones, α,β-unsaturated carbonyl compounds, or any combination of the above, in ammonia or ammonia derivatives.[66] In particular, unsubstituted pyridine is produced from formaldehyde and acetaldehyde, which are inexpensive and widely available. First, acrolein is formed in a Knoevenagel condensation from the acetaldehyde and formaldehyde. It is then condensed with acetaldehyde and ammonia into dihydropyridine, and then oxidized with a solid-state catalyst to pyridine. This process is carried out in a gas phase at 400–450 °C. The product consists of a mixture of pyridine, simple methylated pyridines (picoline), and lutidine; its composition depends on the catalyst used and can be adapted to the needs of the manufacturer. The catalyst is usually a transition metal salt such as cadmium(II) fluoride or manganese(II) fluoride, but cobalt and thallium compounds can also be used. The recovered pyridine is separated from byproducts in a multistage process.[48]

Formation of acrolein from acetaldehyde and formaldehyde
Condensation of pyridine from acrolein and acetaldehyde

Practical application of the traditional Chichibabin pyridine synthesis are limited by its consistently low yield, typically about 20%. This low yield, together with the high prevalence of byproducts, render unmodified forms of Chichibabin's method unpopular.[66]

Dealkylation of alkylpyridines[edit]

Pyridine can be prepared by dealkylation of alkylated pyridines, which are obtained as byproducts in the syntheses of other pyridines. The oxidative dealkylation is carried out either using air over vanadium(V) oxide catalyst,[67] by vapor-dealkylation on nickel-based catalyst,[68][69] or hydrodealkylation with a silver- or platinum-based catalyst.[70] Yields of pyridine up to be 93% can be achieved with the nickel-based catalyst.[48]

Hantzsch pyridine synthesis[edit]

The first major synthesis of pyridine derivatives was described in 1881 by Arthur Rudolf Hantzsch.[71] The Hantzsch pyridine synthesis typically uses a 2:1:1 mixture of a β-keto acid (often acetoacetate), an aldehyde (often formaldehyde), and ammonia or its salt as the nitrogen donor. First, a double hydrogenated pyridine is obtained, which is then oxidized to the corresponding pyridine derivative. Emil Knoevenagel showed that asymmetrically-substituted pyridine derivatives can be produced with this process.[72]

Hantzsch pyridine synthesis with acetoacetate, formaldehyde and ammonium acetate, and iron(III) chloride as the catalyst.

Bönnemann cyclization[edit]

Bönnemann cyclization

The trimerization of a part of a nitrile molecule and two parts of acetylene into pyridine is called Bönnemann cyclization. This modification of the Reppe synthesis can be activated either by heat or by light. While the thermal activation requires high pressures and temperatures, the photoinduced cycloaddition proceeds at ambient conditions with CoCp2(cod) (Cp = cyclopentadienyl, cod = 1,5-cyclooctadiene) as a catalyst, and can be performed even in water.[73] A series of pyridine derivatives can be produced in this way. When using acetonitrile as the nitrile, 2-methylpyridine is obtained, which can be dealkylated to pyridine.

Other methods[edit]

The Kröhnke pyridine synthesis provides a fairly general method for generating substituted pyridines using pyridine itself as a reagent which does not become incorporated into the final product. The reaction of pyridine with α-bromoesters give the related pyridinium salt, wherein the methylene group is highly acidic. This species undergoes a Michael-like addition to α,β-unsaturated carbonyls in the presence of ammonium acetate to undergo ring closure and formation of the targeted substituted pyridine as well as pyridinium bromide.[74]

Figure 1

The Ciamician–Dennstedt rearrangement entails the ring-expansion of pyrrole with dichlorocarbene to 3-chloropyridine.[75][76][77]

Ciamician–Dennstedt Rearrangement

In the Gattermann–Skita synthesis,[78] a malonate ester salt reacts with dichloromethylamine.[79]

Gattermann–Skita synthesis

Another method is the Boger pyridine synthesis.


Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals. Mammals synthesize nicotinic acid through oxidation of the amino acid tryptophan, where an intermediate product, aniline, creates a pyridine derivative, kynurenine. On the contrary, the bacteria Mycobacterium tuberculosis and Escherichia coli produce nicotinic acid by condensation of glyceraldehyde 3-phosphate and aspartic acid.[80]


Many reactions that are characteristic of benzene proceed with pyridine either at more complicated conditions or with low yield or both. Owing to the decreased electron density in the aromatic system, electrophilic substitutions are suppressed in pyridine and its derivatives in favor of addition of nucleophiles at the electron-rich nitrogen atom. The nucleophilic addition at the nitrogen atom leads to a further deactivation of the aromatic properties and hindering of the electrophilic substitution. On the other hand, free-radical and nucleophilic substitutions occur more readily in pyridine than in benzene.[6][27]

Electrophilic substitutions[edit]

Many electrophilic substitutions on pyridine either do not proceed or proceed only partially; however, the heteroaromatic character can be activated by electron-donating functionalization. Common alkylations and acylations, such as Friedel–Crafts alkylation or acylation, usually fail for pyridine because they lead only to the addition at the nitrogen atom. Substitutions usually occur at the 3-position, which is the most electron-rich carbon atom in the ring and is, therefore, more susceptible to an electrophilic addition.

substitution in the 2-position
substitution in the 3-position
Substitution in 4-position
Structure of pyridine N-oxide

Substitutions to pyridine at the 2- or 4-position result in an energetically unfavorable σ complex. They can be promoted, however, using experimental techniques, such as conducting electrophilic substitution on the pyridine N-oxide followed by deoxygenation of the nitrogen atom. Addition of oxygen reduces electron density on the nitrogen atom and promotes substitution at the 2- and 4-carbons. The oxygen atom can then be removed via several routes, most commonly with compounds of trivalent phosphorus or divalent sulfur, which are easily oxidized. Triphenylphosphine is a frequently used reagent, which is oxidized in this reaction to triphenylphosphine oxide. The following paragraphs describe representative electrophilic substitution reactions of pyridine.[27]

Direct nitration of pyridine requires harsh conditions and has very low yields. The 3-nitropyridine can be obtained instead by reacting pyridine with dinitrogen pentoxide in presence of sodium.[81][82][83] Pyridine derivatives wherein the nitrogen atom is screened sterically and/or electronically can be obtained by nitration with nitronium tetrafluoroborate (NO2BF4). In this way, 3-nitropyridine can be obtained via the synthesis of 2,6-dibromopyridine followed by removal of the bromine atoms.[84][85] Direct sulfonation of pyridine is even more difficult than direct nitration. However, pyridine-3-sulfonic acid can be obtained at acceptable yield by boiling pyridine in an excess of sulfuric acid at 320 °C.[86] Reaction with the SO3 group also facilitates addition of sulfur to the nitrogen atom, especially in the presence of a mercury(II) sulfate catalyst.[27][87]

In contrast to the nitration and sulfonation, the direct bromination and chlorination of pyridine proceed well. The reaction of pyridine with molecular bromine in sulfuric acid at 130 °C readily produced 3-bromopyridine. The yield is lower for 3-chloropyridine upon chlorination with molecular chlorine in the presence of aluminium chloride at 100 °C. Both 2-bromopyridine and 2-chloropyridine can be produced by direct reaction with halogen with a palladium(II) chloride catalyst.[88]

Nucleophilic substitutions[edit]

In contrast to benzene, pyridine efficiently supports several nucleophilic substitutions. The reason for this is relatively lower electron density of the carbon atoms of the ring. These reactions include substitutions with elimination of a hydride ion and elimination-additions with formation of an intermediate aryne configuration, and usually proceed at the 2- or 4-position.[27][28]

Nucleophilic substitution in 2-position
Nucleophilic substitution in 3-position
Nucleophilic substitution in 4-position

Many nucleophilic substitutions occur more easily not with bare pyridine but with pyridine modified with bromine, chlorine, fluorine, or sulfonic acid fragments that then become a leaving group. So fluorine is the best leaving group for the substitution with organolithium compounds. The nucleophilic attack compounds may be alkoxides, thiolates, amines, and ammonia (at elevated pressures).[89]

In general, the hydride ion is a poor leaving group and occurs only in a few heterocyclic reactions. They include the Chichibabin reaction, which yields pyridine derivatives aminated at the 2-position. Here, sodium amide is used as the nucleophile yielding 2-aminopyridine. The hydride ion released in this reaction combines with a proton of an available amino group, forming a hydrogen molecule.[28][90]

Analogous to benzene, nucleophilic substitutions to pyridine can result in the formation of pyridyne intermediates as heteroaryne. For this purpose, pyridine derivatives can be eliminated with good leaving groups using strong bases such as sodium and potassium tert-butoxide. The subsequent addition of a nucleophile to the triple bond has low selectivity, and the result is a mixture of the two possible adducts.[27]

Radical reactions[edit]

Pyridine supports a series of radical reactions, which is used in its dimerization to bipyridines. Radical dimerization of pyridine with elemental sodium or Raney nickel selectively yields 4,4′-bipyridine,[91] or 2,2′-bipyridine,[92] which are important precursor reagents in the chemical industry. One of the name reactions involving free radicals is the Minisci reaction. It can produce 2-tert-butylpyridine upon reacting pyridine with pivalic acid, silver nitrate and ammonium in sulfuric acid with a yield of 97%.[27]

Reactions on the nitrogen atom[edit]

Additions of various Lewis acids to pyridine

Lewis acids easily add to the nitrogen atom of pyridine, forming pyridinium salts. The reaction with alkyl halides leads to alkylation of the nitrogen atom. This creates a positive charge in the ring that increases the reactivity of pyridine to both oxidation and reduction. The Zincke reaction is used for the selective introduction of radicals in pyridinium compounds (it has no relation to the chemical element zinc).

Hydrogenation and reduction[edit]

Reduction of pyridine to piperidine with Raney nickel

Hydrogen-saturated piperidine is obtained through reaction with hydrogen gas in the presence of Raney nickel.[93] This reaction releases 193.8 kJ·mol−1 of energy,[94] which is slightly less than the energy of the hydrogenation of benzene (205.3 kJ·mol−1).[94]

Partially hydrogenated derivatives are obtained under milder conditions. For example, reduction with lithium aluminium hydride yields a mixture of 1,4-dihydropyridine, 1,2-dihydropyridine, and 2,5-dihydropyridine.[95] Selective synthesis of 1,4-dihydropyridine is achieved in the presence of organometallic complexes of magnesium and zinc,[96] and (Δ3,4)-tetrahydropyridine is obtained by electrochemical reduction of pyridine.[97]


Use of pyridine in the chemical industry, VEB Berlin-Chemie, 1959.

Pyridine is an important raw material in the chemical industry, with the 1989 production of 26,000 tonnes worldwide.[48] Among the largest 25 production sites for pyridine, eleven are located in Europe (as of 1999).[25] The major producers of pyridine include Evonik Industries, Rütgers Chemicals, Imperial Chemical Industries, and Koei Chemical.[48] Pyridine production has significantly increased in the early 2000s, with an annual production capacity of 30,000 tonnes in mainland China alone.[98] The US–Chinese joint venture Vertellus is currently the world leader in pyridine production.[99]


The main use of pyridine is as a precursor to the herbicides paraquat and diquat.[48] The first synthesis step of insecticide chlorpyrifos consists of the chlorination of pyridine. Pyridine is also the starting compound for the preparation of pyrithione-based fungicides.[25] Cetylpyridinium and laurylpyridinium, which can be produced from pyridine with a Zincke reaction, are used as antiseptic in oral and dental care products.[6] Pyridine is easily attacked by alkylating agents to give N-alkylpyridinium salts. One example is cetylpyridinium chloride.

Synthesis of paraquat[100]


Pyridine is used as a polar, basic, low-reactive solvent, for example in Knoevenagel condensations.[25] It is especially suitable for the dehalogenation, where it acts as the base of the elimination reaction and bonds the resulting hydrogen halide to form a pyridinium salt. In esterifications and acylations, pyridine activates the carboxylic acid halides or anhydrides. Even more active in these reactions are the pyridine derivatives 4-dimethylaminopyridine (DMAP) and 4-(1-pyrrolidinyl) pyridine. Pyridine is also used as a base in condensation reactions.[101]

Elimination reaction with pyridine to form pyridinium

Pyridine is used as a solvent in the manufacture of dyes and rubber.[102] It is also used in the textile industry to improve network capacity of cotton.[6] Pyridine is added to ethanol to make it unsuitable for drinking.[6] In low doses, pyridine is added to foods to give them a bitter flavor, and such usage is approved by the US Food and Drug Administration.[25] The detection threshold for pyridine in solutions is about 1–3 mmol·L−1 (79–237 mg·L−1).[103] As a base, pyridine can be used as the Karl Fischer reagent, but it is usually replaced by alternatives with a more pleasant odor, such as imidazole.[104]

Precursor to piperidine[edit]

Piperidine, a fundamental nitrogen heterocycle, is important synthetic building-block. Piperidines are produced by hydrogenation of pyridine with a nickel-, cobalt-, or ruthenium-based catalyst at elevated temperatures.[105]

Specialty reagents based on pyridine[edit]

Pyridinium chlorochromate was developed by Elias James Corey and William Suggs in 1975 and is used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones.[106] It is obtained by adding pyridine to a solution of chromic acid and concentrated hydrochloric acid:

C5H5N + HCl + CrO3 → [C5H5NH][CrO3Cl]

The carcinogenicity of the side-product chromyl chloride (CrO2Cl2) urged to look for alternative routes, such as treating chromium(VI) oxide with pyridinium chloride:[107]

[C5H5NH+]Cl + CrO3 → [C5H5NH][CrO3Cl]

The Cornforth reagent (pyridinium dichromate, PDC),[108] pyridinium chlorochromate (PCC), the Collins reagent (complex of chromium(VI) oxide with pyridine in dichloromethane)[109][110] and the Sarret reagent (complex of chromium(VI) oxide with pyridine in pyridine) are similar chromium-based pyridine compounds, which are also used for oxidation, namely conversion of primary and secondary alcohols to ketones. The Collins and Sarret reagents are both difficult and dangerous to prepare, they are hygroscopic and can inflame during preparation. For this reason, the use of PCC and PDC was preferred. Those reagents were rather popular in the 1970s and 1980s, but because of their toxicity and confirmed carcinogenic status, they are rarely used nowadays.[111]

Oxidation of an alcohol to aldehyde with the Collins reagent.

Ligand and Lewis base[edit]

structure of the Crabtree's catalyst

Pyridine is widely used as a ligand in coordination chemistry, as are its derivative 2,2′-bipyridine, consisting of two pyridine molecules joined by a single bond, and terpyridine, a molecule of three pyridine rings linked together.

When a pyridine ligand is part of a metal complex, it can be easily replaced by a stronger Lewis base. This property is exploited in catalysis of polymerization[112][113] and hydrogenation reactions, using, for example, Crabtree's catalyst.[114] The pyridine ligand replaced during the reaction is restored after its completion.

Useful adducts of pyridine include pyridine-borane, C5H5NBH3 (melting point 10–11 °C), a mild reducing agent with improved stability relative to NaBH4 in protic solvents and improved solubility in aprotic organic solvents. Pyridine-sulfur trioxide, C5H5NSO3 (melting point 175 °C) is a sulfonation agent used to convert alcohols to sulfonates, which in turn undergo C–O bond scission upon reduction with hydride agents.


Pyridine has a flash point (the lowest temperature at which it can vaporize to form an ignitable mixture in air) of only 17 °C and is, therefore, highly flammable. Its ignition temperature is 550 °C, and mixtures of 1.7–10.6 vol% of pyridine with air are explosive. The thermal modification of pyridine starts above 490 °C, resulting in bipyridine (mainly 2,2′-bipyridine and to a lesser extent 2,3′-bipyridine and 2,4′-bipyridine), nitrogen oxides, and carbon monoxide.[17] Pyridine easily dissolves in water and harms both animals and plants in aquatic systems.[115] The permitted maximum allowable concentration of pyridine was 15–30 parts per million (ppm, or 15–30 mg·m−3 in air) in most countries in the 1990s,[25] but was reduced to 5 ppm in the 2000s.[116] For comparison, indoor air contaminated with tobacco smoke may contain up to 16 µg·m−3 of pyridine, and one cigarette contains 21–32 µg.[25]

Health issues[edit]

Metabolism of pyridine

Pyridine is harmful if inhaled, swallowed or absorbed through the skin.[117] Effects of acute pyridine intoxication include dizziness, headache, lack of coordination, nausea, salivation, and loss of appetite. They may progress into abdominal pain, pulmonary congestion and unconsciousness.[118] One person died after accidental ingestion of half a cup of pyridine.[25] The lowest known lethal dose (LDLo) for the ingestion of pyridine in humans is 500 mg·kg−1. In high doses, pyridine has a narcotic effect and its vapor concentrations of above 3600 ppm pose a health risk.[48] The oral LD50 in rats is 891 mg·kg−1. Pyridine is flammable.

Evaluations as a possible carcinogenic agent showed that there is inadequate evidence in humans for the carcinogenicity of pyridine, although there is limited evidence of carcinogenic effects on animals.[118] Available data indicate that "exposure to pyridine in drinking-water led to reduction of sperm motility at all dose levels in mice and increased estrous cycle length at the highest dose level in rats".[118]

Pyridine might also have minor neurotoxic, genotoxic, and clastogenic effects.[17][25][119] Exposure to pyridine would normally lead to its inhalation and absorption in the lungs and gastrointestinal tract, where it either remains unchanged or is metabolized. The major products of pyridine metabolism are N-methylpyridiniumhydroxide, which are formed by N-methyltransferases (e.g., pyridine N-methyltransferase), as well as pyridine N-oxide, and 2-, 3-, and 4-hydroxypyridine, which are generated by the action of monooxygenase. In humans, pyridine is metabolized only into N-methylpyridiniumhydroxide.[17][119] Pyridine is readily degraded by bacteria to ammonia and carbon dioxide.[120] The unsubstituted pyridine ring degrades more rapidly than picoline, lutidine, chloropyridine, or aminopyridines,[121] and a number of pyridine degraders have been shown to overproduce riboflavin in the presence of pyridine.[122] Ionizable N-heterocyclic compounds, including pyridine, interact with environmental surfaces (such as soils and sediments) via multiple pH-dependent mechanisms, including partitioning to soil organic matter, cation exchange, and surface complexation.[123] Such adsorption to surfaces reduces bioavailability of pyridines for microbial degraders and other organisms, thus slowing degradation rates and reducing ecotoxicity.[124]

Minor amounts of pyridine are released into environment from some industrial processes such as steel manufacture,[125] processing of oil shale, coal gasification, coking plants and incinerators.[25] The atmosphere at oil shale processing plants can contain pyridine concentrations of up to 13 µg·m−3,[126] and 53 µg·m−3 levels were measured in the groundwater in the vicinity of a coal gasification plant.[127] According to a study by the US National Institute for Occupational Safety and Health, about 43,000 Americans work in contact with pyridine.[128]

See also[edit]


  1. ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 141. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. 
  2. ^ a b c d e f g "NIOSH Pocket Guide to Chemical Hazards #0541". National Institute for Occupational Safety and Health (NIOSH). 
  3. ^ Lide, p. 3-474
  4. ^ Linnell, Robert (1960). "Notes – Dissociation Constants of 2-Substituted Pyridines". Journal of Organic Chemistry. 25 (2): 290. doi:10.1021/jo01072a623. 
  5. ^ Pearson, Ralph G.; Williams, Forrest V. (1953). "Rates of Ionization of Pseudo Acids.1V. Steric Effects in the Base-catalyzed Ionization of Nitroethane". Journal of the American Chemical Society. 75 (13): 3073. doi:10.1021/ja01109a008. 
  6. ^ a b c d e f RÖMPP Online – Version 3.5. Thieme Chemistry. Stuttgart: Georg Thieme. 2009. 
  7. ^ a b "Pyridine". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH). 
  8. ^ "Pyridine MSDS". Fisher. 
  9. ^ "Iodine Solution (0.02 M in THF/pyridine/H2O 70:20:10)". Sigma-Aldrich. Retrieved 28 November 2011. 
  10. ^ "Pyridine". Encyclopædia Britannica Online. 
  11. ^ a b Lide, p. 3-448
  12. ^ a b Mootz, D. (1981). "Crystal structures of pyridine and pyridine trihydrate". The Journal of Chemical Physics. 75 (3): 1517. Bibcode:1981JChPh..75.1517M. doi:10.1063/1.442204. 
  13. ^ Lide, p. 3-673
  14. ^ Lide, p. 5-28
  15. ^ Lide, p. 6-211
  16. ^ Lide, p. 6-221
  17. ^ a b c d Record of Pyridine in the GESTIS Substance Database of the IFA
  18. ^ Majer, V.; Svoboda, V. (1985). Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation. Oxford: Blackwell Scientific Publications. ISBN 0-632-01529-2. 
  19. ^ Domalski, Eugene S.; Hearing, Elizabeth D. (1996). "Heat Capacities and Entropies of Organic Compounds in the Condensed Phase". Journal of Physical and Chemical Reference Data. 25: 1. Bibcode:1996JPCRD..25....1D. doi:10.1063/1.555985. 
  20. ^ Cox, E. (1958). "Crystal Structure of Benzene". Reviews of Modern Physics. 30: 159. Bibcode:1958RvMP...30..159C. doi:10.1103/RevModPhys.30.159. 
  21. ^ Lide, p. 6-67
  22. ^ McCullough, J. P.; Douslin, D. R.; Messerly, J. F.; Hossenlopp, I. A.; Kincheloe, T. C.; Waddington, Guy (1957). "Pyridine: Experimental and Calculated Chemical Thermodynamic Properties between 0 and 1500 °K.; a Revised Vibrational Assignment". Journal of the American Chemical Society. 79 (16): 4289. doi:10.1021/ja01573a014. 
  23. ^ Joule, p. 14
  24. ^ Joule, p. 16
  25. ^ a b c d e f g h i j k l "Pyridine" (PDF). IARC Monographs 77. Washington DC: OSHA. 1985. 
  26. ^ "Pyridine hydrochloride MSDS" (PDF). Alfa Aesar. Retrieved 26 June 2010. 
  27. ^ a b c d e f g Joule, pp. 125–141
  28. ^ a b c Davies, D. T. (1992). Aromatic Heterocyclic Chemistry. Oxford University Press. ISBN 0-19-855660-8. 
  29. ^ Milcent, R.; Chau, F. (2002). Chimie organique hétérocyclique: Structures fondamentales. EDP Sciences. pp. 241–282. ISBN 2-86883-583-X. 
  30. ^ Krygowski, T. M.; Szatyowicz, H.; Zachara, J. E. (2005). "How H-bonding Modifies Molecular Structure and π-Electron Delocalization in the Ring of Pyridine/Pyridinium Derivatives Involved in H-Bond Complexation". J. Org. Chem. 70 (22): 8859–8865. doi:10.1021/jo051354h. PMID 16238319. 
  31. ^ "IUPAC SC-Database: A comprehensive database of published data on equilibrium constants of metal complexes and ligands". 
  32. ^ Nakamoto, K. (1997). Infrared and Raman spectra of Inorganic and Coordination compounds. Part A (5th ed.). Wiley. ISBN 0-471-16394-5. 
  33. ^ Nakamoto, K. Infrared and Raman spectra of Inorganic and Coordination compounds. Part B (5th ed.). p. 24. ISBN 0-471-16392-9. 
  34. ^ Mendham, J.; Denney, R. C.; Barnes, J. D.; Thomas, M. J. K. (2000), Vogel's Quantitative Chemical Analysis (6th ed.), New York: Prentice Hall, p. 418, ISBN 0-582-22628-7 
  35. ^ a b Elschenbroich, C. (2008). Organometallchemie (6th ed.). Vieweg & Teubner. pp. 524–525. ISBN 3-8351-0167-6. 
  36. ^ Joule, p. 7
  37. ^ Weissberger, A.; Klingberg, A.; Barnes, R. A.; Brody, F.; Ruby, P.R. (1960). Pyridine and its Derivatives. 1. New York: Interscience. 
  38. ^ Anderson, T. (1849). Transactions of the Royal Society of Edinburgh. 16: 123.
  39. ^ a b Anderson, T. (1849). "Producte der trocknen Destillation thierischer Materien" [Products of the dry distillation of animal matter]. Annalen der Chemie und Pharmacie. 70: 32. doi:10.1002/jlac.18490700105. 
  40. ^ Anderson, T. (1851). "Ueber die Producte der trocknen Destillation thierischer Materien" [On the products of dry distillation of animal matter]. Annalen der Chemie und Pharmacie. 80: 44. doi:10.1002/jlac.18510800104. 
  41. ^ Körner, W. (1869). Giornale academico di Palermo. 5.
  42. ^ Dewar, J. (1871). Chemical News. 23: 38.
  43. ^ Rocke, Alan J. (1988). "Koerner, Dewar and the Structure of Pyridine". Bulletin for the History of Chemistry. 2: 4.  open access publication - free to read
  44. ^ Ladenburg, Albert. Lectures on the history of the development of chemistry since the time of Lavoisier. (PDF). pp. 283–287.  open access publication - free to read
  45. ^ Bansal, Raj K. (1999). Heterocyclic Chemistry. p. 216. ISBN 81-224-1212-2. 
  46. ^ "A. Henninger, aus Paris. 12. April 1877". Berichte der deutschen chemischen Gesellschaft (Correspondence). 10: 727. 1877. doi:10.1002/cber.187701001202. 
  47. ^ a b Chichibabin, A. E. (1924). "Über Kondensation der Aldehyde mit Ammoniak zu Pyridinebasen" [On condensation of aldehydes with ammonia to make pyridines]. Journal für Praktische Chemie. 107: 122. doi:10.1002/prac.19241070110. 
  48. ^ a b c d e f g h Shimizu, S.; Watanabe, N.; Kataoka, T.; Shoji, T.; Abe, N.; Morishita, S.; Ichimura, H. (2005), "Pyridine and Pyridine Derivatives", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a22_399 
  49. ^ Burdock, G. A., ed. (1995). Fenaroli's Handbook of Flavor Ingredients. 2 (3rd ed.). Boca Raton: CRC Press. ISBN 0-8493-2710-5. 
  50. ^ Täufel, A.; Ternes, W.; Tunger, L.; Zobel, M. (2005). Lebensmittel-Lexikon (4th ed.). Behr. p. 450. ISBN 3-89947-165-2. 
  51. ^ Tang, Jian; Jin, Qi Zhang; Shen, Guo Hui; Ho, Chi Tang; Chang, Stephen S. (1983). "Isolation and identification of volatile compounds from fried chicken". Journal of Agricultural and Food Chemistry. 31 (6): 1287. doi:10.1021/jf00120a035. 
  52. ^ Shibamoto, Takayuki; Kamiya, Yoko; Mihara, Satoru (1981). "Isolation and identification of volatile compounds in cooked meat: sukiyaki". Journal of Agricultural and Food Chemistry. 29: 57. doi:10.1021/jf00103a015. 
  53. ^ Aeschbacher, HU; Wolleb, U; Löliger, J; Spadone, JC; Liardon, R (1989). "Contribution of coffee aroma constituents to the mutagenicity of coffee". Food and Chemical Toxicology. 27 (4): 227–232. doi:10.1016/0278-6915(89)90160-9. PMID 2659457. 
  54. ^ Buttery, Ron G.; Seifert, Richard M.; Guadagni, Dante G.; Ling, Louisa C. (1971). "Characterization of Volatile Pyrazine and Pyridine Components of Potato Chips". Journal of Agricultural and Food Chemistry. Washington, DC: ACS. 19 (5): 969–971. doi:10.1021/jf60177a020. 
  55. ^ Ho, Chi Tang; Lee, Ken N.; Jin, Qi Zhang (1983). "Isolation and identification of volatile flavor compounds in fried bacon". Journal of Agricultural and Food Chemistry. 31 (2): 336. doi:10.1021/jf00116a038. 
  56. ^ Dumont, Jean Pierre; Adda, Jacques (1978). "Occurrence of sesquiterpene in mountain cheese volatiles". Journal of Agricultural and Food Chemistry. 26 (2): 364. doi:10.1021/jf60216a037. 
  57. ^ Labows, John N., Jr.; Warren, Craig B., (1981). "Odorants as Chemical Messengers". In Moskowitz, Howard R. Odor Quality and Chemical Structure. Washington, DC: American Chemical Society. pp. 195–210. doi:10.1021/bk-1981-0148.fw001. ISBN 9780841206076. 
  58. ^ Vitzthum, Otto G.; Werkhoff, Peter; Hubert, Peter (1975). "New volatile constituents of black tea flavor". Journal of Agricultural and Food Chemistry. 23 (5): 999. doi:10.1021/jf60201a032. 
  59. ^ Kostelc, J. G.; Preti, G.; Nelson, P. R.; Brauner, L.; Baehni, P. (1984). "Oral Odors in Early Experimental Gingivitis". Journal of Periodontology Research. 19 (3): 303–312. doi:10.1111/j.1600-0765.1984.tb00821.x. PMID 6235346. 
  60. ^ Täufel, A.; Ternes, W.; Tunger, L.; Zobel, M. (2005). Lebensmittel-Lexikon (4th ed.). Behr. p. 226. ISBN 3-89947-165-2. 
  61. ^ Curvall, Margareta; Enzell, Curt R.; Pettersson, Bertil (1984). "An evaluation of the utility of four in vitro short term tests for predicting the cytotoxicity of individual compounds derived from tobacco smoke". Cell Biology and Toxicology. 1 (1): 173–193. doi:10.1007/BF00125573. PMID 6400922. 
  62. ^ Schmeltz, Irwin; Hoffmann, Dietrich (1977). "Nitrogen-containing compounds in tobacco and tobacco smoke". Chemical Reviews. 77 (3): 295. doi:10.1021/cr60307a001. 
  63. ^ Powell, W. H. (1983). "Revision of the extended Hantzsch-Widman system of nomenclature for hetero mono-cycles" (PDF). Pure and Applied Chemistry. 55 (2): 409–416. doi:10.1351/pac198855020409. 
  64. ^ Hellwinkel, D. (1998). Die systematische Nomenklatur der Organischen Chemie (4th ed.). Berlin: Springer. p. 45. ISBN 3-540-63221-2. 
  65. ^ Gossauer, A. (2006). Struktur und Reaktivität der Biomoleküle. Weinheim: Wiley-VCH. p. 488. ISBN 3-906390-29-2. 
  66. ^ a b Frank, R. L.; Seven, R. P. (1949). "Pyridines. IV. A Study of the Chichibabin Synthesis". Journal of the American Chemical Society. 71 (8): 2629–2635. doi:10.1021/ja01176a008. 
  67. ^ DE patent 1917037, ICI, issued 1968 
  68. ^ JP patent 7039545, Nippon Kayaku, issued 1967 
  69. ^ BE patent 758201, Koei Chemicals, issued 1969 
  70. ^ Mensch, F. (1969). Erdöl Kohle Erdgas Petrochemie. 2: 67–71
  71. ^ Hantzsch, A. (1881). "Condensationsprodukte aus Aldehydammoniak und ketonartigen Verbindungen" [Condensation products from aldehyde ammonia and ketone-type compounds]. Berichte der deutschen chemischen Gesellschaft. 14 (2): 1637. doi:10.1002/cber.18810140214. 
  72. ^ Knoevenagel, E.; Fries, A. (1898). "Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese" [Syntheses in the pyridine series. On an extension of the Hantzsch dihydropyridine synthesis]. Berichte der deutschen chemischen Gesellschaft. 31: 761. doi:10.1002/cber.189803101157. 
  73. ^ Behr, A. (2008). Angewandte homogene Katalyse. Weinheim: Wiley-VCH. p. 722. ISBN 3-527-31666-3. 
  74. ^ Kroehnke, Fritz (1976). "The Specific Synthesis of Pyridines and Oligopyridines". Synthesis. 1976 (1): 1–24. doi:10.1055/s-1976-23941. .
  75. ^ Skell, P. S.; Sandler, R. S. (1958). "Reactions of 1,1-Dihalocyclopropanes with Electrophilic Reagents. Synthetic Route for Inserting a Carbon Atom Between the Atoms of a Double Bond". Journal of the American Chemical Society. 80 (8): 2024. doi:10.1021/ja01541a070. 
  76. ^ Jones, R. L.; Rees, C. W. (1969). "Mechanism of heterocyclic ring expansions. Part III. Reaction of pyrroles with dichlorocarbene". Journal of the Chemical Society C: Organic (18): 2249. doi:10.1039/J39690002249. 
  77. ^ Gambacorta, A.; Nicoletti, R.; Cerrini, S.; Fedeli, W.; Gavuzzo, E. (1978). "Trapping and structure determination of an intermediate in the reaction between 2-methyl-5-t-butylpyrrole and dichlorocarbene". Tetrahedron Letters. 19 (27): 2439. doi:10.1016/S0040-4039(01)94795-1. 
  78. ^ Gattermann, L.; Skita, A. (1916). "Eine Synthese von Pyridin-Derivaten" [A synthesis of pyridine derivatives]. Chemische Berichte. 49 (1): 494–501. doi:10.1002/cber.19160490155. 
  79. ^ "Gattermann–Skita". Institute of Chemistry, Skopje. Archived from the original on 2006-06-16. 
  80. ^ Tarr, J. B.; Arditti, J. (1982). "Niacin Biosynthesis in Seedlings of Zea mays". Plant Physiology. 69 (3): 553–556. doi:10.1104/pp.69.3.553. PMC 426252Freely accessible. PMID 16662247. 
  81. ^ Joule, p. 129
  82. ^ Bakke, Jan M.; Hegbom, Ingrid; Verne, Hans Peter; Weidlein, Johann; Schnöckel, Hansgeorg; Paulsen, Gudrun B.; Nielsen, Ruby I.; Olsen, Carl E.; Pedersen, Christian; Stidsen, Carsten E. (1994). "Dinitrogen Pentoxide-Sulfur Dioxide, a New nitrate ion system". Acta Chemica Scandinavica. 48: 181. doi:10.3891/acta.chem.scand.48-0181. 
  83. ^ Ono, Noboru; Murashima, Takashi; Nishi, Keiji; Nakamoto, Ken-Ichi; Kato, Atsushi; Tamai, Ryuji; Uno, Hidemitsu (2002). "Preparation of Novel Heteroisoindoles from nitropyridines and Nitropyridones". Heterocycles. 58: 301. doi:10.3987/COM-02-S(M)22. 
  84. ^ Duffy, Joseph L.; Laali, Kenneth K. (1991). "Aprotic Nitration (NO+
    ) of 2-Halo- and 2,6-Dihalopyridines and Transfer-Nitration Chemistry of Their N-Nitropyridinium Cations". The Journal of Organic Chemistry. 56 (9): 3006. doi:10.1021/jo00009a015.
  85. ^ Joule, p. 126
  86. ^ Gabriel, S. (1882). "Note on nicotinic acid from pyridine". Berichte der deutschen chemischen Gesellschaft. 15: 834. doi:10.1002/cber.188201501180. 
  87. ^ Möller, Ernst Friedrich; Birkofer, Leonhard (1942). "Konstitutionsspezifität der Nicotinsäure als Wuchsstoff bei Proteus vulgaris und Streptobacterium plantarum" [Constitutional specificity of nicotinic acid as a growth factor in Proteus vulgaris and Streptobacterium plantarum]. Berichte der deutschen chemischen Gesellschaft (A and B Series). 75 (9): 1108. doi:10.1002/cber.19420750912. 
  88. ^ Joule, p. 130
  89. ^ Joule, p. 133
  90. ^ Shreve, R. Norris; Riechers, E. H.; Rubenkoenig, Harry; Goodman, A. H. (1940). "Amination in the Heterocyclic Series by Sodium amide". Industrial & Engineering Chemistry. 32 (2): 173. doi:10.1021/ie50362a008. 
  91. ^ Badger, G; Sasse, W (1963). "The Action of Metal Catalysts on Pyridines". Advances in Heterocyclic Chemistry. Advances in Heterocyclic Chemistry. 2. p. 179. doi:10.1016/S0065-2725(08)60749-7. ISBN 9780120206025. 
  92. ^ Sasse, W. H. F. (1966). "2,2′-bipyridine" (PDF). Organic Syntheses. 46: 5–8. doi:10.1002/0471264180.os046.02. ISBN 0471264229. 
  93. ^ Burrows, George H.; King, Louis A. (1935). "The Free Energy Change that Accompanies Hydrogenation of pyridines to piperidines". Journal of the American Chemical Society. 57 (10): 1789. doi:10.1021/ja01313a011. 
  94. ^ a b Cox, J. D.; Pilcher, G. (1970). "Thermochemistry of Organic and Organometallic Compounds". New York: Academic Press: 1–636. ISBN 0-12-194350-X. 
  95. ^ Tanner, Dennis D.; Yang, Chi Ming (1993). "On the structure and mechanism of formation of the Lansbury reagent, lithium tetrakis(N-dihydropyridyl) aluminate". The Journal of Organic Chemistry. 58 (7): 1840. doi:10.1021/jo00059a041. 
  96. ^ De Koning, A.; Budzelaar, P. H. M.; Boersma, J.; Van Der Kerk, G. J. M. (1980). "Specific and selective reduction of aromatic nitrogen heterocycles with the bis-pyridine complexes of bis(1,4-dihydro-1-pyridyl)zinc and bis(1,4-dihydro-1-pyridyl)magnesium". Journal of Organometallic Chemistry. 199 (2): 153. doi:10.1016/S0022-328X(00)83849-8. 
  97. ^ Ferles, M. (1959). Collection of Czechoslovak Chemical Communications. 24: 1029–1033.
  98. ^ "Pyridine's Development in China". AgroChemEx. 11 May 2010. 
  99. ^ "About Vertellus". 
  100. ^ "Environmental and health criteria for paraquat and diquat". Geneva: World Health Organization. 1984. 
  101. ^ Sherman, A. R. (2004). "Pyridine". In Paquette, L. Encyclopedia of Reagents for Organic Synthesis. e-EROS (Encyclopedia of Reagents for Organic Synthesis). New York: J. Wiley & Sons. doi:10.1002/047084289X.rp280. ISBN 0471936235. 
  102. ^ Terry, C. E.; Ryan, R. P.; Leffingwell, S. S. Toxicology Desk Reference: The Toxic Exposure & Medical Monitoring Index: The Toxic Exposure and Medical Monitoring Index (5th ed.). Taylor & Francis. p. 1062. ISBN 1-56032-795-2. 
  103. ^ Täufel, A.; Ternes, W.; Tunger, L.; Zobel, M. (2005). Lebensmittel-Lexikon (4th ed.). Behr. p. 218. ISBN 3-89947-165-2. 
  104. ^ "Wasserbestimmung mit Karl-Fischer-Titration" [Water analysis with the Karl Fischer titration] (PDF). Jena University. 
  105. ^ Eller, K.; Henkes, E.; Rossbacher, R.; Hoke, H. (2005), "Amines, aliphatic", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH 
  106. ^ Corey, E. J.; Suggs, W. (1975). "Pyridinium Chlorochromate. An Efficient Reagent for Oxidation of Primary and Secondary Alcohols to Carbonyl Compounds". Tetrahedron Letters. 16 (31): 2647–2650. doi:10.1016/S0040-4039(00)75204-X. 
  107. ^ Agarwal, S; Tiwari, H. P.; Sharma, J. P. (1990). "Pyridinium Chlorochromate: an Improved Method for its Synthesis and use of Anhydrous acetic acid as catalyst for oxidation reactions". Tetrahedron. 46 (12): 4417–4420. doi:10.1016/S0040-4020(01)86776-4. 
  108. ^ Cornforth, R. H.; Cornforth, J. W.; Popjak, G. (1962). "Preparation of R- and S-mevalonolactones". Tetrahedron. 18 (12): 1351–1354. doi:10.1016/S0040-4020(01)99289-0. 
  109. ^ Collins, J. C.; Hess, W. W.; Frank, F. J. (1968). "Dipyridine-chromium(VI) oxide oxidation of alcohols in dichloromethane". Tetrahedron Lett. 9 (30): 3363–3366. doi:10.1016/S0040-4039(00)89494-0. 
  110. ^ Collins, J. C.; Hess, W. W. (1988). "Aldehydes from Primary Alcohols by Oxidation with Chromium Trioxide: Heptanal". Org. Synth. ; Coll. Vol., 6, p. 644 
  111. ^ Tojo, G.; Fernandez, M. (2006). Oxidation of alcohols to aldehydes and ketones: a guide to current common practice. New York: Springer. pp. 28, 29, 86. ISBN 0-387-23607-4. 
  112. ^ Bamford, C. H.; Tipper, C. F. H (1980). Comprehensive Chemical Kinetics: Non-radical Polymerisation. Amsterdam: Elsevier. ISBN 0-444-41252-2. 
  113. ^ Hopper, A. V. (2007). Recent Developments in Polymer Research. Nova Science. ISBN 1-60021-346-4. 
  114. ^ Crabtree, Robert (1979). "Iridium compounds in catalysis". Accounts of Chemical Research. 12 (9): 331. doi:10.1021/ar50141a005. 
  115. ^ "Database of the (EPA)". U.S. Environmental Protection Agency. 
  116. ^ "Pyridine MSDS" (PDF). Alfa Aesar. Retrieved 3 June 2010. 
  117. ^ Aylward, G (2008). SI Chemical Data (6th ed.). ISBN 978-0-470-81638-7. 
  118. ^ a b c International Agency for Research on Cancer (IARC) (22 August 2000). "Pyridine Summary & Evaluation". IARC Summaries & Evaluations. IPCS INCHEM. Retrieved 17 January 2007. 
  119. ^ a b Bonnard, N.; Brondeau, M. T.; Miraval, S.; Pillière, F.; Protois, J. C.; Schneider, O. "Pyridine" (PDF). Fiche Toxicologique (in French). INRS. 
  120. ^ Sims, G. K.; O'Loughlin, E. J. (1989). "Degradation of pyridines in the environment". CRC Critical Reviews in Environmental Control. 19 (4): 309–340. doi:10.1080/10643388909388372. 
  121. ^ Sims, G. K.; Sommers, L.E. (1986). "Biodegradation of pyridine derivatives in soil suspensions". Environmental Toxicology and Chemistry. 5 (6): 503–509. doi:10.1002/etc.5620050601. 
  122. ^ Sims, G. K.; O'Loughlin, E.J. (1992). "Riboflavin production during growth of Micrococcus luteus on pyridine". Applied and Environmental Microbiology. 58 (10): 3423–3425. PMC 183117Freely accessible. PMID 16348793. 
  123. ^ Bi, E.; Schmidt, T. C.; Haderlein, S. B. (2006). "Sorption of heterocyclic organic compounds to reference soils: column studies for process identification". Environ Sci Technol. 40 (19): 5962–5970. doi:10.1021/es060470e. PMID 17051786. 
  124. ^ O'Loughlin, E. J; Traina, S. J.; Sims, G. K. (2000). "Effects of sorption on the biodegradation of 2-methylpyridine in aqueous suspensions of reference clay minerals". Environmental Toxicology and Chemistry. 19 (9): 2168–2174. doi:10.1002/etc.5620190904. 
  125. ^ Junk, G. A.; Ford, C. S. (1980). "A review of organic emissions from selected combustion processes". Chemosphere. 9 (4): 187. doi:10.1016/0045-6535(80)90079-X. 
  126. ^ Hawthorne, Steven B.; Sievers, Robert E. (1984). "Emissions of organic air pollutants from shale oil wastewaters". Environmental Science & Technology. 18 (6): 483. Bibcode:1984EnST...18..483H. doi:10.1021/es00124a016. 
  127. ^ Stuermer, Daniel H.; Ng, Douglas J.; Morris, Clarence J. (1982). "Organic contaminants in groundwater near to underground coal gasification site in northeastern Wyoming". Environmental Science & Technology. 16 (9): 582. Bibcode:1982EnST...16..582S. doi:10.1021/es00103a009. 
  128. ^ National Occupational Exposure Survey 1981–83. Cincinnati, OH: Department of Health and Human Services, Public Health Service, Centers for Disease Control, National Institute for Occuptional Safety and Health. 


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