| Nitroglycerin | |
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1,2,3-Trinitroxypropane |
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2,3-Bis(nitrooxy)propyl nitrate |
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Other names
1,3-Dinitrooxypropan-2-yl nitrate |
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| Identifiers | |
| CAS number | 55-63-0 |
| PubChem | 4510 |
| ChemSpider | 4354 |
| UNII | G59M7S0WS3 |
| EC number | 200-240-8 |
| UN number | 0143, 0144, 1204, 3064, 3319 |
| DrugBank | DB00727 |
| KEGG | D00515 |
| MeSH | Nitroglycerin |
| ChEBI | CHEBI:28787 |
| ChEMBL | CHEMBL730 |
| ATC code | C01,C05AE01 |
| Beilstein Reference | 1802063 |
| Gmelin Reference | 165859 |
| Jmol-3D images | Image 1 Image 2 |
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| Properties | |
| Molecular formula | C3N3H5O9 |
| Molar mass | 227.0865 g mol−1 |
| Exact mass | 227.002578773 g mol−1 |
| Appearance | Colorless liquid |
| Density | 1.6 g cm−3 (at 15 °C) |
| Melting point |
14 °C, 287 K, 57 °F |
| Boiling point |
50-60 °C, 323-333 K, 122-140 °F (decomposes) |
| log P | 2.154 |
| Structure | |
| Coordination geometry |
Tetragonal at C1, C2, and C3 Trigonal planar at N7, N8, and N9 |
| Molecular shape | Tetrahedral at C1, C2, and C3 Dihedral at N7, N8, and N9 |
| Thermochemistry | |
| Std enthalpy of formation ΔfH |
-370 kJ mol-1 |
| Std enthalpy of combustion ΔcH |
-1.529 MJ mol-1 |
| Pharmacology | |
| Bioavailability | <1% |
| Routes of administration |
Intravenous, Oral, Sublingual, Topical, Transdermal |
| Metabolism | Hepatic |
| Elimination half-life |
3 min |
| Legal status | Pharmacist Only (S3)(AU) |
| Pregnancy category |
C(US) |
| Explosive data | |
| Shock sensitivity | high |
| Friction sensitivity | high |
| Explosive velocity | 7700 m s−1 |
| RE factor | 1.50 |
| Hazards | |
| EU Index | 603-034-00-X |
| EU classification | E (Explosive) T+ N |
| R-phrases | R3, R26/27/28, R33, R51/53 |
| S-phrases | (S1/2), S33, S35, S36/37, S45, S61 |
| NFPA 704 |
3
3
4
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| (verify) (what is: /?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Nitroglycerin (NG), also known as nitroglycerine, trinitroglycerin, trinitroglycerine, 1,2,3-trinitroxypropane and glyceryl trinitrate, is a heavy, colorless, oily, explosive liquid produced by nitrating glycerol. Since the 1860s, nitroglycerin has been used as an active ingredient in the manufacture of explosives, mostly dynamite, and as such it is employed in the construction, demolition, and mining industries. Similarly, since the 1880s, it has been used by the military as an active ingredient, and a gelatinizer for nitrocellulose, in some solid propellants, such as Cordite and Ballistite.
Nitroglycerin is also used medically as a vasodilator to treat heart conditions, such as angina and chronic heart failure. It is one of the oldest and most useful drugs for treating heart disease by shortening or even preventing attacks of angina pectoris. Nitroglycerin comes in forms of tablets, sprays or patches.[1] Nitroglycerin may be able to be used to help destroy prostate cancer.[2]
Contents |
Nitroglycerin was the first practical explosive ever produced that was stronger than black powder. Nitroglycerin was synthesized by the chemist Ascanio Sobrero in 1847, working under Théophile-Jules Pelouze at the University of Turin. Sobrero initially called his discovery pyroglycerine, and warned vigorously against its use as an explosive. It was later adopted as a commercially useful explosive by Alfred Nobel. Nobel experimented with several safer ways to handle the dangerous nitroglycerin after his younger brother Emil Oskar Nobel and several factory workers were killed in a nitroglycerin explosion at the Nobel's armaments factory in 1864 in Heleneborg, Sweden.[3]
One year later, Alfred Nobel founded Alfred Nobel & Company in Germany and built an isolated factory in the Krümmel hills of Geesthacht near Hamburg. This business exported a liquid combination of nitroglycerin and gunpowder called "Blasting Oil", but this was extremely unstable and difficult to handle, as shown in numerous catastrophes. The buildings of the Krümmel factory were destroyed twice.[4]
In April 1866, three crates of nitroglycerin were shipped to California for the Central Pacific Railroad, which planned to experiment with it as a blasting explosive to expedite the construction of the 1,659-foot (506 m)-long Summit Tunnel through the Sierra Nevada Mountains. One of these crates exploded, destroying a Wells Fargo company office in San Francisco and killing 15 people. This led to a complete ban on the transportation of liquid nitroglycerin in California. The on-site manufacture of nitroglycerin was thus required for the remaining hard-rock drilling and blasting required for the completion of the First Transcontinental Railroad in North America.[5]
Liquid nitroglycerin was widely banned elsewhere as well, and these legal problems led to Alfred Nobel and his company's developing dynamite in 1867. This was made by mixing nitroglycerin with diatomaceous earth (called kieselguhr) found in the Krümmel hills. Similar mixtures, such as "dualine" (1867), "lithofracteur" (1869), and "gelignite" (1875), were formed by mixing nitroglycerin with other inert absorbents, and many combinations were tried by other companies in attempts to get around Nobel's tightly-held patents for dynamite.
Dynamite mixtures containing nitrocellulose, which increases the viscosity of the mix, are commonly known as "gelatins".
Following the discovery that amyl nitrite helped alleviate chest pain, Dr. William Murrell experimented with the use of nitroglycerin to alleviate angina pectoris and to reduce the blood pressure. He began treating his patients with small doses of nitroglycerin in 1878, and this treatment was soon adopted into widespread use after Murrell published his results in the journal The Lancet in 1879. The medical establishment used the name "glyceryl trinitrate" or "trinitrin" to avoid alarming patients who associated nitroglycerin with explosions.[6]
Large quantities of nitroglycerin were manufactured during World War I and World War II for use as military propellants and in military engineering work. During World War I, HM Factory, Gretna, the largest propellant factory in the Great Britain, produced about 800 long tons (812 tonnes) of Cordite RDB per week. This amount took at least 336 tons of nitroglycerin per week (assuming no losses in production). The Royal Navy had its own factory at Royal Navy Cordite Factory, Holton Heath in Dorset, England. A large cordite factory was also built in Canada during World War I. The Canadian Explosives Limited cordite factory at Nobel, Ontario, was designed to produce 1,500,000 lb (680 t) of cordite per month. This required about 286 tonnes of nitroglycerin per month.
In its pure form, nitroglycerin is a primary contact explosive, with physical shock causing it to explode, and it degrades over time to even more unstable forms. This makes nitroglycerin highly dangerous to transport or use. In this undiluted form, it is one of the world's more powerful explosives, comparable to the more recently-developed RDX and PETN, as well as the plastic explosive C-4—which contains 90 to 92 percent of RDX as its active ingredient.
Early in the history of nitroglycerin, it was discovered that liquid nitroglycerin can be "desensitized" by cooling it to about 5 to 10 °C (40 to 50 °F). At this temperature nitroglycerin freezes, contracting upon solidification. However, thawing it out can be extremely sensitizing, especially if impurities are present or if the warming is too rapid.[7] It is possible to chemically "desensitize" nitroglycerin to a point where it can be considered approximately as "safe" as modern high explosives, such as by the addition of approximately 10 to 30 percent ethanol, acetone,[8] or dinitrotoluene. (The percentage varies with the desensitizing agent used.) Desensitization requires extra effort to reconstitute the "pure" product. Failing this, it must be assumed that desensitized nitroglycerin is substantially more difficult to detonate, possibly rendering it useless as an explosive for practical application.
A serious problem in the use of nitroglycerin results from its high freezing point 13 °C (55 °F). Solid nitroglycerin is much less sensitive to shock than the liquid, a feature that is common in explosives. In the past, nitroglycerin was often shipped in the frozen state, but this resulted in a high number of accidents during the thawing process just before its use. This disadvantage is overcome by using mixtures of nitroglycerin with other polynitrates. For example, a mixture of nitroglycerin and ethylene glycol dinitrate freezes at −29 °C (−20 °F).[9]
Nitroglycerin and any dilutents can certainly deflagrate, i.e. burn. However, the explosive power of nitroglycerin is derived from detonation: energy from the initial decomposition causes a pressure wave or gradient that detonates the surrounding fuel. This is a self-sustained shock wave that propagates through the explosive medium at some 30 times the speed of sound as a near-instantaneous pressure-induced decomposition of the fuel into a white hot gas. Detonation of nitroglycerin generates gases that would occupy more than 1,200 times the original volume at ordinary room temperature and pressure. Moreover, the heat liberated raises the temperature to about 5,000 °C (9,030 °F).[10] This is totally different from deflagration, which depends solely upon available fuel regardless of pressure or shock.
The industrial manufacturing process often uses a nearly 1:1 mixture of concentrated sulfuric acid and concentrated nitric acid. This can be produced by mixing white fuming nitric acid—a quite expensive pure nitric acid in which the oxides of nitrogen have been removed, as opposed to red fuming nitric acid, which contains nitrogen oxides—and concentrated sulfuric acid. More often, this mixture is attained by the cheaper method of mixing fuming sulfuric acid, also known as oleum—sulfuric acid containing excess sulfur trioxide—and azeotropic nitric acid (consisting of about 70 percent nitric acid, with the rest being water).
The sulfuric acid produces protonated nitric acid species, which are attacked by glycerin's nucleophilic oxygen atoms. The nitro group is thus added as an ester C-O-NO2 and water is produced. This is different from an aromatic nitration reaction in which nitronium ions are the active species in an electrophilic attack on the molecule's ring system.
The addition of glycerin results in an exothermic reaction (i.e., heat is produced), as usual for mixed-acid nitrations. However, if the mixture becomes too hot, it results in "runaway", a state of accelerated nitration accompanied by the destructive oxidizing of organic materials of nitric acid and the release of very poisonous brown nitrogen dioxide gas at high risk of an explosion. Thus, the glycerin mixture is added slowly to the reaction vessel containing the mixed acid (not acid to glycerin). The nitrator is cooled with cold water or some other coolant mixture and maintained throughout the glycerin addition at about 22 °C (72 °F), much below which the esterification occurs too slowly to be useful. The nitrator vessel, often constructed of iron or lead and generally stirred with compressed air, has an emergency trap door at its base, which hangs over a large pool of very cold water and into which the whole reaction mixture (called the charge) can be dumped to prevent an explosion, a process referred to as drowning. If the temperature of the charge exceeds about 30 °C (86 °F) (actual value varying by country) or brown fumes are seen in the nitrator's vent, then it is immediately drowned.
The main use of nitroglycerin, by tonnage, is in explosives such as dynamite and in propellants.
Nitroglycerin is an oil that may explode with heat, pressure or when it burns. It is extremely unstable, therefore dropping or bumping a container can also make it explode.[11]
Alfred Nobel developed the use of nitroglycerin as a blasting explosive by mixing the nitroglycerin with inert absorbents particularly diatomaceous earth. He named this explosive dynamite and patented it in 1867. It was supplied ready for use in the form of sticks, individually wrapped in greased water-proof paper. Dynamite and similar explosives were widely adopted for civil engineering tasks, such as in drilling highway and railroad tunnels, for mining, in quarrying, and in demolition work. Likewise, military engineers have used dynamite for construction and demolition work.
Nitroglycerin was also adapted as a military propellant, for use in guns and rifles.
Nitroglycerin is a high explosive which is so unstable that the slightest jolt, friction, or impact can cause it to detonate. The molecule contains oxygen, nitrogen, and carbon with weak chemical bonds. Hence when it explodes, great energy is released as the atoms rearrange to form new molecules with strong, stable bonds such as N2, H2O, and CO2. It is the speed of the decomposition reaction which makes it such a violent explosive. A supersonic wave passing through the material causes it to decompose almost instantly. This instantaneous destruction of all molecules is called a detonation, and the destructive blast results from the rapid expansion of hot gases. Nitroglycerin has an advantage over some other high explosives, that practically no visible smoke is produced, therefore it acts as a "smokeless powder".[12]
Because of its extreme sensitivity, nitroglycerin was rendered obsolete as a military explosive, and was replaced by less sensitive explosives such as TNT, RDX, and HMX. Combat engineers still use dynamite.
Alfred Nobel then developed ballistite, by combining nitroglycerin and guncotton. He patented it in 1887. Ballistite was adopted by a number of European governments, as a military propellant. Italy was the first to adopt it. However, it was not adopted by the British Government. This government and the Commonwealth governments, adopted cordite, which had been developed by Sir Frederick Abel and Sir James Dewar of the United Kingdom in 1889. The original Cordite Mk I consisted of 58% nitroglycerin, 37% guncotton, and 5.0% petroleum jelly. Ballistite and cordite were both manufactured in the forms of cords.
Smokeless powders were originally developed using nitrocellulose as the sole explosive ingredient. Therefore they were known as single base propellants. A range of smokeless powders that contain both nitrocellulose and nitroglycerin, known as double base propellants, were also developed. Smokeless powders were originally supplied only for military use, but they were also soon developed for civilian use and were quickly adopted for sports. Some are known as sporting powders. Triple base propellants contain nitrocellulose, nitroglycerin, and nitroguanidine, but are reserved mainly for extremely high caliber ammunition rounds such as those used in tank cannons and naval artillery.
Blasting gelatin, also known as gelignite, was invented by Nobel in 1875, using nitroglycerin, wood pulp, and sodium or potassium nitrates. This was an early low-cost, flexible explosive.
Alfred Nobel discovered that mixing nitroglycerin with diatomaceous earth would turn the liquid into a paste, called dynamite. An advantage of dynamite was that it could be cylinder-shaped for insertion into the drilling holes used for mining and tunneling. Nobel received the American patent number 78,317 for his dynamite in 1867.[13]
Nitroglycerin belongs to a group of drugs called nitrates, which includes many other nitrates like isosorbide dinitrate (Isordil) and isosorbide mononitrate (Imdur, Ismo, Monoket).[14] In medicine, where it is generally called glyceryl trinitrate, nitroglycerin is used as a heart medication. It is used as a medicine for angina pectoris (ischemic heart disease) in tablets, ointment, solution for intravenous use, transdermal patches, or sprays administered sublingually. Patients who experience angina when doing certain physical activities can often prevent symptoms by taking nitroglycerin 5 to 10 minutes before the activity. Some forms of nitroglycerin last much longer in the body than others. These may come in the form of a pill taken one, two, or three times per day, or even as a patch. It has been shown that round-the-clock exposure to nitrates can cause the body to stop responding normally to this medicine. Experts recommend that the patches be removed at night, allowing the body a few hours to restore its responsiveness to nitrates. Shorter-acting preparations can be used several times a day with less risk of the body getting used to this drug.[15] Nitroglycerin was first used to treat anginal attacks in 1879.
Angina pectoris is due to an inadequate flow of blood and oxygen to the heart. It is believed that nitroglycerin corrects the imbalance between the flow of oxygen and blood to the heart.[16] The principal action of nitroglycerin is vasodilation—widening of the blood vessels. Nitroglycerin will dilate veins more than arteries. It also lowers the pressure in the arteries against which the heart must pump.[14] Dilating the veins decreases cardiac preload and leads to the following therapeutic effects during episodes of angina pectoris: subsiding of chest pain, decrease of blood pressure, increase of heart rate, and orthostatic hypotension.
These effects arise because nitroglycerin is converted to nitric oxide in the body by mitochondrial aldehyde dehydrogenase,[17] and nitric oxide is a natural vasodilator. Recently, it has also become popular in an off-label use at reduced (0.2%) concentration in ointment form as an effective treatment for anal fissure.
Infrequent exposure to high doses of nitroglycerin can cause severe headaches known as "NG head". These headaches can be severe enough to incapacitate some people; however, humans develop a tolerance to and dependence on nitroglycerin after long-term exposure. Withdrawal can (rarely) be fatal; withdrawal symptoms include headaches and heart problems; with re-exposure to nitroglycerin, these symptoms may disappear.
For workers in nitroglycerin (NTG) manufacturing facilities, this can result in a "Monday morning headache" phenomenon for those who experience regular nitroglycerin exposure in the workplace leading to the development of NTG tolerance for the vasodilating effects. Over the weekend the workers lose the tolerance to NTG and when they are reexposed on Monday the prominent vasodilation produces tachycardia, dizziness, and a headache.