Pentaerythritol tetranitrate Chemical Properties

Melting point:

140°

Boiling point:

455.59°C (rough estimate)

Density 

d420 1.773

refractive index 

1.7900 (estimate)

storage temp. 

-20°C

solubility 

Practically insoluble in water, soluble in acetone, slightly soluble in ethanol (96 per cent). The solubility of diluted pentaerythrityl tetranitrate depends on the diluent and its concentration.

color 

Crystals or prisms from Me2CO/EtOH

Water Solubility 

2mg/L(temperature not stated)

Stability:

Stable, but decomposes readily and possibly explosively if heated. Incompatible with strong oxidizing agents. Store cold and keep away from sources of ignition.

NIST Chemistry Reference

Pentaerythritol, tetranitrate(78-11-5)

EPA Substance Registry System

Pentaerythritol tetranitrate (78-11-5)

Safety Information

Hazard Codes 

E,Xn

Risk Statements 

3-36-20/21/22-11

Safety Statements 

35-36/37-26-16

RIDADR 

0473

HazardClass 

1.1A

PackingGroup 

II

Hazardous Substances Data

78-11-5(Hazardous Substances Data)

Toxicity

LD50 oral in rat: 1660mg/kg

Pentaerythritol tetranitrate Usage And Synthesis

Chemical Properties

white crystalline powder

Chemical Properties

Pentaerythrite tetranitrate (PETN) is a high explosive, especially when dry. PETN is a sand-like, white crystalline solid. Piratically odorless.

Originator

Pentanitrine, Promedica ,France,1948

Uses

Pentaerythritol tetranitrate is used for chronic cardiac insufficiency. It prevents angina pectoris attacks and eases their course.

Uses

Pentaerythritol tetranitrate (PETN) is a high explosive, often used as the booster in artillery ammunition. It is frequently used as a detonation fuse, which is a form of primacord in which PETN powder is wrapped in waterproof fabric.

Uses

Mainly in the manufacture of detonating fuse (Primacord), a waterproof textile filled with powdered PETN.

Definition

ChEBI: A pentaerythritol nitrate in which all four hydroxy groups of pentaerythritol have been converted to the corresponding nitrate ester. It is a vasodilator with properties similar to those of glyceryl trinitrate, but with a more prolonged duration of action, and is used for treatment of angina pectoris. It is also one of the most powerful high explosives known and is a component of the plastic explosive known as Semtex.

Manufacturing Process

Cooling water was turned on and 420 parts nitric acid of 94% strength was introduced into the nitrator. The amount of acid was such that the ratio of nitric acid to pentaerythritol was 4.29. The agitator was started and the agitator speed adjusted to 120 rpm. 92 parts pentaerythritol, which had been screened previously through a 14-mesh screen was used in each charge. About 45 parts pentaerythritol was added to the nitrator at such a rate that the temperature in the nitrator gradually rose to 110°F. This required about 12 minutes. Time was allowed for the temperature rise to cease before each succeeding increment of material was added.
After reaching 110°F the charge was maintained at about said temperature from 12 to 14 minutes during which time approximately 30 parts pentaerythritol was added to the nitrator. During the following 14 minutes, approximately, the remainder of the 92 parts pentaerythritol was added in like manner to the charge and the temperature gradually reduced. The pentaerythritol was introduced into the acid in finely divided and welldispersed particles and not in large unitary quantities. The entire 92 parts of pentaerythritol tetranitrate was introduced in 35 to 40 minutes. The pentaerythritol thus obtained was separated from the spent acid by filtering or drowning in water. To recover the spent acid the charge was passed onto a nutsch and filtered. The crude product was washed with water, then with a weak water-soluble alkali solution, such as sodium carbonate for example, and subsequently with water in order to remove the acid.
After the removal of acid, the nitrate was dried by suction on the nutsch for about 15 minutes. The dried material was refined by means of acetone treatment or other suitable refining means. About 210 parts refined pentaerythritol tetranitrate per charge was obtained.

brand name

Pentritol Tempules (Rhone-Poulenc Rorer); Peritrate (Parke-Davis).

Therapeutic Function

Coronary vasodilator

Reactivity Profile

Pure PENTAERYTHRITE TETRANITRATE is an explosive. Severe explosion hazard when shocked or exposed to heat. Explodes when heated to 205-215°C. Highly dangerous when mixed with oxidizing agents. On decomposition Pentaerythritol tetranitrate emits highly toxic fumes of NOx (Sax and Lewis, 1987 pp. 699-700).

Health Hazard

Some are toxic and may be fatal if inhaled, swallowed or absorbed through skin. Contact may cause burns to skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may cause pollution.

Health Hazard

Skin contact can cause dermatitis. There is no report of any major adverse effects in humans. However, drawing a parallelism with other nitroorganics of similar structures, PETN is expected to cause poisoning with symptoms of headache, nausea, abdominal pain, and dyspnea.

Fire Hazard

PETN is a high explosive, as powerful as cyclonite. It is more sensitive than TNT to shock. It explodes on percussion or heating. The detonating temperature is 210°C (410°F). The detonation velocity is 7.9 km/s.

Safety Profile

Human systemic effects by ingestion: dermatitis. Effects are sirmlar to those of nitroglycerin, i.e., headache, weakness, and fall in blood pressure. Very low oral toxicity. Severe explosion hazard when shocked or exposed to heat. It explodes at 215’C. On decomposition it emits hghly toxic fumes of NO,; can react vigorously with oxidizing materials. Used in detonators and explosive specialities. See also NITRATES and EXPLOSIVES, HIGH.

Synthesis

Pentaerythritol tetranitrate, 2,2-bis(hydroxymethyl)-1,3- propandioltetranitrate (19.1.2), is also synthesized by a nitration reaction of pentaerythritol with nitric acid, but using 2,2-bis(hydroxymethyl)-1,3-propandiol instead of glycerol as the starting material.

Potential Exposure

First introduced following WWII, PETN shares the same chemical family as nitroglycerine. It is 70% more powerful than TNT. Used in the manufacture of fuses for detonation and explosive specialties, including the plastic explosive, Semtex, and in blasting caps. PETN is also used as a medical vasodilator to lower blood pressure by widening blood vessels to improve blood flow. PRTN has been used in terrorism attempts in 2001 by the so-called “shoe bomber,” in 2009 by the “underwear bomber,” and most recently in October 2010, hidden in printer cartridges being shipped internationally by passenger jet.

Shipping

UN3344 Pentaerythrite tetranitrate mixture, desensitized, solid, n.o.s. with ＞10% but not ＞20% PETN, by mass, Hazard Class: 4.1; Labels: 4.1-Flammable solid. UN0150 Pentaerythrite tetranitrate, wetted or Pentaerythritol tetranitrate, wetted, or PETN, wetted or Pentaerythrite tetranitrate, or Pentaerythritol tetranitrate or PETN, desensitized, Hazard Class: 1D; Labels:1DExplosive (with a mass explosion hazard); D-Substances or articles which may mass detonate (with blast and/or fragment hazard) when exposed to fire.

Purification Methods

Crystallise pentaerythritol tetranitrate from acetone or acetone/EtOH. When crystallised from H2O at 0o, it may have m 26-28o (hydrate). It detonates more easily than TNT on percussion. The O-acetate, when crystallised from EtOH, has m 87-88o. Although it has been distilled at 60o/2mm, distillation should NOT be attempted as it is VERY EXPLOSIVE. Itis a vasodilator. [Marans et al. J Am Chem Soc 76 1304 1954, Camp et al. J Am Chem Soc 77 751 1955, Beilstein 1 IV 2816, 2 IV 264.]

Incompatibilities

Treat PETN as an unstable explosive. Rapid heating can cause detonation when heated to 210C. PETN is a dangerous high explosive and a strong oxidizer. PETN normally requires a blasting cap or other kind of detonator but may decompose explosively from concussion, shock, friction, static charges. Keep away from combustible materials; other oxidizers, for example, nitrates and permanganates. Contact with sulfur trioxide may cause detonation. Contact with reducing agents, e.g., zinc and alkaline metals may cause explosion. May explode in the presence of strong bases (i.e., sodium or potassium hydroxide). May react with heavy metals.

Waste Disposal

Seek expert help with this explosive material. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. governing storage, transportation, treatment, and waste disposal.

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