124-47-0 Usage
Description
Urea nitrate, is a colorless crystal shipped with not less than 20% water by mass. It is a dangerous fire and explosion risk, and is slightly soluble in water. It decomposes at 305.6°F (152°C). The four-digit UN identification number is 1357. It is used in the manufacture of explosives and urethane.
Chemical Properties
Colorless crystals. Decomposes at
152C. Slightly soluble in water; soluble in alcohol.
Uses
As sensitizer for explosives; fertilizer; organic reagent; manufacture of urethane.
General Description
A crystalline compound arising from the neutralization of urea with nitric acid. Melting point 152°C. Slightly soluble in water. Soluble in alcohol. Primary hazard is blast of an instantaneous explosion, not flying projectiles or fragments.
Air & Water Reactions
Easily ignited. Burns very vigorously to generate toxic oxides of nitrogen. Slightly soluble in water.
Reactivity Profile
UREA NITRATE is explosive when left in dry state. Wetting reduces possibility of explosion but may explode under prolonged exposure to heat or fire, even when wet. Urea nitrate reacts with strong oxidizer such as perclorates and hypochlorites. With hypochlorites Urea nitrate forms a compound nitrogen trichloride which explodes spontaneously in air (J. Am. Chem. Soc. 63:3530-32). Organic nitrates may explode when shocked, exposed to heat or flame or by spontaneous chemical reaction. Urea nitrate must be stored in a cool, ventilated place, away from acute fire hazards and easily oxidized materials. Also reacts violently with Al; BP; cyanides; esters; PN2H; P; NaCN; SnCl2; sodium hypophosphite; thiocyanates. Dangerous disaster hazard due to fire and explosion hazard. On decomposition, they emit toxic fumes. They are powerful oxidizing agents which may cause violent reaction with reducing materials. Nitrates should be protected carefully in storage. (SAX and Lewis, 1987) p.664. Decomposition is catalyzed by the presence of heavy metals such as lead or iron in trace amounts [Bretherick, 1995, pg. 201]. Produces toxic oxides of nitrogen during combustion. Decomposed with explosive evolution of gas during the evaporation of an alkaline solution. [Bretherick, 1995, p. 201].
Health Hazard
Fire may produce irritating, corrosive and/or toxic gases.
Fire Hazard
MAY EXPLODE AND THROW FRAGMENTS 1600 meters (1 MILE) OR MORE IF FIRE REACHES CARGO.
Safety Profile
A mild irritant.
Flammable when exposed to heat or flame.
The dry nitrate may explode when heated.
The presence of heavy metals (e.g., lead,
iron) catalyzes the thermal decomposition of
urea nitrate. When heated to decomposition
it emits toxic fumes of NOx.
Purification Methods
Crystallise it from dilute HNO3 or EtOH (m 157-158o) and dry it in a vacuum over P2O5. [Beilstein 3 H 54, 3 I 25, 3 II 45, 3 III 105, 3 IV 94.]
Check Digit Verification of cas no
The CAS Registry Mumber 124-47-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124-47:
(5*1)+(4*2)+(3*4)+(2*4)+(1*7)=40
40 % 10 = 0
So 124-47-0 is a valid CAS Registry Number.
InChI:InChI=1/CH4N2O.NO3/c2*2-1(3)4/h(H4,2,3,4);/q;-1/p+1
124-47-0Relevant articles and documents
Urea nitrate catalyzed synthesis of 2-arylbenzothiazoles using the grindstone technique
Gandhi, Divyani,Agarwal, Shikha
, p. 307 - 310 (2018)
An efficient, green and environmentally friendly grindstone method for the synthesis of 2-arylbenzothiazole derivatives in the presence of urea nitrate as the catalyst under solvent-free conditions was developed. All products were characterized by elemental analysis and spectral methods.
Studies of Cyanamide Derivatives. Part 110. A facile Synthesis of 2,4,6-Triureido-1,3,5-triazine and 2-Amino-4,6-diureido-1,3,5-triazine
Iio, Kokoro,Ichikawa, Eiichi
, p. 2009 - 2010 (2007/10/02)
2,4,6-Triureido-1,3,5-triazine and 2-amino-4,6-diureido-1,3,5-triazine were readily synthetized in high yields, 94 and 85percent respectively, by the alcoholysis of 2,4,6-tris(cyanoamino)-1,3,5-triazine and 2-amino-4,6-bis(cyanoamino)-1,3,5-triazine in the presence of hydrogen chloride
