UreaChemical structure History Occurrence Physical properties Chemical Properties Productions Production methods Uses Hazards Reference
- Product Name
- CAS No.
- Chemical Name
- Molecular Formula
- Formula Weight
- MOL File
- Melting point:
- 132-135 °C(lit.)
- Boiling point:
- 332.48°C (estimate)
- 1.335 g/mL at 25 °C(lit.)
- vapor pressure
- <0.1 hPa (20 °C)
- refractive index
- n20/D 1.40
- storage temp.
- H2O: 8 M at 20 °C
- 0.10(at 25℃)
- Specific Gravity
- 8.0-10.0 (20℃, 8M in H2O)
- Water Solubility
- 1080 g/L (20 ºC)
- λ: 260 nm Amax: 0.03
λ: 280 nm Amax: 0.02
- Substances to be avoided include strong oxidizing agents. Protect from moisture.
- CAS DataBase Reference
- 57-13-6(CAS DataBase Reference)
- NIST Chemistry Reference
- EPA Substance Registry System
- Urea (57-13-6)
- Product number
- Product name
- free-flowing, Redi-Dri?, Bioreagent, ≥98%
- 100 g
- Product number
- Product name
- for biochemistry
- 250 g
- Product number
- Product name
- granulated, Emprove? Expert, Ph. Eur., BP, JP, USP, ACS reagent
- Product number
- Product name
- for synthesis
- 1 kg
- Product number
- Product name
- Urea solution
- suitable for microbiology, 40% in H2O
- 10 vials
Urea Chemical Properties,Usage,Production
Urea, also known as carbamide, is an organic compound with chemical formula CO (NH2)2. This amide has two –NH2 groups joined by a carbonyl (C=O) functional group.
Pure urea was first isolated from urine in 1727 by the Dutch scientist Herman Boerhaave, and he extracted urea from urine by working with the concentated-by-boiling residue. But if only not considering the purity of urea, the discovery of urea should be attributed to the French chemist Hilaire Rouelle, and he prepared urea (or its addition compound with sodium chloride) from urine some time before 1727.
In 1828, just 55 years after its discovery, urea became the first organic compound to be synthetically formulated, this time by a German chemist named Friedrich Wöhler, one of the pioneers of organic chemistry. It was found when Wohler attempted to synthesis ammonium cyanate, to continue a study of cyanates which he had been carrying out for several years. On treating silver cyanate with ammonium chloride solution he obtained a white crystalline material which proved identical to urea obtained from urine.
AgNCO + NH4Cl → (NH2)2CO + AgCl
Synthetic urea is created from synthetic ammonia and carbon dioxide and can be produced as a liquid or a solid. The process of dehydrating ammonium carbamate under conditions of high heat and pressure to produce urea was first implemented in 1870 and is still in use today. Uses of synthetic urea are numerous and therefore production is high. Approximately one million pounds of urea is manufactured in the United States alone each year, most of it used in fertilizers. Nitrogen in urea makes it water soluble, a highly desired property in this application.
Urea is the chief nitrogenous end product of the metabolic breakdown of proteins in all mammals and some fishes. The material occurs not only in the urine of all mammals but also in their blood, bile, milk, and perspiration. In the course of the breakdown of proteins, amino groups (NH2) are removed from the amino acids that partly comprise proteins. These amino groups are converted to ammonia (NH3), which is toxic to the body and thus must be converted to urea by the liver. The urea then passes to the kidneys and is eventually excreted in the urine.
Fig.1 The urea cycle in animals
Fig.2 Urea crystal
It is a colourless, crystalline substance that melts at 132.7°C (271°F) and decomposes before boiling. Its density is 1.32 g/cm3 and It is highly soluble in water and contains 46.7% nitrogen.
The urea molecule is planar in the crystal structure, but the geometry around the nitrogens is pyramidal in the gas-phase minimum-energy structure. In solid urea, the oxygen center is engaged in two N-H-O hydrogen bonds. The resulting dense and energetically favourable hydrogen-bond network is probably established at the cost of efficient molecular packing: The structure is quite open, the ribbons forming tunnels with square cross-section. The carbon in urea is described as sp2 hybridized, the C-N bonds have significant double bond character, and the carbonyl oxygen is basic compared to, say, formaldehyde. Urea's high aqueous solubility reflects its ability to engage in extensive hydrogen bonding with water.
Urea dissolved in water is in equilibrium with the isomeric ammonium cyanate. The resulting activity of the isocyanic acid ions do result in carbamylation (formation of long-chain carbamides, liberating ammonia molecule as byproduct) of proteins if proteins are present in the solution too. The carbamylation reaction may occurs at elevated temperatures even without catalysts. At room temperature, water solutions of urea are prone to same decomposition reaction in the presence of urease. The isomerization of urea in solution at room temperature without catalysts is a slow process (taking days to reach equilibrium), and freshly prepared, unheated solutions had negligible carbamylation rates.Urea can react with alcohols to form urethanes and react with malonic esters to make barbituric acids.
The primary raw material used to manufacture urea is natural gas, which ties the costs directly to gas prices. Consequently, new plants are only being built in areas with large natural gas reserves where prices are lower. Finished product is transported around the globe in large shipments of 30,000 metric tons. The market price for urea is directly related to the world price of natural gas and the demand for agricultural products. Prices can be very volatile, and at times, unpredictable. TCC is positioned to know the world markets and keep your prices competitive.
Annual production of sulfuric acid
1. Potash Corporation, 2013
2. International Fertilizer Industry Association, 2014
Urea was first noticed by Hermann Boerhaave in the early 18th century from evaporates of urine. In 1773, Hilaire Rouelle obtained crystals containing urea from human urine by evaporating it and treating it with alcohol in successive filtrations. This method was aided by Carl Wilhelm Scheele's discovery that urine treated by concentrated nitric acid precipitated crystals. Antoine François, comte de Fourcroy and Louis Nicolas Vauquelin discovered in 1799 that the nitrated crystals were identical to Rouelle's substance and invented the term "urea." Berzelius made further improvements to its purificationand finally William Prout, in 1817, succeeded in obtaining and determining the chemical composition of the pure substance. In the evolved procedure, urea was precipitated as urea nitrate by adding strong nitric acid to urine. To purify the resulting crystals, they were dissolved in boiling water with charcoal and filtered. After cooling, pure crystals of urea nitrate form. To reconstitute the urea from the nitrate, the crystals are dissolved in warm water, and barium carbonate added. The water is then evaporated and anhydrous alcohol added to extract the urea. This solution is drained off and evaporated, leaving pure urea.
For use in industry, urea is produced from synthetic ammonia and carbon dioxide. As large quantities of carbon dioxide are produced during the ammonia manufacturing process as a byproduct from hydrocarbons (predominantly natural gas, less often petroleum derivatives), or occasionally from coal, urea production plants are almost always located adjacent to the site where the ammonia is manufactured.
Urea can be produced as prills, granules, pellets, crystals, and solutions. The prills are formed by spraying molten urea down a tower up which air is pumped. They are slightly smaller than urea sold as granules and are particularly useful when the fertilizer is being applied by hand. In admixture, the combined solubility of ammonium nitrate and urea is so much higher than that of either component alone that it is possible to obtain a stable solution (known as UAN) with a total nitrogen content (32%) approaching that of solid ammonium nitrate (33.5%), though not, of course, that of urea itself (46%).
Fig.3 Industrial process of urea
Fig.4 An aerial view of a large plant in Alberta, Canada, in which ammonia is synthesized and then converted to urea.( By kind permission of Agrium Inc.)
Fig.5 Prills(small spheres of urea)
Fig.6 UAN(admixture of urea and ammonium nitrate) Laboratory process
Ureas in the more general sense can be accessed in the laboratory by reaction of phosgene with primary or secondary amines, proceeding through an isocyanate intermediate. Non-symmetric ureas can be accessed by reaction of primary or secondary amines with an isocyanate.
Also, urea is produced when phosgene reacts with ammonia:
COCl2 + 4 NH3 → (NH2)2CO + 2 NH4Cl
Urea is byproduct of converting alkyl halides to thiols via a S-alkylation of thiourea. Such reactions proceed via the intermediacy of isothiouronium salts:
RX + CS(NH2)2 → RSCX(NH2)2X
RSCX(NH2)2X + MOH → RSH + (NH2)2CO + MX
In this reaction R is alkyl group, X is halogen and M is alkali metal.
More than 90% of world industrial production of urea is destined for use as a nitrogen-release fertilizer. Urea has the highest nitrogen content of all solid nitrogenous fertilizers in common use. Therefore, it has the lowest transportation costs per unit of nitrogen nutrient.
In the soil, it hydrolyses back to ammonia and carbon dioxide. The ammonia is oxidized by bacteria in the soil to nitrate, which can be absorbed by the plants. Urea is also used in many multi-component solid fertilizer formulations. Urea is highly soluble in water, therefore, very suitable for use in fertilizer solutions (in combination with ammonium nitrate: UAN), e.g., in ‘foliar feed’ fertilizers. For fertilizer use, granules are preferred because of their narrower particle size distribution, an advantage for mechanical application. The most common impurity of synthetic urea, biuret, must be present at less than 2 percent of the time, as it impairs plant growth.
Fig.7 Urea fertilizer and farmer’s fertilization process
Urea and malonic acid react to form barbituric acid. This was discovered by Adolf Bayer in 1864. But the barbiturates were not exploited as hypnotics until the early 1900's.Urea is also used in the production of various acylureas and urethanes for use as sedatives and hypnotics.
Urea is a raw material for the manufacture of two main classes of materials: urea-formaldehyde resins and urea-melamine-formaldehyde used in marine plywood. They all have very varied uses including adhesives, laminates, moulding compounds, coatings and textile finishes.
Urea has the ability to trap many organic compounds in the form of clathrates. The organic compounds are held in channels formed by interpenetrating helices comprising of hydrogen-bonded urea molecules. This behavior can be used to separate mixtures, and has been used in the production of aviation fuel and lubricating oils, and in the separation of paraffin.
As the helices are interconnected, all helices in a crystal must have the same molecular handedness. This is determined when the crystal is nucleated and can thus be forced by seeding. The resulting crystals have been used to separate racemic mixtures.
Urea in concentrations up to 10 M is a powerful protein denaturant as it disrupts the noncovalent bonds in the proteins. This property can be exploited to increase the solubility of some proteins. A mixture of urea and choline chloride is used as a deep eutectic solvent, a type of ionic liquid.
Urea can in principle serve as a hydrogen source for subsequent power generation in fuel cells. Urea present in urine/wastewater can be used directly (though bacteria normally quickly degrade urea.) Producing hydrogen by electrolysis of urea solution occurs at a lower voltage (0.37 V) and thus consumes less energy than the electrolysis of water (1.2 V).
Urea in concentrations up to 8 M can be used to make fixed brain tissue transparent to visible light while still preserving fluorescent signals from labeled cells. This allows for much deeper imaging of neuronal processes than previously obtainable using conventional one photon or two photon confocal microscopes.
Urea is used in SNCR and SCR reactions to reduce the NOx pollutants in exhaust gases from combustion, for example, from power plants and diesel engines. The BlueTec system, for example, injects water-based urea solution into the exhaust system. The ammonia produced by decomposition of the urea reacts with the nitrogen oxide emissions and is converted into nitrogen and water within the catalytic converter.
Fig.9 A line diagram of the car above illustrating five key elements in the design of the exhaust system.
1 The oxidation catalyst is used to remove unwanted hydrocarbons, ensuring that they are oxidised to carbon dioxide and water. The catalyst is usually based on platinum or palladium.
2 Known as an NOx catalytic convertor, it contains aluminium oxide on whose surface, platinum and barium oxide are present. It traps the oxides of nitrogen. When the solid is saturated with the oxides, unburnt hydrocarbons are allowed to flow through, converting much of the mixture to nitrogen, carbon dioxide and water vapour.
3 A filter which traps particulates (small pieces of carbon and other solids).
4 A tank containing the solution of urea.
5 The SCR-catalytic convertor which contains another catalyst, for example an oxide of vanadium (or tungsten) on titanium dioxide, which allows the exhaust gases, still containing some nitrogen oxides, to react with ammonia formed from the urea solution, to produce exhaust gases with only traces of the oxides. By kind permission of Daimler AG
A stabilizer in nitrocellulose explosive
A component of animal feed, providing a relatively cheap source of nitrogen to promote growth
A non-corroding alternative to rock salt for road de-icing, and the resurfacing of snowboarding half pipes and terrain parks
A flavor-enhancing additive for cigarettes
A main ingredient in hair removers such as Nair or Veet
A browning agent in factory-produced pretzels
An ingredient in some hair conditioners, facial cleansers, bath oils, skin softeners, and lotions
A reactant in some ready-to-use cold compresses for first-aid use, due to the endothermic reaction it creates when mixed with water
A cloud seeding agent, along with other salts
A flame-proofing agent, commonly used in dry chemical fire extinguisher charges such as the urea-potassium bicarbonate mixture.
An ingredient in many tooth whitening products
An ingredient in dish soap
Along with ammonium phosphate, as a yeast nutrient, for fermentation of sugars into ethanol
A nutrient used by plankton in ocean nourishment experiments for geoengineering purposes
As an additive to extend the working temperature and open time of hide glue
As a solubility-enhancing and moisture-retaining additive to dye baths for textile dyeing or printing
Causes irritation to the respiratory tract. Symptoms may include coughing, shortness of breath. May be absorbed into the bloodstream with symptoms similar to ingestion.
Causes irritation to the gastrointestinal tract. Symptoms may include nausea, vomiting and diarrhea. May also cause headache, confusion and electrolyte depletion.
Causes irritation to skin. Symptoms include redness, itching, and pain.
Causes irritation, redness, and pain.
A study of 67 workers in an environment with high airborne concentrations of urea found a high incidence of protein metabolism disturbances, moderate emphysema, and chronic weight loss.
Aggravation of Pre-existing Conditions:
Supersensitive individuals with skin or eye problems, kidney impairment or asthmatic condition should have physician's approval before exposure to urea dust.
Behavior in Fire: Melting and decomposing to generate ammonia.
Not combustible. Gives off irritating or toxic fumes (or gases) in a fire.
Handling and Storage
Keep in a tightly closed container, stored in a cool, dry, ventilated area. Protect against physical damage. Isolate from incompatible substances. Containers of this material may be hazardous when empty since they retain product residues (dust, solids); observe all warnings and precautions listed for the product.
Urea is a stable highly water-soluble compound
of high nitrogen content (47%), with good storage
properties that make it the most commonly used nitrogen
fertilizer. The synthesis process has remained essentially
unchanged since it was first developed by the BASF
Corporation in 1922. In this process, liquid ammonia
is reacted with carbon dioxide to produce ammonium
carbamate, which is then dehydrated to form urea. The
2NH3 + CO2 ===? NH2·CO2·NH4
NH2·CO2·NH4 ===? (NH2)2CO + H2O
Urea,CO(HN2)2, also known as carbamide, is a white crystalline powder that has a melting point of l32.7 °C (270 °F). It is a natural product of animal protein metabolism and is the chief nitrogen constituent of urine. Commercially, urea is produced by the reaction of ammonia and carbon dioxide. It is soluble in water, alcohol, and benzene.
Urea is a white crystalline so lid.
The compound was discovered by Hilaire Rouelle in 1773 as a constituent of urine.
Urea has the distinction of being the first synthesized organic compound. Until the mid-18th century, scientists believed organic compounds came only from live plants and animals. The first serious blow to the theory of vitalism, which marked the beginning of modern organic chemistry, occurred when Friedrich W?hler (1800 1882) synthesized urea from the two inorganic substances, lead cyanate and ammonium hydroxide: Pb(OCN)2 + 2NH4OH→2(NH2)2CO + Pb(OH)2. W?hler's discoveries on urea occurred while he was studying cyanates; he was attempting to synthesize ammonium cyanate when he discovered crystals of urea in his samples. He first prepared urea in 1824, but he did not identify this product and report his findings until 1828. W?hler's synthesis of urea signaled the birth of organic chemistry.
The primary use of urea is as a nitrogen source in fertilizers, with about 90% of the urea production being used for this purpose. Urea's high nitrogen content (46%) makes it a concentrated source for adding fixed nitrogen to soils. It can be applied to the soil alone, but its high nitrogen content can stress plants and impact the soil negatively, so it is often blended with other nutrients. Blending also reduces the nitrogen content of the fertilizer. For example, blending with ammonium nitrate, NH4NO3, in different proportions produces fertilizers with various nitrogen contents. Urea in the soil is converted to ammonium nitrogen and taken up by plants. It can be applied in solid granule form or dissolved in water and used as a spray. Urea is also used agriculturally as a supplement in livestock feeds to assist protein synthesis.
Another use of urea is for resins, which are used in numerous applications including plastics, adhesives, moldings, laminates, plywood, particleboard, textiles, and coatings. Resins are organic liquid substances exuded from plants that harden on exposure to air. The term now includes numerous synthetically produced resins. Urea resins are thermosetting, which means they harden when heated, often with the aid of a catalyst. The polymerization of urea and formaldehyde produces urea-formaldehyde resins, which is the second most abundant use of urea. Urea is dehydrated to melamine, which, when combined with formaldehyde, produces melamine-formaldehyde resins.
urea is incorporated into cosmetics for a variety of purposes, including moisturizing, desquamating, anti-microbial, and buffering. urea is regarded as a “true” moisturizer rather than a humectant because it attracts and retains moisture in the corneum layer. It facilitates the natural exfoliation of keratinocytes given its ability to dissolve intercellular cement in the corneum layer. Through its anti-microbial properties that inhibit the growth of micro-organisms in a product, urea can also be part of a larger preservative system. This ingredient’s buffering action is attributed to its ability to regulate the hydrolipid mantle. In addition, urea is found to enhance the penetration and absorption of other active ingredients, relieve itchiness, and help leave the skin feeling soft and supple. Anti-inflammatory, anti-septic, and deodorizing actions allow it to protect the skin’s surface against negative changes and help maintain healthy skin. Studies show that urea does not induce photoallergy, phototoxicity, or sensitization. The safest concentration of use in skin care preparations is between 2 and 8 percent. High concentrations of urea seem to be unstable when incorporated into skin care preparations and can also cause irritation. Acidic urea solutions can produce burning or stinging sensations.
Used for the denaturation of proteins and as a mild solubilization agent for insoluble or denatured proteins. Useful for renaturing proteins from samples already denatured with 6 M guanidine chloride such as inclusion bodies. May be used with guanidine hydrochloride and dithiothreitrol (DTT) in the refolding of denatured proteins into their native or active form.
anticholelithogenic; LD50(rat) 890 mg/kg ip
Urea is a physiological regulator of nitrogen excretion in mammals; synthesized in the liver as an end-product of protein catabolism and excreted in urine. Also occurs normally in skin. Emollient; diu retic.
1) UREA, FCC is an odorless and colorless solid that is an important nitrogen-containing substance found in mammal urine.2) Urea has little or no nutritional value to monogastric mammals but Urea is used in sugar-free chewing gum to adjust the texture
ChEBI: A carbonyl group with two C-bound amine groups.
Urea is an important industrial compound. The synthesis of urea was discovered in 1870.Commercial production of urea involves the reaction of carbon dioxide and ammonia at highpressure and temperature to produce ammonium carbamate. Ammonium carbamate is thendehydrated to produce urea (Figure 96.1). The reaction uses a molar ratio of ammonia tocarbon dioxide that is approximately 3:1 and is carried out at pressures of approximately 150atmospheres and temperatures of approximately 180°C.
A white crystalline compound made from ammonia and carbon dioxide. It is used in the manufacture of urea–formaldehyde (methanal) resins. Urea is the end product of metabolism in many animals and is present in urine.
Urea-containing preparations have a softening and moisturizing effect on the stratum
corneum and, at times, may provide good therapy for dry skin and the pruritus
associated with it. They appear to have an antipruritic effect apart from their hydrating
qualities. Urea compounds disrupt the normal hydrogen bonds of epidermal
proteins; therefore, their effect in dry hyperkeratotic diseases such as ichthyosis
vulgaris and psoriasis is not only to make the skin more pliable but also to help
remove adherent scales. Lactic acid also has a softening and moisturizing effect on
the stratum corneum.
Urea 40% ointment may be useful in removing hypertrophic or dystrophic psoriatic nails. Subsequent topical therapy to the denuded nail bed and proximal nail fold may result in regrowth of ‘‘normal’’ nails in half of those treated.
The use of urea (Ureaphil, Urevert) has declined in recent years owing both to its disagreeable taste and to the increasing use of mannitol for the same purposes. When used to reduce cerebrospinal fluid pressure, urea is generally given by intravenous drip. Because of its potential to expand the extracellular fluid volume, urea is contraindicated in patients with severe impairment of renal, hepatic, or cardiac function or active intracranial bleeding.
Solid odorless white crystals or pellets. Density 1.335 g /cc. Noncombustible.
Air & Water Reactions
Urea is a weak base. Reacts with hypochlorites to form nitrogen trichloride which explodes spontaneously in air [J. Am. Chem. Soc. 63:3530-32]. Same is true for phosphorus pentachloride. Urea reacts with azo and diazo compounds to generate toxic gases. Reacts with strong reducing agents to form flammable gases (hydrogen). The heating of improper stoichiometric amounts of Urea and sodium nitrite lead to an explosion. Heated mixtures of oxalic acid and Urea yielded rapid evolution of gases, carbon dioxide, carbon monoxide and ammonia (if hot, can be explosive). Titanium tetrachloride and Urea slowly formed a complex during 6 weeks at 80°C., decomposed violently at 90°C., [Chem. Abs., 1966, 64, 9219b]. Urea ignites spontaneously on stirring with nitrosyl perchlorate, (due to the formation of the diazonium perchlorate). Oxalic acid and Urea react at high temperatures to form toxic and flammable ammonia and carbon monoxide gasses, and inert CO2 gas [Von Bentzinger, R. et al., Praxis Naturwiss. Chem., 1987, 36(8), 41-42].
May irritate eyes.
Behavior in Fire: Melts and decomposes, generating ammonia.
Fertilizer, Fungicide: Used in fertilizers and animal feeds, as a fungicide, in the manufacture of resins and plastics, as a stabilizer in explosives and in medicines, and others. Urea is used to protect against frost and is used in some pesticides as an inert ingredient as a stabilizer, as an inhibitor and as an intensifier for herbicides. Registered for use in EU countries . Registered for use in the U.S.
Urea, CO(NH2)2, also referred to as carbamide, is a
white, crystalline, organic, water-soluble fertilizer. It
contains around 46 % nitrogen, the highest N percentage
any solid fertilizer can have.
Apart from its major use as a fertilizer, urea is also employed in the manufacture of paints, glues, plastics, paper, textiles, feed and weed control chemicals as well as a source of non-protein nitrogen.
Urea is an acceptable fertilizer for rice and preferable to nitrates for flooded rice because of the reduction of nitrates to N,O and/or nitrogen (in anaerobic conditions) which is lost to the atmosphere. Also, rice can utilize the ammonium form of nitrogen efficiently. Hydrolysis and nitrification (in aerobic conditions) are rapid in tropical, sub-tropical and warm climates.
Urea can thus be used efficiently but its use requires a better understanding than that required for other inorganic salts. It is applied to flooded soil three times: at the time of planting, tillering and panicle development. Similar to other nitrogenous fertilizers, urea promotes the growth of both weeds and crops. Urea solution after evaporation in vacuum evaporators, can be finally spraydried into pellets or prills. When protected from moisture (to which it is susceptible), urea is non-caking, freeflowing and suitable for storage and handling.
However, the benefits of urea outweigh its disadvantages. Insofar as the weed growth is concerned, effective methods should be devised to minimize it to a manageable level.
Urea is converted rapidly to ammonia by hydrolysis in the soil via the ammonium carbonate formation route, the latter being unstable (decomposing to ammonia and carbon dioxide). Urea is not as quick acting as ammonium nitrate because the nitrifying bacteria require a few days of warm and moist soil conditions to convert ammonia to the nitrate form. The formation of ammonium ion is slightly acidic in its ultimate reaction with the soil.
Urea is decomposed by the enzyme urease and a part of urea is lost as gaseous nitrogen. The time between urea application and the first availability of water to the soil is important, as also the temperature, because the enzyme is less reactive in cold than at high temperature (25 to 30°C). Prevention and retardation of the hydrolytic action of urease is important following the addition of urea to soil. This may help to avoid difficulties associated with ammonia formation and alkalization.
Many substances are urease inhibitors, but very few meet the rather specific requirements of being (a) effective at low concentrations, (b) relatively non-toxic to higher forms of life, (c) inexpensive, and (d) compatible with urea.
Urea can be sprayed on leaves and can also be mixed with insecticides or herbicides for soil application. A urea-ammonium nitrate mixture with herbicide is also used for weed control.
Urea, although an excellent fertilizer, suffers from the following drawbacks: (i) When applied to a bare soil surface, urea hydrolyzes rapidly and loses a significant quantity of ammonia by volatilization. Such losses vary from soil to soil and are greater for urea in a pellet form rather than in a solution form. Burning residues on the field is suggested as a practical means to control the ammonia loss because the burning reduces the concentration of the enzyme urease in plants. (ii) Rapid hydrolysis of urea in soils can cause injury to the seedlings by ammonia, if large quantities of the fertilizer are placed too close to the seeds. (iii) The fertilizer grade urea may contain toxic biuret which is formed during urea manufacture by an excessive temperature rise. A large concentration of biuret in urea ( > 2 %) causes injury to plants. Feed-grade urea is sometimes referred to by the number 262 which is the product of its nitrogen content (42%) multiplied by 6.25, the latter being the factor used by chemists to convert nitrogen to its protein equivalent. Urea is sometimes phytotoxic when placed close to seeds or seedlings. The phytotoxicity is caused by high local concentrations of ammonia during the hydrolysis stage or by accumulation of nitrite during the nitrification step. Another possible cause is the presence of biuret impurity in urea.
The whole series of urea-formaldehyde compounds, ranging from soluble to completely water-insoluble, are produced by reacting urea with formaldehyde in different ratios. The fertilizer grade contains a minimum of 35% nitrogen, largely water-insoluble but in a gradually available form. The suitability of these compounds as fertilizers also depends on the quantity and quality of cold-water-insoluble nitrogen. The solubility reflects the rate at which the nitrogen becomes available. Formaldehyde-treated urea seems to be more waterproof and less subject to dissolution by light showers or heavy dew.
In addition to the marked improvements in the size, strength and density of granular urea, urea has a number of good characteristics compared to ammonium nitrate. These include its (a) lesser tendency to stick and cake than ammonium nitrate, (b) insensitivity to fire and explosion, and (c) resistance to corrosion during handling and A popular urea-formaldehyde product in the USA contains 38% nitrogen (of which 28 % is water-insoluble) and has an activity index of 50. Urea-formaldehyde products are used to fertilize sod and certain speciality crops. As a result of the slow nitrification pattern, ureaformaldehyde prevents excessive leaching of nitrates.
The use of urea-formaldehyde is not popular because it is costlier than the other nitrogenous fertilizers.
The condensation product of urea and acetaldehyde is commercially known as urea-z. It is a slow-release nitrogen fertilizer containing around 31 % nitrogen. Urea crotonaldehyde, a derivative of urea (also known as crotonylidene diurea), is also a slow-release nitrogen fertilizer.
Urea-sulphur is a relatively new compound containing 40% nitrogen and 10% sulphur. The prilled material has excellent physical properties. Its urea part dissolves after being applied to the soil, leaving elemental sulphur that is converted into sulphate by the oxidizing bacteria.
Adding urea slurry to diammonium phosphate slurry (before or during granulation) makes urea-phosphate which has a higher nitrogen-to-phosphorus ratio than the ammonium phosphate does; the product contains 29% nitrogenand 12.7% phosphorus (29.0% P2O5).
A new liquid fertilizer material [CO(NH2)2?H3PO4] is made by the reaction of urea, phosphoric acid and water. Depending on the ratio of the reactants, the nitrogen content varies from 10% to 28% and the phosphorus content from 9 to 18%.
PRESPERSION, 75 UREA®; SUPERCEL 3000®; UREAPHIL®; UREOPHIL®; UREVERT®; VARIOFORM II®
Moderately toxic by intravenous and subcutaneous routes. Human reproductive effects by intraplacental route: ferthty effects. Experimental reproductive effects. Human mutation data reported. A human skin irritant. Questionable carcinogen with experimental carcinogenic and neoplastigenic data. Reacts with sodium hypochlorite or calcium hypochlorite to form the explosive nitrogen trichloride. Incompatible with NaNO2, P2Cl5, nitrosyl perchlorate. Preparation of the 15N-labeled urea is hazardous. When heated to decomposition it emits toxic fumes of NOx.
Urea is used in ceramics, cosmetics, paper processing; resins, adhesives, in animal feeds; in the manufacture of isocyanurates; resins, and plastics; as a stabilizer in explosives; in medicines; anticholelithogenic, and others.
Urea is expected to have very high mobility in soil. Urea is not expected to volatilize from dry soil surfaces based on its vapor pressure. Various field and laboratory studies have demonstrated that urea degrades rapidly in most soils. Urea is rapidly hydrolyzed to ammonium ions through soil urease activity, which produces volatile gases, that is, ammonia and carbon dioxide. However, the rate of hydrolysis can be much slower, depending on the soil type, moisture content, and urea formulation.
Urea is not expected to adsorb to suspended solids and sediments. Volatilization from water surfaces is not expected. Urea is rapidly hydrolyzed to ammonia and carbon dioxide in environmental systems by the extracellular enzyme urease, which originates from microorganisms and plant roots.
According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere, urea, which has a vapor pressure of 1.2×10-5mm Hg at 251°C, will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase urea is degraded in the atmosphere by reaction with photochemically produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 9.6 days.
The high analysis and good handling properties of urea have made it the leading nitrogen fertilizer, both as a source of nitrogen alone or when compounded with other materials in mixed fertilizers. Although an excellent source of nitrogen, urea can present problems unless properly managed; due to its rapid hydrolysis to ammonia, significant volatilization loss of this may occur if prilled or granular urea is applied to and left on the soil surface without timely incorporation. Mixtures of urea and ammonium nitrate for use in mixed fertilizers are also more highly hygroscopic than ammonium nitrate itself.
Crystallise urea twice from conductivity water using centrifugal drainage and keeping the temperature below 60o. The crystals are dried under vacuum at 55o for 6hours. Levy and Margouls [J Am Chem Soc 84 1345 1962] prepared a 9M solution in conductivity water (keeping the temperature below 25o) and, after filtering through a medium-porosity glass sinter, added an equal volume of absolute EtOH. The mixture was set aside at -27o for 2-3 days and filtered cold. The precipitate was washed with a small amount of EtOH and dried in air. Crystallisation from 70% EtOH between 40o and -9o has also been used. Ionic impurities such as ammonium isocyanate have been removed by treating the concentrated aqueous solution at 50o with Amberlite MB-1 cation-and anion-exchange resin, and allowing it to crystallise on evaporation. [Benesch et al. J Biol Chem 216 663 1955.] It can also be crystallised from MeOH or EtOH, and is dried under vacuum at room temperature. [Beilstein 3 H 42, 3 I 19, 3 II 35, 3 III 80.]
The primary mechanism of toxicity appears to be inhibition of the citric acid cycle. It leads to blockade of electron transport and a decrease in energy production and cellular respiration, which leads to convulsions.
Violent reaction with strong oxidizers, chlorine, permanganates, dichromates, nitrites, inorganic chlorides; chlorites, and perchlorates. Contact with hypochlorites can result in the formation of explosive compounds.
Controlled incineration in equipment containing a scrubber or thermal unit to reduce nitrogen oxide emissions.
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