Shopping on line can be easy, simple and save you lots of money. It can also take a lot of your time, frustrate you, and result in unwanted purchases. Now the same can be said for regular high street shopping, but with the vast opportunity presented by the Internet it will pay you to spend a few minutes reading this and understanding how to better optimize your Urea shopping experience:

1. Compare - without doubt the biggest advantage that the Urea offers shoppers today is the ability to compare thousands of Urea at a time. This is a great thing, but not necessarily all the time! Too much can be daunting at times so take advantage of the great comparison sites and where possible let them do the hard work for you.

2. Research - if it has been said it will be on the internet. Ignorance is no longer a justifiable reason for buying the wrong thing. Take the time to research in detail everything that you could possible want to know about

3. Testimonials - don't know anybody that has bought a Urea? Wrong! If the Urea is good the internet will let you know. Use the Internet as a friend and get testimonials before you buy.

4. Questions - Got a question about Urea then search the Forums, FAQ's, Blogs etc. Don't be afraid to ask .....

5. Reputation - Never heard of the company selling Urea? Don't worry, no reason why you should know every company in the world, but you know someone that does! Use the internet to find out what people are saying about Urea and build up a picture of their reputation for sales, returns, customer service, delivery etc.

6. Returns - still worried that even after all of the above your Urea wont be what you want? Check out the returns policy. There is so much competition now that someone, somewhere is bound to offer the terms that you are comfortable with.

7. Feedback - happy with your Urea then let people know, after all you are depending on others people input in your buying decision, so why not give a little back.

8. Security - check for the yellow padlock on the Urea site before you buy, and the s after http:/ /i.e. https:// = a secure site

9. Contact - got a question about Urea, or want to leave a comment then check out the sites contact page. Reputable companies have them and respond.

10. Payment - ready to pay for your Urea, then use your credit card or PayPal! Be aware of companies that don't accept them, there may be genuine reasons but given the huge amount of choice you have when buying online there is no reason at all not to buy via credit card or PayPal.

{{Chembox new| Name = Urea| ImageFile = Urea.png| ImageFile1 = Urea-3D-vdW.png| IUPACName = Diaminomethanal| OtherNames = carbamide| Section1 = {{Chembox Identifiers| SMILES = NC(=O)N| CASNo = 57-13-6| RTECS = --> | Section2 = {{Chembox Properties| Formula = (NH2)2CO| MolarMass = 60.07 g/mol| Appearance = white odourless solid| Density = 1.33·10³ kg/m³http://webmineral.com/data/Urea.shtml, solid| Solubility = 108 g/100 ml (20 °C)167 g/100 ml (40 °C)251 g/100 ml (60 °C)400 g/100 ml (80 °C)733 g/100 ml (100 °C)| MeltingPt = 132.7 °C (406 K)decomposes| BoilingPt = n.a.| pKa = 0.18| pKb = 13.82 --> | Section3 = {{Chembox Structure| Dipole = 4.56 Debye --> | Section7 = {{Chembox Hazards| ExternalMSDS = ScienceLab.com| MainHazards = Toxic| FlashPt =| NFPA-H = 2| NFPA-F = 1 --> -->Urea is an organic compound with the chemical formula (nitrogenhydrogen2)2carbonoxygen.

Urea is also known as carbamide, especially in the recommended International Nonproprietary Names (rINN) in use in Europe. For example, the medicinal compound hydroxyurea (old British Approved Name) is now hydroxycarbamide. Other names include carbamide resin, isourea, carbonyl diamide, and carbonyldiamine.

It was the first organic compound to be artificially synthesized from inorganic starting materials, thus dispelling the concept of vitalism.

Discovery Urea was discovered by Hilaire Rouelle in 1773. It was the first organic compound to be artificially synthesized from inorganic starting materials, in 1828 by Friedrich Wöhler, who prepared it by the reaction of potassium cyanate with ammonium sulfate. Although Woehler was attempting to prepare ammonium cyanate, by forming urea, he inadvertently disproved vitalism, the theory that the chemicals of living organisms are fundamentally different from inanimate matter, thus starting the discipline of organic chemistry.

This discovery prompted Wohler to write triumphantly to Berzelius:

"I must tell you that I can make urea without the use of kidneys, either man or dog. Ammonium cyanate is urea."

It is found in mammalian and amphibian urine as well as in some fish. Birds and reptiles excrete uric acid, comprising a different form of nitrogen metabolism that requires less water.

Structure Urea is highly soluble in water and is therefore an efficient way for the human body to expel excess nitrogen. Due to extensive hydrogen bonding with water (up to six hydrogen bonds may form, two from the oxygen atom and one from each hydrogen), it is very soluble and thus is also a good fertilizer.

The urea molecule is planar and retains its full molecular point symmetry, due to conjugation of one of each nitrogen's P orbital to the carbonyl double bond. Each carbonyl oxygen atom accepts four N-H-O hydrogen bonds, a very unusual feature for such a bond type. This dense (and energetically quite 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.

Physiology The individual atoms that make up a urea molecule come from carbon dioxide, water, aspartate and ammonia in a metabolic pathway known as the urea cycle, an Anabolism. This expenditure of energy is necessary because ammonia, a common metabolism waste product, is toxic and must be neutralized. Urea production occurs in the liver and is under the regulatory control of N-acetylglutamate.

The urea cycle was originally known as the Krebs-Henseleit cycle after it was partially deduced by Hans Adolf Krebs and Kurt Henseleit in 1932. Its details were clarified in the 1940s as the roles of citrulline and argininosuccinate as intermediates were understood. In this cycle, amino groups donated by ammonia and L-aspartate are converted to urea, while L-ornithine, citrulline, L-argininosuccinate, and L-arginine act as intermediates.

Most organisms have to deal with the excretion of nitrogen waste originating from protein and amino acid catabolism. In marine biology organisms the most common form of nitrogen waste is ammonia, while land-dwelling organisms convert the toxic ammonia to either urea or uric acid. Generally, birds and saurian reptiles excrete uric acid, while the remaining species, including mammals, excrete urea. Remarkably, tadpoles excrete ammonia, and shift to urea production during Metamorphosis (biology). In veterinary medicine, Dalmatian breeds of dogs are noteworthy in that they excrete urea in the form of uric acid in the urine rather than in the urea form. This is due to a defect in one of the genes controlling expression of the conversion enzymes in the urea cycle.

Despite the generalization above, the pathway has been documented not only in mammals and amphibians, but in many other organisms as well, including birds, invertebrates, insects, plants, yeast, fungi, and even microorganisms.

Urea is essentially a waste product, but is vital for forming hypertonic (concentrated) urine. In the distal portions of the kidney collecting duct, urea is reintroduced into the kidney medulla to raise osmolarity. Afterwards, water flowing through the collecting tubule flows back into the body by osmosis through aquaporins.

Urea is dissolved in blood (in humans in a concentration of 2.5 - 7.5 mmol/liter) and excreted by the kidney in the urine.

In addition, a small amount of urea is excreted (along with sodium chloride and water) in human sweat.

Hazards Urea can be irritating to skin and eyes. Too high concentrations in the blood can cause damage to organs of the body. Low concentrations of urea such as in urine are not dangerous.

It has been found that urea can cause algal blooms to produce toxins, and urea in runoff from fertilizers may play a role in the increase of toxic blooms.

Repeated or prolonged contact with urea in fertiliser form on the skin may cause dermatitis. The substance also irritates the eyes, the skin and the respiratory tract. The substance decomposes on heating above melting point producing toxic gases. Reacts violently with strong oxidants, nitrites, inorganic chlorides, chlorites and perchlorates causing fire and explosion hazard

Production Urea is a nitrogen-containing chemical product which is produced on a scale of some 100,000,000 tonnes per year worldwide.

Urea is produced commercially from synthetic ammonia and carbon dioxide. Urea can be produced as prills, granules, flakes, pellets, crystals and solutions.

More than 90% of world production is destined for use as a fertilizer. Urea has the highest nitrogen content of all solid nitrogenous fertilizers in common use (46.4%) It therefore has the lowest transportation costs per unit of nitrogen nutrient.

Urea is highly soluble in water and is therefore also very suitable for use in fertilizer solutions (in combination with ammonium nitrate: UAN), e.g. in 'foliar feed' fertilizers.

Solid urea is marketed as prills or granules. The advantage of prills is that in general they can be produced more cheaply than granules which, because of their narrower particle size distribution have an advantage over prills if applied mechanically to the soil. Properties such as impact strength, crushing strength and free-flowing behaviour are particularly important in product handling, storage and bulk transportation.

Commercial production Urea is produced commercially from two raw materials, ammonia and carbon dioxide. Large quantities of carbon dioxide are produced during the manufacture of ammonia from coal or from hydrocarbons such as natural gas and petroleum derived raw materials. This allows direct synthesis of urea from these raw materials.

The production of urea from ammonia and carbon dioxide takes place in an equilibrium reaction, with incomplete conversion of the reactants. The various urea processes are characterized by the conditions under which urea formation takes place and the way in which unconverted reactants are further processed.

Unconverted reactants can be used for the manufacture of other products, for example ammonium nitrate or sulphate, or they can be recycled for complete conversion to urea in a total-recycle process.

Two principal reactions take place in the formation of urea from ammonia and carbon dioxide. The first reaction is exothermic: 2NH3 + CO2 → H2N-COONH4 (ammonium carbamate)
While the second reaction is endothermic: H2N-COONH4 → (NH2)2CO + H2O Both reactions combined are exothermic.

The process is also called the Bosch-Meiser urea process after its discoverers (1922).

Uses Agricultural Use Urea is used as a nitrogen release fertilizer as it hydrolyses back to ammonia and carbon dioxide, but its most common impurity (biuret,NH2-CO-NH-CO-NH2) must be present at less than 2% as it impairs plant growth. It is also used in many multi-component solid fertilizer formulations.Its action of nitrogen release is due to the conditions favouring the reagent side of the equilibriums which produce urea.

Urea is usually spread at rates of between 40 and 300 kg/ha, but actual spreading rates will vary according to farm type and region. It is better to make several small to medium applications at intervals to minimise leaching losses and increase efficient use of the N applied compared with single heavy applications. During summer, urea should be spread just before, or during rain to reduce possible losses from volatilisation (process where nitrogen is lost to the atmosphere as ammonia gas). Urea should not be mixed for any length of time with other fertilizers as problems of physical quality may result.

Because of the high N concentration in urea, it is very important to achieve an even spread. Make sure that the application equipment has been correctly calibrated and is properly used. Do not drill on contact with or close to seed, due to the risk of germination damage. Urea dissolves in water for application as a spray or through irrigation systems.

In grain and cotton crops, urea is often applied at the time of the last cultivation before planting. It should be applied into, or be incorporated into the soil. In high rainfall areas and on sandy soils (where nitrogen can be lost through leaching) and where good in-season rainfall is expected, urea can be side or top-dressed during the growing season. Top-dressing is also popular on pasture and forage crops. In sugarcane, urea is side-dressed after planting, and applied to each ratoon crop.

In irrigated crops, urea can be applied dry to the soil, or dissolved and applied through the irrigation water. Urea will dissolve in its own weight in water, but it becomes increasingly difficult to dissolve as the concentration increases. Dissolving urea in water is endothermic, causing the temperature of the solution to fall when urea dissolves.

As a practical guide, when preparing urea solutions for fertigation (injection into irrigation lines), dissolve no more than 30 kg urea per 100 L water.

In foliar sprays, urea concentrations of 0.5 – 2.0% are often used in horticultural crops. As urea sprays may damage crop foliage, specific advice should be sought before use. Low biuret grades of urea should be used if urea sprays are to be applied regularly or to sensitive horticultural crops.

Storage of Urea Fertilizer Like most nitrogen products, urea absorbs moisture from the atmosphere. Therefore it is should be stored either in closed/sealed bags on pallets, or if stored in bulk, covered with a tarpaulin. As with most solid fertilizers, it should also be stored in a cool, dry, well ventilated area.

Industrial Use Urea has the ability to form 'loose compounds' with many organic compounds. The organic compounds are held in channels formed by interpenetrating helices comprising of hydrogen bonded urea molecules. This behaviour can be used to separate mixtures and has been used in the production of aviation fuel and lubricating oils.As the helices are interconnected all helices in a crystal must have the same 'handedness'. This is determined when the crystal is nucleated and can thus be forced by seeding. This property has been used to separate racemic mixtures.

Further commercial uses include:

Laboratory use Urea is a powerful protein denaturation (biochemistry). This property can be exploited to increase the solubility of some proteins. For this application it is used in concentrations up to 10 Molar volume.Urea is used to effectively disrupt the noncovalent bonds in proteins.Urea is an ingredient in the synthesis of urea nitrate.Urea nitrate is also a high explosive very similar to ammonium nitrate, however it may even be more powerful because of its complexity. VOD is 11,000 fps to 15,420 fps.

Medical use Drug use Urea is used in topical Dermatology products to promote rehydration of the skin. If covered by an occlusive dressing, 40% urea preparations may also be used for nonsurgical debridement of Nail (anatomy). This drug is also used as an earwax removal aid.

Clinical diagnosis See blood urea nitrogen ("BUN") for a commonly performed urea test, and marker of renal function.

Other diagnostic use Isotopically-labeled urea (carbon-14 - radioactive, or Carbon-13 - stable isotope) is used in the Urea breath test, which is used to detect the presence of Helicobacter pylori (H. pylori, a bacterium) in the stomach and duodenum of humans. The test detects the characteristic enzyme urease, produced by H. pylori, by a reaction that produces ammonia from urea. This increases the pH (reduces acidity) of the stomach environment around the bacteria.

Similar bacteria species to H. pylori can be identified by the same test in animals (apes, dogs, cats - including big cats).

Textile use Urea in textile laboratories are frequently used both in dyeing and printing as an important auxiliary which provides solubility to the bath and retains some moisture which is required for the dyeing or printing process.

Ureas Ureas or carbamides are a class of chemical compounds sharing the same functional group RR'N-CO-NRR' based on a carbonyl group flanked by two organic amine residues. They can be accessed in the laboratory by reaction of phosgene with primary or secondary amines. Example of ureas are the compounds carbamide peroxide, allantoin and Hydantoin. Ureas are closely related to biurets and structurally related to amides, carbamates, diimides, carbodiimides and thiocarbamides.

Reactions Urea reacts with alcohols to form urethanes. Urea reacts with malonic acid esters to make barbituric acids.

References

External links

{{Chembox new| Name = Urea| ImageFile = Urea.png| ImageFile1 = Urea-3D-vdW.png| IUPACName = Diaminomethanal| OtherNames = carbamide| Section1 = {{Chembox Identifiers| SMILES = NC(=O)N| CASNo = 57-13-6| RTECS = --> | Section2 = {{Chembox Properties| Formula = (NH2)2CO| MolarMass = 60.07 g/mol| Appearance = white odourless solid| Density = 1.33·10³ kg/m³http://webmineral.com/data/Urea.shtml, solid| Solubility = 108 g/100 ml (20 °C)167 g/100 ml (40 °C)251 g/100 ml (60 °C)400 g/100 ml (80 °C)733 g/100 ml (100 °C)| MeltingPt = 132.7 °C (406 K)decomposes| BoilingPt = n.a.| pKa = 0.18| pKb = 13.82 --> | Section3 = {{Chembox Structure| Dipole = 4.56 Debye --> | Section7 = {{Chembox Hazards| ExternalMSDS = ScienceLab.com| MainHazards = Toxic| FlashPt =| NFPA-H = 2| NFPA-F = 1 --> -->Urea is an organic compound with the chemical formula (nitrogenhydrogen2)2carbonoxygen.

Urea is also known as carbamide, especially in the recommended International Nonproprietary Names (rINN) in use in Europe. For example, the medicinal compound hydroxyurea (old British Approved Name) is now hydroxycarbamide. Other names include carbamide resin, isourea, carbonyl diamide, and carbonyldiamine.

It was the first organic compound to be artificially synthesized from inorganic starting materials, thus dispelling the concept of vitalism.

Discovery Urea was discovered by Hilaire Rouelle in 1773. It was the first organic compound to be artificially synthesized from inorganic starting materials, in 1828 by Friedrich Wöhler, who prepared it by the reaction of potassium cyanate with ammonium sulfate. Although Woehler was attempting to prepare ammonium cyanate, by forming urea, he inadvertently disproved vitalism, the theory that the chemicals of living organisms are fundamentally different from inanimate matter, thus starting the discipline of organic chemistry.

This discovery prompted Wohler to write triumphantly to Berzelius:

"I must tell you that I can make urea without the use of kidneys, either man or dog. Ammonium cyanate is urea."

It is found in mammalian and amphibian urine as well as in some fish. Birds and reptiles excrete uric acid, comprising a different form of nitrogen metabolism that requires less water.

Structure Urea is highly soluble in water and is therefore an efficient way for the human body to expel excess nitrogen. Due to extensive hydrogen bonding with water (up to six hydrogen bonds may form, two from the oxygen atom and one from each hydrogen), it is very soluble and thus is also a good fertilizer.

The urea molecule is planar and retains its full molecular point symmetry, due to conjugation of one of each nitrogen's P orbital to the carbonyl double bond. Each carbonyl oxygen atom accepts four N-H-O hydrogen bonds, a very unusual feature for such a bond type. This dense (and energetically quite 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.

Physiology The individual atoms that make up a urea molecule come from carbon dioxide, water, aspartate and ammonia in a metabolic pathway known as the urea cycle, an Anabolism. This expenditure of energy is necessary because ammonia, a common metabolism waste product, is toxic and must be neutralized. Urea production occurs in the liver and is under the regulatory control of N-acetylglutamate.

The urea cycle was originally known as the Krebs-Henseleit cycle after it was partially deduced by Hans Adolf Krebs and Kurt Henseleit in 1932. Its details were clarified in the 1940s as the roles of citrulline and argininosuccinate as intermediates were understood. In this cycle, amino groups donated by ammonia and L-aspartate are converted to urea, while L-ornithine, citrulline, L-argininosuccinate, and L-arginine act as intermediates.

Most organisms have to deal with the excretion of nitrogen waste originating from protein and amino acid catabolism. In marine biology organisms the most common form of nitrogen waste is ammonia, while land-dwelling organisms convert the toxic ammonia to either urea or uric acid. Generally, birds and saurian reptiles excrete uric acid, while the remaining species, including mammals, excrete urea. Remarkably, tadpoles excrete ammonia, and shift to urea production during Metamorphosis (biology). In veterinary medicine, Dalmatian breeds of dogs are noteworthy in that they excrete urea in the form of uric acid in the urine rather than in the urea form. This is due to a defect in one of the genes controlling expression of the conversion enzymes in the urea cycle.

Despite the generalization above, the pathway has been documented not only in mammals and amphibians, but in many other organisms as well, including birds, invertebrates, insects, plants, yeast, fungi, and even microorganisms.

Urea is essentially a waste product, but is vital for forming hypertonic (concentrated) urine. In the distal portions of the kidney collecting duct, urea is reintroduced into the kidney medulla to raise osmolarity. Afterwards, water flowing through the collecting tubule flows back into the body by osmosis through aquaporins.

Urea is dissolved in blood (in humans in a concentration of 2.5 - 7.5 mmol/liter) and excreted by the kidney in the urine.

In addition, a small amount of urea is excreted (along with sodium chloride and water) in human sweat.

Hazards Urea can be irritating to skin and eyes. Too high concentrations in the blood can cause damage to organs of the body. Low concentrations of urea such as in urine are not dangerous.

It has been found that urea can cause algal blooms to produce toxins, and urea in runoff from fertilizers may play a role in the increase of toxic blooms.

Repeated or prolonged contact with urea in fertiliser form on the skin may cause dermatitis. The substance also irritates the eyes, the skin and the respiratory tract. The substance decomposes on heating above melting point producing toxic gases. Reacts violently with strong oxidants, nitrites, inorganic chlorides, chlorites and perchlorates causing fire and explosion hazard

Production Urea is a nitrogen-containing chemical product which is produced on a scale of some 100,000,000 tonnes per year worldwide.

Urea is produced commercially from synthetic ammonia and carbon dioxide. Urea can be produced as prills, granules, flakes, pellets, crystals and solutions.

More than 90% of world production is destined for use as a fertilizer. Urea has the highest nitrogen content of all solid nitrogenous fertilizers in common use (46.4%) It therefore has the lowest transportation costs per unit of nitrogen nutrient.

Urea is highly soluble in water and is therefore also very suitable for use in fertilizer solutions (in combination with ammonium nitrate: UAN), e.g. in 'foliar feed' fertilizers.

Solid urea is marketed as prills or granules. The advantage of prills is that in general they can be produced more cheaply than granules which, because of their narrower particle size distribution have an advantage over prills if applied mechanically to the soil. Properties such as impact strength, crushing strength and free-flowing behaviour are particularly important in product handling, storage and bulk transportation.

Commercial production Urea is produced commercially from two raw materials, ammonia and carbon dioxide. Large quantities of carbon dioxide are produced during the manufacture of ammonia from coal or from hydrocarbons such as natural gas and petroleum derived raw materials. This allows direct synthesis of urea from these raw materials.

The production of urea from ammonia and carbon dioxide takes place in an equilibrium reaction, with incomplete conversion of the reactants. The various urea processes are characterized by the conditions under which urea formation takes place and the way in which unconverted reactants are further processed.

Unconverted reactants can be used for the manufacture of other products, for example ammonium nitrate or sulphate, or they can be recycled for complete conversion to urea in a total-recycle process.

Two principal reactions take place in the formation of urea from ammonia and carbon dioxide. The first reaction is exothermic: 2NH3 + CO2 → H2N-COONH4 (ammonium carbamate)
While the second reaction is endothermic: H2N-COONH4 → (NH2)2CO + H2O Both reactions combined are exothermic.

The process is also called the Bosch-Meiser urea process after its discoverers (1922).

Uses Agricultural Use Urea is used as a nitrogen release fertilizer as it hydrolyses back to ammonia and carbon dioxide, but its most common impurity (biuret,NH2-CO-NH-CO-NH2) must be present at less than 2% as it impairs plant growth. It is also used in many multi-component solid fertilizer formulations.Its action of nitrogen release is due to the conditions favouring the reagent side of the equilibriums which produce urea.

Urea is usually spread at rates of between 40 and 300 kg/ha, but actual spreading rates will vary according to farm type and region. It is better to make several small to medium applications at intervals to minimise leaching losses and increase efficient use of the N applied compared with single heavy applications. During summer, urea should be spread just before, or during rain to reduce possible losses from volatilisation (process where nitrogen is lost to the atmosphere as ammonia gas). Urea should not be mixed for any length of time with other fertilizers as problems of physical quality may result.

Because of the high N concentration in urea, it is very important to achieve an even spread. Make sure that the application equipment has been correctly calibrated and is properly used. Do not drill on contact with or close to seed, due to the risk of germination damage. Urea dissolves in water for application as a spray or through irrigation systems.

In grain and cotton crops, urea is often applied at the time of the last cultivation before planting. It should be applied into, or be incorporated into the soil. In high rainfall areas and on sandy soils (where nitrogen can be lost through leaching) and where good in-season rainfall is expected, urea can be side or top-dressed during the growing season. Top-dressing is also popular on pasture and forage crops. In sugarcane, urea is side-dressed after planting, and applied to each ratoon crop.

In irrigated crops, urea can be applied dry to the soil, or dissolved and applied through the irrigation water. Urea will dissolve in its own weight in water, but it becomes increasingly difficult to dissolve as the concentration increases. Dissolving urea in water is endothermic, causing the temperature of the solution to fall when urea dissolves.

As a practical guide, when preparing urea solutions for fertigation (injection into irrigation lines), dissolve no more than 30 kg urea per 100 L water.

In foliar sprays, urea concentrations of 0.5 – 2.0% are often used in horticultural crops. As urea sprays may damage crop foliage, specific advice should be sought before use. Low biuret grades of urea should be used if urea sprays are to be applied regularly or to sensitive horticultural crops.

Storage of Urea Fertilizer Like most nitrogen products, urea absorbs moisture from the atmosphere. Therefore it is should be stored either in closed/sealed bags on pallets, or if stored in bulk, covered with a tarpaulin. As with most solid fertilizers, it should also be stored in a cool, dry, well ventilated area.

Industrial Use Urea has the ability to form 'loose compounds' with many organic compounds. The organic compounds are held in channels formed by interpenetrating helices comprising of hydrogen bonded urea molecules. This behaviour can be used to separate mixtures and has been used in the production of aviation fuel and lubricating oils.As the helices are interconnected all helices in a crystal must have the same 'handedness'. This is determined when the crystal is nucleated and can thus be forced by seeding. This property has been used to separate racemic mixtures.

Further commercial uses include:

Laboratory use Urea is a powerful protein denaturation (biochemistry). This property can be exploited to increase the solubility of some proteins. For this application it is used in concentrations up to 10 Molar volume.Urea is used to effectively disrupt the noncovalent bonds in proteins.Urea is an ingredient in the synthesis of urea nitrate.Urea nitrate is also a high explosive very similar to ammonium nitrate, however it may even be more powerful because of its complexity. VOD is 11,000 fps to 15,420 fps.

Medical use Drug use Urea is used in topical Dermatology products to promote rehydration of the skin. If covered by an occlusive dressing, 40% urea preparations may also be used for nonsurgical debridement of Nail (anatomy). This drug is also used as an earwax removal aid.

Clinical diagnosis See blood urea nitrogen ("BUN") for a commonly performed urea test, and marker of renal function.

Other diagnostic use Isotopically-labeled urea (carbon-14 - radioactive, or Carbon-13 - stable isotope) is used in the Urea breath test, which is used to detect the presence of Helicobacter pylori (H. pylori, a bacterium) in the stomach and duodenum of humans. The test detects the characteristic enzyme urease, produced by H. pylori, by a reaction that produces ammonia from urea. This increases the pH (reduces acidity) of the stomach environment around the bacteria.

Similar bacteria species to H. pylori can be identified by the same test in animals (apes, dogs, cats - including big cats).

Textile use Urea in textile laboratories are frequently used both in dyeing and printing as an important auxiliary which provides solubility to the bath and retains some moisture which is required for the dyeing or printing process.

Ureas Ureas or carbamides are a class of chemical compounds sharing the same functional group RR'N-CO-NRR' based on a carbonyl group flanked by two organic amine residues. They can be accessed in the laboratory by reaction of phosgene with primary or secondary amines. Example of ureas are the compounds carbamide peroxide, allantoin and Hydantoin. Ureas are closely related to biurets and structurally related to amides, carbamates, diimides, carbodiimides and thiocarbamides.

Reactions Urea reacts with alcohols to form urethanes. Urea reacts with malonic acid esters to make barbituric acids.

References

External links



UREA
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Urea - Wikipedia, the free encyclopedia
Urea is an organic compound with the chemical formula (N H 2) 2 C O. Urea is also known by the International Nonproprietary Name (rINN) carbamide, as established by the World ...

Definition: urea from Online Medical Dictionary
The Online Medical Dictionary is a searchable dictionary of definitions from medicine, science and technology.

Definition: urea cycle from Online Medical Dictionary
The Online Medical Dictionary is a searchable dictionary of definitions from medicine, science and technology.

Urea (Renal PatientView)
Urea - [also known as BUN] Urea is a small molecule produced from protein and put out by the kidneys, so blood levels rise in kidney failure. It is not such an accurate test for ...

Urea - definition of Urea in the Medical dictionary - by the Free ...
Definition of Urea in the Medical Dictionary. Urea explanation. Information about Urea in Free online English dictionary. What is Urea? Meaning of Urea medical term. What does Urea ...

Amazon.co.uk: urea
The World Market for Carboxyamide-Function Compounds and Amide-Function Compounds of Carbonic Acid Excluding Urea: A 2007 Global Trade Perspective by Philip M.

UREA FORMALDEHYDE FOAM INSULATION
urea formaldehyde foam insulation ... Health and Safety Executive / Local Authorities Enforcement Liaison Committee (HELA)

Urea
Urea (also known as carbamide) is a waste product of many living organisms, and is the major organic component of human urine. This is because it is at the end of chain of ...

urea definition of urea in the Free Online Encyclopedia.
Encyclopedia article about urea. Information about urea in the Columbia Encyclopedia, Computer Desktop Encyclopedia, computing dictionary. urea cycle, blood urea nitrogen, urea ...

 

Urea



 
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