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Molar Mass of Urea (CH₄N₂O)

Learn how chemists calculate the molar mass of Urea (CH₄N₂O), with a clear formula breakdown, worked steps, and study notes · IUPAC name: Carbamide.

Quick answer

The molar mass of Urea (CH₄N₂O) is

60.056g/mol

One mole of Urea therefore has a mass of 60.056 grams—the value you use for stoichiometry and laboratory preparation.

Reviewed for educational accuracy · Accuracy policy

CAS Registry Number
57-13-6
PubChem CID
1176
SMILES
C(=O)(N)N

Step-by-step calculation

Let's find the molar mass of Urea (CH₄N₂O) together—step by step, as if you are seeing the formula for the first time.

Step 1 — Look at the chemical formula

The formula is CH₄N₂O. Each letter stands for an element. The little number after a letter (the subscript) tells you how many atoms of that element are in one molecule or formula unit.

  • 1 Carbon atom (C)
  • 4 Hydrogen atoms (H)
  • 2 Nitrogen atoms (N)
  • 1 Oxygen atom (O)

Step 2 — Look up each atomic mass

Atomic mass comes from the periodic table. It is the average mass of one mole of atoms of that element, in grams per mole (g/mol). Think of it as the "price tag" for one mole of that element.

  • Carbon (C) = 12.011 g/mol
  • Hydrogen (H) = 1.008 g/mol
  • Nitrogen (N) = 14.007 g/mol
  • Oxygen (O) = 15.999 g/mol

Step 3 — Multiply atoms × atomic mass

Why multiply? If one oxygen atom "costs" about 16 g/mol, then two oxygen atoms cost twice as much. Each element's contribution is: number of atoms × atomic mass.

  • 1 × 12.011 = 12.011 g/mol (Carbon)
  • 4 × 1.008 = 4.032 g/mol (Hydrogen)
  • 2 × 14.007 = 28.014 g/mol (Nitrogen)
  • 1 × 15.999 = 15.999 g/mol (Oxygen)

Step 4 — Add the contributions

Why add? The molar mass of the whole compound is simply the total mass of every atom in the formula. Add each element's contribution:

12.011 + 4.032 + 28.014 + 15.999 = 60.056 g/mol

Step 5 — Final answer

Molar mass of Urea = 60.056 g/mol

That means one mole of Urea (CH₄N₂O) has a mass of about 60.06 grams.

Quick summary

Read the formula → count atoms → look up atomic masses → multiply → add → report g/mol. For CH₄N₂O, the total is 60.056 g/mol.

Common beginner mistakes

  • Writing urea's formula incorrectly as CON₂H₄ without recognizing the correct connectivity CO(NH₂)₂.
  • Confusing urea (CH₄N₂O, 60.06 g/mol) with ammonium nitrate (NH₄NO₃, 80.04 g/mol) — both nitrogen fertilizers but chemically distinct.
  • Assuming urea itself is toxic like ammonia — it is specifically the far less toxic detoxification product the body produces to safely eliminate excess nitrogen.

Memory trick

Remember the Wöhler synthesis as the historical turning point separating organic chemistry from vitalism — a favorite exam and general chemistry history question.

Mini practice

Without looking above, list the atoms in CH₄N₂O and write one multiplication line for the heaviest element. Then check your work against Step 3.

Real-world example

If a recipe asks for 0.100 mol of Urea, mass needed = 0.100 × 60.056 = 6.006 g. That is how chemists turn a mole amount into a weighable sample.

Atomic contribution table

Each row shows how much mass one element contributes to the total for CH₄N₂O.

ElementAtomsAtomic massContributionMass %
C112.01112.011 g/mol20.0%
H41.0084.032 g/mol6.7%
N214.00728.014 g/mol46.6%
O115.99915.999 g/mol26.6%
Total molar mass60.056 g/mol100%

Mass contribution chart

Mass contribution by element
Mass%C 20.0%H 6.7%N 46.6%O 26.6%
Formula unit — Urea
CH4N2O

Count every atom in this formula, multiply by atomic mass, then add. That total is the molar mass used in lab weighing.

Download study sheets

Save a printable summary, revision sheet, practice worksheet, or laboratory reference for Urea (CH₄N₂O).

Practice this calculation

Without looking above, write the atom count for CH₄N₂O, then compute the molar mass. Check your answer against 60.056 g/mol.

Next challenge: how many grams are in 0.250 mol of Urea? Multiply 0.250 × 60.056 to get 15.014 g.

Physical and chemical properties

Physical properties

AppearanceWhite crystalline solid or prilled granules (fertilizer form)
ColorWhite
OdorOdorless (fresh); ammonia-like odor if decomposing
State (STP)Solid
Density1.32 g/cm³
Melting point133–135 °C
Boiling pointDecomposes before boiling
Solubility1,080 g/L water at 20 °C (highly soluble)
Crystal structureTetragonal

Chemical properties

ClassificationOrganic diamide / carbamide (carbonic acid diamide)
FamilyAmides / carbamide derivatives
BasicityVery weakly basic (amide nitrogen lone pairs, much weaker than simple amines)
PolarityHighly polar (strong hydrogen-bonding carbonyl and amine groups)
GeometryPlanar around the carbonyl carbon (sp² hybridized)
Oxidation statesNot typically described by oxidation states (organic covalent compound)

Applications

Industrial uses

  • Nitrogen fertilizer manufacturing (highest nitrogen content of common solid fertilizers)
  • Urea-formaldehyde resin production for adhesives and particleboard
  • Diesel exhaust fluid (AdBlue) for selective catalytic reduction of NOₓ emissions
  • Feed additive (as a non-protein nitrogen source for ruminant livestock)

Laboratory uses

  • Protein denaturant in biochemistry (disrupts hydrogen bonding in solution)
  • Reference compound for teaching the Wöhler synthesis and history of organic chemistry
  • Urease enzyme activity assays

Ammonia volatilization from applied urea fertilizer contributes to air quality and nitrogen deposition concerns; excess agricultural nitrogen runoff can contribute to waterway eutrophication.

The primary nitrogenous waste product of mammalian protein metabolism, synthesized via the liver's urea cycle and excreted in urine; blood urea nitrogen is a standard clinical kidney function marker.

Preparation and production

Industrially synthesized by reacting ammonia with carbon dioxide under high pressure and temperature to form ammonium carbamate, which then dehydrates to urea: 2 NH₃ + CO₂ → NH₂COONH₄ → CO(NH₂)₂ + H₂O. This is known as the Bosch–Meiser urea process, closely linked to the Haber–Bosch ammonia synthesis that supplies its nitrogen feedstock.

Global urea production exceeds 180 million tonnes annually, making it the highest-volume manufactured nitrogen compound, overwhelmingly destined for agricultural fertilizer use.

Important reactions of Urea

2 NH₃(g) + CO₂(g) → CO(NH₂)₂(s) + H₂O(l)

Reaction type
Industrial synthesis (Bosch–Meiser process)
Conditions
High temperature and pressure, via ammonium carbamate intermediate
Explanation
Ammonia and carbon dioxide combine under industrial conditions to form ammonium carbamate, which dehydrates to yield urea, the dominant industrial production route.
Products
Urea and water
Why it matters
Global industrial urea fertilizer production

Related ideas: Industrial synthesis · Haber-Bosch integration · Condensation reactions

CO(NH₂)₂(aq) + H₂O(l) → 2 NH₃(g) + CO₂(g)

Reaction type
Enzymatic hydrolysis (urease-catalyzed)
Conditions
Aqueous, urease enzyme (soil bacteria or biological systems)
Explanation
Urease-catalyzed hydrolysis breaks down urea into ammonia and carbon dioxide, the mechanism by which soil bacteria release plant-available nitrogen from applied urea fertilizer.
Products
Ammonia and carbon dioxide
Why it matters
Soil nitrogen release from fertilizer, urease assay chemistry

Related ideas: Enzyme catalysis · Hydrolysis · Agricultural chemistry

2 CO(NH₂)₂(l, heated) → NH₂CONHCONH₂ (biuret) + NH₃(g)

Reaction type
Thermal decomposition (condensation side reaction)
Conditions
Heating above melting point (~135 °C)
Explanation
Prolonged heating of molten urea drives a condensation reaction forming biuret with loss of ammonia, an undesirable side reaction monitored in fertilizer manufacturing quality control.
Products
Biuret and ammonia
Why it matters
Fertilizer quality control, understanding thermal decomposition limits

Related ideas: Thermal decomposition · Condensation reactions · Fertilizer chemistry

4 NH₃(from urea) + 4 NO(g) + O₂(g) → 4 N₂(g) + 6 H₂O(g)

Reaction type
Selective catalytic reduction (industrial emissions control)
Conditions
Catalyst (e.g., vanadium or zeolite-based), diesel exhaust temperature
Explanation
Ammonia generated from thermally decomposed urea (diesel exhaust fluid) reacts catalytically with nitrogen oxides in diesel exhaust, converting them to harmless nitrogen gas and water vapor.
Products
Nitrogen gas and water vapor
Why it matters
Diesel vehicle emissions control (AdBlue/SCR systems)

Related ideas: Catalysis · Redox reactions · Emissions control chemistry

History and discovery

Urea was first isolated from urine by Hilaire Rouelle in 1773, but its true chemical significance emerged in 1828 when Friedrich Wöhler synthesized it by heating ammonium cyanate, an inorganic salt — a discovery credited with undermining vitalism and helping establish organic chemistry as a discipline governed by the same physical laws as inorganic chemistry. Hans Krebs and Kurt Henseleit elucidated the biological urea cycle in 1932, and industrial urea synthesis from ammonia and CO₂ (the Bosch–Meiser process) was developed in the early 20th century alongside the broader growth of the nitrogen fertilizer industry.

Hilaire Rouelle isolated urea from urine in 1773; Friedrich Wöhler achieved its landmark inorganic-to-organic synthesis in 1828.

Interesting facts

  • Urea's 1828 synthesis by Friedrich Wöhler is widely taught as the experiment that helped end the doctrine of vitalism in chemistry.
  • Urea has the highest nitrogen content by mass (46%) of any commonly used solid nitrogen fertilizer.
  • The human body produces roughly 25–30 grams of urea daily as a byproduct of normal protein metabolism, excreted primarily through urine.
  • Diesel exhaust fluid, essentially a purified urea solution, has become a common sight at fuel stations as more vehicles adopt selective catalytic reduction emissions technology.

Comparison with similar compounds

Urea (CH₄N₂O, 60.06 g/mol, 46% nitrogen by mass) has a substantially higher nitrogen content than ammonium nitrate (NH₄NO₃, 80.04 g/mol, 35% nitrogen), explaining urea's dominance in bulk nitrogen fertilizer markets despite ammonium nitrate's faster initial nitrogen release.

Storage, handling, and safety

Store in a dry, sealed container, as urea is hygroscopic and can cake or degrade with moisture absorption. Keep away from strong oxidizers and avoid prolonged storage above its melting point, which can promote biuret formation.

Low acute hazard; treat as a mild irritant. Standard gloves and eye protection are sufficient for typical laboratory or agricultural handling. Avoid inhaling fine fertilizer-grade dust in bulk handling situations.

Low toxicity; generally recognized as safe in food-grade and pharmaceutical contexts at appropriate concentrations. Fertilizer-grade dust may cause mild respiratory or eye irritation.

  • Mild eye and respiratory irritation from dust
  • Ammonia release possible on prolonged heating or microbial decomposition
  • Environmental nitrogen loading concerns with excessive agricultural application

Classification: Not classified as hazardous under GHS for standard fertilizer or laboratory-grade material

Exam notes and student tips

Exam notes

  • Molar mass CH₄N₂O = 12.01 + 4(1.008) + 2(14.01) + 16.00 = 60.06 g/mol.
  • Wöhler synthesis: NH₄OCN (ammonium cyanate) → CO(NH₂)₂ (urea), an inorganic-to-organic isomerization.
  • Industrial synthesis: 2 NH₃ + CO₂ → CO(NH₂)₂ + H₂O (Bosch–Meiser process).
  • Urea hydrolysis (urease-catalyzed): CO(NH₂)₂ + H₂O → 2 NH₃ + CO₂.

Student tips

  • Remember the Wöhler synthesis as the historical turning point separating organic chemistry from vitalism — a favorite exam and general chemistry history question.
  • Link urea's high nitrogen percentage (46%) directly to its dominance as the world's most-used nitrogen fertilizer.
  • Connect the urea cycle's role in ammonia detoxification to clinical blood urea nitrogen (BUN) testing for kidney function.

Common mistakes

  • Writing urea's formula incorrectly as CON₂H₄ without recognizing the correct connectivity CO(NH₂)₂.
  • Confusing urea (CH₄N₂O, 60.06 g/mol) with ammonium nitrate (NH₄NO₃, 80.04 g/mol) — both nitrogen fertilizers but chemically distinct.
  • Assuming urea itself is toxic like ammonia — it is specifically the far less toxic detoxification product the body produces to safely eliminate excess nitrogen.

Misconceptions

  • Urea used in fertilizer and diesel exhaust fluid is not derived from animal urine — virtually all commercial urea is synthetically manufactured from ammonia and carbon dioxide.
  • Urea is not itself a strong base or strongly reactive compound — its amide nitrogens make it only very weakly basic compared to typical amines.
  • The biuret test for proteins does not use biuret derived from decomposed urea directly — it uses a copper(II)/alkaline reagent that reacts with peptide bonds structurally similar to biuret's own linkage.

Practice questions

  1. 1. Calculate the molar mass of urea (CH₄N₂O).

    Show answer

    12.01 + 4(1.008) + 2(14.01) + 16.00 = 60.06 g/mol

  2. 2. What is the percent nitrogen by mass in urea?

    Show answer

    (2 × 14.01) / 60.06 × 100 = 46.6%

  3. 3. How many moles of ammonia are released from complete hydrolysis of 30.03 g of urea?

    Show answer

    30.03 g ÷ 60.06 g/mol = 0.500 mol urea → 0.500 × 2 = 1.00 mol NH₃

  4. 4. Why is the Wöhler synthesis considered a landmark event in the history of chemistry?

    Show answer

    It demonstrated that an organic compound (urea) could be synthesized from inorganic starting materials (ammonium cyanate), challenging vitalism and helping unify organic and inorganic chemistry under the same natural laws.

Frequently asked questions about Urea

60.06 g/mol.

Chemistry of Urea

The sections above give the number you need for calculations. Here we look more closely at how Urea (CH₄N₂O) behaves chemically—so the molar mass connects to real reactions, properties, and laboratory practice.

Urea (CH₄N₂O, more descriptively written CO(NH₂)₂) is a simple organic compound with molar mass 60.06 g/mol (C 12.01 + H 4 × 1.008 + N 2 × 14.01 + O 16.00), consisting of a carbonyl group flanked by two amine groups. It holds a unique place in the history of chemistry as the first organic compound ever synthesized from inorganic starting materials, a landmark 1828 achievement by Friedrich Wöhler that helped dismantle the doctrine of vitalism — the belief that organic compounds could only be produced by living organisms through some special "vital force."

Biologically, urea is the primary nitrogenous waste product of protein and amino acid metabolism in mammals, produced in the liver through the urea cycle, which safely converts toxic ammonia (a byproduct of amino acid breakdown) into the far less toxic, highly water-soluble urea for excretion in urine. This detoxification pathway is so central to nitrogen metabolism that blood urea nitrogen (BUN) is a standard clinical marker of kidney function, since impaired renal filtration causes urea to accumulate in the bloodstream.

Industrially, urea is overwhelmingly the world's most widely used nitrogen fertilizer, prized for its high nitrogen content (46% by mass, the highest of any solid nitrogen fertilizer) and relatively low cost of production from ammonia and carbon dioxide. Beyond agriculture, urea serves as a key feedstock for urea-formaldehyde resins used in adhesives and particleboard, as the active reducing agent in diesel exhaust fluid (AdBlue) that helps catalytically reduce nitrogen oxide emissions, and in a striking twist of chemical history, as the compound whose accidental overheating with ammonium cyanate first revealed the biuret side reaction that still bears practical relevance in fertilizer quality control today.

CH₄N₂O, more informatively written CO(NH₂)₂, contains a central carbon double-bonded to oxygen (carbonyl) and single-bonded to two amine (–NH₂) groups. This arrangement makes urea the diamide of carbonic acid, structurally bridging simple carbonyl chemistry and amine/amide functionality, and gives the molecule strong hydrogen-bonding capacity despite its small size.

Urea is a weakly basic compound (due to its amide nitrogen lone pairs, though far weaker than a simple amine) and undergoes hydrolysis, especially enzymatically via urease, to ammonia and carbon dioxide — the reaction exploited by soil bacteria to release plant-available nitrogen from urea fertilizer. On heating above its melting point, urea can decompose to biuret and ammonia, and at higher temperatures further condenses to cyanuric acid and other products; controlling these side reactions is important in fertilizer manufacturing and quality.

Wöhler synthesis: the birth of organic chemistry from inorganic materials

In 1828, Friedrich Wöhler heated ammonium cyanate, an inorganic salt, and unexpectedly obtained urea — a compound previously known only as a product of animal metabolism. This landmark synthesis of an organic compound from purely inorganic starting materials directly challenged vitalism, the prevailing belief that organic substances required a mysterious 'vital force' unique to living organisms, and is widely credited with launching organic chemistry as a rigorous, unified scientific discipline rather than a separate domain governed by different natural laws.

The urea cycle and ammonia detoxification

In the liver, the urea cycle converts toxic ammonia — generated from amino acid catabolism — into water-soluble, far less toxic urea for excretion in urine. This multistep enzymatic pathway, elucidated by Hans Krebs and Kurt Henseleit in 1932, is essential to mammalian nitrogen metabolism, and genetic defects in urea cycle enzymes cause serious, sometimes life-threatening ammonia accumulation disorders.

The world's dominant nitrogen fertilizer

Urea's exceptionally high nitrogen content (46% by mass) and relatively straightforward industrial synthesis from ammonia and carbon dioxide have made it the most widely used solid nitrogen fertilizer on Earth, feeding a substantial share of global crop nitrogen demand. Soil urease enzymes hydrolyze applied urea to ammonium and eventually nitrate, making its nitrogen available for plant uptake, though volatilization losses as ammonia gas are a practical agronomic concern requiring careful application timing.

Biuret formation: urea's accidental decomposition product

Heating urea above its melting point can drive a condensation side reaction forming biuret (a compound of two urea units minus ammonia), which is undesirable in fertilizer because it can be phytotoxic to certain sensitive crops at elevated concentrations. This same biuret molecule lends its name to the classic biuret test for proteins, in which a copper(II) sulfate/alkaline reagent produces a violet color with peptide bonds structurally reminiscent of the biuret linkage — an unrelated but memorably connected piece of chemical nomenclature.

Diesel exhaust fluid and selective catalytic reduction

Urea dissolved in purified water (commercially sold as AdBlue or diesel exhaust fluid) is injected into modern diesel vehicle exhaust systems, where it thermally decomposes to ammonia that reacts with nitrogen oxides over a catalyst in a process called selective catalytic reduction, converting harmful NOₓ pollutants into harmless nitrogen gas and water vapor — a major technology enabling modern diesel engines to meet strict emissions standards.

Recalculate any formula with the molar mass calculator, compare atoms on the periodic table, or browse more compounds in the organic library.

References and further reading

  • PubChem CID 1176: Urea compound data
  • NIST Chemistry WebBook: Thermodynamic properties
  • FAO: Global nitrogen fertilizer production and use statistics