Urea CAS#57-13-6

Environmentally Responsive Behavior: Exhibits controlled moisture absorption and release depending on temperature and humidity conditions, ensuring adaptable performance.

Strong Chemical Reactivity: Easily forms a wide range of crystalline addition compounds and complex salts with inorganic substances, supporting diverse chemical applications.

High Functional Versatility: Reacts with multiple compounds such as carbohydrates, acids, and formaldehyde, enabling the production of derivatives like urea resins and slow-release urea.

Broad Industrial Utility: Widely applicable in chemical synthesis and material production due to its ability to undergo various controlled reactions and transformations.

Products Description of Urea CAS#57-13-6

When the temperature stays below 20°C and relative humidity remains under 70%, urea exhibits no moisture absorption; it may even release water, leading to a drop in its moisture content. Once the temperature rises above 20°C and relative humidity exceeds 80%, urea starts absorbing moisture and can turn into a pasty mass under extreme circumstances. When ambient humidity subsequently declines, caking will recur. Its caking tendency is second only to ammonium nitrate.

Aqueous urea solution hydrolyzes and decomposes at 80°C to generate ammonium carbamate, ammonia and carbon dioxide. Heating accelerates the decomposition rate under both acidic and alkaline environments.

Urea easily reacts with linear carbohydrates to form crystalline adducts. It is capable of forming multiple complex salts with inorganic compounds, including Ca(NO₃)₂·4CO(NH₂)₂, NH₄Cl·CO(NH₂)₂, CaSO₄·4CO(NH₂)₂, MgSO₄·4CO(NH₂)₂·3H₂O and Mg(NO₃)₂·4CO(NH₂)₂·2H₂O. Moreover, it reacts with monocalcium phosphate to yield urea phosphate, dicalcium phosphate and water, following the reaction equation: Ca(H₂PO₄)₂·H₂O + CO(NH₂)₂ → H₃PO₄·CO(NH₂)₂ + CaHPO₄ + H₂O. Urea can also combine with nitric acid to produce urea nitrate: CO(NH₂)₂ + HNO₃ → CO(NH₂)₂·HNO₃. Additionally, it undergoes condensation with formaldehyde to form urea-formaldehyde derivatives. A high formaldehyde proportion facilitates the synthesis of urea resins, whereas a lower proportion generates slow-release urea.

Urea Chemical Properties

Melting point 

132-135 °C(lit.)

Boiling point 

332.48°C (estimate)

density 

1.335 g/mL at 25 °C(lit.)

vapor pressure 

<0.1 hPa (20 °C)

refractive index 

n20/D 1.40

storage temp. 

2-8°C

solubility 

H2O: 8 M at 20 °C

form 

powder

pka

0.10(at 25℃)

color 

white

Specific Gravity

1.335

PH

8.0-10.0 (20℃, 8M in H2O)

Odor

almost odorless

Water Solubility 

1080 g/L (20 ºC)

λmax

λ: 260 nm Amax: 0.03

λ: 280 nm Amax: 0.02

Merck 

149867

BRN 

635724

Dielectric constant

3.5(Ambient)

Stability:

Substances to be avoided include strong oxidizing agents. Protect from moisture.

InChIKey

XSQUKJJJFZCRTK-UHFFFAOYSA-N

LogP

-1.660 (est)

CAS DataBase Reference

57-13-6(CAS DataBase Reference)

NIST Chemistry Reference

Urea(57-13-6)

EPA Substance Registry System

Urea (57-13-6)

Safety Information

Hazard Codes 

Xn,Xi

Risk Statements 

36/37/38-40-38

Safety Statements 

26-36-24/25-37

RIDADR 

Not regulated

WGK Germany 

1

RTECS 

YR6250000

TSCA 

Yes

HS Code 

31021010

Hazardous Substances Data

57-13-6(Hazardous Substances Data)

Toxicity

LD50 orally in Rabbit: 8471 mg/kg LD50 dermal Rat 8200 mg/kg

Urea CAS#57-13-6

Product Application of Urea CAS# 57-13-6

Urea finds its major application as an agricultural fertilizer. For industrial purposes, it acts as a key feedstock to manufacture urea-formaldehyde resins, polyurethane and melamine-formaldehyde resins. It also has extensive applications across pharmaceuticals, explosives, leather treatment, flotation reagents, pigments and petroleum dewaxing processes.When heated to approximately 200°C, urea converts into solid cyanuric acid. Derivatives of cyanuric acid cover trichloroisocyanuric acid, sodium dichloroisocyanurate, tris(2-hydroxyethyl) isocyanurate, triallyl isocyanurate, tris(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate, triglycidyl isocyanurate, as well as cyanuric acid-melamine complexes. These derivatives possess wide-ranging and valuable uses. Specifically, trichloroisocyanuric acid and sodium dichloroisocyanurate are premium disinfectants and bleaching agents, and the worldwide production capacity of trichloroisocyanuric acid surpasses 80,000 tons.

Urea CAS# 57-13-6

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