Urea peroxide
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Product Description
Urea peroxide is a white, odorless, water-soluble crystalline adduct that couples the oxidizing power of hydrogen peroxide with the softening action of urea in a storage-stable solid. This dual personality lets it release H₂O₂ slowly on contact with water, giving a sustained yet mild oxidative punch that is exploited far beyond the bathroom cabinet: in tooth-whitening strips, ear-wax drops, acne creams and hair-bleach it cleans, disinfects and brightens without the harshness of liquid peroxide, while in agriculture it moonlights as a “soil doctor,” breaking down allelopathic phenolic acids that cause replant failure, cutting arsenic uptake in rice through in-situ Fenton chemistry, accelerating glyphosate and volatile-chlorinated solvent degradation, and re-igniting soil nitrogen-cycling enzymes. Textile, paper, organic-synthesis and coal-desulfurization industries likewise value it as a selective, low-temperature bleaching and oxidizing agent. Although concentrations and compatibility must be managed—keep it away from acids, chlorinated cleaners and light—the compound’s benign footprint and easy handling are now driving research into greener farming, contaminated-land remediation and sustainable chemical manufacturing.
Other Information
Commercial Products
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Multiple brand-name earwax removal products
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Dental bleaching systems (e.g., Opalescence)
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Topical antiseptics and disinfectants
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Professional hair care products
Synthesis and Production
Synthesis Methods
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Traditional Chemical Synthesis: Formed by combining equimolar amounts of urea and hydrogen peroxide through hydrogen bonding to create a stable 1:1 adduct (CO(NH₂)₂·H₂O₂)
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Electrochemical Synthesis (Novel Method): Using an oxygen-coordinated cobalt single-atom catalyst (Co–O–C) for ambient electrosynthesis:
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Urea synthesis from CO₂ and NO₃⁻ with yield rate of 2704.2 ± 183.9 μg h⁻¹ mgcat⁻¹
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Hydrogen peroxide synthesis via two-electron oxygen reduction reaction (2e⁻ ORR) with yield rate of 538.8 ± 2.7 mmol h⁻¹ gcat⁻¹
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Subsequent combination to produce urea peroxide
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Industrial Production: Commercial production through reaction of urea with hydrogen peroxide solution followed by crystallization
Production Characteristics
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Solid form offers safer storage and transportation compared to liquid hydrogen peroxide
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Gradual decomposition upon contact with water, releasing hydrogen peroxide and urea
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Mature industrial production with CAS number 124-43-6
Uses and Applications
Medical and Personal Care
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Dental Bleaching: Active ingredient in tooth whitening agents (typically 10-35% concentrations)
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Earwax Removal: 5-6.5% otic solutions to soften, loosen and remove excessive earwax (e.g., Debrox, Murine)
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Oral Wound Healing: Treatment for oral mucosal injuries
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Topical Anti-infective: Disinfectant for minor wounds and skin infections
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Cosmetics: Oxidizing agent in hair bleaching, permanent wave oxidation, and hair relaxing products
Agricultural and Environmental Applications
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Soil Remediation:
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Alleviating continuous cropping obstacles: BC-UP (biochar-urea peroxide) composite degrades phenolic acids in soil, improving growth of medicinal plants like patchouli and ginseng
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Reducing arsenic contamination in rice: Alternative nitrogen source that inhibits arsenic reduction and methylation
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Pesticide residue degradation: Degrades glyphosate with half-life reduced to ~12 days
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Volatile organic compound control: With iron-loaded bentonite, degrades trichloroethylene and controls vapor emissions
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Biomass Pretreatment: KOH-UHP-Si combined pretreatment significantly increases cellulose content in lignocellulose to 81.4%, removes 97.3% lignin, and increases glucose yield by 9-fold
Industrial Applications
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Textile and Paper Industry: Mild bleaching agent for cotton, linen, wool, and paper whitening
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Organic Synthesis: Mild oxidizing agent for epoxidation and other reactions
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Coal Desulfurization: Microwave-assisted removal of organic sulfur from coal
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Plastics Manufacturing: Used in production of certain plastics
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Blueprint Development and Starch Modification: Historical uses
Household and Commercial Products
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Earwax removal kits and drops
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Tooth whitening kits and gels
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Topical disinfectants
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Landscaping/yard products
Chemical and Physical Properties
Physicochemical Properties
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Chemical Formula: CH₆N₂O₃ (CO(NH₂)₂·H₂O₂)
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Molecular Weight: 94.07 g/mol
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Appearance: White crystalline solid or paste-like semisolid, odorless
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Melting Point: 75-85°C (decomposes)
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Solubility: Highly water soluble (≥500 g/L)
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Density: 0.8 g/cm³ (less dense than water)
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Stability: Stable at room temperature, decomposes when moistened or heated
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Autoignition Temperature: >680°F (>360°C)
Structural Characteristics
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Hydrogen-bonded adduct of urea and hydrogen peroxide
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Crystal structure: Space group P nca, unit cell parameters a=6.7317Å, b=4.8207Å, c=12.873Å
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Four molecules per unit cell, Z'=0.5
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Crystallography Open Database (COD) Number: 2106955
Computed Properties
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Hydrogen Bond Donor Count: 4
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Hydrogen Bond Acceptor Count: 3
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Rotatable Bond Count: 0
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Topological Polar Surface Area: 110 Ų
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Complexity: 29
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Covalently-Bonded Unit Count: 2
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Exact Mass: 94.03784206 Da
Safety and Handling
Hazard Classification (GHS)
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Pictograms: Oxidizer, Corrosive, Irritant
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Signal Word: Danger
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Hazard Statements:
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H272: May intensify fire; oxidizer
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H314: Causes severe skin burns and eye damage
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H315: Causes skin irritation
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H318: Causes serious eye damage
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Precautionary Statements: P210, P220, P260, P264, P280, etc.
Physical Hazards
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Oxidizer: May intensify fire, combustible when heated or in contact with organic substances
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Thermal Decomposition: Melts and decomposes when heated, releasing oxygen and ammonia
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Explosion Hazard: Containers may explode when heated; serious explosion hazard from shock or heat
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Reactivity: Strong oxidizing agent; liable to spontaneous combustion with organic materials
Health Hazards
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Inhalation: Dust causes irritation of nose from hydrogen peroxide formed when heated
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Eye Contact: Causes severe damage, potentially corneal damage
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Skin Contact: Moist skin contact causes temporary itching or burning sensation; may cause skin blistering
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Ingestion: Causes irritation of mouth and stomach
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Specific Effects: Dermatotoxin (skin burns), toxic pneumonitis
Emergency Response
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Fire Fighting: Use water only; do not use dry chemicals or foams
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Small Spills: Place material into clean, dry container with clean shovel
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Large Spills: Dike far ahead of liquid spill for later disposal
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Isolation Distance: 50 meters for liquids, 25 meters for solids
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First Aid: Flush eyes/skin with water for 20-30 minutes; do not induce vomiting if ingested
Personal Protective Equipment
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Rubber gloves and protective goggles
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Positive pressure self-contained breathing apparatus (SCBA)
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Chemical protective clothing
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Structural firefighters' protective clothing for thermal protection
Storage Requirements
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Store in sealed containers
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Protect from light and moisture
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Keep in cool, dry place
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Separate from organic materials and combustibles
Regulatory Approvals
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United States: FDA-approved OTC drug ingredient, UN Number 1511 (Oxidizer), DOT Hazard Class 5.1
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European Union: REACH registered (EC Number 204-701-4), active status
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Australia: Listed on AICIS inventory
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New Zealand: HSNO approved with controls (HSR001360)
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Japan: NITE GHS classification available
Environmental Considerations
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Decomposition products: urea, oxygen, and water
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May form irritating ammonia gas during combustion
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Runoff from fire control may cause environmental contamination
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Considered for various environmental applications including soil remediation