Hydrogen peroxide - urea

Hydrogen peroxide - urea (also called Hyperol, artizone, urea hydrogen peroxide, and UHP) is a solid composed of equal amounts of hydrogen peroxide and urea. This compound is a white crystalline solid which dissolves in water to give free hydrogen peroxide. Hydrogen peroxide - urea contains solid and water-free hydrogen peroxide, which offers a higher stability and better controllability than liquid hydrogen peroxide when used as an oxidizing agent. Often called carbamide peroxide in the dental office, it is used as a source of hydrogen peroxide for bleaching, disinfection, and oxidation.

Hydrogen peroxide - urea
Names
Other names
Urea peroxide, percarbamide, UHP
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.004.275
PubChem CID
UNII
InChI
  • InChI=1S/CH4N2O.H2O2/c2-1(3)4;1-2/h(H4,2,3,4);1-2H Y
    Key: AQLJVWUFPCUVLO-UHFFFAOYSA-N Y
SMILES
  • O=C(N)N.OO
Properties
Chemical formula
 CH6N2O3
Molar mass 94.070 g·mol−1
Appearance White solid
Density 1.50 g/cm3
Melting point 75 to 91.5 °C (167.0 to 196.7 °F; 348.1 to 364.6 K) (decomposes)
Pharmacology
D02AE01 (WHO)
Hazards
GHS labelling:[1]
Pictograms
Signal word
 Danger
Hazard statements
 H272, H315, H318
Precautionary statements
 P210, P220, P264, P280, P302+P352, P305+P351+P338
Flash point 60 °C (140 °F; 333 K)
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Production

For the preparation of the complex, urea is dissolved in 30% hydrogen peroxide (molar ratio 2:3) at temperatures below 60 °C. upon cooling this solution, hydrogen peroxide - urea precipitates in the form of small platelets.[2]

Determination of the hydrogen peroxide content by titration with potassium permanganate solution gives a value of 35.4% which corresponds to 97.8% of the theoretical maximum value. The remaining impurity consists of urea.

Akin to water of crystallization, hydrogen peroxide cocrystallizes with urea with the stoichiometry of 1:1. The compound is simply produced (on a scale of several hundred tonnes a year) by the dissolution of urea in excess concentrated hydrogen peroxide solution, followed by crystallization.[3] The laboratory synthesis is analogous.[4]

Structure and properties

The solid state structure of this adduct has been determined by neutron diffraction.[5]

Hydrogen peroxide-urea is a readily water-soluble, odorless, crystalline solid, which is available as white powder or colorless needles or platelets.[2] Upon dissolving in various solvents, the 1:1 complex dissociates back to urea and hydrogen peroxide. So just like hydrogen peroxide, the (erroneously) so-called adduct is an oxidizer but the release at room temperature in the presence of catalysts proceeds in a controlled manner. Thus the compound is suitable as a safe substitute for the unstable aqueous solution of hydrogen peroxide. Because of the tendency for thermal decomposition, which accelerates at temperatures above 82 °C,[6] it should not be heated above 60 °C, particularly in pure form.

The solubility of commercial samples varies from 0.05 g/mL[7] to more than 0.6 g/mL.[8]

Applications

Disinfectant and bleaching agent

Hydrogen peroxide - urea is mainly used as a disinfecting and bleaching agent in cosmetics and pharmaceuticals.[3] As a drug, this compound is used in some preparations for the whitening of teeth.[3][9][10] It is also used to relieve minor inflammation of gums, oral mucosal surfaces and lips including canker sores and dental irritation,[11] and to emulsify and disperse earwax.[12]

Carbamide peroxide is also suitable as a disinfectant, e.g. for germ reduction on contact lens surfaces or as an antiseptic for mouthwashes, ear drops or for superficial wounds and ulcers.

Reagent in organic synthesis

In the laboratory, it is used as a more easily handled replacement for hydrogen peroxide.[4][13][14] It has proven to be a stable, easy-to-handle and effective oxidizing agent which is readily controllable by a suitable choice of the reaction conditions. It delivers oxidation products in an environmentally friendly manner and often in high yields especially in the presence of organic catalysts such as cis-butenedioic anhydride[15] or inorganic catalysts such as sodium tungstate.[16]

Reaktionen mit Carbamidperoxid

It converts thiols selectively to disulfides,[15] secondary alcohols to ketones,[16] sulfides to sulfoxides and sulfones,[17] nitriles to amides,[17][18] and N-heterocycles to amine oxides.[17][19]

Reaktionen von Methoxyphenolen mit UHP

Hydroxybenzaldehydes are converted to dihydroxybenzenes (Dakin reaction)[17][20] and give, under suitable conditions, the corresponding benzoic acids.[20]

Baeyer-Villiger-Oxidation mit UHP

It oxidizes ketones to esters, in particular cyclic ketones, such as substituted cyclohexanones[21] or cyclobutanones[22] to give lactones (Baeyer-Villiger oxidation).

The epoxidation of various alkenes in the presence of benzonitrile yields oxiranes in yields of 79 to 96%.[23]

Epoxidierung von Cyclohexen mit UHP

The oxygen atom transferred to the alkene originates from the peroxoimide acid formed intermediately from benzonitrile. The resulting imidic acid tautomerizes to the benzamide.

Safety

The compound acts as a strong oxidizing agent and can cause skin irritation and severe eye damage.[24]

See also
  • Sodium percarbonate

References
  1. GHS: Sigma-Aldrich 289132
  2. C.-S. Lu, E.W. Hughes, P.A. Giguère (1941), "The crystal structure of the urea-hydrogen peroxide addition compound CO(NH2)2 H2O2", J. Am. Chem. Soc., vol. 63, no. 6, pp. 1507–1513, doi:10.1021/ja01851a007{{citation}}: CS1 maint: multiple names: authors list (link)
  3. Harald Jakob, Stefan Leininger, Thomas Lehmann, Sylvia Jacobi, Sven Gutewort. "Peroxo Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_177.pub2.{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link)
  4. Yu, Lei; Meng, Bo; Huang, Xian (2008). "Urea-Hydrogen Peroxide Complex: A Selective Oxidant in the Synthesis of 2-Phenylselenyl-1,3-butadienes". Synthetic Communications. 38 (18): 3142. doi:10.1080/00397910802109224. S2CID 98323467.
  5. Fritchie, C. J. Jr.; McMullan, R. K. (1981). "Neutron Diffraction Study of the 1:1 Urea:Hydrogen Peroxide complex at 81 K". Acta Crystallographica Section B. 37 (5): 1086. doi:10.1107/S0567740881005116.
  6. H. Heaney, F. Cardona, A. Goti, A.L. Frederick (2013). "Hydrogen Peroxide-Urea". Encyclopedia of Reagents for Organic Synthesis. E-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rh047.pub3. ISBN 978-0471936237.{{cite book}}: CS1 maint: multiple names: authors list (link)
  7. Sigma-Aldrich specification sheet
  8. Chemicalland data sheet
  9. Mokhlis, G. R.; Matis, B. A.; Cochran, M. A.; Eckert, G. J. (2000). "A Clinical Evaluation of Carbamide Peroxide and Hydrogen Peroxide Whitening Agents during Daytime Use". Journal of the American Dental Association. 131 (9): 1269–77. doi:10.14219/jada.archive.2000.0380. PMID 10986827. Archived from the original on 2013-02-23.
  10. Toothwhitening Archived 2008-03-17 at the Wayback Machine from the UMD of New Jersey website
  11. Center for Integrative Medicine: Carbamide Peroxide from the University of Maryland Medical Center website Archived October 18, 2007, at the Wayback Machine
  12. "Ear Drops GENERIC NAME(S): CARBAMIDE PEROXIDE". WebMD. Retrieved July 3, 2021.
  13. Varma, Rajender S.; Naicker, Kannan P. (1999). "The Urea−Hydrogen Peroxide Complex: Solid-State Oxidative Protocols for Hydroxylated Aldehydes and Ketones (Dakin Reaction), Nitriles, Sulfides, and Nitrogen Heterocycles". Organic Letters. 1 (2): 189. doi:10.1021/ol990522n.
  14. Harry Heaney, Francesca Cardona, Andrea Goti, "Hydrogen Peroxide–Urea" Encyclopedia of Reagents for Organic Synthesis 2008. doi:10.1002/047084289X.rh047.pub2
  15. B. Karami, M. Montazerozohori, M. H. Habibi (2005), "Urea-Hydrogen Peroxide (UHP) oxidation of thiols to the corresponding disulfides promoted by maleic anhydride as mediator" (PDF), Molecules (in German), vol. 10, no. 10, pp. 1358–1363, doi:10.3390/10101385, PMC 6147623, PMID 18007530{{citation}}: CS1 maint: multiple names: authors list (link)
  16. M. Lukasiewicz; D. Bogdal; J. Pielichowski. "Microwave-assisted oxidation of alcohols using urea hydrogen peroxide". 8th International Electronic Conference on Synthetic Organic Chemistry. ECSOC-8. Retrieved 2016-05-10.
  17. R.S. Varma, K.P. Naicker, "The Urea-Hydrogen Peroxide Complex: Solid-State Oxidative Protocols for Hydroxylated Aldehydes and Ketones (Dakin Reaction), Nitriles, Sulfides, and Nitrogen Heterocycles", Org. Lett. (in German), vol. 1, no. 2, pp. 189–191, doi:10.1021/ol990522n
  18. US 0
  19. D. Rong, V.A. Phillips, R.S. Rubio, M.A. Castro, R.T. Wheelhouse, "A safe, convenient and efficient method for the preparation of heterocyclic N-oxides using urea-hydrogen peroxide", Tetrahedron Lett. (in German), vol. 49, no. 48, pp. 6933–6935, doi:10.1016/j.tetlet.2008.09.124{{citation}}: CS1 maint: multiple names: authors list (link)
  20. H. Heaney, A.J. Newbold (2001), "The oxidation of aromatic aldehydes by magnesium monoperoxyphthalate and urea-hydrogen peroxide", Tetrahedron Lett. (in German), vol. 42, no. 37, pp. 6607–6609, doi:10.1016/S0040-4039(01)01332-6
  21. M.Y. Rios, E. Salazar, H.F. Olivo (2007), "Baeyer–Villiger oxidation of substituted cyclohexanones via lipase-mediated perhydrolysis utilizing urea–hydrogen peroxide in ethyl acetate", Green Chem. (in German), vol. 9, no. 5, pp. 459–462, doi:10.1039/B618175A{{citation}}: CS1 maint: multiple names: authors list (link)
  22. A. Watanabe, T. Uchida, K. Ito, T. Katsuki (2002), "Highly enantioselective Baeyer-Villiger oxidation using Zr(salen) complex as catalyst", Tetrahedron Lett. (in German), vol. 43, no. 25, pp. 4481–4485, doi:10.1016/S0040-4039(02)00831-6{{citation}}: CS1 maint: multiple names: authors list (link)
  23. L. Ji, Y.-N. Wang, C. Qian, X.-Z. Chen (2013), "Nitrile-promoted alkene epoxidation with urea-hydrogen peroxide (UHP)", Synth. Commun. (in German), vol. 43, no. 16, pp. 2256–2264, doi:10.1080/00397911.2012.699578, S2CID 93770740{{citation}}: CS1 maint: multiple names: authors list (link)
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