Date published: 2026-2-1

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Urea, 2M (CAS 57-13-6)

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Alternate Names:
Carbamide solution
Application:
Urea, 2M is stock solution used routinely as a cleaning and regeneration buffer for affinity columns
CAS Number:
57-13-6
Molecular Weight:
60.06
Molecular Formula:
CH4CONH2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Urea, 2M, is a highly concentrated solution of urea, a small organic compound that plays a pivotal role in biochemical and molecular biology research, particularly in the study of protein structures. Urea acts primarily as a protein denaturant; it disrupts the hydrogen bonding that holds proteins in their three-dimensional structures without breaking peptide bonds, thereby unfolding proteins into their linear form. This mechanism is crucial for studying protein sequences and conformations, as it allows researchers to reduce the complex native structure of proteins and examine their polypeptide backbones. In protein research, urea solutions are commonly used in denaturing polyacrylamide gel electrophoresis (PAGE), a technique that separates proteins based on their molecular weight under denaturing conditions, providing valuable insights into protein composition and purity. Additionally, urea is used in the refolding of proteins, where controlled removal of urea can aid in the renaturation process after initial denaturation. This is particularly useful in recombinant protein production where high yields of properly folded proteins are desirable. Moreover, urea finds application in the solubilization of nucleic acids, facilitating the manipulation and analysis of RNA and DNA in various experimental protocols. Its ability to disrupt secondary and tertiary structures without degrading nucleic acid chains makes it a useful reagent in molecular biology for processes such as nucleic acid extraction and purification. Overall, 2M urea is an essential tool in the arsenal of life sciences research, enabling detailed structural and functional analyses of biomolecules.


Urea, 2M (CAS 57-13-6) References

  1. Biologically inspired synthesis of bone-like composite: self-assembled collagen fibers/hydroxyapatite nanocrystals.  |  Tampieri, A., et al. 2003. J Biomed Mater Res A. 67: 618-25. PMID: 14566805
  2. A chemical-responsive supramolecular hydrogel from modified cyclodextrins.  |  Deng, W., et al. 2007. Angew Chem Int Ed Engl. 46: 5144-7. PMID: 17526038
  3. Cooperative effects of urea and L-arginine on protein refolding.  |  Chen, J., et al. 2009. Protein Expr Purif. 66: 82-90. PMID: 19233287
  4. Jk(a-b-) phenotype screening by the urea lysis test in Thai blood donors.  |  Deelert, S., et al. 2010. Blood Transfus. 8: 17-20. PMID: 20104274
  5. Solubilization of inclusion body proteins using n-propanol and its refolding into bioactive form.  |  Singh, SM., et al. 2012. Protein Expr Purif. 81: 75-82. PMID: 21964443
  6. Novel porous soy protein-based blend structures for biomedical applications: Microstructure, mechanical, and physical properties.  |  Barkay-Olami, H. and Zilberman, M. 2016. J Biomed Mater Res B Appl Biomater. 104: 1109-20. PMID: 26038233
  7. Primaquine hybrids as promising antimycobacterial and antimalarial agents.  |  Pavić, K., et al. 2018. Eur J Med Chem. 143: 769-779. PMID: 29220797
  8. Use of isoelectric focusing and a chromophoric organomercurial to monitor urea-induced conformational changes of yeast phosphoglycerate kinase.  |  Stinson, RA. 1977. Biochem J. 167: 65-70. PMID: 337969
  9. Urea and oxalate inhibition of the serum lactate dehydrogenase.  |  Emerson, PM. and Wilkinson, JH. 1965. J Clin Pathol. 18: 803-7. PMID: 5844214

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Urea, 2M, 500 ml

sc-296684
500 ml
$41.00