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EDTA, 0.5 M, pH 8.0 (CAS 60-00-4)

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Alternate Names:
Ethylenediaminetetraacetic Acid Sodium Salt Solution
Application:
EDTA, 0.5 M, pH 8.0 is a sterile-filtered solution of 0.5 M EDTA in H2O treated with DEPC, for use in molecular biology applications
CAS Number:
60-00-4
Molecular Weight:
292.24
Molecular Formula:
C10H16N2O8•xNa
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ethylenediaminetetraacetic acid (EDTA) is a versatile chemical compound widely utilized in scientific research due to its exceptional chelating properties. In laboratories, it is commonly prepared as a 0.5 M solution with a pH of 8.0. In research, EDTA is primarily employed as a chelating agent, meaning it forms stable complexes with metal ions. This property makes it invaluable in various biochemical and molecular biology applications. For instance, EDTA is frequently used in molecular biology to chelate divalent cations like magnesium (Mg^2+) that are essential for nucleic acid polymerases. By sequestering these ions, EDTA inhibits enzyme activity, enabling researchers to manipulate and study nucleic acids without unwanted enzymatic reactions. Moreover, EDTA finds extensive use in analytical chemistry, particularly in metal ion detection and titrations. Its ability to selectively bind to specific metal ions allows for precise determination and quantification of metals in complex mixtures. In addition to its role as a chelator, EDTA serves as a stabilizing agent in various laboratory reagents and solutions. Its ability to prevent metal ion-mediated catalysis or degradation enhances the stability and shelf-life of many biochemical and molecular biology reagents.


EDTA, 0.5 M, pH 8.0 (CAS 60-00-4) References

  1. Final report on the safety assessment of EDTA, calcium disodium EDTA, diammonium EDTA, dipotassium EDTA, disodium EDTA, TEA-EDTA, tetrasodium EDTA, tripotassium EDTA, trisodium EDTA, HEDTA, and trisodium HEDTA.  |  Lanigan, RS. and Yamarik, TA. 2002. Int J Toxicol. 21 Suppl 2: 95-142. PMID: 12396676
  2. Some further observations on the interaction of EDTA with the myosin-ATP system.  |  FRIESS, EG., et al. 1954. Arch Biochem Biophys. 53: 311-3. PMID: 13208306
  3. Bismuth EDTA complex.  |  SAPEIKA, N. 1955. S Afr Med J. 29: 137-9. PMID: 14358876
  4. The inhibition of hematopoietic action of cobalt by ethylenediamine. tetraacetic acid (EDTA).  |  CHILD, GP. 1951. Science. 114: 466-7. PMID: 14892768
  5. RNase footprinting to map sites of RNA-protein interactions.  |  Nilsen, TW. 2014. Cold Spring Harb Protoc. 2014: 677-82. PMID: 24890210
  6. Necroptosis mediates the antineoplastic effects of the soluble fraction of polysaccharide from red wine in Walker-256 tumor-bearing rats.  |  Stipp, MC., et al. 2017. Carbohydr Polym. 160: 123-133. PMID: 28115086
  7. Stable chelating linkage for reversible immobilization of oligohistidine tagged proteins in the BIAcore surface plasmon resonance detector.  |  Gershon, PD. and Khilko, S. 1995. J Immunol Methods. 183: 65-76. PMID: 7602140
  8. Determining EDTA in blood.  |  Sheppard, RL. and Henion, J. 1997. Anal Chem. 69: 477A-480A. PMID: 9253241

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

EDTA, 0.5 M, pH 8.0, 100 ml

sc-203932
100 ml
$19.00