Diethyl dicarbonate, 97%, Thermo Scientific Chemicals
Diethyl dicarbonate, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Diethyl dicarbonate, 97%, Thermo Scientific Chemicals

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Quantity:
100 g
5 g
25 g
Catalog number B22753.22
also known as B22753-22
Price (USD)/ Each
286.65
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318.00 
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Quantity:
100 g
Request bulk or custom format
Price (USD)/ Each
286.65
Online exclusive
318.00 
Save 31.35 (10%)
Add to cart
Diethyl dicarbonate, 97%, Thermo Scientific Chemicals
Catalog numberB22753.22
Price (USD)/ Each
286.65
Online exclusive
318.00 
Save 31.35 (10%)
-
Add to cart
Chemical Identifiers
CAS1609-47-8
IUPAC Namediethyl dicarbonate
Molecular FormulaC6H10O5
InChI KeyFFYPMLJYZAEMQB-UHFFFAOYSA-N
SMILESCCOC(=O)OC(=O)OCC
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
FormLiquid
Acid-base back titration≥96.0 to ≤104.0% (non-U.S. specification)
Assay from Suppliers CofA≥96.0% (U.S. specification)
CommentSpecification differs for U.S. and non-U.S. material where indicated
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Ribonuclease inhibitorDiethyl dicarbonate acts as an inhibitor of ryanodine binding to ryanodine/calcium(II) receptor channel. It is useful for specific inactivation of nucleases during isolation of undegraded polynucleotides. Further, it inhibits platelet-activating factor acetyl hydrolase. In addition to this, it is involved in the modification reagent for His and Tyr residues in proteins.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ribonuclease inhibitorDiethyl dicarbonate acts as an inhibitor of ryanodine binding to ryanodine/calcium(II) receptor channel. It is useful for specific inactivation of nucleases during isolation of undegraded polynucleotides. Further, it inhibits platelet-activating factor acetyl hydrolase. In addition to this, it is involved in the modification reagent for His and Tyr residues in proteins.

Solubility
Miscible with chloroform, ethanol, esters, ketones and hydrocarbons. Slightly miscible with water.

Notes
Store in cool place. Incompatible with strong oxidizing agents, strong reducing agents, strong acids, strong bases and ammonia.
RUO – Research Use Only

General References:

  1. In the presence of the hindered base lithium dicyclohexylamide (from Dicyclohexyl amine, A15671), ɑ -ethoxycarbonylation of ketones occurs to give ß -keto esters: Synthesis, 1014 (1984).
  2. Dogandzhiyski, P.; Ghidini, A.; Danneberg, F.; Strömberg, R.; Göbel, M. W. Studies on Tris(2-aminobenzimidazole)-PNA Based Artificial Nucleases: A Comparison of Two Analytical Techniques. Bioconjugate Chem. 2015, 26 (12), 2514-2519.
  3. Zuldesmi, M.; Waki, A.; Kuroda, K.; Okido, M. Hydrothermal treatment of titanium alloys for the enhancement of osteoconductivity. Mater. Sci. Eng., C 2015, 49, 430-435.