TCEP

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TCEP
Skeletal formula of TCEP
Space-filling model of the TCEP molecule
Names
IUPAC name
3,3′,3′′-Phosphanetriyltripropanoic acid
Other names
TCEP
Tris(2-carboxyethyl)phosphine
Identifiers
51805-45-9 YesY
ChemSpider 106653 N
Jmol 3D model Interactive image
PubChem 119411
  • InChI=1S/C9H15O6P/c10-7(11)1-4-16(5-2-8(12)13)6-3-9(14)15/h1-6H2,(H,10,11)(H,12,13)(H,14,15) N
    Key: PZBFGYYEXUXCOF-UHFFFAOYSA-N N
  • InChI=1/C9H15O6P/c10-7(11)1-4-16(5-2-8(12)13)6-3-9(14)15/h1-6H2,(H,10,11)(H,12,13)(H,14,15)
    Key: PZBFGYYEXUXCOF-UHFFFAOYAQ
  • OC(CCP(CCC(O)=O)CCC(O)=O)=O
Properties
C9H15O6P
Molar mass 250.19 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

TCEP (tris(2-carboxyethyl)phosphine) is a reducing agent frequently used in biochemistry and molecular biology applications.[1] It is often prepared and used as a hydrochloride salt (TCEP-HCl) with a molecular weight of 286.65 gram/mol. It is soluble in water and available as a stabilized solution at neutral pH and immobilized onto an agarose support to facilitate removal of the reducing agent.

Applications

TCEP is often used as a reducing agent to break disulfide bonds within and between proteins as a preparatory step for gel electrophoresis.

Compared to the other two most common agents used for this purpose (dithiothreitol and β-mercaptoethanol), TCEP has the advantages of being odorless, a more powerful reducing agent, an irreversible reducing agent (in the sense that TCEP does not regenerate--the end product of TCEP-mediated disulfide cleavage is in fact two free thiols/cysteines), more hydrophilic, and more resistant to oxidation in air.[2] It also does not reduce metals used in immobilized metal affinity chromatography.

TCEP is particularly useful when labeling cysteine residues with maleimides. TCEP can keep the cysteines from forming di-sulfide bonds and unlike dithiothreitol and β-mercaptoethanol, it will not react as readily with the maleimide.[2] However, TCEP has been reported to react with maleimide under certain conditions.[3][4]

TCEP is also used in the tissue homogenization process for RNA isolation.[5]

References

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  2. 2.0 2.1 TCEP technical information, from Interchim
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