EGTA

EGTA
Names
	Preferred IUPAC name 3,12-Bis(carboxymethyl)-6,9-dioxa-3,12-diazatetradecane-1,14-dioic acid
	Other names Triethylene glycol diamine tetraacetic acid
Identifiers
CAS Number	67-42-5 (free acid) ; 13368-13-3 (tetrasodium salt) ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:30740 ;
ChEMBL	ChEMBL240390 ;
ChemSpider	5972 ;
ECHA InfoCard	100.000.592
KEGG	D00569 ;
PubChem CID	6207;
UNII	526U7A2651 ;
CompTox Dashboard (EPA)	DTXSID2045151 ;
	InChI InChI=1S/C14H24N2O10/c17-11(18)7-15(8-12(19)20)1-3-25-5-6-26-4-2-16(9-13(21)22)10-14(23)24/h1-10H2,(H,17,18)(H,19,20)(H,21,22)(H,23,24) Key: DEFVIWRASFVYLL-UHFFFAOYSA-N ; InChI=1/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12) Key: CPJSUEIXXCENMM-UHFFFAOYAO; InChI=1/C14H24N2O10/c17-11(18)7-15(8-12(19)20)1-3-25-5-6-26-4-2-16(9-13(21)22)10-14(23)24/h1-10H2,(H,17,18)(H,19,20)(H,21,22)(H,23,24) Key: DEFVIWRASFVYLL-UHFFFAOYAF;
	SMILES O=C(O)CN(CC(=O)O)CCOCCOCCN(CC(=O)O)CC(=O)O;
Properties
Chemical formula	C14H24N2O10
Molar mass	380.350 g·mol−1
Melting point	241 °C (466 °F; 514 K)
Acidity (pKa)	2.0, 2.68, 8.85, 9.43
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

EGTA (ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid), also known as egtazic acid (INN, USAN),^[2] is an aminopolycarboxylic acid, a chelating agent. It is a white solid that is related to the better known EDTA. Compared to EDTA, it has a lower affinity for magnesium, making it more selective for calcium ions. It is useful in buffer solutions that resemble the environment in living cells^[3] where calcium ions are usually at least a thousandfold less concentrated than magnesium.

The pK_a for binding of calcium ions by tetrabasic EGTA is 11.00, but the protonated forms do not significantly contribute to binding, so at pH 7, the apparent pK_a becomes 6.91. See Qin et al. for an example of a pK_a calculation.^[4]

EGTA has also been used experimentally for the treatment of animals with cerium poisoning and for the separation of thorium from the mineral monazite. EGTA is used as a compound in elution buffer in the protein purification technique known as tandem affinity purification, in which recombinant fusion proteins are bound to calmodulin beads and eluted out by adding EGTA.

EGTA is often employed in dentistry and endodontics for the removal of the smear layer.

References

^ Raaflaub, Jürg (1956). "Applications of Metal Buffers and Metal Indicators in Biochemistry". Methods of Biochemical Analysis. Vol. 3. pp. 301–325. doi:10.1002/9780470110195.ch10. ISBN 978-0-470-30492-1. PMID 13369167.
^ Pubchem. "EGTA | C14H24N2O10 - PubChem". pubchem.ncbi.nlm.nih.gov. Retrieved 2017-04-24.
^ Bett, Glenna C. L.; Rasmusson, Randall L. (2002). "1. Computer Models of Ion Channels". In Cabo, Candido; Rosenbaum, David S. (eds.). Quantitative Cardiac Electrophysiology. Marcel Dekker. p. 48. ISBN 0-8247-0774-5.
^ Ning Qin; Riccardo Olcese; Michael Bransby; Tony Lin; Lutz Birnbaumer (March 1999). "Ca²⁺-induced inhibition of the cardiac Ca²⁺ channel depends on calmodulin". PNAS. 96 (5): 2435–2438. Bibcode:1999PNAS...96.2435Q. doi:10.1073/pnas.96.5.2435. PMC 26802. PMID 10051660.

[1] Raaflaub, Jürg (1956). "Applications of Metal Buffers and Metal Indicators in Biochemistry". Methods of Biochemical Analysis. Vol. 3. pp. 301–325. doi:10.1002/9780470110195.ch10. ISBN 978-0-470-30492-1. PMID 13369167.

[2] Pubchem. "EGTA | C14H24N2O10 - PubChem". pubchem.ncbi.nlm.nih.gov. Retrieved 2017-04-24.

[3] Bett, Glenna C. L.; Rasmusson, Randall L. (2002). "1. Computer Models of Ion Channels". In Cabo, Candido; Rosenbaum, David S. (eds.). Quantitative Cardiac Electrophysiology. Marcel Dekker. p. 48. ISBN 0-8247-0774-5.

[4] Ning Qin; Riccardo Olcese; Michael Bransby; Tony Lin; Lutz Birnbaumer (March 1999). "Ca²⁺-induced inhibition of the cardiac Ca²⁺ channel depends on calmodulin". PNAS. 96 (5): 2435–2438. Bibcode:1999PNAS...96.2435Q. doi:10.1073/pnas.96.5.2435. PMC 26802. PMID 10051660.

[1]

[2]

[3]

[4]

v t e Chelating agents / chelation therapy (V03AC, others)
Copper	Penicillamine^#
Iron	Deferasirox Deferiprone Deferoxamine^#
Lead	BAL^# EDTA^# Dexrazoxane
Thallium	Prussian blue^#
Other	ALA BAPTA DMPS DMSA^# DTPA EGTA
^#WHO-EM ^‡Withdrawn from market Clinical trials: ^†Phase III ^§Never to phase III

Names


Preferred IUPAC name 3,12-Bis(carboxymethyl)-6,9-dioxa-3,12-diazatetradecane-1,14-dioic acid
Other names Triethylene glycol diamine tetraacetic acid
Identifiers
CAS Number	67-42-5 (free acid)^Y 13368-13-3 (tetrasodium salt)^N
3D model (JSmol)	Interactive image
ChEBI	CHEBI:30740^Y
ChEMBL	ChEMBL240390^Y
ChemSpider	5972^Y
ECHA InfoCard	100.000.592
KEGG	D00569^Y
PubChem CID	6207
UNII	526U7A2651^Y
CompTox Dashboard (EPA)	DTXSID2045151
InChI InChI=1S/C14H24N2O10/c17-11(18)7-15(8-12(19)20)1-3-25-5-6-26-4-2-16(9-13(21)22)10-14(23)24/h1-10H2,(H,17,18)(H,19,20)(H,21,22)(H,23,24)^Y Key: DEFVIWRASFVYLL-UHFFFAOYSA-N^Y InChI=1/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12) Key: CPJSUEIXXCENMM-UHFFFAOYAO InChI=1/C14H24N2O10/c17-11(18)7-15(8-12(19)20)1-3-25-5-6-26-4-2-16(9-13(21)22)10-14(23)24/h1-10H2,(H,17,18)(H,19,20)(H,21,22)(H,23,24) Key: DEFVIWRASFVYLL-UHFFFAOYAF
SMILES O=C(O)CN(CC(=O)O)CCOCCOCCN(CC(=O)O)CC(=O)O
Properties
Chemical formula	C₁₄H₂₄N₂O₁₀
Molar mass	380.350 g·mol⁻¹
Melting point	241 °C (466 °F; 514 K)
Acidity (pK_a)	2.0, 2.68, 8.85, 9.43^[1]
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

EGTA

See also

References

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