203806-08-0

203806-08-0 structure
203806-08-0 structure
  • Name: EDTA-d12
  • Chemical Name: 2-[[2-[bis[carboxy(dideuterio)methyl]amino]-1,1,2,2-tetradeuterioethyl]-[carboxy(dideuterio)methyl]amino]-2,2-dideuterioacetic acid
  • CAS Number: 203806-08-0
  • Molecular Formula: C10H4D12N2O8
  • Molecular Weight: 304.317
  • Catalog: Signaling Pathways Others Others
  • Create Date: 2018-03-08 08:00:00
  • Modify Date: 2024-01-02 18:57:41
  • EDTA-d12 is the deuterium labeled Ethylenediaminetetraacetic acid[1]. Ethylenediaminetetraacetic acid (EDTA) is a metal chelators (binds to metal divalent and trivalent cations including calcium), which shows activities of anticoagulant and anti-hypercalcemic. Ethylenediaminetetraacetic acid decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid can also decrease the formation of disulfide bonds[2][3][4].

Name 2-[[2-[bis[carboxy(dideuterio)methyl]amino]-1,1,2,2-tetradeuterioethyl]-[carboxy(dideuterio)methyl]amino]-2,2-dideuterioacetic acid
Synonyms 2,2',2'',2'''-[(H)Ethane-1,2-diyldinitrilo]tetra(H)acetic acid
2,2',2'',2'''-[(H)-1,2-Ethanediyldinitrilo]tetra(H)acetic acid
Ethylenediaminetetraacetic-d12 acid
MFCD00144285
EDTA-d12
Description EDTA-d12 is the deuterium labeled Ethylenediaminetetraacetic acid[1]. Ethylenediaminetetraacetic acid (EDTA) is a metal chelators (binds to metal divalent and trivalent cations including calcium), which shows activities of anticoagulant and anti-hypercalcemic. Ethylenediaminetetraacetic acid decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid can also decrease the formation of disulfide bonds[2][3][4].
Related Catalog
In Vitro Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.  

[2]. Chumanov RS, et al. Artifact-inducing enrichment of ethylenediaminetetraacetic acid and ethyleneglycoltetraacetic acid on anion exchange resins. Anal Biochem. 2011 May 1;412(1):34-9.  

[3]. Banfi G, et al. The role of ethylenediamine tetraacetic acid (EDTA) as in vitro anticoagulant for diagnostic purposes. Clin Chem Lab Med. 200745(5):565-76.  

[4]. Ibad A, et al. Chelation therapy in the treatment of cardiovascular diseases. J Clin Lipidol. 2016 Jan-Feb10(1):58-62.  

Density 1.6±0.1 g/cm3
Boiling Point 614.2±55.0 °C at 760 mmHg
Melting Point 250ºC (dec.)(lit.)
Molecular Formula C10H4D12N2O8
Molecular Weight 304.317
Flash Point 325.2±31.5 °C
Exact Mass 304.165985
PSA 155.68000
LogP -0.43
Vapour Pressure 0.0±3.8 mmHg at 25°C
Index of Refraction 1.580
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H319
Precautionary Statements P305 + P351 + P338
Hazard Codes Xi
RIDADR UN 3077 9 / PGIII