Physicochemical Properties
| Molecular Formula | C6H10N2O5 |
| Molecular Weight | 190.1540 |
| Exact Mass | 190.058 |
| CAS # | 26239-55-4 |
| PubChem CID | 117765 |
| Appearance | White to off-white solid powder |
| Density | 1.5±0.1 g/cm3 |
| Boiling Point | 524.9±45.0 °C at 760 mmHg |
| Melting Point | 219 °C (dec.)(lit.) |
| Flash Point | 271.3±28.7 °C |
| Vapour Pressure | 0.0±3.0 mmHg at 25°C |
| Index of Refraction | 1.558 |
| LogP | -3.9 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Heavy Atom Count | 13 |
| Complexity | 211 |
| Defined Atom Stereocenter Count | 0 |
| InChi Key | QZTKDVCDBIDYMD-UHFFFAOYSA-N |
| InChi Code | InChI=1S/C6H10N2O5/c7-4(9)1-8(2-5(10)11)3-6(12)13/h1-3H2,(H2,7,9)(H,10,11)(H,12,13) |
| Chemical Name | 2-[(2-amino-2-oxoethyl)-(carboxymethyl)amino]acetic acid |
| HS Tariff Code | 2934.99.9001 |
| Storage |
Powder-20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition | Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs) |
Biological Activity
| References |
[1]. T Minami, et al. Identification of metallothionein isoforms with capillary zone electrophoresis using a polyacrylamide-coated tube. J Chromatogr B Biomed Appl. 1996 Oct 25;685(2):353-9. [2]. Birte M Gerken, et al. Tweezing-adsorptive bubble separation. Analytical method for the selective and high enrichment of metalloenzymes. Anal Chem. 2005 Oct 1;77(19):6113-7. |
| Additional Infomation | 2,2'-[(2-amino-2-oxoethyl)imino]diacetic acid is a tricarboxylic acid amide that is a Good's buffer substance, pKa = 6.6 at 20 ℃. It is a dicarboxylic acid, a tricarboxylic acid amide and an ADA. It is functionally related to a nitrilotriacetic acid. It is a conjugate acid of a 2,2'-[(2-amino-2-oxoethyl)imino]diacetate(1-). |
Solubility Data
| Solubility (In Vitro) | H2O: 5 mg/mL (26.30 mM) |
| Solubility (In Vivo) |
Solubility in Formulation 1: 10 mg/mL (52.59 mM) in PBS (add these co-solvents sequentially from left to right, and one by one), clear solution; with sonication.  (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 5.2590 mL | 26.2950 mL | 52.5901 mL | |
| 5 mM | 1.0518 mL | 5.2590 mL | 10.5180 mL | |
| 10 mM | 0.5259 mL | 2.6295 mL | 5.2590 mL |