Identification |
Name: | Glycine,N,N'-[(1S)-1-[[4-[(bromoacetyl)amino]phenyl]methyl]-1,2-ethanediyl]bis[N-(carboxymethyl)-(9CI) |
Synonyms: | Glycine,N,N'-[1-[[4-[(bromoacetyl)amino]phenyl]methyl]-1,2-ethanediyl]bis[N-(carboxymethyl)-,(S)-; BABE |
CAS: | 81677-64-7 |
Molecular Formula: | C19H24 Br N3 O9 |
Molecular Weight: | 518.31256 |
InChI: | InChI=1/C19H24BrN3O9/c20-6-15(24)21-13-3-1-12(2-4-13)5-14(23(10-18(29)30)11-19(31)32)7-22(8-16(25)26)9-17(27)28/h1-4,14H,5-11H2,(H,21,24)(H,25,26)(H,27,28)(H,29,30)(H,31,32) |
Molecular Structure: |
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Properties |
Flash Point: | 462.4°C |
Boiling Point: | 840.9°C at 760 mmHg |
Density: | 1.669g/cm3 |
Refractive index: | 1.649 |
Specification: | Off-White Solid usageEng:A bifunctional iron chelating agent that has been employed to couple metal ions to biological molecules, including radiopharmaceutical synthesis and targeted protein hydrolysis. Bifunctional chelating reagents possess both a strong metal-binding moiety and a group that binds to a biological molecule. |
Flash Point: | 462.4°C |
Storage Temperature: | Hygroscopic, -20?C Freezer, Under Inert Atmosphere |
Usage: | A bifunctional iron chelating agent that has been employed to couple metal ions to biological molecules, including radiopharmaceutical synthesis and targeted protein hydrolysis. Bifunctional chelating reagents possess both a strong metal-binding moiety a |
Safety Data |
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