M.F.
C₆₂H₈₉CoN₁₃O₁₅P·C₂H₄O₂
Smiles
CC([O-][Co+3]123([N]4=CN(C(OC(CO)C5O[P]6([O-])=O)C5O)C7=C4C=C(C)C(C)=C7)[N]8=C9C(CCC(N)=O)C(CC(N)=O)(C)C8(C)C(C(CC(N)=O)C%10(CCC(NCC(C)O6)=O)C)[N-]1C%10=C(C)C(C(CCC(N)=O)C%11(C)C)=[N]2C%11=CC%12=[N]3C(C(CC(N)=O)(C)C%12CCC(N)=O)=C9C)=O
API Family
Hydroxocobalamin Acetate
Storage Condition
Store at refrigerator (2-8°C) for long term storage
IUPAC Name
Coα-[α-(5,6-dimethylbenzimidazolyl)]-Coβ-hydroxocobamide acetate
References
"Kaczka, E,A,, et al,: Science, 112, 354 (1950), Friedrich, W,, et al,: Vitamins, 837 (1988), Forsyth, J,C,, et al,: Clin, Toxicol,, 31, 277 (1993), "
Synonyms
Cyanocobalamin EP impurity H
Application Notes
Physiological analog of vitamin B12 where the CN group is replaced with OH. Exists in aqueous solution as an equilibrium mixture of the hydroxy isomer and the ionic aqua isomer (aquacobalamin). Precursor of the coenzymes methylcobalamin and cobamamide. Coordination Compound
Purity by HPLC
Not less than 95 %
Hazard Compound
Refer MSDS for accurate information
Physiological analog of vitamin B12 where the CN group is replaced with OH. Exists in aqueous solution as an equilibrium mixture of the hydroxy isomer and the ionic aqua isomer (aquacobalamin). Precursor of the coenzymes methylcobalamin and cobamamide. Coordination Compound
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