Hydroxocobalamin

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Revision as of 01:59, 4 December 2024 by Admin (talk | contribs) (Created page with "{{Compound|aka=Hydrox<u>o</u>cobalamin, Vitamin B<sub>12</sub>|chemf=C62H89CoN13O15P|group=Bioproducts |complexo=yes|mm=1346.37 |stp_p=crystals|stp_q=dark red |medicine=yes|listed_who=yes|med_class=Dietary Supplements }} Hydroxocobalamin, along with related compounds '''cyano'''cobalamin, '''methyl'''cobalamin, and '''adenosyl'''cobalamin, represent bioavailable forms of vitamin B12. Cobalamin coordinates five out of six points on the cobalt atom, leaving the sixth f...")
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Hydroxocobalamin
aka Hydroxocobalamin, Vitamin B12
Chemical formula C62H89CoN13O15P
OTP appearance dark red crystals 
Molar Mass(g/mol) 1346.37
NFPA 704
NFPA704.png
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Hydroxocobalamin, along with related compounds cyanocobalamin, methylcobalamin, and adenosylcobalamin, represent bioavailable forms of vitamin B12. Cobalamin coordinates five out of six points on the cobalt atom, leaving the sixth for a hydroxy, nitrile, methyl, or andenosine ligand. The ligands are easily exchanged in vivo and in vitro, and metabolism of cyanocobalamin to hydroxocobalamin + thiocyanate in the kidney is the body's primary way of eliminating cyanide compounds.

Uses

Primary

  • Pharm: WHO LEM dietary supplement (vitamin B12a) and cyanide antidote

Natural occurrence

  • Occurs in most living beings, produced only by monads.

Hazards

Production

Extraction

  1. Fermentation of streptomyces griseus produces vitamin B12, cyanocobalamin.[1]
  2. Cyanocobalamin is converted to hydroxocobalamin by reduction with Zn/HCl, (a dark red solution), aeration, neutralization with NaCO3, and recrystallizing from aqueous acetone.[2]

Synthesis

Testing

Purification

Storage

Disposal

See Also

References

  1. US patent 2695862 "Process for obtaining vitamin b12"
    Link courtesy Google
  2. US patent 3138583 "Process for the industrial manufacture of hydroxocobalamin"
    Link courtesy Google