Pyridoxine is the alcohol form of Vitamin B6, with molecular formula . Its pyridine ring has a methyl group at position 2, a hydroxyl group at position 3 and hydroxymethyl groups at positions 4 and 5.[ref]
At position 4, pyridoxine differs from the aldehyde pyridoxal and the amine pyridoxamine. Replacing by changes the formula by two hydrogen atoms; replacing it by changes both the oxygen and nitrogen counts. This provides a concrete structural meaning for the three names, beyond their membership of the same vitamin family.
The distinction also matters for biochemistry. Pyridoxal phosphate and pyridoxamine phosphate are active coenzyme forms; free pyridoxine is not simply another name for either phosphorylated molecule.[ref]
Vitamin B6 Fact Sheet for Health Professionals by the Office of Dietary Supplements. Introduction, chemical forms and active coenzymes
For example, an experiment comparing equal molar amounts of two B6 forms holds the number of molecules constant, while their functional groups and ability to enter a particular reaction can still differ. Equal mass would additionally fail to hold molecular amount constant because the forms have different molar mass values.Pyridoxine phosphate is the 5′-phosphate derivative of pyridoxine, one of the forms of Vitamin B6. Attaching a phosphate group and changing an alcohol group into an aldehyde are different chemical modifications. Pyridoxine phosphate still differs from pyridoxal phosphate, the form used as a coenzyme in many reactions.[ref]
Vitamin B6 Fact Sheet for Health Professionals by the Office of Dietary Supplements. Introduction: six vitamin B6 forms and their phosphorylated derivatives
An important connection is the oxidation of pyridoxine phosphate by pyridoxal 5'-phosphate synthase. The official reaction isHere oxygen accepts the reducing equivalents, producing hydrogen peroxide; the phosphate group is retained. The enzyme contains flavin mononucleotide.[ref]
For a constructed material-balance example, complete conversion of 4 micromoles of pyridoxine phosphate through this reaction consumes 4 micromoles of oxygen and forms 4 micromoles each of pyridoxal phosphate and hydrogen peroxide. There is no net release of free phosphate in that reaction. Measuring only total phosphorus would therefore miss the conversion: the substrate and product each retain one phosphorus atom. A measurement that distinguishes their functional groups can answer a question that elemental accounting cannot.
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