AssayIndex
Cross-section

NAD+ impurity profile

Every named species the index has reported alongside NAD+, how often, at what level, and what its presence implies about the synthesis or the handling. Reporting threshold is 0.05 % area; anything below it is invisible to this page and is silently added to the main peak.

48 recordsmedian 98.88 %spec 97.0 %
Median total impurities 1.12% n=48
Median largest single 0.60% n=48
Worst single observed 1.21% n=48
Named species observed 5 / 5 n=5
Named speciesΔRT (min)Δ mass (Da)Seen inMedian % areaMax % area
nicotinamide (−541 Da)-0.68-541.05296%0.101.13
nicotinamide mononucleotide (NMN, −331 Da)-0.42-331.05892%0.351.21
ADP-ribose (−121 Da)-0.26-121.04092%0.211.00
NADH (reduced, +2 Da)+0.34+2.01692%0.110.62
α-NAD anomer+0.18mass-identical88%0.080.92

nicotinamide (−541 Da)

Retention offset from the main peak
-0.68 min on RG-2
Mass difference
-541.052 Da
Reported in
46 of 48 records (96 %)
Level when reported
median 0.10 %, max 1.13 %
Resolution requirement
Baseline-resolved on the reference method.

nicotinamide mononucleotide (NMN, −331 Da)

Retention offset from the main peak
-0.42 min on RG-2
Mass difference
-331.058 Da
Reported in
44 of 48 records (92 %)
Level when reported
median 0.35 %, max 1.21 %
Resolution requirement
Baseline-resolved on the reference method.

ADP-ribose (−121 Da)

Retention offset from the main peak
-0.26 min on RG-2
Mass difference
-121.040 Da
Reported in
44 of 48 records (92 %)
Level when reported
median 0.21 %, max 1.00 %
Resolution requirement
Close-eluting — resolution below 1.2 is common and the peaks merge on short gradients.

NADH (reduced, +2 Da)

Retention offset from the main peak
+0.34 min on RG-2
Mass difference
+2.016 Da
Reported in
44 of 48 records (92 %)
Level when reported
median 0.11 %, max 0.62 %
Resolution requirement
Baseline-resolved on the reference method.

α-NAD anomer

Retention offset from the main peak
+0.18 min on RG-2
Mass difference
mass-identical — chromatography only
Reported in
42 of 48 records (88 %)
Level when reported
median 0.08 %, max 0.92 %
Resolution requirement
A gradient long enough to separate it. No mass spectrometer will.

Degradation pathways

Degradants are a handling finding rather than a synthesis finding. A lot that shipped clean and arrived oxidised tells you about the courier, not the chemist.

  • glycosidic hydrolysis to nicotinamide + ADP-ribose, fast above pH 8 and above 30 °C
  • anomerisation to the inactive α form