Technical Data

R2005
CAS Number
130-40-5
Grade
Highly Purified
MDL Number
MFCD00150992
Molecular Formula
C₁₇H₂₀N₄NaO₉P
Molecular Weight
478.33
EU Commodity Code
38220090
Shipping Temp
Blue Ice
Storage Temp
-20°C
Riboflavin-5’-Phosphate Disodium Salt (Flavin mononucleotide, FMN)
Flavin mononucleotide disodium salt; FMN; 7,8-Dimethyl-10-ribitylisoalloxazine Phosphate Sodium; 5'-(Dihydrogen Phosphate)riboflavin Sodium; Riboflavine 5-Phosphate Sodium; Riboflavin Mononucleotide Sodium; Riboflavine Monophosphate Sodium; Riboflavine Phosphate Sodium; Vitamin B2 Phosphate Sodium

Flavin mononucleotide (FMN), or riboflavin-5′-phosphate, is a biomolecule produced from riboflavin (vitamin B2) by the enzyme riboflavin kinase and functions as prosthetic group of various oxidoreductases including NADH dehydrogenase as well as cofactor in biological blue-light photo receptors. During the catalytic cycle, a reversible interconversion of the oxidized (FMN), semiquinone (FMNH•) and reduced (FMNH2) forms occurs in the various oxidoreductases. FMN is a stronger oxidizing agent than NAD and is particularly useful because it can take part in both one- and two-electron transfers. In its role as blue-light photo receptor, (oxidized) FMN stands out from the 'conventional' photo receptors as the signaling state and not an E/Z isomerization. It is the principal form in which riboflavin is found in cells and tissues. It requires more energy to produce, but is more soluble than riboflavin.

Synonyms
Flavin mononucleotide disodium salt; FMN; 7,8-Dimethyl-10-ribitylisoalloxazine Phosphate Sodium; 5'-(Dihydrogen Phosphate)riboflavin Sodium; Riboflavine 5-Phosphate Sodium; Riboflavin Mononucleotide Sodium; Riboflavine Monophosphate Sodium; Riboflavine Phosphate Sodium; Vitamin B2 Phosphate Sodium
CAS No
130-40-5 Free Acid: 146-17-8
Molecular Formula
C17H21N4O9P•Na
Molecular Weight
478.33
Purity
≥98%
Appearance
Yellow or orange-yellow crystalline hygrosopic powder
Storage and Stability
May be stored at RT for short-term only. Long-term storage is recommended at -20°C. For maximum recovery of product, centrifuge the original vial prior to removing the cap.

Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.

References
1. Unna, K., et al.: J. Pharmacol. Exp. Ther., 76, 75 (1942). 2. Rivlin, et al.: N. Engl. J. Med., 283, 463 (1970). 3. Al-Shammary, F.J., et al.: Anal. Profiles Drug Subs., 19, 429 (1990)
USBio References
No references available
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