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R0630000

Riboflavin sodium phosphate

European Pharmacopoeia (EP) Reference Standard

Synonyme(s) :

Riboflavin 5′-monophosphate sodium salt, Riboflavin Sodium phosphate

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About This Item

Formule empirique (notation de Hill):
C17H20N4NaO9P
Numéro CAS:
130-40-5
Poids moléculaire :
478.33
Numéro Beilstein :
4106529
Numéro CE :
204-988-6
Numéro MDL:
MFCD00065362
Code UNSPSC :
41116107
ID de substance PubChem :
329823989
Nomenclature NACRES :
NA.24

Source biologique

synthetic

Qualité

pharmaceutical primary standard

Agence

EP

Famille d'API

riboflavin

Forme

solid

Fabricant/nom de marque

EDQM

Technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

[Na+].Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)COP(O)([O-])=O)c2cc1C

InChI

1S/C17H21N4O9P.Na/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29;/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29);/q;+1/p-1/t11-,12+,14-;/m0./s1

Clé InChI

OHSHFZJLPYLRIP-BMZHGHOISA-M

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Description générale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Riboflavin sodium phosphate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Conditionnement

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Autres remarques

Sales restrictions may apply.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

PHR1054

(−)-Riboflavine, Pharmaceutical Secondary Standard; Certified Reference Material

1603006

(−)-Riboflavine, United States Pharmacopeia (USP) Reference Standard

R0600000

(−)-Riboflavine, European Pharmacopoeia (EP) Reference Standard

Y0000757

(−)-Riboflavine, European Pharmacopoeia (EP) Reference Standard

1535700

Phosphated Riboflavin, United States Pharmacopeia (USP) Reference Standard

PHR1936

Riboflavin Impurity A, Pharmaceutical Secondary Standard; Certified Reference Material

BP459

Riboflavin sodium phosphate, British Pharmacopoeia (BP) Reference Standard

PHR2570

Riboflavin Impurity B, Pharmaceutical Secondary Standard; Certified Reference Material

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Carlos Marcuello et al.
Biochimica et biophysica acta, 1834(3), 665-676 (2013-01-08)
Biochemical characterization of Corynebacterium ammoniagenes FADS (CaFADS) pointed to certain confusion about the stoichiometry of this bifunctional enzyme involved in the production of FMN and FAD in prokaryotes. Resolution of its crystal structure suggested that it might produce a hexameric
Sarah Raffelberg et al.
Biological chemistry, 394(11), 1517-1528 (2013-07-06)
Flavin-binding light, oxygen, and voltage (LOV) domains are UVA/blue-light-sensing protein units that form a reversible flavin mononucleotide-cysteine adduct upon light induction. In their dark-adapted state, LOV domains exhibit the typical spectral features of fully oxidized riboflavin derivatives. A survey on
Ruchanok Tinikul et al.
Biochemistry, 52(39), 6834-6843 (2013-09-06)
Bacterial luciferase (LuxAB) is a two-component flavin mononucleotide (FMN)-dependent monooxygenase that catalyzes the oxidation of reduced FMN (FMNH(-)) and a long-chain aliphatic aldehyde by molecular oxygen to generate oxidized FMN, the corresponding aliphatic carboxylic acid, and concomitant emission of light.
Yulia V Bertsova et al.
The Journal of biological chemistry, 288(20), 14276-14286 (2013-04-06)
Na(+)-translocating NADH:quinone oxidoreductase (Na(+)-NQR) contains two flavin residues as redox-active prosthetic groups attached by a phosphoester bond to threonine residues in subunits NqrB and NqrC. We demonstrate here that flavinylation of truncated Vibrio harveyi NqrC at Thr-229 in Escherichia coli
Jinrok Oh et al.
Organic letters, 15(6), 1210-1213 (2013-03-07)
A new application of a fluorescent sensor (PyDPA) for the discrimination of redox-responsible molecules is reported. Nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide phosphate (NAD(+)/NADP(+)) and flavin mononucleotide/flavin adenine dinucleotide (FMN/FAD) were differentiated by means of ratiometric fluorescence change from excimer-monomer equilibrium
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