Riboflavine - Moligand™, ≥98% , CAS No.83-88-5

CAS: 83-88-5 Cat. No.: R104137 Formule: C₁₇H₂₀N₄O₆ Poids moléculaire: 376.36 Beilstein Registry Number: 97825 Numéro CE: 201-507-1 PubChem CID: 493570

GRADE & PURITY Moligand™, ≥98%

Synonyms

Ribovel | Vitamin G | Ribotone | Beflavin | Riboflavinum | Flavin BB | vitamin B2 | Lactobene | Riboflavine | Vitaflavine | Ribocrisina | Beflavine | Lactoflavine | Russupteridine Yellow III | (-)-riboflavin | Riboflavina | Ribosyn | Flaxain | Ribipca | r

Storage

Store at 2-8°C

Shipped In

Wet ice

Vue d’ensemble

Riboflavin belongs to the vitamin-B family and contains a pentose side chain ribitol.

Specifications

Synonymes

Ribovel | Vitamin G | Ribotone | Beflavin | Riboflavinum | Flavin BB | vitamin B2 | Lactobene | Riboflavine | Vitaflavine | Ribocrisina | Beflavine | Lactoflavine | Russupteridine Yellow III | (-)-riboflavin | Riboflavina | Ribosyn | Flaxain | Ribipca | r

Spécifications et pureté

Moligand™, ≥98%

Mécanismes biochimiques et physiologiques

Riboflavin is a key component of the redox cofactors flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) that are used by a wide variety of flavoprotein oxidoreductases, dehydrogenase(s), decarboxylase(s) and electron transporters.Vitamin an

Conditions de stockage de stockage

Store at 2-8°C

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureté

≥98%

Noms et identifiants

Pubchem Sid

488189937

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488189937

Sourires canoniques

CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(CO)O)O)O

IUPAC Name

7,8-dimethyl-10-[(2S,3S,4R)-2,3,4,5-tetrahydroxypentyl]benzo[g]pteridine-2,4-dione

InChIKey

AUNGANRZJHBGPY-SCRDCRAPSA-N

INCHI

1S/C17H20N4O6/c1-7-3-9-10(4-8(7)2)21(5-11(23)14(25)12(24)6-22)15-13(18-9)16(26)20-17(27)19-15/h3-4,11-12,14,22-25H,5-6H2,1-2H3,(H,20,26,27)/t11-,12+,14-/m0/s1

Isomères SMILES

CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO)O)O)O

WGK Allemagne

1

RTECS

VJ1400000

PubChem CID

493570

Poids moléculaire

376.36

Beilstein

97825

Reaxy-Rn

97825

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Pteridines and derivatives
      • Subclass Alloxazines and isoalloxazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Pteridines and derivatives
• Subclass: Alloxazines and isoalloxazines
• Intermediate Tree Nodes: Not available
• Direct Parent: Flavins
• Alternative Parents: Quinoxalines Pyrimidones Pyrazines Benzenoids Vinylogous amides Heteroaromatic compounds Secondary alcohols Lactams Polyols Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Flavin - Diazanaphthalene - Quinoxaline - Pyrimidone - Pyrazine - Pyrimidine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Secondary alcohol - Lactam - Polyol - Azacycle - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as flavins. These are compounds containing a flavin (7,8-dimethyl-benzo[g]pteridine-2,4-dione) moiety, with a structure characterized by an isoalloaxzine tricyclic ring.
• External Descriptors: Water-soluble vitamins

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water, absolute ethanol and dimethyl sulfoxide. Insoluble in acetone and chloroform.
• Sensibilité: Light sensitive.
• Rotation spécifique [α]: -128.0 to -142.0 deg (C=0.5, JP Method)
• Point de fusion (°C): 290°C
• Poids moléculaire: 376.400 g/mol
• XLogP3: -1.500
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 376.138 Da
• Monoisotopic Mass: 376.138 Da
• Topological Polar Surface Area: 155.000 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 680.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1