Acriflavine(Neutral) - Cl,13.3-15.8% , CAS No.8048-52-0

CAS: 8048-52-0 Cat. No.: A103028 Molecular Weight: 259.73 EC Number: 623-012-3

GRADE & PURITY Cl,13.3-15.8%

Synonyms

Acriflavinium chloride 3,6-Acridinediamine mix | AMY22363 | CAS-69235-50-3 | AKOS015902524 | Tox21_111337 | 3,6-Diamino-10-methylacridinium chloride-3,6-acridinediamine mixt | Acriflavine dihydrochloride | AMY3317 | Flavacridine | HY-100575 | RKL10102 | 1

Storage

Room temperature

Shipped In

Normal

Overview

Acriflavine is a fluorescent label for high molecular weight RNA.
Fluorescent label for high molecular weight RNA

Specifications

Synonyms

Acriflavinium chloride 3, 6-Acridinediamine mix | AMY22363 | CAS-69235-50-3 | AKOS015902524 | Tox21_111337 | 3, 6-Diamino-10-methylacridinium chloride-3, 6-acridinediamine mixt | Acriflavine dihydrochloride | AMY3317 | Flavacridine | HY-100575 | RKL10102 | 1

Specifications & Purity

Cl, 13.3-15.8%

Storage

Room temperature

Shipped In

Normal

Names and Identifiers

• Pubchem Sid: 488189800
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488189800
• Canonical Smiles: C[N+]1=C2C=C(C=CC2=CC3=C1C=C(C=C3)N)N.C1=CC(=CC2=NC3=C(C=CC(=C3)N)C=C21)N.[Cl-]
• IUPAC Name: acridine-3,6-diamine;10-methylacridin-10-ium-3,6-diamine;chloride
• InChIKey: PEJLNXHANOHNSU-UHFFFAOYSA-N
• INCHI: 1S/C14H13N3.C13H11N3.ClH/c1-17-13-7-11(15)4-2-9(13)6-10-3-5-12(16)8-14(10)17;14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10;/h2-8H,1H3,(H3,15,16);1-7H,14-15H2;1H
• Isomeric SMILES: C[N+]1=C2C=C(C=CC2=CC3=C1C=C(C=C3)N)N.C1=CC(=CC2=NC3=C(C=CC(=C3)N)C=C21)N.[Cl-]
• WGK Germany: 3
• RTECS: AR9660000
• UN Number: 3077
• Molecular Weight: 259.73
• Reaxy-Rn: 13329365
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13329365&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Quinolines and derivatives
      • Subclass Benzoquinolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Quinolines and derivatives
• Subclass: Benzoquinolines
• Intermediate Tree Nodes: Not available
• Direct Parent: Acridines
• Alternative Parents: Aminoquinolines and derivatives Pyridinium derivatives Benzenoids Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Acridine - Aminoquinoline - Pyridine - Pyridinium - Benzenoid - Heteroaromatic compound - Azacycle - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organopnictogen compound - Amine - Organic chloride salt - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as acridines. These are organic compounds containing the acridine moiety, a linear tricyclic heterocycle which consists of two benzene rings joined by a pyridine ring.
• External Descriptors: Not available

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

Chemical and Physical Properties

• Solubility: Soluble in water (330 mg/ml), ethanol, and alcohol (1:40). Insoluble in ether, and chloroform
• Melt Point(°C): 179-181°C
• Molecular Weight: 469.000 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 468.183 Da
• Monoisotopic Mass: 468.183 Da
• Topological Polar Surface Area: 121.000 Ų
• Heavy Atom Count: 34
• Formal Charge: 0
• Complexity: 486.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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: 3

XLogP3

References

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