APTS - for fluorescence analysis , CAS No.196504-57-1

CAS: 196504-57-1 Cat. No.: A113925 Fórmula: C₁₆H₈NNa₃O₉S₃ Peso molecular: 523.4 Número EC: 634-973-3

CALIDAD & PUREZA for Fluorescence analysis

Synonyms

Trisodium 8-aminopyrene-1,3,6-trisulfonate;Sodium 8-aminopyrene-1,3,6-trisulfonate;8-Aminopyrene-1,3,6-trisulfonic acid trisodium salt | AKOS015903157 | 8-Aminopyrene-1,3,6-trisulfonic acid (trisodium salt) | 8-amino trisodium salt | Trisodium 8-aminopyre

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

Fluorescent label for saccharides and glycoproteins. APTS is a fluorescence reagent that has been demonstrated to have a high level of detection sensitivity for sugars The LOD for APTS-derivatized sugars has been shown to be 0.4 nM when using a 488 nm argon-ion laser. The multi-anionic nature of APTS makes it ideal for the studies of carbohydrate molecules and small hormone molecules by high resolution capillary electrophoresis.

Especificaciones

Sinónimos

Trisodium 8-aminopyrene-1,3,6-trisulfonate;Sodium 8-aminopyrene-1,3,6-trisulfonate;8-Aminopyrene-1,3,6-trisulfonic acid trisodium salt | AKOS015903157 | 8-Aminopyrene-1,3,6-trisulfonic acid (trisodium salt) | 8-amino trisodium salt | Trisodium 8-aminopyre

Especificaciones y pureza

for fluorescence analysis

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C,Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

for Fluorescence analysis

Nombres e identificadores

Pubchem Sid

528762864

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528762864

Sonrisas canónicas

C1=CC2=C3C(=C(C=C2S(=O)(=O)[O-])S(=O)(=O)[O-])C=CC4=C(C=C(C1=C43)N)S(=O)(=O)[O-].[Na+].[Na+].[Na+]

IUPAC Name

trisodium;8-aminopyrene-1,3,6-trisulfonate

InChIKey

XSTNYACEWLNWPY-UHFFFAOYSA-K

INCHI

1S/C16H11NO9S3.3Na/c17-11-5-12(27(18,19)20)8-3-4-10-14(29(24,25)26)6-13(28(21,22)23)9-2-1-7(11)15(8)16(9)10;;;/h1-6H,17H2,(H,18,19,20)(H,21,22,23)(H,24,25,26);;;/q;3*+1/p-3

Isómeros SMILES

C1=CC2=C3C(=C(C=C2S(=O)(=O)[O-])S(=O)(=O)[O-])C=CC4=C(C=C(C1=C43)N)S(=O)(=O)[O-].[Na+].[Na+].[Na+]

WGK Alemania

3

Peso molecular

523.4

Reaxy-Rn

7330049

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7330049&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Pyrenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Pyrenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrenes
• Alternative Parents: Phenanthrenes and derivatives 2-naphthalene sulfonic acids and derivatives 2-naphthalene sulfonates 1-naphthalene sulfonic acids and derivatives 1-naphthalene sulfonates 1-sulfo,2-unsubstituted aromatic compounds Sulfonyls Organosulfonic acids Primary amines Organic sodium salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Pyrene - Phenanthrene - 2-naphthalene sulfonate - 1-naphthalene sulfonate - Naphthalene sulfonic acid or derivatives - 2-naphthalene sulfonic acid or derivatives - 1-naphthalene sulfonic acid or derivatives - Naphthalene sulfonate - Naphthalene - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Organic alkali metal salt - Amine - Organic nitrogen compound - Organic salt - Organic sodium salt - Hydrocarbon derivative - Primary amine - Organic oxide - Organosulfur compound - Organonitrogen compound - Organic oxygen compound - Organic cation - Aromatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyrenes. These are compounds containing a pyrene moiety, which consists four fused benzene rings, resulting in a flat aromatic system.
• 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

Propiedades químicas y físicas

• Solubilidad: DMF: soluble;DMSO: soluble;H2O: soluble
• Sensibilidad: Moisture sensitive；Light sensitive
• Punto de fusión (°C): ≥250°C
• Peso molecular: 523.400 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 0
• Exact Mass: 522.905 Da
• Monoisotopic Mass: 522.905 Da
• Topological Polar Surface Area: 223.000 Ų
• Heavy Atom Count: 32
• Formal Charge: 0
• Complexity: 936.000
• 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: 4

XLogP3