APTS - ≥95% , CAS No.196504-57-1

CAS: 196504-57-1 Cat. No.: A359191 Formule: C₁₆H₈NNa₃O₉S₃ Poids moléculaire: 523.4 Numéro CE: 634-973-3

QUALITÉ & PURETÉ ≥95%

Synonyms

8-aminopyrène-1,3,6-trisulfonate de trisodium;8-aminopyrène-1,3,6-trisulfonate de sodium;Acide 8-aminopyrène-1,3,6-trisulfonique sel trisodique | AKOS015903157 | Acide 8-aminopyrène-1,3,6-trisulfonique (sel trisodique) | Sel trisodique de 8-amino | Sel tr

Storage

Stocker à 2-8°C, chargé d'argon

Shipped In

Glace humide

Vue d’ensemble

Marqueur fluorescent pour les saccharides et les glycoprotéines. L'APTS est un réactif fluorescent dont la sensibilité de détection des sucres a été démontrée. La limite de détection des sucres dérivés de l'APTS est de 0,4 nM avec un laser à argon de 488 nm. La nature multi-anionique de l'APTS le rend idéal pour l'étude des molécules d'hydrates de carbone et des petites molécules hormonales par électrophorèse capillaire à haute résolution.

Spécifications

Synonymes

8-aminopyrène-1,3,6-trisulfonate de trisodium;8-aminopyrène-1,3,6-trisulfonate de sodium;Acide 8-aminopyrène-1,3,6-trisulfonique sel trisodique | AKOS015903157 | Acide 8-aminopyrène-1,3,6-trisulfonique (sel trisodique) | Sel trisodique de 8-amino | Sel tr

Spécifications et pureté

≥95%

Conditions de stockage de stockage

Stocker à 2-8°C, chargé d'argon

Expédié en

Glace humide

Pureté

≥95%

Noms et identifiants

Pubchem Sid

508810261

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508810261

Sourires canoniques

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

Isomères 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 Allemagne

3

Poids moléculaire

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
    • Classe Pyrenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: 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
• Description: 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

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive；Light sensitive
• Point de fusion (°C): ≥250°C
• Poids moléculaire: 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

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