1-Pyrenemethylamine hydrochloride - ≥95% , CAS No.93324-65-3

CAS: 93324-65-3 Cat. No.: P346131 Peso molecular: 267.75 Número EC: 628-261-1 PubChem CID: 11601427

GRADE & PURITY ≥95%

Synonyms

HY-W090065 | STR09035 | RGNMXKKNDSHTFD-UHFFFAOYSA-N | 1-Pyrenemethylamine hydrochloride | E78136 | SCHEMBL466304 | YSWG257 | MFCD00192425 | 1-Aminomethylpyrene,hydrochloride | 1-Pyrenemethanamine, hydrochloride | 1-Pyrenemethylamine hydrochloride, 95% | 1

Storage

Room temperature

Shipped In

Normal

Descripción general

1-Pyrenemethylamine hydrochloride is used to label carbonyl-containing biomolecules. It is used for synthesizing probes that have excited-state lifetimes of ~100 nanoseconds and also for preparing derivatives of carboxylic acids for chromatographic analysis.

Specifications

Sinónimos

HY-W090065 | STR09035 | RGNMXKKNDSHTFD-UHFFFAOYSA-N | 1-Pyrenemethylamine hydrochloride | E78136 | SCHEMBL466304 | YSWG257 | MFCD00192425 | 1-Aminomethylpyrene, hydrochloride | 1-Pyrenemethanamine, hydrochloride | 1-Pyrenemethylamine hydrochloride, 95% | 1

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 488197614
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197614
• Sonrisas canónicas: C1=CC2=C3C(=C1)C=CC4=C(C=CC(=C43)C=C2)CN.Cl
• IUPAC Name: pyren-1-ylmethanamine;hydrochloride
• InChIKey: RGNMXKKNDSHTFD-UHFFFAOYSA-N
• INCHI: 1S/C17H13N.ClH/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12;/h1-9H,10,18H2;1H
• Isómeros SMILES: C1=CC2=C3C(=C1)C=CC4=C(C=CC(=C43)C=C2)CN.Cl
• WGK Alemania: 3
• PubChem CID: 11601427
• Peso molecular: 267.75

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 Naphthalenes Aralkylamines Monoalkylamines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Pyrene - Phenanthrene - Naphthalene - Aralkylamine - Organic nitrogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - 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

Mecanismos de acción

Propiedades químicas y físicas

• Punto de fusión (°C): 258° C
• Peso molecular: 267.800 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 267.081 Da
• Monoisotopic Mass: 267.081 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 313.000
• 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: 2

XLogP3

Referencias

1. Guo Si-hua, Zheng Fang-yuan, Zeng Fang, Wu Shui-zhu.  (2016)  Temperature-responsive behavior of polymer fluorescent system via electrostatic interaction mediated aggregation/deaggregation.  CHINESE JOURNAL OF POLYMER SCIENCE,  34  (7): (830-837).  [PMID:] [10.1007/s10118-016-1793-5]