5,6-Diamino-1,10-phenanthroline - ≥96% , CAS No.168646-54-6

CAS: 168646-54-6 Cat. No.: D191440 Peso molecular: 210.24

GRADE & PURITY ≥96%

Synonyms

1,10-phenanthroline-5,6-diamine | SMSSF-0625473 | SCHEMBL2355988 | AMY23542 | 5,6-Diamine-1,10-phenanthroline | MNXMBMNXSPNINS-UHFFFAOYSA-N | YSWG187 | 5,6-diamino-1,10-phenanthroline | DTXSID30448072 | MFCD12913573 | 5,6-diamino-1,10-phenathroline

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

1, 10-phenanthroline-5, 6-diamine | SMSSF-0625473 | SCHEMBL2355988 | AMY23542 | 5, 6-Diamine-1, 10-phenanthroline | MNXMBMNXSPNINS-UHFFFAOYSA-N | YSWG187 | 5, 6-diamino-1, 10-phenanthroline | DTXSID30448072 | MFCD12913573 | 5, 6-diamino-1, 10-phenathroline

Especificaciones y pureza

≥96%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

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

Pureza

≥96%

Nombres e identificadores

• Pubchem Sid: 504765720
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504765720
• Sonrisas canónicas: C1=CC2=C(C(=C3C=CC=NC3=C2N=C1)N)N
• IUPAC Name: 1,10-phenanthroline-5,6-diamine
• InChIKey: MNXMBMNXSPNINS-UHFFFAOYSA-N
• INCHI: 1S/C12H10N4/c13-9-7-3-1-5-15-11(7)12-8(10(9)14)4-2-6-16-12/h1-6H,13-14H2
• Isómeros SMILES: C1=CC2=C(C(=C3C=CC=NC3=C2N=C1)N)N
• Peso molecular: 210.24
• Reaxy-Rn: 7294811
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7294811&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Phenanthrolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Phenanthrolines
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenanthrolines
• Alternative Parents: Aminoquinolines and derivatives Pyridines and derivatives Benzenoids Heteroaromatic compounds Azacyclic compounds Primary amines Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 1,10-phenanthroline - Aminoquinoline - Quinoline - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene 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

Propiedades químicas y físicas

• Peso molecular: 210.230 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 210.091 Da
• Monoisotopic Mass: 210.091 Da
• Topological Polar Surface Area: 77.800 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 231.000
• 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: 1

Referencias

1. W. Sun, B. Shi, Z. Xia, C. Lü.  (2022)  Visible-light-excited long-lived organic room-temperature phosphorescence of phenanthroline derivatives in PVA matrix by H-bonding interaction for security applications.  Materials Today Chemistry,      [PMID:] [10.1016/j.mtchem.2022.101297]

2. Xuexue Xu, Shuang Wang, Yaxuan Mi, Huaqian Zhao, Zebao Zheng, Xiaolong Zhao.  (2019)  A hydroxyquinoline-appended ruthenium(II)-polypyridyl complex that induces and stabilizes G-quadruplex DNA.  JOURNAL OF COORDINATION CHEMISTRY,      [PMID:] [10.1080/00958972.2018.1548703]

3. Ke Jia, Xiaochen Lu, Yidong Zhou, Jing Han, Xiaoyu Zhou, Huihui Liu, Zongxiu Nie.  (2025)  MALDI Mass Spectrometry Imaging of Metal Ions and Metabolites in Tissues Using a Bifunctional Matrix.  ANALYTICAL CHEMISTRY,      [PMID:40994224] [10.1021/acs.analchem.5c02995]

4. Song Zhang, Yucong Zhou, Zhitao Shen, Yingying Li, Jian Song, Yicong Gao, Zezhi Wang, Bohao Zhang, Chong Chen, Rong Liu, Ying Liu, Ruirui Cao, Huilin Li, Fumin Li.  (2025)  High-efficiency and stable perovskite solar cells via bidentate chelation for facet-engineered growth of FAPbI3 (111) crystals.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.164079]