66-71-7,MFCD00149973
Catalog No.:AA0032GS

66-71-7 | 1,10-Phenanthroline

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$9.00   $6.00
- +
10g
98%
in stock  
$10.00   $7.00
- +
25g
98%
in stock  
$13.00   $9.00
- +
50g
98%
in stock  
$23.00   $16.00
- +
100g
98%
in stock  
$46.00   $32.00
- +
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0032GS
Chemical Name:
1,10-Phenanthroline
CAS Number:
66-71-7
Molecular Formula:
C12H8N2
Molecular Weight:
180.2053
MDL Number:
MFCD00149973
SMILES:
c1ccc2c(n1)c1ncccc1cc2
NSC Number:
203545
Properties
Properties
 
BP:
365°C at 760 mmHg  
Form:
Solid  
MP:
114-117 °C(lit.)  
Refractive Index:
1.5200 (estimate)  
Solubility:
2.69g/l  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
183  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.8  

Synonyms
 
  
Literature

Title: Guan NanMu, et al. Synergistic inhibition between o-phenanthroline and chloride ion on cold rolled steel corrosion in phosphoric acid. Materials Chemistry and Physics Volume 86, Issue 1, 15 July 2004, Pages 59-68.

Title: Zi-Qiang Liu, et al. The role of matrix metalloprotease (MMP) to the autolysis of sea cucumber (Stichopus japonicus). J Sci Food Agric. 2019 Oct;99(13):5752-5759.

Application
1,10-Phenanthroline emerges as a versatile compound with diverse applications across various fields of chemistry. Firstly, it acts as a cathode buffer layer, enhancing the efficiency of organic solar cells by facilitating charge transport. Secondly, it serves as a conventional chelator, employed to investigate its effectiveness in the Fenton′s reaction-luminol chemiluminescence system, contributing to analytical chemistry studies. Additionally, 1,10-Phenanthroline acts as a ligand in mild, copper(II)-catalyzed cross-coupling reactions, enabling the synthesis of aryl- and alkenylsulfones, valuable organic compounds. Moreover, it finds utility as a versatile ligand in spectrophotometric metal determination and photocatalytic reduction of carbon dioxide, crucial for environmental and analytical chemistry applications. Lastly, 1,10-Phenanthroline serves as a building block for metallomacrocycles, paving the way for the development of intricate molecular architectures with unique properties. Overall, its multifunctional properties make it indispensable in various chemical endeavors, from catalysis to materials science.
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SDS
Tags:66-71-7 Molecular Formula|66-71-7 MDL|66-71-7 SMILES|66-71-7 1,10-Phenanthroline
Catalog No.: AA0032GS
66-71-7,MFCD00149973
66-71-7 | 1,10-Phenanthroline
Pack Size: 5g
Purity: 98%
in stock
$9.00 $6.00
Pack Size: 10g
Purity: 98%
in stock
$10.00 $7.00
Pack Size: 25g
Purity: 98%
in stock
$13.00 $9.00
Pack Size: 50g
Purity: 98%
in stock
$23.00 $16.00
Pack Size: 100g
Purity: 98%
in stock
$46.00 $32.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA0032GS
Chemical Name: 1,10-Phenanthroline
CAS Number: 66-71-7
Molecular Formula: C12H8N2
Molecular Weight: 180.2053
MDL Number: MFCD00149973
SMILES: c1ccc2c(n1)c1ncccc1cc2
NSC Number: 203545
Properties
BP: 365°C at 760 mmHg  
Form: Solid  
MP: 114-117 °C(lit.)  
Refractive Index: 1.5200 (estimate)  
Solubility: 2.69g/l  
Stability: Hygroscopic  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 183  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.8  
166:   
Application fold
1,10-Phenanthroline emerges as a versatile compound with diverse applications across various fields of chemistry. Firstly, it acts as a cathode buffer layer, enhancing the efficiency of organic solar cells by facilitating charge transport. Secondly, it serves as a conventional chelator, employed to investigate its effectiveness in the Fenton′s reaction-luminol chemiluminescence system, contributing to analytical chemistry studies. Additionally, 1,10-Phenanthroline acts as a ligand in mild, copper(II)-catalyzed cross-coupling reactions, enabling the synthesis of aryl- and alkenylsulfones, valuable organic compounds. Moreover, it finds utility as a versatile ligand in spectrophotometric metal determination and photocatalytic reduction of carbon dioxide, crucial for environmental and analytical chemistry applications. Lastly, 1,10-Phenanthroline serves as a building block for metallomacrocycles, paving the way for the development of intricate molecular architectures with unique properties. Overall, its multifunctional properties make it indispensable in various chemical endeavors, from catalysis to materials science.
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