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Phthalocyanine - >93.0%(N), high purity , CAS No.574-93-6

    Grade & Purity:
  • ≥93%(N)
In stock
Item Number
P160721
Grouped product items
SKU Size
Availability
Price Qty
P160721-1g
1g
10
$23.90
P160721-5g
5g
9
$89.90

最大吸收波长:689(THF) nm

Basic Description

Synonyms HSDB 4350 | 5,28-Dihydro-29H,31H-phthaloCyanine | Phthalocyanine (purified by sublimation) [for organic electronics] | PHTHALOCYANINE [HSDB] | UNII-V5PUF4VLGY | EC 209-378-3 | Phthalocyanin | YSWG725 | AKOS015912687 | Lionol Blue KW | NCGC00259070-01 | PH
Specifications & Purity ≥93%(N)
Storage Temp Protected from light
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Tetrapyrroles and derivatives
Subclass Phthalocyanines
Intermediate Tree Nodes Not available
Direct Parent Phthalocyanines
Alternative Parents Isoindoles  Benzenoids  Pyrroles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Phthalocyanine skeleton - Isoindole or derivatives - Isoindole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as phthalocyanines. These are cyclic tetrapyrroles that contain a phthalocyanine skeleton, which consists of four isoindole-type units, with the connecting carbon atoms in the macrocycle replaced by nitrogen.
External Descriptors tetrapyrrole fundamental parent - phthalocyanines

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488202414
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488202414
IUPAC Name 2,11,20,29,37,38,39,40-octazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13,15,17,19(39),20,22,24,26,28,30(37),31,33,35-nonadecaene
INCHI InChI=1S/C32H18N8/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25/h1-16H,(H2,33,34,35,36,37,38,39,40)
InChIKey IEQIEDJGQAUEQZ-UHFFFAOYSA-N
Smiles C1=CC=C2C(=C1)C3=NC4=NC(=NC5=C6C=CC=CC6=C(N5)N=C7C8=CC=CC=C8C(=N7)N=C2N3)C9=CC=CC=C94
Isomeric SMILES C1=CC=C2C(=C1)C3=NC4=NC(=NC5=C6C=CC=CC6=C(N5)N=C7C8=CC=CC=C8C(=N7)N=C2N3)C9=CC=CC=C94
Molecular Weight 514.55
Reaxy-Rn 15026350
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=15026350&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot Number Certificate Type Date Item
C2526807 Certificate of Analysis Dec 14, 2024 P160721
C2517506 Certificate of Analysis Dec 14, 2024 P160721
H2421423 Certificate of Analysis Aug 13, 2024 P160721
H2421425 Certificate of Analysis Aug 13, 2024 P160721
H2421424 Certificate of Analysis Aug 13, 2024 P160721
L2418698 Certificate of Analysis Jun 27, 2024 P160721
D2325173 Certificate of Analysis May 13, 2022 P160721
F2209241 Certificate of Analysis May 13, 2022 P160721
F2209218 Certificate of Analysis May 13, 2022 P160721
C2422083 Certificate of Analysis May 13, 2022 P160721
D2325189 Certificate of Analysis May 13, 2022 P160721
F2210157 Certificate of Analysis May 13, 2022 P160721

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Chemical and Physical Properties

Solubility Insoluble in water.
Sensitivity light sensitive
Melt Point(°C) >300 °C
Molecular Weight 514.500 g/mol
XLogP3 6.400
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 0
Exact Mass 514.165 Da
Monoisotopic Mass 514.165 Da
Topological Polar Surface Area 109.000 Ų
Heavy Atom Count 40
Formal Charge 0
Complexity 777.000
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

Citations of This Product

1. Cao Peike, Quan Xie, Nie Xiaowa, Zhao Kun, Liu Yanming, Chen Shuo, Yu Hongtao, Chen Jingguang G..  (2023)  Metal single-site catalyst design for electrocatalytic production of hydrogen peroxide at industrial-relevant currents.  Nature Communications,  14  (1): (1-12). 
2. Menghui Chen, Yongting Chen, Jialin Cai, Zhili Yang, Meihua Tang, Joey Chung-Yen Jung, Shengli Chen, Jiujun Zhang, Shiming Zhang.  (2023)  Multi-sites synergistic modulation in oxygen reduction electrocatalysis.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  629  (697). 
3. Yueqi Li, Minjuan Cai, Bingbing Ji, Feng Wu, Li-Zhi Huang.  (2022)  Pyridinic nitrogen enables dechlorination of trichloroethylene to acetylene by green rust: Performance, mechanism and applications.  SCIENCE OF THE TOTAL ENVIRONMENT,  824  (153825). 
4. Kejun Chen, Maoqi Cao, Ganghai Ni, Shanyong Chen, Hanxiao Liao, Li Zhu, Hongmei Li, Junwei Fu, Junhua Hu, Emiliano Cortés, Min Liu.  (2022)  Nickel polyphthalocyanine with electronic localization at the nickel site for enhanced CO2 reduction reaction.  APPLIED CATALYSIS B-ENVIRONMENTAL,  306  (121093). 
5. Yilin Huang, Weidong Xue, Xingwang Hou, Rui Zhao.  (2021)  Metal Oxide/Nitrogen-Doped Carbon Nanosheet Heteronanostructures as Highly Efficient Electromagnetic Wave Absorbing Materials.  MOLECULES,  26  (24): (7537). 
6. Yangke Long, Jian Dai, Shiyin Zhao, Yiping Su, Zhongying Wang, Zuotai Zhang.  (2021)  Atomically Dispersed Cobalt Sites on Graphene as Efficient Periodate Activators for Selective Organic Pollutant Degradation.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,  55  (8): (5357–5370). 
7. Qingshan Zhao, Xiaojie Tan, Tianwen Ma, Fengliang Cao, Zhengzheng Xia, Hui Liu, Hui Ning, Zhongtao Li, Han Hu, Mingbo Wu.  (2021)  Reinforced atomically dispersed FeNC catalysts derived from petroleum asphalt for oxygen reduction reaction.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  587  (810). 
8. Xiao-Cheng Liu, Chuan-Shu He, Zi-Yang Shen, Wen-Qiang Li, Ning Chen, Jun-Sheng Song, Xiao-Guo Zhou, Yang Mu.  (2020)  Mechanistic study of Fe(III) chelate reduction in a neutral electro-Fenton process.  APPLIED CATALYSIS B-ENVIRONMENTAL,  278  (119347). 
9. Chen Jin-ping, Zhang Xue-song.  (2018)  Phosphorous Phthalocyanine Analogues as Degradable Corrosion Inhibitor of Mild Steel in 1 mol/L HCl.  TRANSACTIONS OF THE INDIAN INSTITUTE OF METALS,  71  (5): (1113-1126). 
10. Yangke Long, Guicong Xiao, Jian Dai, Yanyun Chen, Hua-Yue Zhu, Dan Peng, Huosheng Li.  (2025)  Efficacy and durability of cobalt sulfide nanoparticles and axial sulfur-coordinated cobalt single-atom composite sites in hydrogenative nitroaromatics decontamination.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  684  (540). 
11. Sheng Li, Wentong Fan, Qiulin Chen, Xinfeng Zhang.  (2024)  Facile Light-Driven Synthesis of Highly Luminous Sulfur Quantum Dots for Fluorescence Sensing and Cell Imaging.  ACS Applied Materials & Interfaces,  16  (31): (41281-41292). 
12. Zhongliang Huang, Qi Xiao, Tianyi Ding, Jing Xia, Changhong Zhan, Xiangmin Meng, Chih-Wen Pao, Zhiwei Hu, Wei-Hsiang Huang, Yingru Wang, Nanjun Chen, Liang Cao, Xiaoqing Huang.  (2025)  Interfacial metal–coordinated bifunctional PtCo for practical fuel cells.  Science Advances,    (11(10)). 
13. Shanlei Chang, Kai Rong, Yuchen Wang, Zhixuan Yu, Junfeng Zhai, Hongwei Tian, Youxing Fang, Shaojun Dong.  (2024)  Polymerizable deep eutectic solvent enables flexible gel formation for motion sensor and anti-UV film.  CHEMICAL ENGINEERING JOURNAL,  499  (156597). 
14. Weiting Yu, Zhe Yang, Rendan Zhu, Mengzhi Lu, Tingjiang Lu, Yan Yu, Shuang Song.  (2024)  Suppression of hydrogen evolution reaction in CO2 reduction by functionalizing Ag-decorated Si electrode with phthalocyanine.  SEPARATION AND PURIFICATION TECHNOLOGY,  343  (127080). 
15. Xiaoyu Chu, Xinrui Wang, Shuo Tian, Yongkuo Zhao, Shikai Liu, Hong Yan, Yan Shang.  (2024)  Synthesis of Iron Phthalocyanine/CeO2 Z-scheme nanocomposites as efficient photocatalysts for degradation of 2, 4-chlorophenol.  DALTON TRANSACTIONS,     

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