The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser.
For the best experience on our site, be sure to turn on Javascript in your browser.
This is a demo store. No orders will be fulfilled.
We use cookies to keep things working smoothly and to improve your experience.
Choose what’s okay for you below. See our Cookie Policy .
Accept Cookies
Tetraphenylphosphonium chloride - for the spectrophotometric det. of Bi, Co, ≥97.0%, high purity , CAS No.2001-45-8
Basic Description
Synonyms
Ph4PCl | A855066 | Tetraphenylphosphonium chloride, for the spectrophotometric det. of Bi, Co, >=97.0% | C24H20ClP | Q7706653 | SY032650 | Phosphonium, tetraphenyl-, chloride | EINECS 217-890-3 | SCHEMBL126056 | Tetraphenylphosphonium chloride | WAGFXJQAI
Specifications & Purity
≥97%, for the spectrophotometric det. of Bi, Co
Storage Temp
Argon charged
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Phenylphosphines and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Phenylphosphines and derivatives
Alternative Parents
Organopnictogen compounds Organophosphorus compounds Organic chloride salts Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Triphenylphosphine - Phenylphosphine - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organophosphorus compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as phenylphosphines and derivatives. These are compounds containing a phenylphosphine, which consists of phosphine substituent bound to a phenyl group.
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.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
tetraphenylphosphanium;chloride
INCHI
InChI=1S/C24H20P.ClH/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;1H/q+1;/p-1
InChIKey
WAGFXJQAIZNSEQ-UHFFFAOYSA-M
Smiles
C1=CC=C(C=C1)[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Cl-]
Isomeric SMILES
C1=CC=C(C=C1)[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Cl-]
WGK Germany
3
PubChem CID
164911
Molecular Weight
374.85
Beilstein
3922390
Reaxy-Rn
3922393
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Hygroscopic
Melt Point(°C)
272-274 °C
Molecular Weight
374.800 g/mol
XLogP3
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
4
Exact Mass
374.099 Da
Monoisotopic Mass
374.099 Da
Topological Polar Surface Area
0.000 Ų
Heavy Atom Count
26
Formal Charge
0
Complexity
301.000
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
Citations of This Product
1.
R. Teng, P. Cai, X. Pu, X. Wang, Q. Ai, J. Si, X. Yao, Z. Liu.
(2023)
Modified luminescent properties from green afterglow to efficient orange emission in zirconium-based organometallic chloride scintillator by Sb3+ doping. Materials Today Chemistry,
30
(101527).
2.
Yuan Wang, Guangmin Xie, Jinglei Chen, Xiurong Zhang, Cong Chen, Jian Yin, Huanrong Li.
(2022)
Visible-light excitable, highly transparent and luminescent films with an ultrahigh loading of a europium(III) complex. Journal of Materials Chemistry C,
10
(33):
(11924-11930).
3.
Tianmou Xu, Peiqing Cai, Qi Ai, Qi He, Junjie Si, Xin Yao, Zugang Liu.
(2022)
Regulated room temperature phosphorescence from zero-dimensional organometallic halide hybrids for anti-counterfeiting and encryption. JOURNAL OF LUMINESCENCE,
248
(118979).
4.
Haoran Pei, Shaohong Shi, Yinghong Chen, Yu Xiong, Qinniu Lv.
(2022)
Combining Solid-State Shear Milling and FFF 3D-Printing Strategy to Fabricate High-Performance Biomimetic Wearable Fish-Scale PVDF-Based Piezoelectric Energy Harvesters. ACS Applied Materials & Interfaces,
14
(13):
(15346–15359).
5.
Lijun Wang, Fang Wang, Qiang Zhou, Yanfei Wang, Haixiang Song, Haiyang Yang.
(2022)
Metal-free Lewis pairs catalysed synthesis of fluorescently labelled polyester-based amphiphilic polymers for biological imaging. EUROPEAN POLYMER JOURNAL,
166
(111033).
6.
Haoran Pei, Yeping Xie, Yu Xiong, Qinniu Lv, Yinghong Chen.
(2021)
A novel polarization-free 3D printing strategy for fabrication of poly (Vinylidene fluoride) based nanocomposite piezoelectric energy harvester. COMPOSITES PART B-ENGINEERING,
225
(109312).
7.
Huifang Guo, Yuping Chen, Ying-Zi Han, Qingyuan Wu, Lin Wang, Qinghua Xu, Rong Huo, Xuekun Gong, Jing Sun, Qing Tang, Hui Shen.
(2024)
Bulky Ligands Induce Rich Uncoordinated Sites for Boosting Metal Nanocluster Catalysis. CHEMISTRY OF MATERIALS,
36
(15):
(7243-7251).
8.
Gaokuo Du, Huanrong Li, Zixuan Li, Xinchi Ye, Yige Wang.
(2024)
Luminescence Boosting after adding Quaternary ammonium/Phosphine Cations to Europium (III) Laponite Clay. APPLIED CLAY SCIENCE,
261
(107584).
9.
Xiangyan Yun, Yanrong Zhu, Yu Wang, Zutao Fan, Kang Zhou, Hanlin Hu, Haizhe Zhong, Henan Li, Yumeng Shi.
(2024)
Toward an Ideal Light Source for Indoor Photosynthesis: Broadband Red Emission in Zero-Dimensional Hafnium-Based Metal Halide (TPP)2HfCl6·4C2H3N:Sb3+. INORGANIC CHEMISTRY,
63
(39):
(18304-18312).
10.
Yongqiang Zhou, Zixian Wang, linfeng Guo, Lei Huang, Yichen Liu, Mengyue Wu, Qian Zhang, Kang An, Peng He, Fei Wang, Juan Du, Zhengzheng Liu, Zhiping Hu, Yuxin Leng, Yayun Pu, Jun’an Lai, Xiaosheng Tang.
(2024)
Ultrafast and high-resolution X-ray imaging based on zero-dimensional organic silver halides. Materials Chemistry Frontiers,
Solution Calculators
Molarity Calculator
Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator
Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator
Shall we send you a message when we have discounts available?
Remind me later
Allow
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
10 Citations