Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | CC[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Cl-] |
|---|---|
| IUPAC Name | ethyl(triphenyl)phosphanium;chloride |
| InChIKey | NJXBVBPTDHBAID-UHFFFAOYSA-M |
| INCHI | 1S/C20H20P.ClH/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;/h3-17H,2H2,1H3;1H/q+1;/p-1 |
| Isómeros SMILES | CC[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Cl-] |
| Peso molecular | 326.81 |
| Reaxy-Rn | 4170030 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4170030&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | 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 |
| Descripción | 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Apr 25, 2026 | E101567 | |
| Certificate of Analysis | Apr 25, 2026 | E101567 | |
| Certificate of Analysis | Nov 13, 2025 | E101567 | |
| Certificate of Analysis | Nov 13, 2025 | E101567 | |
| Certificate of Analysis | Feb 17, 2025 | E101567 | |
| Certificate of Analysis | Sep 21, 2024 | E101567 | |
| Certificate of Analysis | Feb 20, 2024 | E101567 | |
| Certificate of Analysis | Feb 20, 2024 | E101567 | |
| Certificate of Analysis | Jan 11, 2023 | E101567 | |
| Certificate of Analysis | Mar 10, 2022 | E101567 | |
| Certificate of Analysis | Mar 10, 2022 | E101567 |
| Solubilidad | Soluble in Methanol |
|---|---|
| Sensibilidad | Moisture sensitive |
| Punto de fusión (°C) | 241.0 - 245.0 °C |
| Peso molecular | 326.800 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Exact Mass | 326.099 Da |
| Monoisotopic Mass | 326.099 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 247.000 |
| 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 |
| 1. Tiao Feng, Zi’an Zhou, Yi’ni An, Long Chen, Yuhua Fu, Shuyun Zhou, Nü Wang, Jinxiao Zheng, Chenghua Sun. (2024) Large-Area Transparent Antimony-Based Perovskite Glass for High-Resolution X-ray Imaging. ACS Nano, [PMID:38876985] [10.1021/acsnano.4c01761] |
| 2. Tao Huang, ZiXuan Wang, Tongzhou Li, Xiaodong Shen, Weizheng Liang, Quan Niu, Xianci Zhong, Bingsuo Zou. (2024) Multifunctional Phosphor with High-Efficient Near-Infrared Emission Based on Antimony–Zinc Halides. ACS Applied Materials & Interfaces, [PMID:38857900] [10.1021/acsami.4c04622] |
| 3. Bingning Wang, Yeshuang Wang, Zhen Wang, Song Yang, Chao Yang, Jiawei Kou, Huiling Fan, Ju Shangguan. (2025) Strong interaction of tetrabutylphosphonium chloride and γ-Al2O3 induces dissociation of H2O and generation of basic hydroxyl groups for promoting the carbonyl sulfide hydrolysis at a low temperature. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2025.133279] |
| 4. Zhang Na, Xu Ziwei, Yang Zhou, Zhang Lu, Fan Zihao, Xu Dongfang, Wang Fei, Yuan Ningyi, Ding Jianning, Cui Jian, Liu Zhike. (2025) Three birds with one stone: dual-interfaces and bulk co-passivation enable >21% efficiency of CsPbI3 solar cells with VOC of 1.27 V. Science China-Materials, [PMID:] [10.1007/s40843-025-3547-7] |
| 5. Shibo Gao, Zhigang Li, Mengmeng Jiao, Chuanlu Yang, Kai Wang, Defang Duan, Qinfeng Xu. (2026) Enhanced Cool White Light Emission in Organicinorganic Metal Halides through Pressure-Treated Molecular Configurations Regulation. Journal of Materials Chemistry A, [PMID:] [10.1039/D5TA10428A] |