Determine the necessary mass, volume, or concentration for preparing a solution.
≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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 12 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Trityl chloride is a protecting reagent for amines, alcohols, and thiols.
| Sonrisas canónicas | C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)Cl |
|---|---|
| IUPAC Name | [chloro(diphenyl)methyl]benzene |
| InChIKey | JBWKIWSBJXDJDT-UHFFFAOYSA-N |
| INCHI | 1S/C19H15Cl/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H |
| Isómeros SMILES | C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)Cl |
| WGK Alemania | 3 |
| RTECS | PA6450000 |
| PubChem CID | 6456 |
| Número ONU | 3261 |
| Grupo de embalaje | III |
| Peso molecular | 278.78 |
| Beilstein | 397363 |
| Reaxy-Rn | 397363 |
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 | Triphenyl compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Triphenyl compounds |
| Alternative Parents | Benzene and substituted derivatives Organochlorides Hydrocarbon derivatives Alkyl chlorides |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Triphenyl compound - Monocyclic benzene moiety - Hydrocarbon derivative - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety. |
| 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 | Jan 04, 2026 | T106184 | |
| Certificate of Analysis | Jan 04, 2026 | T106184 | |
| Certificate of Analysis | Feb 08, 2025 | T106184 | |
| Certificate of Analysis | Feb 08, 2025 | T106184 | |
| Certificate of Analysis | Feb 08, 2025 | T106184 | |
| Certificate of Analysis | Feb 08, 2025 | T106184 | |
| Certificate of Analysis | Feb 08, 2025 | T106184 | |
| Certificate of Analysis | Jan 10, 2025 | T106184 | |
| Certificate of Analysis | Aug 10, 2024 | T106184 | |
| Certificate of Analysis | Aug 10, 2024 | T106184 | |
| Certificate of Analysis | Mar 09, 2024 | T106184 | |
| Certificate of Analysis | Mar 09, 2024 | T106184 | |
| Certificate of Analysis | Mar 09, 2024 | T106184 | |
| Certificate of Analysis | Mar 05, 2024 | T106184 | |
| Certificate of Analysis | Jan 17, 2022 | T106184 | |
| Certificate of Analysis | Jan 17, 2022 | T106184 | |
| Certificate of Analysis | Jan 17, 2022 | T106184 |
| Solubilidad | Soluble in Hexane: 20 mg/ml Insoluble in water. Soluble in chloroform, hexane, benzene, ether, acetone and tetrahydrofuran. |
|---|---|
| Sensibilidad | Moisture & heat sensitive. |
| Punto de ebullición (°C) | 310°C |
| Punto de fusión (°C) | 113°C |
| Peso molecular | 278.800 g/mol |
| XLogP3 | 5.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 3 |
| Exact Mass | 278.086 Da |
| Monoisotopic Mass | 278.086 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 235.000 |
| 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 |
| 1. Song Wang, Xiewen Wu, Jing Fang, Feng Zhang, Yanli Liu, Hongbo Liu, Yu He, Min Luo, Run Li. (2023) Direct Z-Scheme Polymer/Polymer Double-Shell Hollow Nanostructures for Efficient NADH Regeneration and Biocatalytic Artificial Photosynthesis under Visible Light. ACS Catalysis, [PMID:] [10.1021/acscatal.2c05722] |
| 2. Shouwan Tang, Fang Wang, Zhenzhong Yan, Ling Huang. (2020) Enantiomer separation on novel cellulose derivatives bearing regioselective phenylcarbamate groups. JOURNAL OF SEPARATION SCIENCE, 44 (2): (489-496). [PMID:33135309] [10.1002/jssc.202000912] |
| 3. Yuhong Zhou, Qian Liang, Zhilun Zhang, Zhaodi Wang, Mingxian Huang. (2020) Chiral separations with crosslinked cellulose derivatives attached onto hybrid silica monolith particles via the thiol–ene click reaction. Analytical Methods, 12 (21): (2727-2734). [PMID:32930304] [10.1039/D0AY00772B] |
| 4. Zhuxin Zhou, Lunjun Qu, Tingting Yang, Jinglan Wen, Yi Zhang, Zhenguo Chi, Siwei Liu, Xudong Chen, Jiarui Xu. (2016) Nonvolatile electrical switching behavior and mechanism of functional polyimides bearing a pyrrole unit: influence of different side groups. RSC Advances, 6 (58): (52798-52809). [PMID:] [10.1039/C6RA11615A] |
| 5. Sun Baishen, Li Xiaofang, Jin Zhaolei, Tian Lili, Wang Fang, Liu Guihua, Tang Shouwan, Pan Fuyou. (2012) Preparation of Regioselectively Modified Amylose Derivatives and Their Applications in Chiral HPLC. CHROMATOGRAPHIA, 75 (23): (1347-1354). [PMID:] [10.1007/s10337-012-2338-x] |
| 6. Shouwan Tang, Xiaofang Li, Fang Wang, Guihua Liu, Yonglong Li, Fuyou Pan. (2011) Synthesis and hplc chiral recognition of regioselectively carbamoylated cellulose derivatives. CHIRALITY, 24 (2): (167-173). [PMID:22213581] [10.1002/chir.21978] |
| 7. Shuqin Xu, Meiling Qiu, Liyuan Liang, Yue Chen, Yajia Wang, Jing Wu, Jinghua Chen. (2025) Multifunctions of Sustainable Chondroitin Sulfates with Predominant Subtypes and Low Molecular Weights on Neurite Outgrowth. BIOMACROMOLECULES, [PMID:39835408] [10.1021/acs.biomac.4c01713] |
| 8. Wang Weiqi, Wang Fan, Wang Yuqing, Zhang Lili, Okamoto Yoshio, Shen Jun. (2024) Synthesis of Bulky Cellulose Derivatives for Efficient Enantioselective Fluorescent Sensing. CELLULOSE, 31 (9): (5779-5794). [PMID:] [10.1007/s10570-024-05959-w] |
| 9. Fan Wang, Yuqing Wang, Lili Zhang, Ting Zheng, Jun Shen. (2025) Synthesis of cellulose derivatives bearing regioselective bulky thiazolyl substituents at 2,3- and 6-positions for efficient fluorescence and UV–visible detection of Cu2+/Fe3+ ions. CARBOHYDRATE POLYMERS, [PMID:40973317] [10.1016/j.carbpol.2025.124339] |
| 10. Shouwan Tang, Zhaolei Jin, Baishen Sun, Fang Wang, Wenyuan Tang. (2017) Preparation and evaluation of regioselectively substituted amylose derivatives for chiral separations. CHIRALITY, 29 (9): (512-521). [PMID:28635058] [10.1002/chir.22720] |
| 11. Zhe Zheng, Songbai Liu. (2026) Curcumin cellular delivery based on assembly of clover shaped trityl polyethylene glycols with ovalbumin. Food Bioscience, [PMID:] [10.1016/j.fbio.2026.108382] |
| 12. Zhou Zhou, Ce Zhao, Xinxin Yan, Lukuan Guo, Shilong Yang, Zhen Chen, Junlong Song, Jiaqi Guo. (2026) Regioselective Synthesis of 6-Triphenylmethyl-2,3-hydroxypropyl Cellulose and Its Application in Colorless Anticounterfeiting Labels. ACS Applied Polymer Materials, [PMID:] [10.1021/acsapm.6c00106] |