Determine the necessary mass, volume, or concentration for preparing a solution.
≥98%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Tributylmethylammonium chloride is a quaternary ammonium salt commonly used as a catalyst in the synthesis of ɛ-caprolactone and 1-substituted tetrazoles.
Application:
Tributylmethylammonium chloride can be used as a phase transfer catalyst in the synthesis of ɛ-caprolactone by Baeyer-Villiger oxidation of cyclohexanone in the presence of KHSO5 as an oxidizing agent.
| Sonrisas canónicas | CCCC[N+](C)(CCCC)CCCC.[Cl-] |
|---|---|
| IUPAC Name | tributyl(methyl)azanium;chloride |
| InChIKey | IPILPUZVTYHGIL-UHFFFAOYSA-M |
| INCHI | 1S/C13H30N.ClH/c1-5-8-11-14(4,12-9-6-2)13-10-7-3;/h5-13H2,1-4H3;1H/q+1;/p-1 |
| Isómeros SMILES | CCCC[N+](C)(CCCC)CCCC.[Cl-] |
| WGK Alemania | 3 |
| PubChem CID | 91822 |
| Peso molecular | 235.84 |
| Beilstein | 6300212 |
| Reaxy-Rn | 6300212 |
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 | Organic nitrogen compounds |
| Clase | Organonitrogen compounds |
| Subclass | Quaternary ammonium salts |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tetraalkylammonium salts |
| Alternative Parents | Organopnictogen compounds Organic chloride salts Hydrocarbon derivatives Amines |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tetraalkylammonium salt - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Amine - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains. |
| 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 | Sep 26, 2025 | T465370 | |
| Certificate of Analysis | Sep 26, 2025 | T465370 | |
| Certificate of Analysis | Dec 12, 2022 | T465370 | |
| Certificate of Analysis | Dec 12, 2022 | T465370 | |
| Certificate of Analysis | Dec 12, 2022 | T465370 | |
| Certificate of Analysis | Dec 12, 2022 | T465370 | |
| Certificate of Analysis | Dec 12, 2022 | T465370 | |
| Certificate of Analysis | Dec 12, 2022 | T465370 |
| Solubilidad | Water solubility 1,000 g/l at 20 °C |
|---|---|
| Sensibilidad | Moisture sensitive |
| Peso molecular | 235.840 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 9 |
| Exact Mass | 235.207 Da |
| Monoisotopic Mass | 235.207 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 98.600 |
| 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. Yan Gao, Shumin Zhao, Miao Yan, Yongxia Li, Jianshe Zhao. (2023) High efficiency extraction oxidation desulfurization of model liquid fuel catalyzed by MIL-101(Fe) supported peroxo-polyoxometalates. MICROPOROUS AND MESOPOROUS MATERIALS, [PMID:] [10.1016/j.micromeso.2023.112857] |
| 2. Wei Wang, Zhensheng Shen, Jiaxiang Zhang, Lun Pan, Chengxiang Shi, Xiangwen Zhang, Ji-Jun Zou. (2023) Synthesis and Performance of Cyclopentadiene-Based Spirocyclopropane High-Energy-Density Fuels. FUEL, [PMID:] [10.1016/j.fuel.2023.129380] |
| 3. Min Wang, Luyao Zhao, Yu Niu, Shu Qin, Lixin Zhang, Liyan Jia, Xu Jing. (2023) Magnetic deep eutectic solvent-based dispersive liquid–liquid microextraction for determination of strobilurin fungicides in water, juice, and vinegar by high-performance liquid chromatography. Food Chemistry-X, [PMID:37397198] [10.1016/j.fochx.2023.100711] |
| 4. Feng Wang, Chao Li, Haohao Wang, Lu Yu, Fuming Zhang, Robert J. Linhardt. (2023) Amphiphilic O(Phe-r-Glu) oligopeptides randomly polymerized via papain exhibiting a pH-insensitive emulsification property. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, [PMID:] [10.1016/j.colsurfa.2023.131141] |
| 5. Xinbo Geng, Qiang Wang, Qiuxia Wang, Zhenghao Kou, Ruitong Xu, Rui Sun, Haowen Yu, Han Jia, Hui Yan. (2025) Investigation on the influence and mechanism of molecular structures on the corrosion inhibition properties of ionic liquids: Symmetry, heteroatom, and functional group. JOURNAL OF MOLECULAR STRUCTURE, [PMID:] [10.1016/j.molstruc.2025.143315] |
| 6. Mengtao Jin, Yu Wang, Lingqi Shen, Xuerong Yang, Peiyu Yan, Zuguang Li, Guohua Zhu. (2025) Green Process for Purification of Menthol from Peppermint Essential Oil based on In-Situ Formation of Deep Eutectic Solvents. JOURNAL OF SEPARATION SCIENCE, 48 (11): (e70296). [PMID:41205144] [10.1002/jssc.70296] |
| 7. Hu Wenxu, Ge Dandan, Fu Feie, Yuan Lin, Yang Chunyan, Weng Zhehui, Huang Yao. (2026) Supramolecular solvents based on deep eutectic solvents and hexafluorobutanol for the extraction of aristolochic acids from natural plants. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, [PMID:41642342] [10.1007/s00216-026-06357-w] |