Determine the necessary mass, volume, or concentration for preparing a solution.
20 wt. % in H2O for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
application:
Triethylmethylammonium hydroxide solution can be used:
To adjust the pH of the reaction mixture in the synthesis of H2VOPO4, which in turn is used to synthesize a vanadium phosphate named ε-VOPO4.
To prepare ionic liquids with amino acid anions, exhibiting bipolar solvent properties.
| Pubchem Sid | 488198710 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488198710 |
| Sorrisi canonici | CC[N+](C)(CC)CC.[OH-] |
| IUPAC Name | triethyl(methyl)azanium;hydroxide |
| InChIKey | JAJRRCSBKZOLPA-UHFFFAOYSA-M |
| INCHI | 1S/C7H18N.H2O/c1-5-8(4,6-2)7-3;/h5-7H2,1-4H3;1H2/q+1;/p-1 |
| Isomeri SMILES | CC[N+](C)(CC)CC.[OH-] |
| PubChem CID | 14647552 |
| Peso molecolare | 133.23 |
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 |
| Classe | Organonitrogen compounds |
| Subclass | Quaternary ammonium salts |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tetraalkylammonium salts |
| Alternative Parents | Organic salts Organic oxoanionic compounds Organic oxides Hydrocarbon derivatives Amines Organic cations |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tetraalkylammonium salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic hydroxide - Amine - Organic cation - Aliphatic acyclic compound |
| Descrizione | 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 |
| Indice di rifrazione | 1.373 |
|---|---|
| Punto di ebollizione (°C) | 102° C at 760 mmHg |
| Peso molecolare | 133.230 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Exact Mass | 133.147 Da |
| Monoisotopic Mass | 133.147 Da |
| Topological Polar Surface Area | 1.000 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 47.100 |
| 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. Yang Wang, Lijuan Liu, Pan Chen, Lina Zhang, Ang Lu. (2018) Cationic hydrophobicity promotes dissolution of cellulose in aqueous basic solution by freezing–thawing. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 20 (20): (14223-14233). [PMID:29761185] [10.1039/C8CP01268G] |