Quaternary ammonium salts
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Filtered Search Results
N-Dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate
CAS: 14933-08-5 Molecular Formula: C17H37NO3S Molecular Weight (g/mol): 335.547 MDL Number: MFCD00036909 InChI Key: IZWSFJTYBVKZNK-UHFFFAOYSA-N Synonym: lauryl sultaine,lauryl sulfobetaine,n-dodecyl-n,n-dimethyl-3-ammonio-1-propanesulfonate,3-dodecyldimethylammonio propane-1-sulfonate,zwittergent 3-12,3-dodecyldimethylammonio propanesulfonate,sulfobetaine 12,unii-r6p3kw3e8u,3-lauryldimethylammonio propanesulfonate,dodecyldimethyl 3-sulphonatopropyl ammonium PubChem CID: 84703 ChEBI: CHEBI:75303 IUPAC Name: 3-[dodecyl(dimethyl)azaniumyl]propane-1-sulfonate SMILES: CCCCCCCCCCCC[N+](C)(C)CCCS(=O)(=O)[O-]
| PubChem CID | 84703 |
|---|---|
| CAS | 14933-08-5 |
| Molecular Weight (g/mol) | 335.547 |
| ChEBI | CHEBI:75303 |
| MDL Number | MFCD00036909 |
| SMILES | CCCCCCCCCCCC[N+](C)(C)CCCS(=O)(=O)[O-] |
| Synonym | lauryl sultaine,lauryl sulfobetaine,n-dodecyl-n,n-dimethyl-3-ammonio-1-propanesulfonate,3-dodecyldimethylammonio propane-1-sulfonate,zwittergent 3-12,3-dodecyldimethylammonio propanesulfonate,sulfobetaine 12,unii-r6p3kw3e8u,3-lauryldimethylammonio propanesulfonate,dodecyldimethyl 3-sulphonatopropyl ammonium |
| IUPAC Name | 3-[dodecyl(dimethyl)azaniumyl]propane-1-sulfonate |
| InChI Key | IZWSFJTYBVKZNK-UHFFFAOYSA-N |
| Molecular Formula | C17H37NO3S |
Sigma Aldrich Tetrabutylammonium Hydroxide Solution
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| Linear Formula | (CH3CH2CH2CH2)4N(OH) |
|---|---|
| CAS | 2052-49-5 |
| Biological Activity | Eyes |
| Molecular Weight (g/mol) | 259.47 g/mol |
| MDL Number | MFCD00009425 |
| Health Hazard 1 | UN 3286 8(6.1)(3) / PGII |
| Refractive Index | n20/D 1.3775 |
| Recommended Storage | Room Temperature |
| Molecular Formula | C16H37NO |
| Density | 0.83 g/mL at 25°C |
Sigma Aldrich 9-Ethylcarbazole
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| CAS | 86-28-2 |
|---|
Sigma Aldrich Benzyltriethylammonium Chloride
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| Linear Formula | C6H5CH2N(Cl)(C2H5)3 |
|---|---|
| CAS | 56-37-1 |
| Molecular Weight (g/mol) | 227.77 g/mol |
| MDL Number | MFCD00011824 |
| Synonym | BTEAC |
| RTECS Number | BO8275000 |
| Recommended Storage | Room Temperature |
| Molecular Formula | C13H22ClN |
| EINECS Number | 200-270-1 |
| Melting Point | 190°C to 192°C |
Sigma Aldrich Tetrabutylammonium Acetate
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| Synonym | TBAAc |
|---|
Sigma Aldrich [Ir(Dfcf3Ppy)2-(5,5'-Dcf3Bpy)]Pf6
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| CAS | 808142-88-3 |
|---|---|
| Recommended Storage | Room Temperature |
Sigma Aldrich Tetramethylammonium Fluoride Tetrahydrate
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Sigma Aldrich Tetrabutylammonium Hydrogensulfate
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| Linear Formula | (CH3CH2CH2CH2)4N(HSO4) |
|---|---|
| CAS | 32503-27-8 |
| Molecular Weight (g/mol) | 339.53 g/mol |
| MDL Number | MFCD00011637 |
| Synonym | Tetrabutylammonium bisulfate |
| Recommended Storage | Room Temperature |
| Molecular Formula | C16H37NO4S |
| EINECS Number | 251-068-5 |
| Melting Point | 169°C to 171°C |
Sigma Aldrich Tetrabutylammonium Bisulfate
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| Synonym | Tetrabutylammonium hydrogen sulfate |
|---|---|
| Recommended Storage | Room Temperature |
Sigma Aldrich Methyltrioctylammonium Hydrogen Sulfate
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| CAS | 625471-18-3 |
|---|
Medchemexpress LLC Tetramethylammonium 25g
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Tetramethylammonium fluoride tetrahydrate (TMAF) is a quaternary ammonium salt TMAF is commonly used as a weak base and a source of fluoride ions in various organic reactions including nucleophilic substitution functional group deprotection and ring-opening polymerization Unlike other fluoride sources TMAF is compatible with many functional groups making it a versatile tool in synthetic chemistry Functional reagents In addition TMAF has been used as a fluorinating agent in medicinal chemistry for the preparation of radiotracers and protein modification in biochemistry and the tetrahydrate form of TMAF is more stable and easier to handle than the anhydrous form
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Medchemexpress LLC Tetrabutylammonium (dihydrogen trifluoride) | 99337-56-1 | MFCD00145365 | 98.0% | 301.47 g·mol⁻¹ | C16H38F3N | 5 G
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Tetrabutylammonium (dihydrogen trifluoride) is a quaternary ammonium salt provided as a high-purity solid reagent for research applications. It is used as a convenient source of dihydrogen trifluoride/fluoride in synthetic chemistry and as an ionic component in specialized electrolyte systems; store sealed and protected from moisture.
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Medchemexpress LLC Tetraethylammonium perchlorate | 2567-83-1 | 98.0% | 229.70 | 25 G
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Tetraethylammonium perchlorate is an organic compound commonly used as an electrolyte in electrochemistry and as a source of perchlorate anion in analytical chemistry. It has various applications in the production of batteries, fuel cells, and electronic components due to its high ionic conductivity and stability under extreme conditions. It can also be used as a reference standard in analytical methods such as ion chromatography.
- Used as an electrolyte in electrochemistry
- Source of perchlorate anion in analytical chemistry
- High ionic conductivity and stability under extreme conditions
- Applications in batteries, fuel cells, and electronic components
- Can be used as a reference standard in analytical methods
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Medchemexpress LLC Tetrabutylammonium 25g
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Tetrabutylammonium triiodideIt is an organic compound and belongs to the category of quaternary ammonium salts It is a strong oxidizing agent and iodinating reagent often used in organic chemical reactions especially the conversion of alkenes and alkynes to the corresponding diiodide or tetraiodide compounds Tetrabutylammonium triiodideThere are various applications in synthetic organic chemistry especially in the synthesis of natural products pharmaceuticals and specialty chemicals
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Medchemexpress LLC Tetrabutylammonium 1g
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Tetrabutylammonium triiodideIt is an organic compound and belongs to the category of quaternary ammonium salts It is a strong oxidizing agent and iodinating reagent often used in organic chemical reactions especially the conversion of alkenes and alkynes to the corresponding diiodide or tetraiodide compounds Tetrabutylammonium triiodideThere are various applications in synthetic organic chemistry especially in the synthesis of natural products pharmaceuticals and specialty chemicals
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