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Product Description
Benzyltributylammonium chloride CAS#23616-79-7
Benzyltributylammonium chloride usually appears as white crystals or powder and is relatively stable under normal environmental conditions. It has a certain hygroscopicity and is relatively sensitive to humidity. Therefore, it is necessary to pay attention to moisture-proofing during storage and use.

Product Name: | Benzyltributylammonium chloride |
Synonyms: | Benzyltributylazanium chloride;Benzyltributylammonium chloride ,99%;Benzyltributylaminium·chloride;Tributylbenzylaminium·chloride;Benzenemethanaminium,N,N,N-tributyl-, chloride (1:1);BENZYL TRIBUTYL AMMONIUM CHLORIDE BTBAC;Benzyltributyl;Benzyltributylammonium chloridepurum |
CAS: | 23616-79-7 |
MF: | C19H34ClN |
MW: | 311.93 |
EINECS: | 245-787-3 |
Product Categories: | Ammonium Salts;Greener Alternatives: Catalysis;Pharmaceutical Intermediates;Ammonium Chlorides (Quaternary);Quaternary Ammonium Compounds;Phase Transfer Catalysts;Quaternary ammonium salt;bc0001 |
Mol File: | 23616-79-7.mol |
Benzyltributylammonium chloride Chemical Properties |
Melting point | 155-163 °C (lit.) |
Boiling point | 466.93°C (rough estimate) |
density | 0.9523 (rough estimate) |
refractive index | 1.6000 (estimate) |
storage temp. | Sealed in dry,Room Temperature |
form | Crystalline Powder |
color | White to ivory |
Water Solubility | soluble |
Sensitive | Hygroscopic |
BRN | 3776210 |
Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. |
InChI | InChI=1S/C19H34N.ClH/c1-4-7-15-20(16-8-5-2,17-9-6-3)18-19-13-11-10-12-14-19;/h10-14H,4-9,15-18H2,1-3H3;1H/q+1;/p-1 |
InChIKey | VJGNLOIQCWLBJR-UHFFFAOYSA-M |
SMILES | [N+](CCCC)(CCCC)(CCCC)CC1=CC=CC=C1.[Cl-] |
CAS DataBase Reference | 23616-79-7(CAS DataBase Reference) |
EPA Substance Registry System | Benzenemethanaminium, N,N,N-tributyl-, chloride (23616-79-7) |
Product Usage
Benzyltributylammonium chloride is used:
As a hydrogen bond acceptor (HBAs) in the synthesis of new series of deep eutectic solvents (DESs) with common hydrogen bond donors.
As a cationic surfactant to study the interactions with anionic dyes such as indigo carmine (IC) and amaranth (Amr)by conductometric method.
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