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Chemodex
Tributylmethylammonium chloride
Product Details | |
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Synonyms | Methyltributylammonium chloride; TBMAC |
Product Type | Chemical |
Properties | |
Formula | C13H30ClN |
MW | 235.84 |
CAS | 56375-79-2 |
Source/Host Chemicals | Synthetic |
Purity Chemicals | ≥98% (T) |
Appearance | White to faint beige powder or crystals. |
Solubility | Soluble in water. |
Identity | Determined by 1H-NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | IPILPUZVTYHGIL-UHFFFAOYSA-M |
Smiles | CCCC[N+](C)(CCCC)CCCC.[Cl-] |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +20°C |
Long Term Storage | +4°C |
Handling Advice |
Keep under inert gas. Very hygroscopic. |
Use/Stability | Stable for at least 2 years after receipt when stored at +4°C. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet | Download PDF |
Tributylmethylammonium chloride (TBMAC) is a quaternary ammonium salt used in various chemical and biochemical applications. It consists of a tetrabutylammonium cation (Bu3N+) and a chloride anion (Cl-), with a methyl group (CH3) attached to the nitrogen atom of the ammonium cation. TBMAC is commonly used as a phase-transfer catalyst (PTC) in organic synthesis. Phase-transfer catalysis involves the transfer of reactants from one phase (usually an aqueous phase) to another phase (usually an organic phase) to facilitate a chemical reaction. TBMAC helps in the transfer of ions or molecules between these phases, allowing reactions that might not occur under standard conditions. Some common applications of TBMAC include, nucleophilic substitution reactions, halogenation reactions or alkylation and acylation reactions.
(1) S.M. Kumar; Synth. Commun. 21, 2121 (1991) | (2) S. Baj, et al.; Appl. Catal. A: General 309, 85 (2006) | (3) M.R. Kalaee, et al.; Macromol. Symp. 277, 81 (2009) | (4) S. Baj, et al.; Appl. Catal. A: General 395, 49 (2011) | (5) M. Sheydaei, et al.; J. Sulf. Chem. 33, 303 (2012) | (6) K. Nagaraju, et al.; Heterocyc. Comm. 23, 365 (2017)