122-19-0 | Stearyldimethylbenzylammonium chloride

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$19.00	$13.00
25g	95%	in stock	$39.00	$27.00
100g	95%	in stock	$100.00	$70.00
500g	95%	in stock	$330.00	$231.00

Description

• Catalog Number: AB47051
• Chemical Name: Stearyldimethylbenzylammonium chloride
• CAS Number: 122-19-0
• Molecular Formula: C27H50ClN
• Molecular Weight: 424.1456
• MDL Number: MFCD00149986
• SMILES: CCCCCCCCCCCCCCCCCC[N+](Cc1ccccc1)(C)C.[Cl-]
• NSC Number: 20199

Computed Properties

• Complexity: 316
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 29
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 19

Upstream Synthesis Route

Benzenemethanaminium, N,N-dimethyl-N-octadecyl-, chloride (1:1) is a crucial compound commonly employed in chemical synthesis processes. This particular compound serves as a versatile catalyst in various organic reactions due to its unique structure and properties. Its application in chemical synthesis is particularly notable in the formation of complex organic molecules and polymers.In organic synthesis, Benzenemethanaminium, N,N-dimethyl-N-octadecyl-, chloride (1:1) acts as a catalyst in promoting reactions such as acylation, alkylation, and polymerization. Its positively charged ammonium group facilitates the activation of substrates, leading to enhanced reaction rates and increased yields of desired products. Moreover, the long octadecyl chain provides hydrophobic interactions, enabling the catalyst to stabilize reactive intermediates and facilitate selective transformations.This compound finds widespread use in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to accelerate key bond-forming reactions and control reaction pathways make it an indispensable tool for chemists engaged in the development of new compounds with desired properties. Additionally, the high purity and stability of Benzenemethanaminium, N,N-dimethyl-N-octadecyl-, chloride (1:1) ensure its reliability and reproducibility in various synthetic protocols.

Literature

• Adsorption of zearalenone by organomodified natural zeolitic tuff.

  Journal of colloid and interface science 20070701

• Adsorption of mycotoxins by organozeolites.

  Colloids and surfaces. B, Biointerfaces 20051125