CAS 103-83-3

N,N-Dimethylbenzylamine

Description:

N,N-Dimethylbenzylamine is an organic compound characterized by its amine functional group, specifically a tertiary amine. It features a benzyl group attached to a nitrogen atom that is further substituted with two methyl groups. This compound is typically a colorless to pale yellow liquid with a distinctive amine odor. It is soluble in organic solvents and exhibits limited solubility in water due to its hydrophobic benzyl group. N,N-Dimethylbenzylamine is known for its role as a catalyst in various chemical reactions, particularly in the production of polyurethanes and as a curing agent in epoxy resins. It can also act as a surfactant and is utilized in the synthesis of other chemical compounds. Safety considerations include its potential to cause skin and eye irritation, and it should be handled with appropriate protective measures. Its chemical structure allows it to participate in nucleophilic reactions, making it a valuable intermediate in organic synthesis.

Formula: C₉H₁₃N

InChI: InChI=1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3

InChI key: InChIKey=XXBDWLFCJWSEKW-UHFFFAOYSA-N

SMILES: C(N(C)C)C1=CC=CC=C1

Synonyms:

• . N,N-Dimethyl Benzylamine
• 4-[(Dimethylamino)methyl]styrene
• Actiron NX 91
• Addocat DB
• Ancamine BDMA
• Araldite Accelerator 062
• Araldite DY 062
• Bdma
• Bencildimetilamina
• Benzyl Dimethylamine
• Benzyl-N,N-dimethylamine
• Benzylamine, N,N-Dimethyl-
• Benzyldimethylamin
• Benzyldimethylamine
• Dabco BDMA
• Desmorapid DB
• Dimethylbenzylamine
• Dy 062
• Dy 62
• Jeffcat BDMA
• Kaolizer 20
• Kh 30
• LCM 1 (catalyst)
• Lcm 1
• N,N-Dimethyl-1-phenylmethanamine
• N,N-Dimethyl-N-benzylamine
• N,N-Dimethylbenzenemethanamine
• N,N-Dimethylbenzylamin
• N,N-Dimethylbenzylamine
• N-(Phenylmethyl)dimethylamine
• N-Benzyl-N,N-dimethylamine
• N-Benzyldimethylamine
• Np 60
• Nsc 5342
• Sumicure BD
• [(Dimethylamino)methyl]benzene
• Benzenemethanamine,N,N-dimethyl-
• Dabco B-16
• Benzenemethamine, N,N-dimethyl-
• Nin-Dimethyl Benzylamine
• N,N-dimethyl(phenyl)methanaminium chloride
• N,N-dimethyl(phenyl)methanaminium
• Benzenemethanamine, N,N-dimethyl-
• aralditeaccelerator062
• N,N-BENZYLDIMETHYLAMINE

N,N-Dimethylbenzylamine

CAS: 103-83-3

Formula: C₉H₁₃N

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 135.21

Ref: 3B-D0688

N-Benzyldimethylamine, 98+%

CAS: 103-83-3

N,N-Dimethylbenzylamine is used in the preparation of bis[(N,N-dimethylamino)benzyl] selenide. It acts as a catalyst in the curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride. It undergoes directed ortho metalation with butyl lithium. It reacts with m

Formula: C₉H₁₃N

Purity: 98+%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 135.21

Ref: 02-A12191

N,N-Dimethylbenzylamine

CAS: 103-83-3

N,N-Dimethylbenzylamine

Formula: C₉H₁₃N

Purity: 95%

Color and Shape: clear. colourless liquid

Molecular weight: 135.21g/mol

Ref: 54-OR54497

N,​N-​Dimethylbenzylamine(Benzyldimethylamine)

Controlled Product

CAS: 103-83-3

Applications Benzyldimethylamine, can be ligated with a N-heterocyclic carbene, to produce a highly active, practical and versatile catalyst for the Heck-Mizoroki reaction. It can also be used for the perpetration of novel electrolyte, dibenzyldimethylammonium fluoride for acylation of cellulose.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Guang-Rong, P., et al.: Org. Biomol. Chem., 7(10), 2110 (2009); Casarano, R., et al.: Carbohydrate Polymers, 101, 444 (2014);

Formula: C₉H₁₃N

Color and Shape: Colourless

Molecular weight: 135.21

Ref: TR-B276200

N,N-Dimethylbenzylamine

CAS: 103-83-3

Dimethylbenzylamine is a colorless, volatile liquid with a low boiling point. It has been shown to be an effective biocide in the form of its copper complex, which may be used in detergent compositions for the inhibition of microbial growth on surfaces. Dimethylbenzylamine is also used as a standard reagent for determining redox potentials and has been studied extensively in kinetic and analytical chemistry. The reaction mechanism of dimethylbenzylamine has been determined to be similar to that of benzalkonium chloride and other quaternary ammonium salts. Dimethylbenzylamine is also used as a ligand in coordination geometry, transfer reactions, and salt metathesis.

Formula: C₉H₁₃N

Purity: Min. 95%

Molecular weight: 135.21 g/mol

Ref: 3D-FD34601