CAS 103-83-3

N,N-Dimetilbenzilamina

Descrição:

N,N-Dimetilbenzilamina é um composto orgânico caracterizado por seu grupo funcional amina, especificamente uma amina terciária. Apresenta um grupo benzila ligado a um átomo de nitrogênio que é ainda substituído por dois grupos metila. Este composto é tipicamente um líquido incolor a amarelo pálido com um odor distintivo de amina. É solúvel em solventes orgânicos e exibe solubilidade limitada em água devido ao seu grupo benzila hidrofóbico. N,N-Dimetilbenzilamina é conhecido por seu papel como catalisador em várias reações químicas, particularmente na produção de poliuretanos e como agente de cura em resinas epóxi. Também pode atuar como surfactante e é utilizado na síntese de outros compostos químicos. Considerações de segurança incluem seu potencial para causar irritação na pele e nos olhos, e deve ser manuseado com as medidas de proteção adequadas. Sua estrutura química permite que participe de reações nucleofílicas, tornando-o um intermediário valioso na síntese orgânica.

Fórmula: C₉H₁₃N

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

Chave InChI: InChIKey=XXBDWLFCJWSEKW-UHFFFAOYSA-N

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

Sinónimos:

• . 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

Fórmula: C₉H₁₃N

Pureza: >98.0%(GC)

Cor e Forma: Colorless to Almost colorless clear liquid

Peso molecular: 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

Fórmula: C₉H₁₃N

Pureza: 98+%

Cor e Forma: Clear colorless to pale yellow, Liquid

Peso molecular: 135.21

Ref: 02-A12191

N,N-Dimethylbenzylamine

CAS: 103-83-3

N,N-Dimethylbenzylamine

Fórmula: C₉H₁₃N

Pureza: 95%

Cor e Forma: clear. colourless liquid

Peso molecular: 135.21g/mol

Ref: 54-OR54497

N,​N-​Dimethylbenzylamine(Benzyldimethylamine)

Produto Controlado

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);

Fórmula: C₉H₁₃N

Cor e Forma: Colourless

Peso molecular: 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.

Fórmula: C₉H₁₃N

Pureza: Min. 95%

Peso molecular: 135.21 g/mol

Ref: 3D-FD34601