D34108

Dibenzylamine

97%

• Sinónimos: (N-Benzylaminomethyl)benzene, Bibenzylamine, DBA, Dibenzylamine (8CI), N,N-Dibenzylamine, N-(Phenylmethyl)benzenemethanamine, N-Benzyl-1-phenylmethanamine, N-Benzylbenzylamine
• Fórmula lineal: (C₆H₅CH₂)₂NH
• Número de CAS: 103-49-1
• Peso molecular: 197.28
• Beilstein: 909664
• Número CE: 203-117-7
• Número MDL: MFCD00004770
• Código UNSPSC: 12352100
• ID de la sustancia en PubChem: 24893752
• NACRES: NA.22

Propiedades

• Nivel de calidad: 200
• Ensayo: 97%
• Formulario: liquid
• índice de refracción: n20/D 1.574 (lit.)
• bp: 300 °C (lit.)
• mp: −26 °C (lit.)
• densidad: 1.026 g/mL at 25 °C (lit.)
• cadena SMILES: C(NCc1ccccc1)c2ccccc2
• InChI: 1S/C14H15N/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10,15H,11-12H2
• Clave InChI: BWLUMTFWVZZZND-UHFFFAOYSA-N

Descripción

Descripción general

Dibenzylamine is mainly used in the production of rubber accelerators, which play a key role in the vulcanization process. It is used as a precursor in the nitrosative cleavage of tertiary amines, aiding in various chemical reactions. It also serves as an intermediate in the synthesis of palladium complexes.

Aplicación

• Environmental monitoring in shale gas wastewater: Dibenzylamine was identified among the hazardous substances in shale gas wastewater, with research characterizing its concentration and distribution in the Upper Yangtze River, contributing to improved environmental management practices (Tang et al., 2024).


• Advancements in organic synthesis: Dibenzylamine was used in a novel synthetic strategy for (L)-Monomethyl Tyrosine via bulky ′forced-traceless′ regioselective Pd-catalyzed C(sp(2))-H activation, showcasing its utility in pharmaceutical compound development (Illuminati et al., 2023).


• Application in crystallography: The crystal structure of di-benzyl-ammonium was elucidated, providing insights into molecular interactions and potential applications in material science and drug design (Traoré et al., 2023).


• Utilization in green chemistry: Dibenzylamine facilitated a green approach towards Triazole forming reactions, aiming to develop anticancer drugs by minimizing environmental impact and enhancing reaction efficiency (Rastogi et al., 2023).

Información de seguridad

• Pictogramas: GHS05,GHS07,GHS09
• Palabra de señalización: Danger
• Frases de peligro: H302,H314,H410
• Consejos de prudencia: P273 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Clasificaciones de peligro: Acute Tox. 4 Oral - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1C
• Código de clase de almacenamiento: 8A - Combustible corrosive hazardous materials
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): 289.4 °F - closed cup
• Punto de inflamabilidad (°C): 143 °C - closed cup
• Equipo de protección personal: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter