D34108

Dibenzylamine

97%

• Synonyme(s) : (N-Benzylaminomethyl)benzene, Bibenzylamine, DBA, Dibenzylamine (8CI), N,N-Dibenzylamine, N-(Phenylmethyl)benzenemethanamine, N-Benzyl-1-phenylmethanamine, N-Benzylbenzylamine
• Formule linéaire : (C₆H₅CH₂)₂NH
• CAS Number: 103-49-1
• Poids moléculaire : 197.28
• Beilstein: 909664
• Numéro CE : 203-117-7
• Numéro MDL: MFCD00004770
• Code UNSPSC : 12352100
• ID de substance PubChem : 24893752
• Nomenclature NACRES : NA.22

Propriétés

• Niveau de qualité: 200
• Essai: 97%
• Forme: liquid
• Indice de réfraction: n20/D 1.574 (lit.)
• pb: 300 °C (lit.)
• Pf: −26 °C (lit.)
• Densité: 1.026 g/mL at 25 °C (lit.)
• Chaîne 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
• Clé InChI: BWLUMTFWVZZZND-UHFFFAOYSA-N

Description

Description générale

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.

Application

• 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).

Informations sur la sécurité

• Pictogrammes: GHS05,GHS07,GHS09
• Mention d'avertissement: Danger
• Mentions de danger: H302,H314,H410
• Conseils de prudence: P273 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Classification des risques: Acute Tox. 4 Oral - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1C
• Code de la classe de stockage: 8A - Combustible corrosive hazardous materials
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): 289.4 °F - closed cup
• Point d'éclair (°C): 143 °C - closed cup
• Équipement de protection individuelle: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter