31719-05-8

Basic information

• Product Name: N,N'-DIBENZYLBUTANE-1,4-DIAMINE
• Synonyms: N,N'-DIBENZYLBUTANE-1,4-DIAMINE
• CAS NO: 31719-05-8
• Molecular Formula: C₁₈H₂₄N₂
• Molecular Weight: 268.4
• Mol File: 31719-05-8.mol
• Article Data: 10

Chemical Properties

• Melting Point: 65 °C
• Boiling Point: 401.5 °C at 760 mmHg
• Flash Point: 235.7 °C
• Appearance: /
• Density: 1.006 g/cm³
• PKA: 9.95±0.19(Predicted)
• CAS DataBase Reference: N,N'-DIBENZYLBUTANE-1,4-DIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-DIBENZYLBUTANE-1,4-DIAMINE(31719-05-8)
• EPA Substance Registry System: N,N'-DIBENZYLBUTANE-1,4-DIAMINE(31719-05-8)

Safety Data

• Hazardous Substances Data: 31719-05-8(Hazardous Substances Data)

Usage

General Description

N,N'-Dibenzylbutane-1,4-diamine is a chemical compound commonly used as a curing agent for epoxy resins. It is a diamine, which means it contains two amino groups, and its chemical structure is derived from butane. N,N'-DIBENZYLBUTANE-1,4-DIAMINE is known for its ability to improve the mechanical and thermal properties of epoxy resins, making them more durable and heat-resistant. It is used in a wide range of applications, including adhesive and coating formulations, as well as in the manufacturing of composite materials. However, it is important to handle N,N'-dibenzylbutane-1,4-diamine with care, as it can be irritating to the skin, eyes, and respiratory system.

Upstream product

• 6970-47-4 N¹,N²-dibenzylidenebutane-1,4-diamine 
• 100-52-7 benzaldehyde 
• 110-60-1 1,4-diaminobutane 
• 6970-47-4 N,N-bis-(phenylmethylene)butane-1,4-diamine 
• 31991-78-3 uvariadiamide 

Downstream Products

• 107886-63-5 N,N'-dibenzyl-N-(3-phthalimidopropyl)-1,4-diaminobutane 
• 107886-62-4 N,N'-dibenzyl-N-(4-phthalimidobutyl)-1,4-diaminobutane 
• 172271-57-7 1,12-biscarbobenzyloxy-4,9-bisbenzyl<1,12-13C2>spermine 
• 361484-36-8 (3S,12S)-N¹,N¹⁴-Bis(trifluoromethanesulfyl)-N⁵,N¹⁰-dibenzyl-N¹,N¹⁴-diethyl-3,12-dihydroxyhomospermine 
• 688763-89-5 C₆₄H₈₄N₂₆O₁₄ 
• 1004318-32-4 C₂₃H₂₇N₃O₂S 
• 785712-80-3 N,N'-Bis-<2-hydroxy-aethyl>-N,N'-dibenzyl-1,4-diamino-butan 
• 1597437-53-0 N-benzyl-N′-benzylidene-1,4-diaminobutane 

Relevant articles and documents

METHODS FOR PRODUCING (6S,15S)-3,8,13,18-TETRAAZAICOSANE-6,15-DIOL

The present invention provides methods of synthesizing (6S,15S)-3,8,13,18-tetraazaicosane-6,15-diol and salts thereof.

Synthesis and investigation of new cyclic haloamidinium salts

The presented work describes the synthesis of new six- and seven-membered haloamidinium salts and their reaction with different metals. The isolated metal complexes were tested in a catalytic reaction. Two different synthetic routes were applied to prepare five different salts. Chloroamidinium salts were very water-sensitive in comparison to their corresponding bromoamidinium salts. Hence, the preparation of the less sensitive bromoamidinium salts was higher prioritized. The formed salts were converted with metal sources to N-heterocyclic carbene (NHC) metal complexes through an oxidative insertion into the C-X bond. This type of formation is less examined for the synthesis of extended NHC metal complexes. Pd(PPh3)4 and cobalt powder were applied as metal sources, whereby two palladium complexes were isolated, characterized, and their crystal and molecular structures determined. The palladium complexes were investigated in the Suzuki-Miyaura reaction and showed promising catalytic activity.

Synthesis and antikinetoplastid activity of a series of N,N×-substituted diamines

A series of 25 N,N×-substituted diamines were prepared by controlled reductive amination of free aliphatic diamines with different substituted benzaldehydes. The library was screened in vitro for antiparasitic activity on the causative agents of human Afr