131991-61-2

Basic information

• Product Name: mono-(6-(1,6-hexamethylenediamine)-6-deoxy)-β-Cyclodextrin
• Synonyms: mono-(6-(1,6-hexamethylenediamine)-6-deoxy)-β-Cyclodextrin;Mono-(6-(1,6-Hexamethylenediamine)-6-Deoxy)-Beta-Cyclodextrin
• CAS NO: 131991-61-2
• Molecular Formula: C₄₈H₈₄N₂O₃₄
• Molecular Weight: 1233.17
• EINECS: 1312995-182-4
• Mol File: 131991-61-2.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 1517.2±65.0 °C(Predicted)
• Appearance: /
• Density: 1.517±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 12.57±0.70(Predicted)
• CAS DataBase Reference: mono-(6-(1,6-hexamethylenediamine)-6-deoxy)-β-Cyclodextrin(CAS DataBase Reference)
• NIST Chemistry Reference: mono-(6-(1,6-hexamethylenediamine)-6-deoxy)-β-Cyclodextrin(131991-61-2)
• EPA Substance Registry System: mono-(6-(1,6-hexamethylenediamine)-6-deoxy)-β-Cyclodextrin(131991-61-2)

Safety Data

• Hazardous Substances Data: 131991-61-2(Hazardous Substances Data)

Usage

General Description

"Mono-(6-(1,6-hexamethylenediamine)-6-deoxy)-β-Cyclodextrin" is a chemical compound that belongs to the family of cyclodextrins, cyclic oligosaccharides composed of sugar molecules bound together in a ring. This specific compound is a derivative of β-Cyclodextrin, which is made up of seven glucopyranose units, featuring a hexamethylenediamine substituent. This means an amine group, derived from 1,6-hexamethylenediamine, has been introduced at one of the sugar units of the cyclodextrin. This complex structure allows the cyclodextrin to form inclusion complexes with a range of molecules, making it useful in a variety of scientific and industrial applications, including drug delivery, food and flavor science, and environmental technology.

Upstream product

• 124-09-4 1,6-Hexanediamine 
• 67217-55-4 mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin 

Relevant articles and documents

Preparation and characterization of 6A-polyamine-mono-substituted β-cyclodextrins

General syntheses for eleven β-cyclodextrins (cyclomaltoheptaoses) mono-substituted at the C6 position by a polyamine are described. The basis of the synthesis is the reaction of 6A-O-(4-methylphenylsulfonyl)-β-cyclodextrin in the presence of KI in 1-methylpyrrolidin-2-one solution. This produces a clean product and obviates the substantial purification procedures which other preparative methods often entail. Systematic studies of the variations of the P-KaS of the protonated amine groups and the 13C NMR spectra of the modified β-cyclodextrins with pH are reported.

Controlled transformation from nanorods to vesicles induced by cyclomaltoheptaoses (β-cyclodextrins)

A modified cyclomaltoheptaose (β-cyclodextrin) containing an anthraquinone moiety, mono[6-deoxy-N-n-hexylamino-(N′-1-anthraquinone)]- β-cyclodextrin (1), which can self-assemble into nanorods in aqueous solution, was synthesized. Interestingly, upon the a

Reversible 2D pseudopolyrotaxanes based on cyclodextrins and cucurbit[6]uril

In this paper, a pseudorotaxane (2) was synthesized by reaction of cucurbit [6]uril with 6-[(6-aminohexyl)amino]-6-deoxy-β-cyclodextrin chloride. Subsequently, pseudorotaxanes 2 were further assembled to form a 2D pseudopolyrotaxane (3) through an α,ω-PPG2000 diamino polymer threading the cavities of cyclodextrins in 2, and the resulting pseudopolyrotaxane was comprehensively characterized by FT-IR, NMR, TG-DTA, elemental analysis, and transmission electron microscopy. Significantly, the 2D pseudopolyrotaxane can turn into a main-chain pseudopolyrotaxane in the presence of base, and then the addition of α-cyclodextrins may result in a reversible switch between two different 2D pseudopolyrotaxanes.

Functional carrier based on alkylamino cyclodextrin in entrapment of ferulic acid

The invention discloses application of a functional carrier based on alkylamino cyclodextrin in entrapment of ferulic acid. On the one hand, alkylamino-modified beta-cyclodextrin is designed as a mainbody to prepare a ferulic acid clathrate compound; and on the other hand, an alkylamino cyclodextrin high-molecular polymer connected with linear polymer molecules is designed to load ferulic acid. Compared with the ferulic acid monomer, the ferulic acid entrapped by the carrier has advantages that the water solubility is obviously improved and the thermal stability is also enhanced; and a certain theoretical reference is provided for developing a novel water-soluble ferulic acid material and expanding the application of ferulic acid in the field of food and medicine.

Synthesis and evaluation of β-cyclodextrin-functionalized hydrophobically associating polyacrylamide

Modified β-cyclodextrin and N-phenethyl-methacrylamide were utilized to react with acrylamide and acrylic acid to synthesize hydrophobically associating polyacrylamide (HMPAM) via photoinitiated free-radical micellar copolymerization. HMPAM was characteri