74426-36-1

Usage

InChI:InChI=1/C8H18N2O6/c9-1-2-10-8(16)7(15)6(14)5(13)4(12)3-11/h4-7,11-15H,1-3,9H2,(H,10,16)/t4-,5-,6+,7-/m1/s1

Upstream product

• 107-15-3 ethylenediamine 
• 90-80-2 D-Glucono-1,5-lactone 
• 526-95-4 gluconic acid 

Downstream Products

• 106683-77-6 N-(β-D-Dluconylamino-ethyl)-phthalsaeure-monoamid 
• 101320-36-9 Terephthalaldehyd-bis-(β-D-gluconoylamino-ethyl-α-imin) 
• 93737-22-5 1-p-Dimethylamino-benzylidenamino-2-D-gluconoyl-amino-aethan 
• 77462-02-3 4-[Bis-(2-diphenylphosphanyl-ethyl)-carbamoyl]-3-[2-((2R,3S,4R,5R)-2,3,4,5,6-pentahydroxy-hexanoylamino)-ethylcarbamoyl]-butyric acid 
• 92328-25-1 1-(2,4,6-Trinitro-anilino)-2-D-gluconoylamino-ethan 

Relevant academic research and scientific papers

METHOD OF STRENGTHENING NON-KERATINOUS FIBERS, AND USES THEREOF

Disclosed is a method of treating non-keratinous fibers using a composition comprising an amide and/or alkyl ammonium carboxylate salt wherein the treating method improves the robust performance of the non-keratinous fibers and simultaneously maintains and/or improve the appearance or look such as color, shine, form, and shape of the fibers even after prolonged use. The method of protecting colored non-keratinous fibers from fading using the composition comprising an amide and/or alkyl ammonium carboxylate salt is also disclosed.

PH-responsive polysaccharide-bortezomib nanosphere and preparation method and application thereof

The invention relates to a pH-responsive polysaccharide-bortezomib nanosphere and a preparation method and application thereof. A nanosphere building unit is glucose modified hyaluronic acid and an anti-cancer drug bortezomib,crosslinking is conducted through borate bond interaction between a boric acid group on pharmaceutical molecules and glucose cis-diols,the nanosphere which takes hydrophilichyaluronic acid as a shell,and takes hydrophobic bortezomib as a kernel is formed,the particle size of the nanosphere is 100-120 nm,and very good drug release responsiveness to the pH is achieved. ThepH-responsive polysaccharide-bortezomib nanosphere has the advantages that hyaluronic acid is biophilic targeting polysaccharide molecules,drugs can be targetedly transported into cancer cells,and toxic and side effects on normal tissue are reduced; the boric acid group and glucose cis-diols can form a pH-responsive borate bond,and stimulus-responsive release of the drugs is achieved; the pH-responsive nanosphere preparation method is simple,easy to implement and low in raw material cost,and the nanosphere has a wide application prospect in the field of cancer targeted therapy.

Synthesis and evaluation of D-gluconamides as green mineral scales

A series of 13 d-gluconamides were synthesized in moderate to good yields and evaluated as green scale inhibitors. The crystal structures of two compounds were determined by X-ray crystallography. The compounds 6c and 6d showed a reasonable inhibition of BaSO4 precipitation from aqueous solution (47% and 51%, respectively) that indicated the potential for these derivatives of δ-gluconolactone.

Synthesis of Functional Chelating Diphosphines Containing the Bisamino Moiety and the Use of These Materials in the Preparation of Water-Soluble Diphosphine Complexes of Transition Metals

Acylation of bisamine provides a flexible synthesis of functionalized chelating diphosphines.This reaction offers a route to diphosphine complexes of transition metals having a wide range of structures and physical properties and especially to water-soluble complexes.The aqueous solubility of the free ligands and of the complexes prepared from them depend on the ligand, on the metal, and on other materials (especially surfactants) present in the solution.We describe typical preparations of ligands and outline the properties of their complexes with certain transition metals.