66080-74-8

Usage

Uses

Used in Chemical Biology and Bioconjugation Chemistry:
O-delta-Aminooxybutylhydroxylamine is used as a reagent for the synthesis of bioconjugates and the modification of proteins and peptides, facilitating the selective modification and functionalization of target molecules for scientific and industrial purposes.
Used in Biomolecular Labeling:
O-delta-Aminooxybutylhydroxylamine is utilized in the creation of oxime linkages and in the labeling of biomolecules, which is essential for biochemical and biophysical studies, enhancing the understanding of molecular interactions and mechanisms.
Used in Drug Delivery Systems and Nanomedicine:
O-delta-Aminooxybutylhydroxylamine has been investigated for its potential use in drug delivery systems and nanomedicine applications, indicating its broad applicability in the development of innovative therapeutic approaches and medical technologies.

InChI:InChI=1/C4H12N2O2/c5-7-3-1-2-4-8-6/h1-6H2

Upstream product

• 94464-30-9 N,N'-butane-1,4-diyldioxy-bis-phthalimide 

Downstream Products

• 1446949-45-6 3,3'-dibromo-1,1'-[butane-1,4-diyldioxybis(nitrilomethylidyne)]dibenzene 

Relevant academic research and scientific papers

Synthesis and characterization of multihalogen substituted salamo-type bisoximes

Four tetrahalogen substituted Salamo-type bisoximes H2L1-H2L4 have been synthesized from 3-bromo-5-chloro-2-hydroxybenzaldehyde and 1,3-bis(aminooxy) propane, 1,4-bis(aminooxy)butane, 1,5-bis(aminooxy)pentane or 1,6-bis(aminooxy)hexane in ethanol solution

Synthesis and characterization of methoxy-substituted salamo-type bisoximes based on bis(aminooxy)alkane and 3-methoxy-2-hydroxybenzaldehyde

Four new methoxy-substituted Salamo-type bisoxime compounds 6,6'-dimethoxy-2,2'-[(propylene-1,3-diyldioxy)bis(nitrilomethylidyne)] diphenol (H2L1), 6,6'-dimethoxy-2,2'-[(butylene-1,4-diyldioxy)bis(nitrilomethylidyne)]diphenol (H2L2), 6,6'-dimethoxy- 2,2'-[(propane-1,5-diyldioxy)bis(nitrilome-thylidyne)]diphenol (H2L3) and 6,6'-dimethoxy-2,2'-[(hexane-1,6-diyldioxy)bis(nitrilomethylidyne)] diphenol (H2L4) have been synthesized through condensation reactions under hot ethanol medium, respectively and characterized by elemental analyses, IR, UV-visible and 1H NMR spectra.

Synthesis and characterization of Salamo-type bisoximes based on 3-ethoxysalicyladehyde and Bis(aminooxy)alkane

A series of ethoxy-substituted Salamo-type bisoximes H2L1-H2L4 have been synthesized from 3-ethoxysalicyladehyde and 1,3-bis(aminooxy)propane, 1,4- bis(aminooxy)butane, 1,5-bis(aminooxy)pentane or 1,6-bis(aminoo

Synthesis and structural characterization of bromo-substituted salamo-type bisoximes based on bis(aminooxy)alkane and 3,5-dibromosalicylaldehyde

A series of bromo-substituted Salamo-type bisoximes H2L1-H2L3 have been synthesized through condensation reactions of 3,5-dibromosalicylaldehyde with 1,2-bis(aminooxy)ethane, 1,3-bis(aminooxy)propane and 1,4-bis

Uracil-directed ligand tethering: An efficient strategy for uracil DNA glycosylase (UNG) inhibitor development

Uracil DNA glycosylase (UNG) is an important DNA repair enzyme that recognizes and excises uracil bases in DNA using an extrahelical recognition mechanism. It is emerging as a desirable target for small-molecule inhibitors given its key role in a wide ran