Description

5-[(3-Aminopropyl)Amino]-1,3-Diazido-1,2,3,5-Tetradeoxy-4-o-(2,6-Diazido-2,6-Dideoxy-D-Glucopyranosyl)-D-Myo-Inositol CAS NO 948916-24-3 is a highly functionalized, multi-azido derivative of a myo-inositol glycoside, representing a sophisticated chemical building block. This compound matters for its unique structural complexity, offering multiple reactive azide groups and an aminoalkyl chain, which are critical for advanced synthetic applications like click chemistry and bioconjugation. It is primarily needed by research institutions and pharmaceutical developers working on novel glycoconjugates, carbohydrate-based drug delivery systems, and complex probe molecules for chemical biology.

Application

• Click Chemistry Reagent: Serves as a multi-valent precursor for copper-catalyzed azide-alkyne cycloaddition (CuAAC) to create complex dendrimers or polymer scaffolds.
• Bioconjugation & Probe Synthesis: Used to label biomolecules (proteins, antibodies, oligonucleotides) with fluorescent or affinity tags via its reactive azide and amine handles.
• Glycoconjugate Research: A key intermediate in the synthesis of novel, structurally defined glycodendrimers and neoglycoproteins for immunological studies.
• Pharmaceutical Intermediate: Potential building block for the development of carbohydrate-based therapeutics and targeted drug delivery vehicles.
• Material Science: Enables the surface functionalization of nanoparticles and polymers to introduce specific biological recognition elements.
• Chemical Biology Tool: Facilitates the study of carbohydrate-protein interactions and cellular processes through activity-based protein profiling (ABPP).

Basic Information

Product Name	5-[(3-Aminopropyl)Amino]-1,3-Diazido-1,2,3,5-Tetradeoxy-4-o-(2,6-Diazido-2,6-Dideoxy-D-Glucopyranosyl)-D-Myo-Inositol
CAS No.	948916-24-3
Molecular Formula	C15H25N11O8
Molecular Weight	487.43 g/mol
Synonyms	1,3,2',6'-Tetraazido-1,3,2',6'-tetradeoxy-4-O-(2,6-diazido-2,6-dideoxy-D-glucopyranosyl)-D-myo-inositol, 5-[(3-Aminopropyl)amino] derivative; 5-(3-Aminopropylamino)-1,3,2',6'-tetraazido-1,3,2',6'-tetradeoxy-4-O-(2,6-diazido-2,6-dideoxy-D-glucopyranosyl)-D-myo-inositol; Multi-azido functionalized inositol glycoside; Azido-inositol glycoside building block; Glyco-click chemistry intermediate; N5-(3-Aminopropyl)-1,3,2',6'-tetraazido-1,3,2',6'-tetradeoxy-4-O-(2,6-diazido-2,6-dideoxy-D-glucopyranosyl)-D-myo-inositol-5-amine
EINECS	Contact for details

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards. We provide material of high purity suitable for research and development applications, with batch-specific Certificates of Analysis (COA) available upon request. Quality is assured through analytical techniques including HPLC, NMR, and mass spectrometry to confirm identity, purity, and the absence of critical impurities.

Storage

Preserve in a tightly closed container, protected from light. Store at -20°C or below under an inert atmosphere for long-term stability. This compound is hygroscopic (moisture-sensitive) and the azide functional groups require careful handling. Allow the sealed container to equilibrate to room temperature before opening to minimize moisture ingress.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 95%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Meets ICH guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.