Description

2-Propenyl O-2,3,4-Tris-O-(phenylmethyl)-α-D-glucopyranosyl-(1→4)-O-2,3,6-tris-O-(phenylmethyl)-α-D-glucopyranosyl-(1→4)-2,3,6-tris-O-(phenylmethyl)-β-D-glucopyranoside is a sophisticated, fully protected trisaccharide derivative, serving as a critical synthetic intermediate in advanced organic chemistry. Its value lies in providing a controlled, reactive scaffold for the precise construction of complex oligosaccharide structures, which are fundamental to biological research and pharmaceutical development. This high-purity building block is essential for researchers and process chemists in pharmaceutical R&D, biotechnology, and academic laboratories focused on glycobiology, carbohydrate-based drug discovery, and the synthesis of novel bioactive compounds.

Application

• Glycoconjugate Synthesis: A key protected intermediate for the chemical synthesis of complex oligosaccharides and glycoconjugates.
• Pharmaceutical Research: Used in the development of carbohydrate-based active pharmaceutical ingredients (APIs) and prodrugs.
• Glycobiology Studies: Serves as a precursor for creating defined glycan structures to study protein-carbohydrate interactions and cell signaling.
• Glycosylation Methodology: Employed in research to develop and optimize new glycosylation protocols and catalysts.
• Diagnostic Reagent Development: Potential use in synthesizing carbohydrate antigens or probes for diagnostic assays.
• Biomimetic Material Synthesis: Building block for creating synthetic polymers that mimic natural polysaccharides.

Basic Information

Item	Detail
Product Name	2-Propenyl O-2,3,4-Tris-O-(phenylmethyl)-α-D-glucopyranosyl-(1→4)-O-2,3,6-tris-O-(phenylmethyl)-α-D-glucopyranosyl-(1→4)-2,3,6-tris-O-(phenylmethyl)-β-D-glucopyranoside
CAS No.	171411-82-8
Molecular Formula	C81H90O16
Molecular Weight	1295.57 g/mol
Synonyms	2-Propenyl 2,3,4,2',3',6',2'',3'',6''-Nona-O-benzyl-α-maltotrioside; Allyl 2,3,4,2',3',6',2'',3'',6''-nona-O-benzyl-α-maltotrioside; Nona-O-benzyl-α-maltotriosyl allyl ether; Fully benzylated allyl α-maltotrioside; Protected maltotriose allyl glycoside; Trisaccharide benzyl ether derivative; Glycosylation donor intermediate
EINECS	Contact for details

Quality Control

Our high-value synthetic intermediates are produced under strict quality-controlled conditions to ensure batch-to-batch consistency and reliability for sensitive research applications. Each lot undergoes comprehensive analytical characterization, including HPLC for purity, NMR for structural confirmation, and mass spectrometry. A detailed Certificate of Analysis (COA) documenting identity, purity, and impurity profile is provided with every shipment to support your quality and regulatory documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store at 2-8°C in a dry, cool place. This compound is light-sensitive (store away from light) and should be handled under an inert atmosphere when appropriate to prevent degradation. Keep away from strong acids and organic solvents.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 95.0%
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.