Description

B-D-Glucopyranoside, Phenyl 3,4,6-Tris-o-(Phenylmethyl)-1-Thio- is a sophisticated, protected thioglycoside building block of significant interest in synthetic organic chemistry. Its primary value lies in its role as a key glycosyl donor for the stereoselective construction of complex carbohydrate structures and glycoconjugates. This high-purity intermediate is essential for researchers and manufacturers in pharmaceutical development, particularly for creating novel glycomimetics, and in academic research focused on glycoscience and chemical biology.

Application

• Glycosylation Reactions: Serves as a crucial glycosyl donor in the synthesis of oligosaccharides and complex glycans.
• Pharmaceutical Intermediates: Used in the research and development of carbohydrate-based drugs, including antibiotics and antiviral agents.
• Glycoconjugate Synthesis: A key precursor for creating glycopeptides, glycolipids, and other biologically active conjugates.
• Chemical Biology Probes: Employed in the synthesis of labeled sugars and probes for studying carbohydrate-protein interactions.
• Academic & Industrial R&D: Fundamental building block for methodological development in stereoselective synthesis and glycoscience.
• Material Science: Potential intermediate for synthesizing specialized polymers and surfactants with sugar-based architectures.

Basic Information

Product Name	B-D-Glucopyranoside, Phenyl 3,4,6-Tris-o-(Phenylmethyl)-1-Thio-
CAS No.	130781-27-0
Molecular Formula	C34H34O5S
Molecular Weight	554.70 g/mol
Synonyms	Phenyl 3,4,6-Tri-O-benzyl-1-thio-β-D-glucopyranoside; 1-Thio-β-D-glucopyranoside, phenyl 3,4,6-tris-O-(phenylmethyl)-; Phenyl 3,4,6-Tri-O-benzyl-1-thio-β-D-glucoside; 3,4,6-Tri-O-benzyl-1-thio-β-D-glucopyranosyl phenyl sulfide; 1-S-Phenyl-3,4,6-tri-O-benzyl-1-thio-β-D-glucopyranose; Thioglycoside donor, benzyl-protected glucose; β-D-Glucopyranosyl phenyl sulfide, 3,4,6-tribenzyl ether
EINECS	Contact for details

Quality Control

Our production of this advanced synthetic intermediate adheres to stringent quality protocols to ensure batch-to-batch consistency and high purity for research and development applications. Each lot is characterized using advanced analytical techniques, including HPLC, NMR, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to support your quality assurance and regulatory documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C) under an inert atmosphere, such as argon or nitrogen, due to its sensitivity to oxidation. Keep the container tightly sealed in a desiccator to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Specific Rotation	Contact for details

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