Description

α-D-Glucopyranoside, Phenylmethyl 2-(Acetylamino)-2-Deoxy-3-o-(Phenylmethyl)-, 6-(4-Methylbenzenesulfonate) is a sophisticated, protected carbohydrate derivative that serves as a critical building block in advanced organic synthesis. This compound is valued for its role in the precise construction of complex oligosaccharides and glycoconjugates, enabling research and development in targeted therapeutic areas. It is primarily utilized by pharmaceutical R&D laboratories, biotechnology companies, and academic institutions focused on glycoscience, medicinal chemistry, and the development of novel bioactive molecules.

Application

• Glycosylation Reagent: A key intermediate for the controlled synthesis of specific glycosidic linkages in oligosaccharide assembly.
• Pharmaceutical Intermediate: Used in the research and development of novel glycoprotein-based drugs, antibiotics, and antiviral agents.
• Glycoconjugate Synthesis: Essential for creating labeled or modified sugars for biochemical studies and diagnostic tool development.
• Medicinal Chemistry Research: Employed in structure-activity relationship (SAR) studies to explore the biological function of carbohydrate motifs.
• Chemical Biology Probes: Serves as a precursor for synthesizing activity-based probes to study glycosyltransferase enzymes.
• Academic & Industrial R&D: A valuable tool for synthetic chemists in both university laboratories and industrial R&D departments specializing in carbohydrate chemistry.

Basic Information

Item	Detail
Product Name	α-D-Glucopyranoside, Phenylmethyl 2-(Acetylamino)-2-Deoxy-3-o-(Phenylmethyl)-, 6-(4-Methylbenzenesulfonate)
CAS No.	50908-12-8
Molecular Formula	C29H33NO8S
Molecular Weight	555.64 g/mol
Synonyms	Benzyl 2-acetamido-2-deoxy-3-O-benzyl-α-D-glucopyranoside 6-(p-toluenesulfonate); Benzyl 2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside 6-tosylate; 6-O-Tosyl-3-O-benzyl-2-deoxy-2-phthalimido-D-glucopyranosyl bromide benzyl glycoside precursor; 2-Acetamido-2-deoxy-3-O-benzyl-α-D-glucopyranoside benzyl 6-tosylate; Protected N-Acetylglucosamine derivative; GlcNAc building block 6-tosylate; Glycosyl donor intermediate.
EINECS	Contact for details

Quality Control

Every batch of our protected carbohydrate intermediates is manufactured and tested under strict quality management protocols to ensure identity, purity, and consistency essential for sensitive synthetic applications. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing key parameters such as assay (HPLC), chiral purity, and impurity profiles. Our commitment to reliable supply and documentation traceability supports critical R&D and cGMP-compliant development workflows.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). This material is light-sensitive and should be handled under appropriate conditions to maintain stability. For long-term storage, consider inert atmosphere conditions to preserve optimal reactivity.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Assay (HPLC)	≥ 95.0%
Purity (HPLC)	≥ 97.0%
Specific Rotation	Contact for details
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Complies with ICH guidelines

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