Description

2,3,4,6-Tetrakis-o-(Phenylmethyl)-β-D-Glucopyranose 1-[3,4,5-Tris(Phenylmethoxy)Benzoate] is a sophisticated, multi-protected carbohydrate derivative, specifically designed as a key synthetic intermediate for advanced organic and medicinal chemistry. Its value lies in its role as a versatile building block for constructing complex molecular architectures, particularly in the synthesis of glycoconjugates, dendrimers, and specialized pharmaceutical agents. This high-purity compound is essential for researchers and process chemists in pharmaceutical R&D, agrochemical development, and advanced material science who require reliable, well-characterized intermediates for critical synthetic pathways.

Application

• Pharmaceutical Intermediate: Serves as a crucial building block in the multi-step synthesis of novel drug candidates, particularly in oncology and metabolic disease research.
• Glycoconjugate Synthesis: Used for the controlled construction of complex carbohydrate structures linked to proteins, lipids, or other aglycones.
• Dendrimer & Polymer Chemistry: Acts as a functionalized core or branching unit for creating precisely defined dendritic macromolecules and specialty polymers.
• Chemical Biology Probes: Employed in the development of labeled saccharide derivatives for studying biological recognition and signaling pathways.
• Agrochemical Research: Utilized as an intermediate in the synthesis of advanced, target-specific crop protection agents.
• Chiral Auxiliary/ Ligand Precursor: Its rigid, multi-functionalized structure makes it a potential precursor for chiral ligands used in asymmetric catalysis.

Basic Information

Product Name	2,3,4,6-Tetrakis-o-(Phenylmethyl)-β-D-Glucopyranose 1-[3,4,5-Tris(Phenylmethoxy)Benzoate]
CAS No.	1195367-79-3
Molecular Formula	C62H58O11
Molecular Weight	979.12 g/mol
Synonyms	1-O-[3,4,5-Tris(benzyloxy)benzoyl]-2,3,4,6-tetra-O-benzyl-β-D-glucopyranose; 2,3,4,6-Tetra-O-benzyl-β-D-glucopyranosyl 3,4,5-tris(benzyloxy)benzoate; Perbenzylated Glucopyranosyl Tris(benzyloxy)benzoate; Benzyl-protected Glucose Benzoate Ester; Glycosyl Donor Intermediate; Tris(benzyloxy)benzoyl Glucoside Derivative
EINECS	Contact for details

Quality Control

Every batch of this advanced synthetic intermediate is produced and analyzed under strict quality protocols to ensure exceptional purity and batch-to-batch consistency, critical for sensitive multi-step syntheses. Our quality system employs advanced analytical techniques including HPLC, NMR, and mass spectrometry for comprehensive characterization. A detailed Certificate of Analysis (COA) is provided with each shipment, confirming identity, purity, and impurity profiles. We adhere to cGMP principles where applicable to support our clients' regulatory and research requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This compound is sensitive to strong acids and organic solvents; ensure the storage area is well-ventilated and separate from incompatible materials. For long-term storage, consider inert atmosphere conditions to maximize stability.

Specification

Item	Specification
Appearance	White to off-white solid
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.