Ethyl β-D-thioglucopyranoside is a chemically synthesized thioglycoside derivative where the anomeric oxygen of β-D-galactopyranose is replaced by a sulfur atom linked to an ethyl group. This modification imparts enhanced stability against hydrolysis compared to O-glycosides, making the compound a valuable glycosyl donor and synthetic intermediate in carbohydrate chemistry. It is a white crystalline powder with a molecular formula of C8H16OS and a molecular weight of about 168.28 g/mol. Produced via thiolysis of protected β-D-galactopyranosyl derivatives with ethyl mercaptan, it is purified by chromatographic methods to a purity typically above 95%. Analytical identification involves NMR, mass spectrometry, and chromatography. Its synthesis route and conditions ensure minimal microbial contamination. The compound should be stored sealed at 2–8 °C, protected from moisture and light, with a shelf life of 1–2 years. Applications include stereoselective oligosaccharide assembly, medicinal chemistry, molecular probe development, and glycobiology research related to carbohydrate-protein interactions and glycosylation processes.
IUPAC Name
- Ethyl 1-thio-β-D-galactopyranoside
Appearance
Source
- Synthesized by thiolysis of protected β-D-galactopyranosyl precursors with ethyl mercaptan
- Purified via chromatographic techniques under controlled laboratory conditions to ensure purity and consistency
Molecular Weight and Structure
- Molecular Formula: C8H16OS
- Molecular Weight: 168.28 g/mol
- Structure: β-D-galactopyranose ring with sulfur substituting anomeric oxygen, bonded to ethyl group
- SMILES: CCOC1OC(CO)C(O)C(O)C1S
Sugar Specificity
- Preserves β-anomeric stereochemistry of D-galactopyranose
- Used as a stable glycosyl donor for selective synthetic transformations
Biological Activity
- Chemically stable intermediate with no direct pharmacological activity
- Functions as substrate mimic in enzymology and glycosylation research
Purity and Microbial Contamination
- High purity (≥95%) confirmed by NMR and chromatographic analysis
- Synthetic origin minimizes microbial contamination
Identity and Quality Control
- Identity confirmed by 1H and 13C NMR, mass spectrometry, and HPLC purity profiles
- Includes Certificates of Analysis and Safety Data Sheets
- Melting point and optical rotation data provided for batch consistency
Shelf Life and Storage
- Store in sealed containers under refrigeration at 2–8 °C
- Protect from moisture, light, and heat
- Stable with a typical shelf life of 1–2 years under recommended conditions
Application
- Used as a glycosyl donor in stereoselective synthesis of oligosaccharides and glycoconjugates
- Supports drug discovery and glycomimetic design
- Facilitates molecular probe development targeting carbohydrate recognition
- Used in enzymatic assays studying glycosidases and glycosyltransferases
Key Characteristics
- Thioglycoside analog of β-D-galactopyranose with ethyl substitution
- CAS Number: 2167-39-1
- Molecular Weight: 168.28 g/mol
- White crystalline solid, hydrolytically stable
- Resistant to enzymatic cleavage enhancing synthetic utility
- Comprehensive analytical data supports identity and quality assurance
- Extended stability under recommended storage conditions
Citations
- Cymit Química
- PubChem
- Sigma-Aldrich
- MedChemExpress
- PMC enzymology articles
- ChemSpider
- Synthose chemical catalog
- Patent Literature
- Thermo Fisher Scientific
- ScienceDirect glycochemistry reviews
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