Boc-Gly-Gly-OH (N-(tert-butoxycarbonyl)glycylglycine) is a Boc-protected dipeptide consisting of two glycine residues linked by an amide bond, with a tert-butyloxycarbonyl (Boc) group protecting the N-terminal amino functionality. The molecular formula is C₉H₁₆N₂O₅ with a molecular weight of 232.23 g/mol. The structure features a tert-butyloxycarbonyl group that serves to shield the glycine residues during complex peptide assembly processes.
Boc-Gly-Gly-OH is a strategically protected dipeptide building block widely recognized for its role in enhancing the efficiency of solid-phase peptide synthesis (SPPS). The Boc group in Boc-Gly-Gly-OH prevents side reactions during peptide assembly, particularly in solid-phase peptide synthesis, while enabling controlled deprotection under standard acidic conditions. As a glycine derivative, Boc-Gly-Gly-OH is valuable for incorporating glycine-glycine sequences into peptides while maintaining control over the deprotection process. Beyond classical peptide synthesis, Boc-Gly-Gly-OH has found application in bioconjugation techniques, where it facilitates the attachment of biomolecules to surfaces or other molecules, supporting the development of targeted drug delivery systems. The pre-formed dipeptide structure of Boc-Gly-Gly-OH makes it an essential reagent in biochemical research and pharmaceutical development.
Product Parameters
Parameter
Specification
Product Name
Boc-Gly-Gly-OH
CAS Number
31972-52-8
Molecular Formula
C₉H₁₆N₂O₅
Molecular Weight
232.23 g/mol
Appearance
White powder
Melting Point
132 °C
Boiling Point
488.1±30.0 °C (Predicted)
Density
1.222±0.06 g/cm³ (Predicted)
Solubility
Soluble in methanol
pKa
3.41±0.10 (Predicted)
Storage Condition
Sealed in dry,Store in freezer, under -20°C
Product Advantages
Pre-Formed Dipeptide Building Block
Boc-Gly-Gly-OH is a protected dipeptide that streamlines peptide synthesis by providing a pre-formed glycine-glycine unit. This eliminates the need for sequential glycine coupling steps, reducing synthesis time, minimizing deletion sequence formation, and improving overall peptide yield.
Robust Boc Protection Strategy
The tert-butyloxycarbonyl (Boc) group in Boc-Gly-Gly-OH provides reliable protection of the N-terminal amino functionality throughout peptide chain assembly. The Boc group prevents side reactions during synthesis and is selectively removed under mild acidic conditions (typically TFA), enabling orthogonal deprotection strategies.
Versatile Applications Beyond Peptide Synthesis
Beyond classical peptide synthesis, Boc-Gly-Gly-OH is used in bioconjugation techniques, where it facilitates the attachment of biomolecules to surfaces or other molecules, supporting the development of targeted drug delivery systems.
High Purity for Reproducible Results
Supplied at ≥98% purity (HPLC) with batch-specific characterization, Boc-Gly-Gly-OH ensures reproducible results across synthetic campaigns.
Essential Reagent for Biochemical Research
Boc-Gly-Gly-OH is widely recognized as an essential reagent in biochemical research and pharmaceutical development, particularly for incorporating glycine residues into peptides while maintaining control over the deprotection process.
Synthetic Route
+→
Under stirring conditions, amino acids or peptides (1 mmol) were added dropwise to an ethanol solution (1 mL) containing guanidine hydrochloride (15 mmol) and diisobutyl carbonate (2.5–3 mmol), with the reaction temperature maintained at 35–40 °C. The mixture was continuously stirred until a clear solution formed. The ethanol was then evaporated under reduced pressure. The residue was successively washed with distilled water (2 mL) followed by hexane or petroleum ether (2 mL) to yield high-purity N-Boc-amino acids or N-Boc-peptides. For further purification of the product, recrystallization may be performed on the crude product.
Product Quality Assurance
Cosperpharm has established a comprehensive quality assurance system for Boc-Gly-Gly-OH that meets the rigorous expectations of pharmaceutical intermediate and research-grade applications:
Thorough analytical characterization. Each batch undergoes multi-technique analytical release testing: HPLC purity (≥98%, with high-purity grades up to 99.5% available), melting point verification (132 °C), and appearance inspection (white powder).
Full batch traceability. From raw material procurement through Boc protection, purification, and final packaging, every step is fully documented and traceable. Each batch receives a unique lot number with retention samples maintained in accordance with Cosperpharm quality procedures.
Documentation ready for research and regulatory submission. Every shipment includes a Certificate of Analysis (COA) with batch-specific purity and characterization data, a Material Safety Data Sheet (SDS), and customs documentation. Custom quality agreements and additional documentation packages are available upon request.
Customer-initiated quality audits. Qualified customers are welcome to audit Cosperpharm‘s manufacturing, quality control, and documentation facilities. Please contact our regulatory team to schedule an audit.
Contact Us
Looking to secure Boc-Gly-Gly-OH for your next peptide synthesis project or bioconjugation study? Cosperpharm makes it simple. Contact our team today for pricing, documentation, or technical support — we‘re ready to help you achieve your research and development goals.
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