Z-Gly-Pro
Z-Gly-Pro (CAS: 1160-54-9), with the molecular formula C15H18N2O5 and a molecular weight of 306.31 g/mol, is a protected amino acid derivative. This compound is primarily utilized in peptide synthesis and chemical biology research. Its specific structure makes it a valuable building block for creating complex peptides and exploring biological pathways. TSS supplies this high-purity reagent for demanding research and development applications.
- IUPAC
- Z-Glycyl-L-proline
Peptide Synthesis
Z-Gly-Pro serves as a crucial protected amino acid building block in solid-phase and solution-phase peptide synthesis. The Z (benzyloxycarbonyl) protecting group facilitates controlled peptide chain elongation.
Chemical Biology Research
This derivative is employed in studies involving peptide-based probes, enzyme inhibitors, and other biologically active molecules. Its incorporation allows for precise structural modifications in research settings.
Organic Synthesis
As an amino acid derivative, Z-Gly-Pro can be utilized in various organic synthesis pathways requiring specific chiral centres and functional groups for molecule construction.
| Molecular weight | 306.31 |
|---|---|
| Empirical formula | C15H18N2O5 |
| Assay | ≥99.0% (TLC) |
| Optical activity | [α]20/D −70±2°, c = 2% in ethanol |
| Melting point | 155-158 °C |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Z-Gly-Pro used for?
+
Z-Gly-Pro is primarily used as a protected amino acid derivative in peptide synthesis and for research applications in chemical biology and organic synthesis.
What are the CAS number and molecular formula for Z-Gly-Pro?
+
The CAS number for Z-Gly-Pro is 1160-54-9, and its molecular formula is C15H18N2O5.
What grade and purity does Tech Serve Solutions supply for Z-Gly-Pro?
+
Tech Serve Solutions supplies Z-Gly-Pro with an assay of ≥99.0% (TLC). This is a research-grade chemical, and TSS does not represent it as USP, BP, EP, or other pharmacopoeia grades.
What are the safety considerations for handling Z-Gly-Pro?
+
Handling Z-Gly-Pro requires appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter should be used if airborne exposure is a risk. Consult the Safety Data Sheet (SDS) for detailed handling procedures.
How is Z-Gly-Pro shipped and exported?
+
Tech Serve Solutions is a specialist global supplier and exporter of fine chemicals, including Z-Gly-Pro, adhering to all necessary regulations for international shipment.
How can I request a sample or quote for Z-Gly-Pro?
+
To request a sample or a quotation for Z-Gly-Pro, please contact our sales team through the TSS website or by phone, referencing the product name and CAS number.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis