CAS 108963-96-8 · Boc-Protected · 4 functional traits · cGMP compliant · Ships from USA in 2-3 days
1-BOC-L-pyroglutamic acid ethyl ester (CAS Number: 108963-96-8) is a Boc (tert-butyloxycarbonyl)-protected amino compound for orthogonal synthesis with defined stereochemistry. ChemContract Research supplies this moderate-complexity compound in high purity from our Huntington Beach, California facility, ensuring consistent quality and reliable domestic delivery throughout the United States.
The Boc group is removed cleanly with TFA or HCl in dioxane, making it orthogonal to Fmoc, Cbz, and Alloc protecting groups — essential for synthesizing complex peptide therapeutics. Carboxylic acids are among the most synthetically versatile functional groups — they can be converted to amides, esters, acid chlorides, anhydrides, alcohols, and aldehydes in a single step. Ester hydrolysis by cellular esterases is the most commonly exploited prodrug activation mechanism — enabling drugs that cannot cross biological membranes as free acids.
Primary applications include solid-phase peptide synthesis (spps) with orthogonal boc/fmoc strategies and amide bond formation via edc/hobt or hatu coupling in peptide synthesis. This compound serves researchers and manufacturers across the pharmaceutical, peptide synthesis, fine chemical sectors. Whether you require 1-BOC-L-pyroglutamic acid ethyl ester for early-stage research, process development, or commercial-scale production, ChemContract Research offers flexible ordering from milligram to multi-kilogram quantities with custom synthesis options and full batch documentation including Certificates of Analysis (CoA) and Safety Data Sheets.
How 1-BOC-L-pyroglutamic acid ethyl ester is used across pharmaceutical and peptide synthesis sectors
Solid-phase peptide synthesis (SPPS) with orthogonal Boc/Fmoc strategies
Amide bond formation via EDC/HOBt or HATU coupling in peptide synthesis
Prodrug development to mask carboxylic acids and improve membrane permeability
Enantiopure building block for single-enantiomer drug development
Multi-step pharmaceutical synthesis requiring selective amine deprotection
Salt formation with amines to improve drug crystallinity and stability
Detailed specifications for this boc-protected, including purity, molecular weight, and analytical data are available upon request. Every batch from ChemContract Research includes:
Boc-protected compounds are generally stable. TFA deprotection generates isobutylene gas — perform in a fume hood. Acids may be corrosive or irritating. Handle with chemical-resistant gloves and eye protection. Use a fume hood for volatile acids. Some esters are volatile and flammable. Handle in a well-ventilated area. Keep away from ignition sources. Handle with standard precautions. Ensure proper labeling of stereochemical identity to prevent mix-ups.
Store at room temperature in a sealed container. Stable under neutral and basic conditions; avoid strong acids during storage. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases. Store at room temperature in a tightly sealed container away from heat and open flame. Store under recommended conditions. Some chiral compounds may racemize at elevated temperatures or in the presence of base.
Boc-protected compounds like 1-BOC-L-pyroglutamic acid ethyl ester are shipped with confirmed protection integrity by NMR. Orthogonal deprotection protocols included on request.
Every batch of 1-BOC-L-pyroglutamic acid ethyl ester is produced under cGMP conditions with full CoA documentation, HPLC purity verification, and lot traceability.
Ship from our Huntington Beach, CA facility with 2-3 business day domestic delivery. No import delays, no customs fees, no tariff surprises.
Need a specific grade, quantity, or derivative of 1-BOC-L-pyroglutamic acid ethyl ester? Our team of PhD chemists can develop custom synthesis solutions for your exact requirements.
Common questions about 1-BOC-L-pyroglutamic acid ethyl ester
1-BOC-L-pyroglutamic acid ethyl ester is a Boc (tert-butyloxycarbonyl)-protected amino compound for orthogonal synthesis used primarily in the pharmaceutical and peptide synthesis industries. Key applications include solid-phase peptide synthesis (spps) with orthogonal boc/fmoc strategies and amide bond formation via edc/hobt or hatu coupling in peptide synthesis.
ChemContract Research is a trusted USA-based supplier of 1-BOC-L-pyroglutamic acid ethyl ester. We offer competitive pricing, fast domestic shipping from our Huntington Beach, California facility, and full quality documentation including Certificates of Analysis (CoA). Request a quote at chemistry@chem-contract.com or call +1 (714) 732-8549.
ChemContract Research supplies 1-BOC-L-pyroglutamic acid ethyl ester in multiple purity grades: ≥95% standard grade, ≥97% high-purity grade, and ≥99% ultra-high-purity grade depending on application requirements. We can also provide custom purity grades through our synthesis capabilities. Contact us for specific purity information and CoA documentation.
Yes. ChemContract Research offers custom synthesis services for 1-BOC-L-pyroglutamic acid ethyl ester from milligram to multi-kilogram scale. Our cGMP-compliant facilities and experienced chemists can accommodate custom specifications, packaging requirements, and delivery timelines. Contact our team to discuss your project.
For amide bond formation from the carboxylic acid in 1-BOC-L-pyroglutamic acid ethyl ester, HATU/DIPEA is recommended for peptide coupling (high yield, low epimerization). EDC/HOBt is a cost-effective alternative for non-peptide amides. T3P (propylphosphonic acid anhydride) offers excellent atom economy with easy workup. For ester formation, DCC/DMAP (Steglich conditions) or Mitsunobu conditions are standard.
The Boc protecting group in 1-BOC-L-pyroglutamic acid ethyl ester is cleanly removed by treatment with trifluoroacetic acid (TFA, 20–50% in DCM) at room temperature, typically within 30–60 minutes. Alternative conditions include HCl in dioxane (4M) or trimethylsilyl triflate with 2,6-lutidine. The Boc group is stable to base, hydrogenation, and many nucleophilic conditions, making it orthogonal to Fmoc and Cbz groups.
Store at room temperature in a sealed container. Stable under neutral and basic conditions; avoid strong acids during storage. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases. Store at room temperature in a tightly sealed container away from heat and open flame. Store under recommended conditions. Some chiral compounds may racemize at elevated temperatures or in the presence of base. Always consult the compound-specific Safety Data Sheet (SDS) provided with your order for detailed storage requirements. ChemContract Research includes handling and storage documentation with every shipment.
The CAS Registry Number for 1-BOC-L-pyroglutamic acid ethyl ester is 108963-96-8. This unique identifier is used worldwide to reference this specific compound in chemical databases, regulatory filings, and scientific literature. ChemContract Research supplies this compound with full quality documentation. Contact us at chemistry@chem-contract.com for availability and pricing.
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