Documentation Center
Access comprehensive guides, technical documentation, compliance certificates, and resources to optimize your logistics operations.
Peptide Synthesis Guide
3 Documents Available
Solid Phase Synthesis Overview
Introduction to Fmoc and Boc SPPS strategies, resin selection, and coupling reagent choice.
Custom Peptide Order Guide
Step-by-step instructions for submitting custom peptide sequences, scale, and purity requirements.
Sequence Notation Standards
Accepted single-letter and three-letter amino acid codes, modification notation, and special residues.
Modifications & Conjugations
4 Documents Available
N- & C-Terminal Modifications
Available acetylation, amidation, biotinylation, and fluorescent label options.
PEGylation Services
Guidelines for PEG chain selection, attachment sites, and impact on solubility and half-life.
Stapled & Cyclic Peptides
Design considerations for lactam bridges, disulfide cyclization, and hydrocarbon stapling.
Isotope Labeling Guide
Stable isotope (¹³C, ¹⁵N, ²H) incorporation for quantitative mass spectrometry workflows.
Analytical & QC Documentation
4 Documents Available
HPLC Purity Analysis
Methodology for reverse-phase HPLC purity assessment and interpretation of chromatograms.
Mass Spectrometry Verification
ESI-MS and MALDI-TOF protocols used to confirm molecular weight and sequence integrity.
Certificate of Analysis (CoA)
Sample CoA template showing purity, mass confirmation, appearance, and storage conditions.
Amino Acid Analysis
Hydrolysis and derivatization procedures for quantitative amino acid composition analysis.
GMP & Regulatory Compliance
4 Documents Available
GMP Manufacturing Overview
Facility standards, batch record documentation, and quality system requirements for GMP peptides.
ICH Q7 Compliance Summary
How our production processes align with ICH Q7 guidelines for active pharmaceutical ingredients.
FDA DMF Filing Support
Documentation support for Drug Master File submissions including peptide API characterization.
Impurity Profiling Standards
Methods for identifying and quantifying related substances, residual solvents, and counterions.
Handling & Storage
4 Documents Available
Lyophilized Peptide Handling
Best practices for reconstitution, aliquoting, and avoiding freeze-thaw degradation.
Solubility Troubleshooting
Strategies for dissolving difficult peptides including hydrophobic, charged, and aggregation-prone sequences.
Long-Term Storage Conditions
Temperature, light, and humidity recommendations for maintaining peptide stability over time.
Cold Chain Shipping Protocol
Dry ice and cold pack packaging standards for temperature-sensitive peptide shipments.
Order Forms & Templates
4 Documents Available
Custom Synthesis Request Form
Downloadable order form for custom peptide sequences, scale, purity grade, and modification requests.
Bulk Order Quotation Template
Spreadsheet template for submitting multi-peptide library or large-scale production quote requests.
NDA / Confidentiality Agreement
Standard non-disclosure agreement for proprietary sequence and project confidentiality.
Incoming Sample Submission Form
Use when sending reference standards or raw materials for analysis or custom conjugation work.
Frequently Asked Questions
Quick answers to common questions about our documentation and resources.
What purity grades do you offer for custom peptides?
We offer crude, >70%, >80%, >90%, >95%, and >98% purity grades by HPLC. Research-grade applications typically use >90%, while therapeutic or analytical reference standards require >95% or >98%. Each order ships with a Certificate of Analysis confirming purity and mass.
What is the typical turnaround time for a custom peptide order?
Standard turnaround is 5–10 business days for most research-grade peptides up to 30 residues at >95% purity. Longer sequences, difficult sequences, or GMP-grade orders may require 3–6 weeks. Rush synthesis options are available — contact us for availability.
Do you synthesize peptides with non-standard or unusual amino acids?
Yes. We routinely incorporate D-amino acids, N-methylated residues, phosphorylated residues (pSer, pThr, pTyr), unnatural amino acids, and a range of fluorescent labels. Please include full modification details when submitting your sequence.
How should I store my lyophilized peptide upon receipt?
Lyophilized peptides should be stored at -20°C in a dry environment, away from light. Avoid repeated freeze-thaw cycles by aliquoting upon first reconstitution. Hydrophilic peptides are generally stable at -20°C for 12+ months; hydrophobic or cysteine-containing peptides may require -80°C for long-term storage.
Can you provide GMP-grade peptides for clinical or pharmaceutical use?
Yes. We offer GMP synthesis services compliant with ICH Q7 guidelines, including full batch documentation, impurity profiling, residual solvent analysis, and support for FDA Drug Master File (DMF) submissions. Contact our team to discuss your regulatory requirements.
What file format should I use to submit my peptide sequence?
Sequences can be submitted using standard single-letter or three-letter amino acid codes. Modifications should be noted in brackets adjacent to the relevant residue (e.g., K[Biotin], pS for phosphoserine). Download our Custom Synthesis Request Form from the Order Forms section for a guided submission template.
Need More Help?
Our team is here to assist you with any questions or support you need.
Have a Synthesis Question?
Our peptide specialists are available to advise on sequence design, modification strategy, scale-up, and analytical requirements.
Contact SupportSynthesis Protocols & Videos
Access step-by-step video walkthroughs covering reconstitution, HPLC interpretation, and handling difficult sequences.
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