| Customization: | Available |
|---|---|
| Application: | Lyophilized Powder |
| Disposable: | Non-Disposable |
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1.All peptides are guaranteed purity greater more than 99%.
2.All peptides are guaranteed overfilled the label weight.
| Items Name | CagriTirz (Research Purpose Only) | Costomize | 2mg 5mg 10mg 15mg 20mg 30mg 60mg |
| CAS Code | Vial size | 3ml/5ml/10ml | |
| Raw Materials | White Powder | Type | Lyophilized process, vaccum seal |
| Package | White Paper Box | GMP | Fully GMP standard operation |
| Test Method | HPLC, MS | Filling Vial | over filled each vial |
| Cap color | Multiple colors customize | Payment Way | SWIFT, ACH, Fedwire, Bank Wire, Wise, Revolut, |
| Purity Content | 99-100% | Reship Policy | Yes |
Test Report
Our Advantages: High purity, Wholesale price, large stock, Stealth Shipping, 100% Delivery Guarantee
Upstream peptide synthesis
Zhaobo Bio production plants are endowed with state-of-the-art equipment for solvent supply, peptide synthesis, purification and isolation of active ingredients and intermediates. All equipment and containment is GMP qualified and cleaning validated. Overlapping capacities and sizes of different equipment trains facilitate a smooth scale-up for increases in demand within the product life cycle.
Downstream purification and isolation of peptides
Zhaobo Bio is committed to the systematic expansion and modernization of its purification equipment in order to ensure the efficient production of ever-increasing amounts of bulk peptide pharmaceuticals.
It uses sophisticated methods for large scale purification campaigns such as preparative high performance liquid chromatography (HPLC), ion exchange (IEX), size-exclusion chromatography (SEC), and ultra-filtration (UF/TFF). The equipment in place permits highly efficient or even continuous manufacturing of extremely pure products up to multi-kg quantities per lot.
For preparative HPLC, dynamic axial compression (DAC) stainless steel columns of up to 60 cm diameter both in batch and continuous mode are packed with the appropriate high performance silica separation phase. For low-pressure chromatography columns up to 80 cm diameter are available. Solvent delivery is ensured from eluent tank farms and containers.
The control of microbiological contamination is a prerequisite for API manufacturing. Class D (ISO 8) and C (ISO 7) clean rooms are supplied via HEPA-filtered, temperature and humidity controlled air, down-flow booths are used for minimizing microbial contamination and protecting operators. Highly active pharmaceutical ingredients are handled in integrated safety workbenches or flexible isolators reaching OEB level 4 (1-10 µg/m3).
Predefined physicochemical properties of the API can only be achieved by a carefully controlled isolation process. Besides precipitation and crystallization, lyophilization of intermediates and final API is a standard unit operation. LaixingPharma have multiple lyophilizers in different sizes (up to 300 liters) located in clean room
Welcome to be our distinguished customer, please do not hesitate to contact us!
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