Octreotide Acetate

Octreotide Acetate

CAS: 79517-01-4
Standard: In-house Standard

Product Introduction

Octreotide Acetate API

High-Purity Synthetic Somatostatin Analogue

Product Overview

 

Octreotide Acetate is a synthetic octapeptide and a long-acting analogue of natural somatostatin. Supplied as a lyophilized powder , this active pharmaceutical ingredient (API) is designed for use in injectable and controlled-release formulations where stable and reproducible peptide activity is essential.

Thanks to its defined purity profile, stability characteristics, and batch-level analytical control, Octreotide Acetate API supports pharmaceutical manufacturing, veterinary formulation, and research applications. Each production lot is fully documented to meet regulatory, quality control, and downstream formulation requirements .

Key Specifications and Quality Data

 

  • CAS Number: 63868-81-9
  • Molecular Formula: C₄₆H₆₈N₁₀O₁₀ · (acetic acid)
  • Molecular Weight: Approx. 1019.3 g/mol
  • Appearance: White to off-white lyophilized powder
  • Purity / Assay: ≥ 98% (HPLC)
  • Solubility: Soluble in sterile water; compatible with standard peptide buffer systems
  • Storage Conditions:

      -Short-term: 2–8 °C, sealed and dry

       -Long-term: −20 °C recommended

  • Packaging Options: Small vials for sampling; bulk packaging for production; OEM/custom formats available
  • Documentation Supplied: COA, MSDS/TDS, impurity profile, stability data

Each lot is accompanied by a Certificate of Analysis and a complete technical data package, allowing procurement and QC teams to verify compliance with internal specifications.

Practical Features and Applications

 

The acetate salt form and well-defined peptide sequence of Octreotide Acetate provide predictable formulation behavior and reliable performance during administration. Typical use scenarios include:

 

  • Pharmaceutical manufacturing of peptide-based injectable or sustained-release dosage forms
  • Veterinary formulations requiring a somatostatin analogue for endocrine modulation
  • Research and development laboratories studying peptide stability, receptor interactions, or controlled-release kinetics

As a lyophilized product, the API supports standard peptide handling practices, including sterile reconstitution, aseptic filtration, and seamless integration into final dosage forms with minimal activity loss.

Quality Assurance and Regulatory Support

 

Octreotide Acetate API is manufactured and released under strict quality control procedures , ensuring batch-to-batch consistency and full traceability. Key quality features include:

 

  • Batch-level analytical testing
  • Complete impurity and stability profiling
  • Documentation suitable for regulatory submissions and audits

These measures support pharmaceutical companies and formulation partners in meeting regional and international regulatory expectations .

Supplier and Procurement Advantages

 

Batch Traceability

Every batch is fully tested and documented, simplifying internal QC review and regulatory filing processes.

Flexible Supply Model

Sample quantities are available for evaluation and formulation trials. After validation, bulk supply can be arranged with consistent quality and agreed lead times.

Custom and OEM Packaging

Tailored packaging and labeling options are available for distributors or manufacturers requiring region-specific formats.

Technical and Logistics Support

Detailed guidance on storage, reconstitution, solvent selection, and transport conditions is provided to minimize formulation risk and maintain peptide integrity.

Packaging and Logistics

 

Octreotide Acetate API is packaged in moisture-barrier vials with desiccant , protecting the peptide from humidity and environmental exposure. Temperature-controlled logistics can be arranged where necessary, and handling instructions are included with each shipment to ensure product stability upon receipt.

Frequently Asked Questions (FAQs)

 

  • Q: Can sample quantities be ordered before bulk purchasing?

  • A: Yes. Sample orders are supported for evaluation, QC comparison, or formulation trials.
  •  
  • Q: What documentation is included with each shipment?

  • A: Certificate of Analysis, MSDS/TDS, and impurity and stability profiles.
  •  
  • Q: How should Octreotide Acetate API be stored?

  • A: Keep sealed and dry. Store at 2–8 °C for short-term use or at −20 °C for long-term storage. Avoid repeated freeze–thaw cycles.
  •  
  • Q: Is custom packaging available?

  • A: Yes. OEM and customized packaging options are offered to meet regulatory or commercial needs.
  •  
  • Q: How can bulk volumes be supplied for production?

  • A: Following successful sample evaluation, bulk supply can be arranged with packaging and delivery schedules aligned to your production plan.

Useful Notes for Procurement Teams

 

 

  • Documentation Readiness: Full analytical packages streamline QC approval and regulatory review
  • Peptide Handling Best Practices: Proper reconstitution and buffer selection help preserve peptide stability
  • Early Validation: Sample testing reduces risk and accelerates scale-up to commercial volumes

 

 

 

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