Fmoc-Asp-Oall CAS 144120-53-6 99% Purity Solid for Pharmaceutical Chemical Synthesis

Product Specifications

Overcoming Purity Challenges in Pharmaceutical Chemical Synthesis with Fmoc-Asp-Oall CAS 144120-53-6

In pharmaceutical chemical synthesis, inconsistent raw material quality can derail production schedules and compromise research outcomes. We’ve witnessed laboratories struggle with impure intermediates causing unexpected副反应, and manufacturers facing costly delays due to supply chain disruptions. For over a decade, these challenges have driven our commitment to delivering reliable chemical solutions that meet the rigorous demands of industrial and research applications.

A Stable Supply Chain for Critical Pharmaceutical Intermediates

Fmoc-Asp-Oall CAS 144120-53-6 addresses these industry pain points through our established supply chain system. With a large warehousing center and annual production capacity of 20 tons, we ensure consistent availability from kilogram to ton-level orders. Our global network serves industrial customers across 50+ countries, providing the stability needed for both small-scale research and large-scale manufacturing.

Industrial Applications of Fmoc-Asp-Oall

This 99% purity solid plays a vital role in pharmaceutical chemical synthesis, serving as a key intermediate in peptide synthesis and organic chemistry research. Its applications extend to laboratory-scale compound development and industrial pharmaceutical manufacturing, where precision and reliability are paramount. The product strictly adheres to industrial research use standards, supporting the development of new chemical entities and process optimization.

Key Specifications Ensuring Synthesis Success

The >99% purity of Fmoc-Asp-Oall minimizes impurity interference, reducing side reactions and improving yield consistency in synthetic processes. Its solid state ensures stable handling and storage, while the precisely determined boiling point (638.5±55.0 °C at 760 mmHg) provides critical data for process temperature control. The molecular formula C22H21NO6 confirms structural integrity, essential for maintaining reaction specificity. Our packaging options (25kgs foil-alum bags, 250kg drums, or 1250kg IBCs) are engineered to preserve product stability during transportation and storage.

Quality Assurance: From Production to Delivery

Choosing our Fmoc-Asp-Oall means investing in quality that translates to operational efficiency. Unlike lower purity alternatives that risk batch failures and rework costs, our pharmaceutical grade intermediate ensures process reproducibility and reduces material waste. Produced in compliance with industrial chemical standards, each batch undergoes rigorous quality control to meet the specifications required for pharmaceutical synthesis applications. Our stable supply capacity eliminates the production delays caused by material shortages, supporting your project timelines.

Our Commitment to Quality and Reliability

Certificate of Analysis & Documentation

Each order of Fmoc-Asp-Oall is accompanied by a detailed Certificate of Analysis (COA) containing batch-specific purity data, physical properties, and quality test results. Material Safety Data Sheets (MSDS) are provided to ensure safe handling and compliance with workplace safety regulations. For research and quality control purposes, additional documentation including detailed chromatographic profiles can be requested for specific batches.

Storage & Handling

• Store in a cool, dry, well-ventilated area, sealed and away from direct sunlight.
• Keep away from incompatible materials, food and feed sources.
• Handle with appropriate personal protective equipment (gloves, goggles, lab coat).
• Follow good industrial hygiene practices. Avoid inhalation and skin contact.
• Refer to MSDS for detailed storage and safety instructions.

Streamlined Ordering Process for Industrial Buyers

Initiate your procurement by submitting a detailed request including required quantity and packaging preferences. Our team will provide a competitive quotation and delivery timeline within 24 hours. For first-time customers, small sample quantities are available for qualification testing. Once specifications are confirmed, we can arrange bulk production and delivery via sea or land transport, with full documentation support to facilitate customs clearance and quality verification.

Frequently Asked Questions