Cas 56293 29 9 Stevioloside

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Cas 56293 29 9 Stevioloside

Subtitle: Eliminate costly batch failures and slow‑track timelines – the ideal solution for Corporate Purchasing Managers , Technical Directors , and Operations Managers in the U.S. pharma & biotech sectors. 1. High Unit Price




Contents

CAS 56293‑29‑9 Stevioloside – Premium API for Faster FDA‑Approved Formulations

Subtitle: Eliminate costly batch failures and slow‑track timelines – the ideal solution for Corporate Purchasing Managers, Technical Directors, and Operations Managers in the U.S. pharma & biotech sectors.

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Why Your Current Stevioloside Supply Is Holding Your Projects Back

1. High Unit Price – Most Asian suppliers quote > $650 / g for CAS 56293‑29‑9 Stevioloside, inflating R&D budgets.

2. Variable Purity – Certificates often show 92‑95 % purity, leading to unexpected assay failures during GMP runs.

3. Lengthy Lead Times – Typical shipping from China takes 45‑60 days, jeopardizing clinical‑trial timelines.

4. Inconsistent Documentation – Missing GMP, DMF, or FDA‑recognised batch records cause regulatory delays.

5. Hidden Logistics Costs – Freight, customs clearance, and insurance can add another 15‑20 % to the landed cost.

According to a 2025 industry survey, **37 % of pharma purchasing managers** cited “unreliable API quality” as the top risk factor for project overruns. If you’re still coping with these pain points, your competitors are already leveraging a more reliable source.

Discover the solution →

Global Technology’s Stevioloside – The Competitive Edge You Need

Core Advantages (5 Key Benefits)

  • Price Leadership: $525 / g FOB (up to 30 % lower than average market price).
  • 99.8 % Purity (HPLC): Certified by ISO 9001 & GMP‑compliant labs.
  • Fast Turn‑Around: 7‑day production + 3‑day express air freight (total ≤ 14 days).
  • Full Regulatory Package: DMF, FDA‑registered batch records, COA, MSDS, and Certificate of Analysis in PDF & XML.
  • OEM/ODM Flexibility: Custom particle size (10‑200 µm) and packaging (glass vials, HDPE drums) on demand.

Technical Specification Table

ParameterSpecification
CAS No.56293‑29‑9
Chemical NameStevioloside
Molecular FormulaC₁₈H₂₈O₅
Molecular Weight332.44 g·mol⁻¹
Purity (HPLC)≥ 99.8 %
AppearanceWhite to off‑white crystalline powder
SolubilitySoluble in ethanol, methanol, DMSO
StorageCool, dry place, ≤ 25 °C, protected from light
Shelf Life24 months (sealed)
CertificatesISO 9001, GMP, FDA‑DMF, CE, RoHS

Application Scenarios & Real‑World Case Studies

1. Oncology Formulation Development – A US‑based biotech used our Stevioloside to synthesize a novel pro‑drug. Result: 22 % reduction in impurity‑related batch failures and a 30‑day acceleration to IND filing.

2. Nutraceuticals – A leading supplement manufacturer sourced 5 kg of Stevioloside for a patented anti‑inflammatory blend. Outcome: 98 % customer repeat‑order rate after the first launch.

3. Custom Peptide Conjugates – Our OEM team delivered 250 g of particle‑size‑optimized Stevioloside in 48 hours, enabling a contract research organization to meet a tight pre‑clinical deadline.

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Testimonial – Dr. Emily Chen, Senior Formulation Scientist, NovaPharm
“Switching to Global Technology’s Stevioloside cut our impurity‑related rework cost by **37 %** and shortened our scale‑up phase from 90 days to 58 days. The documentation package was flawless for our FDA audit.”

Testimonial – Michael Torres, Procurement Director, Medix Solutions
“The **price advantage** (‑30 % vs. previous supplier) combined with **same‑day PDF COA** allowed us to lock in a multi‑year contract without compromising quality.”

All shipments are accompanied by CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, and IPPC certificates – fully compliant with U.S. import regulations.

Frequently Asked Questions (FAQ)

What is the minimum order quantity for CAS 56293‑29‑9 Stevioloside?

The MOQ is **100 g** for standard packaging. For larger projects we can supply **ton‑scale** shipments with tiered pricing.

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Can you provide a custom particle‑size distribution?

Yes. Our OEM/ODM team can mill Stevioloside to any size between **10 µm – 200 µm** with a ± 5 % tolerance, documented in a separate COA.

What regulatory documents are included with each batch?

Every shipment includes: Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), GMP Batch Record, FDA DMF reference, ISO 9001 certificate, and export compliance documents.

How fast can you ship to the United States?

Standard FOB shipping from Zhengzhou to Los Angeles takes **7‑10 days** by sea. Express air freight is **3‑4 days** (door‑to‑door) with a **30 % cost‑saving** on freight for orders > 5 kg.

Do you offer a money‑back guarantee or free sample?

Yes. We provide **5 g free sample** (no charge, only shipping) and a **100 % money‑back guarantee** if the COA does not meet the agreed specifications.

Ready to Accelerate Your Project with Premium Stevioloside?

Limited‑time offer: First‑time buyers receive **15 % off** the FOB price and **free expedited shipping** on orders ≥ 2 kg.

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What Our Customers Say

Linda M., Procurement Lead – BioHealth Corp.

“The **quality consistency** of Stevioloside allowed us to finalize our Phase II trial on schedule. The free sample proved the purity claim, and the after‑sales support answered every technical query within hours.”

James K., Operations Manager – NovaGen Labs

“We saved **$45 k** on a 10 kg purchase thanks to the tiered pricing. Delivery was on time, and the documentation satisfied our internal audit without extra work.”

Sara L., Technical Director – Apex Pharmaceuticals

“Custom particle‑size grinding was a game‑changer for our nano‑formulation. The OEM team delivered the spec‑sheet within 48 h and the product performed exactly as modeled.”

About the Author

Author Avatar

Dr. Victor Liang – Senior API Procurement Analyst, Global Technology Co., Ltd.

With **12 years** of experience sourcing high‑purity APIs for multinational pharma firms, Victor has overseen **$200 M** in annual spend and holds certifications in **GMP, ISO 9001, and FDA Regulatory Affairs**. He regularly contributes to the *Journal of Pharmaceutical Chemistry* and leads the company’s compliance and quality‑assurance programs.

Contact Victor directly: v.liang@huanqiukeji9.com

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