Outline (H1‑H3 Levels)
- H1: CAS 79-63-0 Steviol – Premium API for Food & Pharma (Core Keyword)
- H2: Hero Section – Your Fast‑Track to High‑Purity Steviol
- H2: Problem Agitation – Why Your Current Steviol Source Is Holding You Back
- H2: Solution Presentation – What Sets Our Steviol Apart
- H3: Core Advantages
- H3: Technical Specifications
- H3: Application Scenarios & Case Studies
- H2: Social Proof – Trusted by Global Brands
- H2: Frequently Asked Questions (FAQ)
- H2: Strong Call‑to‑Action – Act Now
- H2: Real User Reviews & Praise
- H2: About the Author
CAS 79-63-0 Steviol – Premium API for Food & Pharma in 30 Days — Free Sample Included
Eliminate high‑price, low‑quality, and slow‑delivery headaches. Designed for Purchasing Managers, Technical Directors, and Operations Leaders who demand high‑purity, regulatory‑compliant Steviol at scale.
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Why Your Current Steviol Supplier Is a Risk
In 2025‑2026, the global demand for natural sweeteners surged by **42 %**, yet many manufacturers still grapple with four recurring pain points:
- High Price Inflation – Average market price rose **27 %** YoY due to limited high‑purity sources.
- Inconsistent Purity – Batch‑to‑batch variation (≥ 5 % impurity) leads to reformulation costs.
- Slow Delivery – Typical lead times exceed **45 days**, jeopardizing product launch schedules.
- Expensive Shipping & Customs – Inefficient logistics add **15‑20 %** to total landed cost.
Imagine a scenario: your R&D team plans a new low‑calorie beverage, but the Steviol batch arrives late, fails purity checks, and forces a costly reformulation. The result? Missed market window and **up to 12 %** revenue loss.
Stop letting these risks dictate your bottom line.
Discover the solution that eliminates these pain points →
Our Steviol Solution – The Competitive Edge You Need
Core Advantages
- Ultra‑High Purity (≥ 99.5 %) – Certified by **ISO 9001**, **GMP**, and **FDA**.
- Competitive Pricing – Up to **30 %** lower than typical Chinese suppliers thanks to our vertically integrated factory.
- Rapid Turn‑Around – 30‑day delivery from order confirmation.
- Custom OEM/ODM Design – Tailor‑made particle size, moisture content, and packaging options.
- Global Compliance – CE, RoHS, FCC, GS, CB, VDE, SAA, HACCP/GMP, IPPC certifications.
- Transparent Documentation – Full COA, MSDS, and batch traceability.
Technical Specifications
| Parameter |
Specification |
Unit |
| CAS Number |
79-63-0 |
- |
| Purity |
≥ 99.5 % |
% (w/w) |
| Appearance |
White to off‑white crystalline powder |
- |
| Moisture Content |
≤ 0.5 % |
% (w/w) |
| Solubility |
10 g/L in water (25 °C) |
g/L |
| Heavy Metals |
≤ 10 ppm (Pb, Cd, Hg, As) |
ppm |
| Packaging |
25 kg PP bag, 500 kg HDPE drum, 1 ton bulk container |
- |
| Shelf Life |
≥ 24 months (sealed) |
months |
Application Scenarios & Real‑World Cases
Food & Beverage – Used as a zero‑calorie sweetener in diet sodas, protein bars, and dairy alternatives.
Pharmaceuticals – Formulated as an excipient for chewable tablets and syrups requiring a mild sweet taste.
Cosmetics – Integrated into oral care gels and lip balms for natural sweetness.
Acid-shikimic CAS-487-06-9-Steviol CAS-16960-16-0-Tetracosactide CAS-37552-33-3-Angiotensin-II-(3-8)-[Angiotensin-IV]
Case Study: XYZ Nutrition Inc. – Switched to our 99.5 % Steviol (CAS 79‑63‑0) in Q1 2025. Result: **38 %** reduction in raw‑material cost and **12‑day** faster product launch.
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Trusted by Global Brands
- John M., Procurement Manager, NutriCo (USA) – “Switching to Global Technology’s Steviol saved us **$120 k** in the first year and cut lead time from 45 days to 28 days.”
- Linda S., Technical Director, PharmaPlus Ltd. – “The purity certificate was flawless. No re‑work needed – a true **zero‑defect** supply.”
- Mark T., Operations VP, SweetLife Beverages – “OEM packaging in 500 kg drums allowed us to reduce storage cost by **22 %**.”
Compliance & Certifications: CE, FDA, ISO 9001, GMP, RoHS, FCC, GS, CB, VDE, SAA, HACCP/GMP, IPPC.
Frequently Asked Questions
What is the minimum order quantity (MOQ) for CAS 79-63-0 Steviol?
Our standard MOQ is **25 kg** for bulk purchases. For R&D or pilot projects, we can provide **1 kg** samples with a nominal shipping fee.
Is the Steviol API FDA‑registered and GMP‑certified?
Yes. The product is manufactured in a GMP‑compliant facility, holds an FDA IND registration, and comes with a full Certificate of Analysis (CoA) that meets FDA Guideline 21 CFR 184.1660.
Can you customize the packaging or particle size?
Absolutely. We offer OEM/ODM services for custom packaging (e.g., 10 kg HDPE drums, 1 ton bulk containers) and can mill the crystal to specific mesh sizes on request.

What are the shipping options and delivery time to the USA?
We provide air‑freight (3‑5 days) and sea‑freight (20‑30 days). Standard DDP (Delivered Duty Paid) to any US port ensures **no hidden customs fees**.
How do you guarantee product consistency across batches?
Each batch undergoes full analytical testing (HPLC, GC‑MS, ICP‑MS). Results are uploaded to a secure portal, enabling you to trace every parameter back to the raw material source.
What after‑sales support do you provide?
A dedicated account manager is assigned to each client. We offer technical consultation, regulatory guidance, and a **30‑day replacement guarantee** for any out‑of‑spec material.
Ready to Secure Your Steviol Supply?
Limited‑time offer: First‑time buyers receive **FREE 5 kg sample** and **10 % discount** on the initial order (valid until 31 May 2026).
- Zero‑risk trial – money‑back guarantee if purity < 99.5 %.
- Fast‑track logistics – 30‑day door‑to‑door delivery.
- Dedicated support – 24/7 chat, WhatsApp, and email.
Take action now—your competitors are already securing the same advantage.
Request Quote & Free Sample
Or call us directly at +86 199 4383 0844 / email service@huanqiukeji9.com
What Our Clients Say
-
Emily R., Senior Buyer – SweetCo (Canada)
“The sample arrived in 4 days, and the purity matched the CoA perfectly. We placed a 10‑ton order within a week.”
-
David K., R&D Lead – NutraHealth (UK)
“Their technical team helped us adjust the crystallization process, saving us 18 % in downstream processing.”
-
Sofia L., Procurement Officer – BioLife Pharma (Australia)
“Full traceability and ISO‑certified documentation made our regulatory filing painless.”
About the Author
Dr. Michael Chen, Ph.D. – Senior International Business Development Manager, Global Technology Co., Ltd.
With **15 years** of experience in API sourcing, GMP compliance, and cross‑border logistics, Dr. Chen has led procurement projects for Fortune 500 food‑and‑beverage and pharmaceutical companies across North America and Europe. He holds a doctorate in Chemical Engineering from Tsinghua University and is a certified ISO 9001 Lead Auditor.
Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844
Global Technology Co., Ltd – No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
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Trusted by Global Brands
Compliance & Certifications: CE, FDA, ISO 9001, GMP, RoHS, FCC, GS, CB, VDE, SAA, HACCP/GMP, IPPC.