High-Purity Bulk Sucralose Powder for Advanced Nutritional Formulations
Backed by FSSC22000, Kosher, and Halal Certifications for Global Export
Sucralose
Heat-Resistant Zero Calorie

Sucralose
Purecium supplies premium-grade Sucralose (CAS Number: 56038-13-2) engineered specifically for the dietary supplement, functional food, and beverage manufacturing industries. As a high-intensity, zero-calorie sweetener derived from sucrose, our bulk Sucralose powder delivers approximately 600 times the sweetness of standard table sugar (sucrose) without contributing to caloric intake, raising blood glucose levels, or promoting dental decay. Formulated to meet rigorous USP, FCC, and EP pharmacopeia specifications, our Sucralose is an indispensable functional ingredient for B2B brands developing sugar-free, keto-friendly, and low-calorie nutritional products.
Product name: Sucralose
Molecular formula: C12H19Cl3O8
Starting material: Sucrose
Grade: Food grade
Heavy Metals: USP
Pesticide residue: USP/EP
Packing size: 25kg/drum
CAS#: 56038-13-2
Molecular weight: 397.63 g/mol
Source: Synthetic
Specification: 98%-102% HPLC
Country of origin: China
Residual solvent: USP/EP
Allergen free/Gluten-free/Non-GMO/Vegan/Non-Irradiation

Sucralose Overview
Sucralose (E955), also known by the chemical name 1',4,6'-trichlorogalactosucrose, is a zero-calorie high-intensity sweetener with the molecular formula C12H19Cl3O8, a molecular weight of 397.63 g/mol and CAS registry number 56038-13-2. It is supplied as a white to off-white crystalline powder, food grade, with an assay of 98% to 102% by HPLC, for use in dietary supplements, functional foods and beverage formulations.
Sucralose is approximately 600 times sweeter than sucrose, yet it contributes no calories and is not metabolized for energy by the body. It is manufactured by the selective chlorination of sucrose, which replaces three hydroxyl groups with chlorine atoms and locks the glycosidic bond, giving the molecule exceptional stability under heat, acidity and prolonged storage.
The ingredient is recognized as safe for food and supplement use by major regulatory authorities, including the FDA, JECFA and EFSA, and carries the European food additive number E955. For B2B formulators, sucralose offers a well-characterized compliance path across the United States, European Union and other major markets.
Source & Ingredient Identity
Purecium Sucralose is synthetic, manufactured from sucrose as the declared starting material through a controlled selective chlorination route. Synthetic production provides supply-chain resilience, consistent purity and full traceability, independent of agricultural crop variability.
Identity and purity are confirmed against USP and EP monographs, with the finished material meeting a food-grade release specification of 98.0% to 102.0% assay by HPLC. The product is manufactured in China in GMP-certified facilities and is verified allergen-free, gluten-free, non-GMO and vegan.
Each batch is documented with a Certificate of Analysis covering identity, assay, heavy metals, pesticide residue, residual solvents and microbiological status, giving buyers complete documentation for supplier qualification and finished-product registration.
Key Characteristics of Sucralose
Key characteristics of Purecium Sucralose include its approximately 600-fold sweetness intensity relative to sucrose, zero-calorie contribution, excellent water solubility and exceptional stability. Unlike many high-intensity sweeteners, sucralose remains stable at high temperatures, making it suitable for baked and heat-processed formats, and it is stable across the typical pH range of foods and supplements.
The ingredient is non-cariogenic, does not promote dental caries, and exhibits a clean, sugar-like sweetness profile with no significant lingering aftertaste at recommended use levels. Its defined particle size and flow properties support consistent dosing in dry-blended tablet and powder applications.
Because sucralose is intensely sweet, typical use levels in finished formulas are very low, often in the range of 0.01% to 0.05% of the formulation by weight. This high potency creates significant formulation flexibility and cost efficiency for manufacturers replacing sugar in calorie-reduced and sugar-free products, while keeping finished-product sweetness profiles clean and consistent.
As a non-nutritive sweetener, sucralose passes through the body largely unchanged and contributes negligible calories, which underpins its widespread use in sugar-free and calorie-reduced product positioning. Its sweetness potency of approximately 600 times that of sucrose means a single kilogram replaces the sweetening power of roughly 600 kilograms of sugar, a key economic advantage in bulk procurement.
Sucralose Manufacturing
Purecium Sucralose is manufactured through a defined synthetic route in facilities certified under ISO 9001 and FSSC 22000 food-safety programs. Production comprises the selective chlorination of sucrose, followed by purification, crystallization, drying, sieving and final blending to specification, with each stage governed by written standard operating procedures.
In-process checks, documented cleaning and changeover procedures, and full batch numbering provide traceability from sucrose starting material to finished drums. The synthetic process is tightly controlled to achieve consistent isomer purity, ensuring the characteristic sweetening profile batch after batch.
Manufacturing capacity and lead times are managed to support both pilot-scale evaluation orders and ongoing contract manufacturing programs, with stability data supporting a defined ambient shelf life in sealed food-grade packaging.
In liquid and ready-to-mix formats, sucralose provides stable sweetness without the browning reactions associated with sugar, preserving product color and flavor over shelf life. Its compatibility with flavors, colors, active ingredients and common excipients is well documented, simplifying formulation development across supplement dosage formats.
Applications of Sucralose
Sucralose is used across dietary supplement and food product categories as a sugar-replacement sweetener: tablets, chewables and gummies, effervescent powders, protein powders and meal replacements, stick-pack beverage mixes, liquid drops and functional-food applications. Its heat stability makes it one of the few high-intensity sweeteners suited to processed and baked formats.
In supplement manufacturing, sucralose is frequently combined with other sweeteners and bulking agents such as dextrose, maltodextrin or sugar alcohols to optimize sweetness curves, mask the taste of active ingredients, and improve mouthfeel in chewable and powder formats. Published research and regulatory bodies recognize sucralose as one of the most thoroughly studied non-nutritive sweeteners, with an acceptable daily intake established by JECFA and EFSA.
Formulators value the ingredient's clean sweetness and stability in combination products containing vitamins, minerals, botanicals and amino acids, where it delivers consistent sweetness without browning or off-flavor development during processing and shelf life.
The manufacturing site operates environmental monitoring and pest-control programs consistent with international food-safety standards, and personnel hygiene and training procedures are documented and audited. Water used in processing meets potable standards, and cleaning validation supports rapid, safe changeover between campaigns.
Manufacturing & Quality Control
Quality control for Purecium Sucralose operates under ISO 9001 and FSSC 22000 food-safety systems in strictly audited GMP facilities. Every production lot is released only after identity confirmation, HPLC assay within 98.0% to 102.0%, heavy-metal analysis to USP limits, pesticide-residue testing to USP/EP expectations, residual-solvent testing and microbiological examination.
Batch-to-batch consistency is guaranteed across campaigns, with related-substance control ensuring the defined chlorination profile of the finished sweetener. Analytical methods align with current USP-NF and European Pharmacopoeia monographs for Sucralose.
Buyers receive a Certificate of Analysis, SDS and specification documentation with each shipment, and facility audits, batch records and additional technical documents are available during supplier qualification.
Sucralose is supplied in sealed, food-grade packaging with moisture protection suitable for global logistics, and can be held under standard ambient warehouse conditions without special storage requirements. CoA documentation for each lot includes identity, assay, related substances, heavy metals, pesticide residue, residual solvents and microbiology, aligned to buyer specification sheets.
Sucralose for B2B Supplement Manufacturing
Purecium supplies bulk Sucralose to dietary supplement manufacturers, beverage and food producers, distributors and finished-product brands worldwide. Standard packaging is 25 kg per drum, with a flexible low MOQ supporting pilot and launch volumes.
Procurement teams benefit from a resilient supply program: food-grade quality standardized by HPLC, full GMP compliance under ISO 9001 and FSSC 22000, allergen-free and non-GMO verification, and documented traceability from sucrose to finished drums. US, Canada and Mexico orders can be picked up from the Purecium US warehouse within two days, and global shipments dispatch from China within one week.
Technical support covers use-level guidance for tablets, chewables, powders and liquid formats, sweetener-blend strategy, specification alignment and regulatory documentation for target markets. Samples for R&D evaluation are available on request, and bulk orders are dispatched by air or sea freight with full export documentation.
Reviewed by the Chief Quality Assurance / Regulatory Affairs Specialist at Purecium for technical accuracy and regulatory alignment.
Sucralose Frequently Asked Questions (FAQ) for B2B Buyers
1. What are the regulatory compliance standards and purity specifications for Purecium bulk Sucralose?
Our bulk Sucralose complies strictly with United States Pharmacopeia (USP), Food Chemicals Codex (FCC), and European Pharmacopoeia (EP) monographs. Each production batch undergoes rigorous HPLC verification to guarantee an assay purity between 98.0% and 102.0%, with strict impurity controls, heavy metal limits below 10 ppm, and moisture content strictly maintained under 0.2%.
2. What manufacturing certifications do Purecium's production facilities hold?
Our manufacturing facilities operate under stringent cGMP guidelines and are certified by internationally recognized bodies for ISO 9001 (Quality Management), FSSC22000 (Food Safety System Certification), HACCP, Kosher, and Halal standards. This ensures complete safety, quality assurance, and legal compliance for brands distributing in the EU, UK, US, and global markets.
3. What is the sweetness profile of Sucralose compared to sucrose, and does it leave an aftertaste?
Sucralose provides an exceptionally clean sweetness profile that is approximately 600 times sweeter than regular table sugar (sucrose). Unlike saccharin or acesulfame potassium (Ace-K), high-purity Sucralose exhibits virtually no bitter metallic aftertaste at standard use levels, making it exceptionally popular for masking vitamin or botanical notes in dietary supplements.
4. How does Sucralose behave under extreme temperatures and varying pH levels in food and supplement manufacturing?
Sucralose possesses outstanding thermal and pH stability. It remains chemically stable during high-temperature manufacturing processes such as baked protein bars, extruded snacks, gummy confectionery cooking, and UHT beverage pasteurization, and it maintains its sweetening power across a wide acidic-to-neutral pH range (pH 3 to 7) over extended shelf lives.
5. What is the standard minimum order quantity (MOQ) for bulk Sucralose purchases from Purecium?
Our standard MOQ for bulk industrial orders is typically one 25 kg fiber drum. However, we fully support our B2B clients' R&D and pilot-scale testing phases by offering smaller sample quantities and flexible trial batch shipments upon request.
6. What packaging options are available for industrial and commercial shipments?
We package our bulk Sucralose in industrial-grade 25 kg fiber drums lined with double food-grade polyethylene bags to ensure optimal moisture barrier protection during transit and storage. Custom packaging sizes, palletization configurations, and private-label container options can be arranged for long-term contract partners.
7. What shipping methods and Incoterms does Purecium support for international B2B clients?
We support a comprehensive range of standard Incoterms, including FOB, CIF, DDP, and EXW, depending on the destination and client preference. We coordinate regular air freight, sea freight container loads (FCL and LCL), and expedited courier dispatch from our export hubs to destinations across North America, Europe, and the UK.
8. What documentation is provided with each commercial shipment of Sucralose?
Every shipment includes a detailed Certificate of Analysis (CoA) matching the specific lot number, a Safety Data Sheet (SDS), an Allergen Declaration, a Non-GMO Statement, a BSE/TSE-Free Certificate, and a Certificate of Origin. Additional regulatory or customs documentation can be provided upon request.
9. Is Purecium's Sucralose non-GMO, allergen-free, and suitable for vegan/vegetarian formulations?
Yes. Our Sucralose is 100% synthetically derived from sucrose through a selective chlorination process, meaning it contains no genetically modified organisms, major food allergens (such as gluten, dairy, soy, nuts, or fish), or animal-derived ingredients, making it fully compliant with vegan, vegetarian, and allergen-free product claims.
10. What is the recommended shelf life and proper storage condition for bulk Sucralose powder?
When stored in its original unopened packaging in a cool, dry, well-ventilated area away from direct sunlight and strong odors, our bulk Sucralose has a recommended shelf life of 24 months from the date of manufacture. The storage area should be maintained at temperatures below 25°C and relative humidity below 65%.
11. How does Sucralose impact blood glucose and insulin levels in human clinical studies?
Clinical and toxicological studies have consistently demonstrated that Sucralose is not metabolized by the human body for energy. It passes through the gastrointestinal tract unabsorbed and unchanged, meaning it has a glycemic index (GI) of zero and does not elevate blood glucose, serum insulin, or caloric intake, making it ideal for diabetic and keto formulations.
12. Can Purecium provide custom particle size specifications (e.g., micro-milled powder vs. granular)?
Yes. We offer different physical grades of Sucralose, including ultra-fine micronized powder (ideal for rapid dispersion in dry powder shakes and instant beverage mixes) and free-flowing granular grades (designed to prevent dusting and segregation in direct compression tablet manufacturing).
13. What support does Purecium offer for contract manufacturers (OEM/ODM) developing new formulations?
We partner closely with contract manufacturers and brand formulators by providing technical advisory support, solubility profiles, recommended usage rates (typically ranging from 0.01% to 0.05% depending on the application), R&D sample kits, and comprehensive regulatory documentation to streamline formula sign-off.
14. What are the typical lead times for order processing and delivery to European and North American ports?
For items in stock at our regional distribution hubs, order dispatch typically occurs within 3 to 5 business days. For direct factory container shipments, standard lead times range from 2 to 4 weeks depending on destination port logistics and seasonal shipping schedules.
15. How can B2B buyers request commercial price quotes, volume discounts, or product samples?
B2B procurement managers, formulators, and distributors can request formal quotations, tier-based volume pricing, and R&D sample packages by contacting our sales engineering team directly through our website contact portal or via corporate email at [email protected].
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