Pure Creatine Monohydrate Powder

Pure Creatine Monohydrate Powder

Full Name: β-Nicotinamide Mononucleotide
Abbreviation: β-NMN
CAS No. : 1094-61-7
Raw Material & Synthesis Route: Chemical enzymatic synthesis using nicotinamide riboside, ribose and phosphate as starting materials; multi-step purification via ultrafiltration & recrystallization
Core Active Marker: β-NMN
Main Specifications: 98%, 99% HPLC
Appearance: White crystalline fine powder, slight characteristic odor
Available Certifications: ISO22000, cGMP, HACCP, HALAL, KOSHER, COA & SDS per batch

Pure Creatine Monohydrate Powder

Micronized Creatine Monohydrate

 
 

Pure Creatine Monohydrate Powder - High-Purity Ergogenic Compound

Shaanxi Rebecca is a leading producer and major supplier of pure creatine monohydrate powder, offering clients worldwide premium components for sports nutrition.We provide creatine monohydrate powder at 98% and 99.9% pharmaceutical grade using three different production lines with an annual production capacity of over 2,000 tons.

Every batch is guaranteed to fulfill USP and EP requirements thanks to our stringent quality control procedures.To verify the quality, we employ sophisticated testing techniques like GC-MS, ICP-MS, and HPLC.Additionally, we offer complete supply chain transparency, which includes raw material tracking and third-party certification support.We provide unique formulation services to companies in the global functional food, sports nutrition, and dietary supplement industries.

Technical Specifications

Parameter

Specification

CAS Number

57-00-1

Molecular Formula

C₄H₉N₃O₂·H₂O

Molecular Weight

149.15 g/mol

Appearance

White crystalline fine powder

Purity (HPLC)

98% / 99.9%

Mesh Size

80–200 mesh (micronized available)

Moisture Content

≤12.5%

Heavy Metals

<1 ppm (Pb, As, Hg, Cd)

Creatinine

<100 ppm

Dicyandiamide (DCD)

<30 ppm

Shelf Life

24–36 months (sealed, cool, dry storage)

Test Item Acceptance Standard Test Result Judgment
Appearance Bright white free-flowing crystalline powder, odorless, no lumps, no foreign particles Bright white uniform crystalline powder with good fluidity Complies
Identification HPLC retention time consistent with creatine monohydrate reference standard Positive identification Complies
Assay Content (HPLC) 99.0% ~ 101.0% 99.71% Complies
Loss on Drying (crystal water) 11.8% ~ 12.4% 12.15% Complies
Residue on Ignition ≤0.10% 0.02% Complies
pH (1% aqueous suspension) 6.5 ~ 8.0 7.1 Complies
Creatinine Impurity ≤0.10% 0.03% Complies
Single Unknown Impurity ≤0.10% 0.03% Complies
Total Related Organic Impurities ≤0.30% 0.12% Complies
Particle Size Conventional: 100 mesh pass rate ≥98%; micronized 200 mesh optional Conventional: 99.8% Complies
Solubility Slightly soluble in cold water, soluble in hot water; insoluble in ethanol, acetone Matches standard solubility features Complies
Lead (Pb) ≤1.0 ppm 0.16 ppm Complies
Total Arsenic (As) ≤1.0 ppm Not Detected Complies
Cadmium (Cd) ≤0.3 ppm Not Detected Complies
Mercury (Hg) ≤0.1 ppm Not Detected Complies
Residual Solvents Comply with ICH Q3C Class 2 & Class 3 limits Fully compliant Complies
Total Aerobic Microbial Count ≤1000 CFU/g 31 CFU/g Complies
Yeast and Mold Count ≤100 CFU/g Not Detected Complies
Escherichia coli Negative per gram Negative Complies
Salmonella spp. Negative per 25g Negative Complies
Staphylococcus aureus Negative per gram Negative Complies
Why Choose Us

Our team has a lot of experience in developing sports nutrition ingredients and creating custom formulas, making sure that each product is innovative and consistent.

With more than 100 different types and more than 2,000 tons produced annually, our capacity to create a broad range of goods enables us to maintain relationships with long-term business partners and provide stable prices on a quarterly basis.

We have sophisticated testing instruments, such as UPLC, HPLC, GC-MS, ICP-MS, and microbiological testing systems, to swiftly and precisely assess the quality of our pure creatine monohydrate powder, including detecting residual solvents and looking for contaminants.

We meet worldwide quality standards with a number of significant certifications, including ISO22000, cGMP, HACCP, HALAL, and KOSHER.

In addition, we give a Safety Data Sheet (SDS) and Certificate of Analysis (COA) for every batch, as well as third-party audits.

From procuring raw ingredients in accordance with GAP criteria to the final packaging, our comprehensive traceability system keeps track of every stage, guaranteeing that everything is appropriately recorded for customs and legal requirements.

Why Choose Us

Source & Traceability

Pharmaceutical-grade raw materials are the first step in production, and they are only obtained from accredited producers who offer comprehensive batch test data. Strict incoming inspection procedures are followed by our chemical synthesis route; any batch that exceeds impurity limits is immediately rejected. To avoid cross-contamination, closed clean workshop production uses separate reaction, separation, and purification zones. This synthesis method produces better batch consistency and comprehensive raw material traceability records appropriate for customs and third-party audits, in contrast to alternatives obtained from fermentation.

Source & Traceability

Solubility & Stability Characteristics

Solubility: 14 g/L at 20°C in water. Micronized 200-mesh powder is perfect for beverage formulations and ready-to-mix powders because it disperses quickly in aqueous systems without leaving behind residue or turbidity.

Thermal Stability: Preserves integrity during brief processing up to 100°C. Extended exposure above 100°C may result in some breakdown.

pH Stability: Stable between 4.0 and 9.0. When formulating, extremely acidic or alkaline conditions should be avoided.

Moisture Sensitivity: When stored correctly, there is little hygroscopicity. In cool, dry settings, sealed packaging keeps the powder from clumping and preserves its free-flowing properties.

Light Stability: Stable in typical warehouse lighting conditions. Long-term UV exposure is not advised.

Solubility & Stability Characteristics

Method of Production

Through carefully regulated sequential procedures, our manufacturing adheres to stringent pharmaceutical requirements. Precise weighing is applied to high-purity raw materials in dust-free conditions.

Crude creatine is created by chemical synthesis reactions that are controlled by temperature and pH. Dicyandiamide and dihydrotriazine are among the contaminants eliminated by multi-stage crystallization and recrystallization.

Thermal deterioration is avoided by vacuum drying at regulated temperatures. Target mesh sizes are obtained via ultrafine pulverization, and batch consistency is achieved by homogenization blending.

The finished goods are vacuum-packed with nitrogen in light-resistant aluminum foil bags within 25 kg fiber drums.

Before being stored with comprehensive documentation, each batch is subjected to comprehensive HPLC purity testing, heavy metal screening, microbiological analysis, and particle size analysis.

Method of Production

Quality Assurance

Strict incoming raw material inspection, in-process monitoring, and final product verification against USP and EP pharmacopeia requirements are all part of our extensive quality control system. Accurate impurity profiling, such as quantification of creatinine (<100 ppm), dicyandiamide (<30 ppm), and dihydrotriazine (non-detectable), is made possible by advanced analytical capabilities. HALAL and KOSHER certifications are available, and each batch comes with COA and SDS paperwork. While complete production records provide total traceability, third-party testing partnerships meet customer-specific validation requirements.

Quality Assurance

Packaging & Delivery

Standard packaging consists of 25 kg plastic-lined fiber drums for large orders and 1 kg aluminum foil packets for samples. Tailored packaging options meet unique transportation security needs.

We provide international shipping by sea freight for economical bulk quantities and air freight for urgent needs. Bulk order production takes 710 working days following deposit confirmation; sample MOQ is 1 kg and preparation takes 35 days.

Packaging & Delivery

FAQ

Q: What distinguishes your 200-mesh micronized grade?

A: Superior dispersion eliminates gritty texture, ensuring rapid dissolution in liquid formulations without sedimentation.

Q: Can you supply material meeting Informed-Sport certification?

A: Yes, third-party verification for WADA-prohibited substances can be arranged per your quality requirements.

Q: What documentation supports customs clearance?

A: Complete COA, SDS, HALAL/KOSHER certificates, and full raw material traceability records accompany shipments.

Q: Do you offer quarterly fixed-price contracts?

A: Long-term framework customers may lock quarterly pricing with guaranteed priority production and stable delivery cycles.

Q: Is this suitable for vegan formulations?

A: Absolutely—synthesis employs no animal-derived precursors, meeting vegetarian and vegan product specifications.

Contact Us

For detailed pure creatine monohydrate powder COA, technical specifications or customized formulation consultation, contact our team at information@sxrebecca.com. Partner with Shaanxi Rebecca Bio-Tech for reliable, high-purity sports nutrition ingredients backed by proven manufacturing excellence and global supply capabilities.

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