Explore our elite portfolio of OEM/ODM plant-derived compounds and active health ingredients engineered for globally recognized brands.
Decoding the technical requirements and strategic sourcing priorities of global pharmaceutical, nutraceutical, and cosmetic corporations.
Global procurement teams prioritize raw active compounds that exhibit validated potency profiles. Our analytical procedures confirm that active components such as Pterostilbene and Quercetin meet standard purity benchmarks through strict HPLC and GC-MS validations. This minimizes batch-to-batch variance and optimizes performance in downstream formulation lines.
Adapting to complex international regulations is vital. Manufacturing facilities must comply with global food and chemical standards, including EFSA Novel Food protocols, US FDA GRAS regulations, and local cosmetic ingredient indexes (such as China's IECIC). Our documentation packages feature full USP/EP solvent residue profiles, heavy metal limits, and microbiological safety controls.
Modern enterprises require complete supply chain transparency. From raw agricultural sourcing to final physical powder milling, every stage must be documented. Sustainable, verifiable sourcing helps brands satisfy ESG compliance requirements while ensuring a consistent raw material flow during market disruptions.
Integrating Research, Scale Production, and Custom Formulation Engineering
Benefiting from the solid foundation provided by its parent company, Xi'an Tianben Bioengineering Co., Ltd., Botanical Cube Inc. focuses on researching, developing, producing, and selling healthy natural ingredients. With more than two decades of industry experience, it has become a leader in the field, specializing in providing high-quality plant extracts and customized solutions to global customers. Services meet the needs of industries including herbal medicine, health foods, dietary supplements, food and beverages, daily chemicals, and cosmetics.
Our operations are supported by three companies—Xi'an Tianben Bioengineering Co., Ltd., Botanical Cube Inc., and Shaanxi Tianben Kangyuan Biotechnology Co., Ltd.—which together operate 3 production bases covering more than 100 acres and process more than 3,000 tons of plant raw materials each year. The product range includes more than 200 plant extracts, and we also provide a variety of certified organic products to meet the global demand for environmentally friendly and healthy solutions. Exporting to 60% of the world's countries, serving more than 200 countries and regions and more than 500 customers from all walks of life.
Translating raw science into functional market applications across critical product categories.
We supply standardized bioactive ingredients optimized for capsule, tablet, and softgel manufacturing. By focusing on flowability, particle size distribution (micronization), and stable active concentrations, we help brands produce high-performance formulas with reliable bio-absorption profiles.
Our cosmetic-grade active ingredients, including L-Glutathione and Niacinamide, are developed for high solubility and formulation compatibility. These active compounds integrate smoothly into emulsions, serums, and creams while meeting clean beauty standards and restricted substance lists.
We refine botanical extracts to improve water solubility and manage bitter sensory properties. This allows clean-label brand owners to fortify RTD beverages, functional powders, and wellness shots without compromising the taste experience or relying on synthetic masking agents.
Operational excellence since 2012, setting cleanroom and processing benchmarks for active botanical materials.
Our first factory was established in 2012 in Sanyuan City, Xi'an, four years after our company was founded. At that time, our production experience was still in its early stages, and we faced many challenges as we worked to refine our processes. However, we remained committed to continuous improvement, investing heavily in technology, training, and quality control to strengthen our capabilities. These early efforts laid a strong foundation for our growth, shaping the high standards of excellence that we uphold today.
Powder collection, crushing and sieving, mixing, and drying processes are all performed in a Class 100,000 cleanroom environment. Our operators strictly follow hygiene protocols and wear sterile gowns, masks, and gloves to maintain product purity and safety, ensuring that we provide our customers with high-quality standards and reliable ingredients.
Developing advanced technologies to improve plant compound performance and enhance bioavailability.
Using pressurized CO2 as a solvent to extract high-purity phytochemicals at lower temperatures, preserving delicate molecular profiles without leaving trace organic residues.
Applying advanced micro-encapsulation and liposomal delivery systems to improve the stability and absorption profiles of lipophilic organic molecules.
Using high-resolution chromatography to isolate specific target molecules, helping to ensure consistent active compound percentages in every batch.
Improving process sustainability through closed-loop solvent recycling systems and by-product processing, aligning with international environmental standards.
Monitored using Gas Chromatography-Headspace (GC-HS) analysis to keep residual solvents well within USP, EP, and ChP guidelines.
Tested using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) to confirm that Arsenic (As), Lead (Pb), Cadmium (Cd), and Mercury (Hg) levels remain low.
Using Class 100,000 cleanroom environments and pasteurization systems to ensure zero pathogen detection (E. coli, Salmonella, Staphylococcus aureus).
Customizing bulk density, tap density, and mesh size distribution (from 80 to 200 mesh) to match specific product manufacturing needs.
We maintain a comprehensive quality system to support international market access.
Our manufacturing sites operate under verified systems including GMP, ISO22000, HACCP, Halal, and Kosher certifications. These systems guide our daily production steps, helping us maintain batch stability and safety.
Every commercial shipment comes with comprehensive quality documentation, including Certificates of Analysis (COA), Allergen Statements, Non-GMO Declarations, MSDS, and detailed process flow diagrams.
We trace every batch from the agricultural source to the finished product. We verify plant identity using TLC and HPTLC testing, preventing raw material substitution and adulteration.
Direct answers from our engineering and regulatory affairs department to support your sourcing process.
For custom ODM formulations, the lead time typically ranges between 3 to 5 weeks. This schedule includes lab-scale pilot batch trials, active ingredient stability validation (HPLC), moisture monitoring, and final packaging assessment. Standard catalog compounds can often be shipped sooner depending on inventory levels.
We employ vacuum low-temperature evaporation and advanced column chromatography purification techniques. Solvent residues are systematically analyzed using Gas Chromatography (GC-FID/Headspace) to confirm they align with standard international pharmacopoeia requirements.
Yes, we offer custom particle size milling. We can micronize powders to 80 mesh, 100 mesh, or 200 mesh to match various formulation types, such as direct compression tablets, powder drink mixes, or cosmetic liquids.
We implement a batch-code tracking system that traces materials from the crop fields through extraction and final packaging. Each step is documented with raw material receipt slips, extraction logs, cleanroom processing data, and laboratory analysis reports.
Explore our specialized functional ingredients developed to meet international regulatory standards.
Botanical
