Tribulus terrestris Extract Powder 45% Protodioscin

What distinguishes your 45% protodioscin standardization?
Our extract is specifically standardized to 45% protodioscin content, representing the highest tier of Tribulus extracts.

How does protodioscin differ from total saponins?
Protodioscin is the primary bioactive compound within the saponin family, offering enhanced potency and specificity.

What is the extract's solubility profile?
The extract demonstrates optimized solubility characteristics, particularly suitable for advanced delivery systems.

How do you quantify protodioscin content?
We employ advanced HPLC-UV analysis with validated protocols specific to protodioscin quantification.

Is this extract suitable for sophisticated plant-based formulations?
Yes, our extract is 100% plant-derived and meets premium vegan standards.

What is the stability profile of protodioscin?
Under controlled storage conditions, protodioscin content remains stable for 24 months.

What analytical documentation is provided?
We furnish comprehensive analytical packages including detailed HPLC profiles and stability data.

What advanced quality parameters are tested?
Each batch undergoes extensive testing including chirality analysis, bioactive profiling, and residual solvent screening.

What are the powder's advanced physical specifications?
The extract achieves pharmaceutical-grade particle distribution with 95% below 80 mesh.

What conditions optimize stability?
Maintains maximum stability in pH range 5-7.5, ideal for specialized formulations.

Can you provide custom protodioscin specifications?
Yes, we can adjust protodioscin levels for specific formulation requirements.

How are source materials selected?
We employ chemotype selection and advanced agricultural protocols to maximize protodioscin yield.

What delivery systems are most effective?
The extract excels in advanced delivery systems including modified release technologies.

What distinguishes your quality system?
Our facility operates under pharmaceutical-grade GMP standards with ISO 9001:2015 certification.

What are the critical storage parameters?
Store under controlled conditions below 25°C with relative humidity below 60%.

Does the extract meet clean label requirements?
Yes, our extract is non-GMO and free from synthetic modification.

What organoleptic standards are maintained?
Consistent light amber color with standardized particle morphology.

How extensive is your stability testing?
We conduct real-time, accelerated, and stress testing under ICH guidelines.

What specialized packaging is available?
Offered in pharmaceutical-grade containers with moisture-barrier properties.

How is allergen control managed?
Produced in isolated suites with advanced air handling and contamination controls.

What moisture limits are enforced?
Loss on drying maintained below 5% with advanced humidity control.

How is extract consistency maintained?
Through process analytical technology and real-time monitoring systems.

What quality control innovations are implemented?
We utilize chemometric analysis and advanced fingerprinting techniques.

Does the extract meet international pharmacopeia standards?
Yes, our extract meets or exceeds global pharmacopeia requirements.