P5P Vitamin B6 Ingredient

Pyridoxal-5-Phosphate Powder (P5P)

Pyridoxal-5-phosphate (P5P) powder for vitamin B6 supplement formulations, including standalone B6, B-complex and multivitamin products. Gensei supplies the ingredient with batch-specific quality documentation for procurement review.

Pyridoxal-5-Phosphate P5P powder

P5P: Pyridoxal-5-Phosphate as a Vitamin B6 Ingredient

Pyridoxal-5-phosphate, commonly abbreviated as P5P, is a coenzyme form of vitamin B6 used in nutritional supplement formulations. The supplied material is a slightly yellow to off-white powder.

For formulation work, its physical properties matter as much as its identity. The specification describes P5P as very slightly soluble in water and includes particle-size, pH, water and density data that can be reviewed against the intended manufacturing process.

MalzemePyridoxal-5-Phosphate (P5P)
Vitamin FormVitamin B6 Coenzyme Form
GörünüşSlightly Yellow or Off-White Powder
İçerik KategorisiNutritional Supplement Ingredient
Teknik Özellikler

Pyridoxal-5-Phosphate Powder Specifications

Review the listed limits alongside the representative batch results and test methods. Confirm acceptance criteria against the requirements for your finished product.

Test ItemŞartnameRepresentative Batch ResultYöntem
Identity & Physical Properties
AçıklamaSlightly yellow or off-white powderUygunlukGörsel
TanımlamaMajor product peak retention time corresponds to the standardUygunlukChP <0512>
ÇözünürlükVery slightly soluble in water; soluble in alkali-OH solutionUygunlukChP General Notices
Erime Noktası140–145°C143°CChP <0612>
pH (0.25% in water)2.6–3.02.9ChP <0631>
Parçacık Boyutu≥90% through 30 meshUygunlukChP <0982>
Yığın Yoğunluğu—0.36 g/mlUSP <616>
Sıkıştırılmış Yoğunluk—0.67 g/mlUSP <616>
Chemical Quality
Water by KF≤10,01 TP3T8.2%ChP <0832>
Free Vitamin B6≤0.05%0.02%ChP <0512>
Assay (as C8H10NO6P, dry basis)98.5–101.0%99.0%ChP <0512>
Elemental Limits
Total Heavy Metals≤10 ppm<10 ppmChP <0821>
Kadmiyum≤0.5 ppm0.010 ppmChP <2321>
Arsenik≤1.5 ppm<0.01 ppmChP <2321>
Kurşun≤0.5 ppm<0.02 ppmChP <2321>
Cıva≤0.1 ppm<0.005 ppmChP <2321>
Kalan Çözücüler
Toluene≤890 ppm8 ppmChP <0861>
Ethanol≤5000 ppm22 ppmChP <0861>
Microbiological Quality
Total Plate Count≤1000 CFU/g<100 CFU/gChP <1105>
Maya ve Küf≤100 CFU/g<10 CFU/gChP <1105>
SalmonellaOlumsuzOlumsuzChP <1106>
E. coliOlumsuzOlumsuzChP <1106>
Staphylococcus aureusOlumsuzOlumsuzChP <1106>
COA BatchC042504816
Batch Size500 kg
ManufacturedApr 14, 2025
Report DateApr 24, 2025
Retest DateApr 14, 2028

The batch results above are representative reference data, not a substitute for the current batch Certificate of Analysis supplied with an order.

Formulation Fit

Working with P5P Powder in Supplement Formulas

P5P is selected for vitamin B6 formulations where the pyridoxal-5-phosphate form is specifically required. Dosage form, blending behavior and finished-product requirements should be considered during development.

Standalone P5P Supplements

For products that specify P5P as the vitamin B6 source, formulation teams should confirm the intended serving level, label declaration and finished-product requirements before scale-up.

B-Complex Formulas

When P5P is combined with other B vitamins, review the ingredient ratios and blending sequence within the complete formula, then verify blend uniformity using the chosen manufacturing process.

Multivitamin Formulas

In broader multi-nutrient systems, assess P5P alongside the other active ingredients and excipients. Confirm the finished blend and product performance under the intended processing conditions.

Dozaj Formuna İlişkin Hususlar

For capsules, tablets and powder blends, consider how particle size and density relate to the wider blend. Flow, filling, compression and blend uniformity should be verified in the actual formulation rather than assumed from individual ingredient data.

Supplier Qualification

From Specification Review to Raw-Material Approval

Use the product specification and batch documentation as part of your normal supplier qualification process, alongside your internal standards and finished-product requirements.

Documentation for Review

The representative COA shows the types of information recorded for a P5P batch. Before placing or releasing an order, request the current documentation and confirm that the supplied material meets your approved raw-material specification.

Any additional documents should be discussed according to your quality system, product category and destination-market requirements.

Specification MatchCompare the supplier specification with your internal raw-material standard, including required test methods and acceptance limits.
Batch COA ReviewCheck the batch-specific results and document identifiers before approving the material for use.
Formulation FitAssess the available physical-property information against the intended blend, dosage form and manufacturing process; verify performance in your own formulation.
Market and Documentation NeedsConfirm any customer, regulatory or destination-market documentation requirements before order confirmation.
Supply & Ordering

P5P Supply for Supplement Manufacturing

Discuss the order and documentation requirements with Gensei before confirming a supply plan for your production schedule.

Paketleme

Standard packing is 25 kg per drum. Confirm the required order quantity and any shipment-specific handling needs when requesting a quotation.

Quality Documents

Batch-specific COA information is available for review. Let the team know if your quality process requires additional documents or a particular document format.

Order Coordination

Share your destination market and expected purchasing schedule so product documentation and commercial details can be discussed before order confirmation.

P5P Ingredient Inquiry

Request a Quote for Pyridoxal-5-Phosphate Powder

For a more relevant quotation and document response, include the project details that matter to your purchasing and formulation team.

Required QuantityShare the quantity needed for sampling, trial production or commercial purchasing.
Destination MarketIdentify the country or market where the finished product will be sold.
Finished-Product FormatLet us know whether the project is a capsule, tablet, powder blend or another dosage form.
Qualification RequirementsNote any supplier-approval documents or project-specific quality requirements your team needs reviewed.

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Share your company details and a short description of your P5P project.

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