Description
COA-BACKED NUTRITIONAL INGREDIENT
Vitamin A Palmitate Oil for B2B Fortification
Vitamin A Palmitate Oil is supplied for B2B fortification and premix projects. Specification centres on the declared potency, the carrier system and the stability behaviour in your finished format.
COA-Backed Specification
| Identity | Vitamin A Palmitate Oil |
|---|---|
| CAS No. | 79-81-2 |
| Form and colour | Yellow to amber oily liquid |
| Assay | 1.5 MIU/g |
| Method | HPLC |
| Loss on drying | <=5.0% |
| Ash | <=5.0% |
| Heavy metals | Within the limits of the approved specification |
| Microbiological limits | Within the limits of the approved specification |
| Representative batch | LXPF260708 |
| Manufacture date | 8 Jul 2026 |
| Shelf life | Two years when stored properly |
Representative values do not replace the current shipment COA.
Buyer Decision Guide
Vitamin grades are specified by potency, carrier and purity, and the same vitamin name can cover several physical forms. Confirm the exact form and the analytical method before comparing quotations; overage and stability requirements are project-specific.
- Confirm the exact physical form and carrier
- Check declared potency and the assay method
- Review stability and overage needs for your format
- Confirm light, heat and oxygen sensitivity in handling
How This Grade Differs
Vitamin A Palmitate Oil must be compared on physical form, carrier and declared potency rather than on the vitamin name alone. Powder, oil, crystal and diluted forms behave differently in blending, dosing and shelf life.
Compare these related grades before approval:
For a substitution review, confirm the vitamin A palmitate identity, 1.5 MIU/g potency and HPLC method, oil delivery form and the current offered-batch COA. Acetate and palmitate, or powder and oil grades, require separate specification approval.
Application Areas
Discuss the intended formulation and processing conditions with the supplier before selecting this oil ingredient.
Packaging and Delivery
Request the available pack sizes, evaluation sample, minimum order quantity and lead time for the offered lot in the quotation.
Quality and Documentation
Representative batch LXPF260708 supports the specification table above. Use the cited record for preliminary comparison and request the offered-lot COA for final technical approval. Batch COA, specification sheet, agreed third-party testing and export documents are available for buyer verification.
Frequently Asked Questions
How do you control related substances?
Related substances are integrated on the same HPLC run used for the 1.5 MIU/g assay.
Which batch is the quotation based on?
The page cites representative batch LXPF260708; the current lot’s certificate governs release.
Which impurity limits are declared?
Moisture and ash are held within the approved specification limits, with heavy metals and microbiology tested on every lot.
How does the material behave in your process?
It is supplied as Yellow to amber oily liquid, so handling and dosing are agreed against your line.
What assay does Vitamin A Palmitate Oil 1.5 MIU/g carry on the certificate of analysis?
Assay 1.5 MIU/g, determined by HPLC.
What is the minimum order quantity?
The regular MOQ is typically 1 kg. An evaluation sample of 10-20 g can usually be arranged before a formal order, subject to stock.
Can I get a sample before placing the order?
Yes. An evaluation sample is normally available before a formal order. Sample quantity, courier account and destination are confirmed at the time of request.
Which documents come with the shipment?
Batch COA, specification sheet, agreed third-party testing where required, commercial invoice, packing list, certificate of origin and transport documents. The exact set is confirmed against the product and destination market.
Request COA, Sample or Quotation
Send your target specification, application, order quantity, destination country and required test limits.
Get the current batch COA, a sample or a quotation
