Acetyl Tetrapeptide-3 CAS 827306-88-7 High-Purity Cosmetic Peptide for Advanced Eye Area Care

Product Overview

Acetyl Tetrapeptide-3 is produced for supplement brands, private label programmes and distributors that need a finished dosage form with a documented specification rather than a generic listing. Capsules are filled under an ISO 22000 management system, checked against a retained reference before release, and shipped with a certificate of analysis traceable to the batch and bottle numbers on the packing list.

Standard presentation is 60 capsules per bottle, bulk packed in 25 kg cartons, and pilot runs are available so a brand can validate label claims, capsule appearance and stability before committing to a production batch.

Typical Specification

Key Features

• Batch to batch consistency controlled against a retained reference sample rather than a catalogue description.
• Active content verified before release, so the label declaration is supported by the certificate rather than by assumption.
• Documentation pack as standard: COA, MSDS, allergen statement, non-GMO statement and heavy metal report.
• Batch numbering from raw material intake through to the bottle that reaches your warehouse.
• Private label support: capsule colour, bottle size, carton artwork and multilingual labels.

Applications

The product is used mainly by dietary supplement brands, private label programmes, e-commerce ranges. Three variables decide whether a launch goes smoothly: the declared active content, the capsule size that carries it, and the label wording the destination market allows. Confirm all three on a pilot batch before artwork is finalised, because changing a claim after printing is the most expensive correction in the project.

Where a brand needs a combination formula, the individual actives can be blended to the target ratio and verified on the finished capsule rather than calculated from input weights.

Quality and Documentation

Every batch is tested for appearance, active content, capsule weight, disintegration and microbiology. Heavy metals and pesticide residue are tested on a scheduled basis, or on request against the requirements of the destination market. Retained samples are kept for 24 months.

Release testing covers appearance, active content per capsule and capsule weight, with microbiology on a scheduled basis. Heavy metals and pesticide residue are tested either on a schedule or against the requirements of the destination market. Retained samples are held for 24 months, which is what allows a deviation to be investigated against the actual lot instead of a memory of it.

Packaging and Delivery

Standard packing is 60 capsules per bottle, bulk packed in 25 kg cartons. Pilot quantities are available for evaluation. Production lead time is typically 15 to 25 working days ex-works depending on capsule colour and label printing, and mixed containers can be consolidated across categories to reach a full load.

Shipping documents are issued in the form your customs broker expects: commercial invoice, packing list, certificate of origin where applicable, and the health or non-GMO declarations some destinations ask for at the border.

Why Buy From Us

We manufacture and export food ingredients and supplement dosage forms for B2B customers in Europe, North America and Asia, and we ship against the documentation the destination market actually requires rather than the documentation that is easiest to issue. Orders are handled by a named contact from quotation through to arrival.

FAQ

Can we order a pilot batch? Yes — the minimum is one production run, and label design can run in parallel.

Is private label possible? Yes, including bottle, carton and multilingual label artwork.

Which documents come with the shipment? COA for the batch, MSDS, allergen statement, non-GMO statement and packing list.

Can the active content be adjusted? Within the production window, yes. Send the target value and we will confirm feasibility with a sample.