Humectant
Vegetable Glycerin USP/EP
CAS 56-81-5
Pharmaceutical-grade glycerol from vegetable feedstocks. Identity and limits aligned to USP and European Pharmacopoeia monographs with batch CoA documentation.
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Quality frameworks
Certifications and food-safety programmes are applied per material and market. Scope and validity are confirmed in your quotation pack and on the certificate of analysis — never assumed site-wide.
How each framework appliesDocumented procedures, change control, supplier qualification.
Batch records, in-process controls, release before dispatch.
Hazard analysis, critical control points, allergen handling.
Per material, line and destination market, where it applies.
Catalogue
Every product page carries the full specification table, available grades, packaging, and minimum order quantity — so your technical team can qualify the material before anyone talks price.
CAS 56-81-5
Pharmaceutical-grade glycerol from vegetable feedstocks. Identity and limits aligned to USP and European Pharmacopoeia monographs with batch CoA documentation.
CAS 57-55-6
High-purity 1,2-propanediol for pharmaceutical and food-adjacent processing. USP monograph limits with identity by IR and refractive index on every release batch.
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Nicotine-free flavor concentrates for e-liquid and oral nicotine pouch programs. Profiles are supplied on declared carrier (PG, VG, liquid pouch, or dry blend) with full ingredient declaration — nicotine is added downstream by the customer.
How supply starts
Four gates between your enquiry and a qualified material. Nothing ships before the paperwork your incoming inspection needs exists.
Grade, volume, packaging, destination market. If you have an internal spec sheet, send that instead — we answer against your document, not a generic datasheet.
Samples are drawn from production stock and shipped with the certificate of analysis for that lot, so your bench results are comparable to what you would receive at volume.
Certificate of analysis, safety data sheet where applicable, regulatory statements, and the declarations your market requires. Requested once during onboarding, reissued per lot afterwards.
Each lot is released against its own test results before it leaves the site, and travels under a documented chain of custody. The lot number on your delivery matches the certificate in your file.
Audit scheduling, retain-sample policy, and quality agreements follow the same rhythm. Details are on quality & compliance.
Global Reach
From our Cyprus headquarters, we deliver to regulated markets across four continents with full chain-of-custody documentation.
Strategic Mediterranean hub with direct EU market access
35.1856° N, 33.3823° E
Indicative figures from current operations; delivery windows and documentation scope are confirmed per shipment at quotation.
TPD notification, GMP documentation, flavor development, and EU logistics — written for the people who have to defend the decision internally.
3 articles
How B2B buyers should align nicotine sourcing, batch documentation, and notification data with EU Tobacco Products Directive expectations before placing regulated liquids on market.
A readiness checklist spanning concentrations and volumes, dossier completeness, labeling, emissions data, and the quality artefacts auditors expect beside a Tobacco Products Directive notification.
A practical map of quality agreements, batch records, and release packs B2B buyers should expect when qualifying glycerin and propylene glycol for regulated formulations.
Next step
Tell us the grade, the annual volume, the packaging, and the destination market. That is enough for us to confirm availability, assign the correct grade and documentation, and price it. If the material is not ours to supply, we will say so rather than quote around it.
Quote-only supply · no public pricing · regulated B2B