Flavour family
For the selected product, review ingredient sources, processing, intended use. Confirm the supporting information available, its scope and language with your Delsa contact. Your regulatory reviewer should assess suitability for the intended application and finished-product claims; do not assume a complete document pack or universal compliance.
Fruit (berry, citrus, tropical, stone fruit) profiles built with vape-suitable carriers; menthol and cooling agent systems (WS-3, WS-23, koolada) for adjustable freshness; tobacco (Virginia, Burley, RY4, Cuban), dessert (custard, vanilla, cheesecake) and beverage (cola, energy, coffee) profiles.
All vape profiles are dosed at 5–15% in PG/VG base and undergo dedicated stability testing against coil temperatures and shelf-life.
Our PG/VG concentrate library covers the full Canadian vape spectrum: fruit, citrus, menthol and koolada cooling, tobacco, dessert, beverage and candy/confectionery. Each is built around a stable base architecture performing consistently across PG/VG ratios from 30/70 to 70/30 and across freebase and salt-nic builds. Most concentrates dose at 5–15% inclusion in the base.
The minimum production order is 5 kg. Share the application, dosage and trial scale to discuss sample availability, quantity, any charges and lead time. Request a quotation for the intended production volume and confirm supply arrangements before ordering.
For each vaping concentrate, request available ingredient information, CAS numbers and composition details, carrier specifications, origin information and relevant analytical results, including any diketone testing. Confirm document scope and suitability with your regulatory reviewer for the intended market and VPRR reporting; a supplier file does not establish inhalation safety or regulatory acceptance.
For the selected product, review ingredient sources, processing, intended use. Confirm the supporting information available, its scope and language with your Delsa contact. Your regulatory reviewer should assess suitability for the intended application and finished-product claims; do not assume a complete document pack or universal compliance.
All e-liquid concentrates supplied under Health Canada Vaping Product Reporting and Disclosure expectations, with full ingredient disclosure.
For the selected product, review CoA, carrier. Confirm the supporting information available, its scope and language with your Delsa contact. Your regulatory reviewer should assess suitability for the intended application and finished-product claims; do not assume a complete document pack or universal compliance.
Custom-profile development with full ingredient transparency is supported under NDA for proprietary vape SKUs.
Yes — full ingredient disclosure, SDS and compositional documentation aligned with Health Canada's Tobacco and Vaping Products Act framework.
Our standard range is formulated without diacetyl, acetyl propionyl and acetoin. Exclusion certificates are issued on request for each commercial reference.
Share the reference, intended product base and attributes to match. Confirm the development scope, reference quantity and timing before trials.
Yes — every commercial concentrate ships with a standardized data pack formatted for direct VPRR submission.
A flavour description is a starting point, not evidence of performance in your recipe. Use a documented trial to decide whether a candidate fits.
Share the product base, processing conditions, target taste and benchmark. Identify the issue: bitterness, aroma loss, an unwanted note or a new flavour direction.
Ask technical support to confirm the selected flavour’s dosage, carrier and handling requirements. Compare candidates in the same recipe and process, including an unflavoured control where useful.
Evaluate aroma, taste, aftertaste and appearance after processing and during your intended storage conditions. Record the formula, dose and observations against your agreed acceptance criteria before scale-up.
Tell us which specification, allergen statement, safety data sheet, certificate of analysis or certification evidence your quality team needs. Availability and certification scope must be confirmed for the specific reference; an ingredient document does not establish compliance of your finished product.
Share your application, product base, target profile and timeline. Our Canadian office reviews your brief with Delsa and confirms the options, sample availability and next steps for your project.
