Cannabinoid Purification (CBD)
Pharmaceutical-grade chromatography resins for high-purity CBD separation and THC remediation
Our always-ready technical support and service teams go the extra step to be your most trusted resource. We're here for you.
Cannabis extracts must be pre-treated before purification of CBD, as they contain many impurities from the plant itself, such as waxes or colors. As CBD is required in a highly purified form to maximize its pharmaceutical effect, all other cannabinoids (over 100) must then be removed from the final product. Due to strict acceptable limits set by countries around the world, removal of Tetrahydrocannabinol (THC) from the final CBD product is a key step in production.
When compared to silica-based alternatives, our Chromalite® chromatographic resins offer a simple, high performance and cost-efficient method to separate THC from CBD, thus maximizing the purity of your CBD extracts.
Why choose Purolite?
Security of Supply
Ensuring reliable availability of resins is vital to customers and is of paramount importance to Purolite. As a leading supplier of resin media to the world’s most regulated industries, we recognise that Purolite’s resins are critical purification products. As such Purolite has a real-world security-of-supply system in place to support your process requirements for business continuity.
Purolite is a global leader in resin technology, and one of the world’s largest developers and manufacturers of high-quality chromatographic resins, enzyme carriers, ion exchange resins, APIs, adsorbents and specialty resins.
All Purolite Life Sciences products are of premium quality and are produced in our ISO-certified production facilities in the UK, Romania, China and the USA.
For over 35 years, Purolite has supplied specialty resin technology to industries within complex regulatory environments including biotechnology, pharmaceutical, food, fine chemical and electric power generation.
Purolite complies with required national and international regulations, as well as many voluntary specialty certifications. These include: • Part II of the EU GMP Guide • US FDA Current Good Manufacturing Practice (CGMP) regulations • US FDA CFR - Code of Federal Regulations including Title 21 • GMO/TSE/BSE free • ResAP(2004)3 • NSF/ANSI 61/WRAS standards • REACH regulations • ISO 9001:2015 quality system specifications, • ISO 14001:2015 Environmental Management System requirements • OHSAS18001:2007 • RoHS Directive 2011/65/EU • Halal and Kosher requirements
We also hold Drug Master Files with the US FDA, Japan, Canada and EU.