Applied Extracts Inc. was founded in 2017 by an MIT Ph.D. engineer and a dedicated team of engineers and extraction scientists in Silicon Valley. We began by designing and manufacturing small-scale supercritical CO₂ extractors in the Bay Area. Through continuous innovation and new product development, we have grown rapidly and built a portfolio of high-pressure materials processing equipment that is unique in the industry.

Over the past nine years, we have steadily expanded our offerings to include supercritical CO₂ extractors, pressurized liquid extraction systems (PLE/Organosolv), hydrocarbon solvent extractors (butane, propane and other volatiles), and supercritical water reactors. Our systems include Class 1 Div 1, fully automated, rated and certified in accordance with UL, CSA, ASME and all applicable state and provincial standards. We currently have systems installed on four continents!

Our equipment serves a wide range of applications, including:

• Botanical oil production (lab- and pilot-scale)
• Lithium-ion battery recycling
• Biorefinery and bioprocessing pilot plants
• Bio-oil and sustainable aviation fuel research and development

If you have a novel process or equipment requirement, contact our engineering team to discuss your application in detail.
We offer custom-engineered process solutions with short delivery times, Made in USA quality, and local support.

Applied Extracts

Client Success Story

A major client in Colorado purchased a set of six AE-150 supercritical CO₂ extraction machines and built a versatile, large-scale processing plant to produce pharmaceutical-grade ingredients for the global market. Their facility obtained a comprehensive set of GMP certifications including:

Certified to meet the World Health Organization Good Manufacturing Practices (WHO GMP).

Certified for compliance with the U.S. FDA’s Code of Federal Regulations: 21 CFR 210/211 (U.S. GMP for finished pharmaceuticals).

Certified to International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Q7 standard (GMP for Active Pharmaceutical Ingredients).

Certified under the Pharmaceutical Inspection Co-operation Scheme (PIC/S) standard, via certification by the Therapeutic Goods Administration (TGA) of Australia.

Registered two Drug Master Files (DMFs) with the U.S. FDA for its APIs (active ingredients).

In-progress regulatory filings: Seeking CBPF certification for Brazil (via Agência Nacional de Vigilância Sanitária / ANVISA) and ASMF/CEP submissions for the European market (via European Medicines Agency / EMA).

Contact us or email us at sales@appliedextracts.com to learn more and discuss your project in detail.