Buyer shall examine Product promptly after receipt for damage, short-weight and non- conformance with the Specifications. Buyer assumes all risks and liabilities (i) arising out of unloading, discharge, storage, handling and use of the Product, or (ii) arising out of compliance or non-compliance with national, state, provincial, or local laws and regulations governing or controlling such activity. In the event of invalidity of a provision of these Terms, the parties shall deem that provision stricken in its entirety (i.e. pro non scripto) and the balance of these Terms shall remain in full force and effect or affecting the validity or enforceability of such provision in any other jurisdiction. 24.

The enhanced “springiness” of FlexSpring insoles also improves vertical jumping performance compared to non-composite reinforced insoles.

Avient offers Gravi-Tech™ high-density formulations that are suitable for alcoholic and non-alcoholic beverages, as well as other premium applications such as beauty and cosmetic products.

And Carbonerro also needed to keep costs down to produce a more economical solution for the non-professional enthusiast.

Cesa™ Stat Antistatic Additives PRODUCT SELECTION GUIDE Polymers are typically non-conductive, allowing the buildup of a static charge on the surface that can attract dust or damage electronics stored within packaging.

Avient provides pre-tested color and additive concentrates based on bio-polymers to minimize the risk of non-compliance and support a more sustainable profile for plastic products used in the healthcare industry.

KEY BENEFITS • Consistent performance with all levels of rPET; 25%, 50% and 100% • Improved haze and color • Can be used with many different resin/grades • Non-nylon based • Simple to use with existing mono-layer equipment • Suitable for use on multi-layer machines Sustainability Spotlight Recycle Solutions TARGET MARKET & APPLICATIONS PET and rPET rigid packaging for food & beverage REGULATORY ColorMatrix Amosorb 4020R meets direct food contact regulatory requirements in major markets.

MEVOPUR COLORANTS • Standard colors in PP and PE to shorten time-to-market • Custom colors matched to Pantone, RAL or other color reference • White colorants for pharmaceutical packaging for LDPE, HDPE and PP with opacity to reach USP chapter MEVOPUR FUNCTIONAL ADDITIVES • Antistatic formulation with good flow/impact for injection molding • Amide- and amine-free antistatic for film in contact with API (Active Pharmaceutical Ingredients) • UV blocking for transparent PP and PE packaging to meet USP chapter • Non-migrating friction reduction/processing aid for PE and PP • Laser marking/welding additive for fast, reliable marking/assembly • MVTR (Moisture Vapor Transmission Rate) reduction for HDPE to improve shelf-life • Thermal protection of the polymer during processing • Gamma/e-beam sterilization protection for PP (up to 50kGy) with color compensation for reduced yellowing REGULATORY SUPPORT • Raw materials tested to: - ISO 10993-1 and USP biological evaluation - European Pharmacopeia 3.1.3/3.1.5 (polyolefin) - USP (polyethylene) - ICH Q3D elemental impurities • Registered Drug Master File (Type III) and/or Device Master File • Food contact established with FDA/EU* APPLICATION BULLETIN * FDA/EU compliance information available upon request Bormed™ is a registered trademark of Borealis Healthcare use limitations apply—see below.

KEY CHARACTERISTICS • Manufactured at four ISO 13485 certified sites, providing global consistency and increased security of supply • Documented change control beyond CAS number level, reducing risk of change • Non-phthalate and formulated without animal-derived substances • Different tones of amber available on request —more or less red or yellow and/or lighter or darker • Also available in liquid form REGULATORY SUPPORT • Pre-tested raw materials: - ISO 10993-1 and USP parts (Class VI) - European Pharmacopeia, monograph 3.1.15, USP and elemental analysis as per ICH Q3D - USP criteria appearance of solution, color • Registered Drug Master File (Type III) by the FDA • Food contact compliance established with FDA/EU* • YBB00102002-2015 (oral liquid pharmaceutical PET bottles) compliance support APPLICATION BULLETIN * FDA/EU compliance information available upon request Healthcare use limitations apply—see below.

KEY BENEFITS • Exceptional recyclability • Compatible with rPET (recommended for >25% rPET content) • Non-nylon based • No scavenging delay or deactivation • Flexibility to employ a wider span of LDR levels to reach long-term shelf life • Excellent bottle aesthetics even at higher LDR • Simple to use with existing mono-layer equipment • Suitable for use on multi-layer machines Copyright © 2025, Avient Corporation.