Inorganic Ventures will be closed Friday, June 19th for Juneteenth National Independence Day. We will resume normal business hours on Monday, June 22nd.

Precision in Every Dose: Certified Standards for Pharmaceutical Elemental Impurity Control

Expert ICP guidance for meeting USP and ICH elemental impurity requirements

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Achieving Accuracy in Mining: A Guide to Metals Testing

Learn to navigate real-world challenges of metals testing using ICP-OES and ICP-MS.

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Consult a Chemist

Our Technical Team is available to help with your lab challenges. Book a meeting to get started!

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Excelling with Standards

5-Year Shelf Life with Transpiration Control Technology (TCT)

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Leading in Learning

Hands-on Lab Training
Virtual ICP Academy
Educational Resources for Chemists

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Struggling with Ion Chromatography (IC) Challenges?

DISCOVER SOLUTIONS
AND RESOURCES!

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Wipe out sticky elements once and for all with ICP TRUE RINSE

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Introducing:
IV IGNITE
Inorganic Ventures’ new online learning platform.

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Effortless Savings.
Efficient Ordering.

With NEW Total Volume Pricing on Custom Standards.

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New Sample Preparation Guides

Samples Containing Antimony, Germanium and Phosphorous

By Dr. Paul Gaines

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New sample preparation guide

Raising Standards by Protecting Yours

Standards Protected Up to 5 Years

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6 Reasons to Stop Preparing Your Own Working Standards

And the formula for creating more bench space and less stress.

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Latest News & Events

Ensuring Accurate pH Measurements: Understanding and Achieving Compliance with USP ⟨791⟩

Introduction: Why pH Accuracy Matters in Pharmaceutical Development

The United States Pharmacopeial Convention (USP) is a nonprofit organization focused on building trust in the quality of medicines, dietary supplements, and foods worldwide. Among its many analytical standards, USP General Chapter ⟨791⟩ pH establishes the mandatory potentiometric method for measuring the pH of pharmaceutical articles, providing a standardized framework laboratories must follow to produce reliable and reproducible res

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USP ⟨541⟩ Titrimetry: Principles, Procedures, and Modernization of Compendial Titrimetric Analysis

Introduction: The Foundation of Quantitative Pharmaceutical Analysis

USP General Chapter ⟨541⟩ Titrimetry establishes the foundational principles and standardized procedures for titrimetric analyses used in compendial pharmaceutical testing. This chapter defines titrimetry as a quantitative analytical technique in which a standardized reagent, known as the titrant, reacts stoichiometrically with an analyte until a reliable endpoint is reached, detected either visually or instrumentally.

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