EU TaxonomyDNSH Appendix CChemicals

EU Taxonomy DNSH Appendix C

Use this page to turn Appendix C chemicals restrictions into a narrow, source-linked EU Taxonomy evidence check.

It focuses on what Appendix C actually requires: activity-specific screening, restricted substances, alternatives, controlled conditions, and documented conclusions.

Author
Sorena AI
Published
May 9, 2026
Updated
May 9, 2026
Sections
5

Structured answer sets in this page tree.

Primary sources
3

Cited legal and guidance references.

Publication metadata
Sorena AI
Published May 9, 2026
Updated May 9, 2026
Overview

DNSH Appendix C is the EU Taxonomy generic DNSH criterion for pollution prevention and control regarding the use and presence of chemicals in activities where the delegated acts point to that appendix. Treat it as an evidence test for the specific activity and product or output, not as a general sustainability policy statement.

Section 1

What does DNSH Appendix C cover?

Appendix C applies only when the relevant EU Taxonomy technical screening criteria for an activity require compliance with Appendix C. The first step is therefore to identify the activity, the applicable delegated-act section, and whether the pollution-prevention DNSH row points to Appendix C.

Where it applies, Appendix C addresses chemicals in substances, mixtures, articles, final products, outputs, manufacturing, placing on the market, use, and presence. The 2023 amendment replaced the earlier essential-use framing with a test based on documented lack of suitable alternatives and use under controlled conditions.

  • Confirm that the activity is covered by EU Taxonomy technical screening criteria before using Appendix C.
  • Check whether the activity's pollution-prevention DNSH criterion expressly requires Appendix C compliance.
  • Define the assessed object: substance, mixture, article, final product, output, manufacturing step, market placement, or use case.
  • Record the exact delegated-act section, Appendix C point, concentration threshold, and exception logic used in the conclusion.
Section 2

What is the Appendix C substance test?

For substances meeting the Article 57 criteria of REACH and identified under Article 59(1), Appendix C point (f) uses a concentration above 0.1% weight by weight and requires an assessment and documentation where an operator relies on the exception.

The added paragraph after point (f) extends the same 0.1% weight-by-weight concentration framing to other substances that meet specified CLP hazard classes or categories linked to Article 57 of REACH. In both cases, the exception depends on documenting that no suitable alternative substances or technologies are available on the market and that the substances are used under controlled conditions.

  • Screen for substances above 0.1% weight by weight in the relevant substance, mixture, article, final product, or output.
  • Separate the REACH Article 57 and Article 59(1) SVHC assessment from the additional CLP hazard-class assessment.
  • If relying on an exception, keep evidence for both limbs: no suitable alternatives on the market and controlled conditions.
  • Do not describe an activity as Taxonomy-aligned until the Appendix C conclusion is tied back to the full activity-level alignment assessment.
Section 3

Which evidence makes an Appendix C conclusion reviewable?

A defensible Appendix C file should let a reviewer trace the conclusion from the activity and delegated-act section to the chemical inventory, concentration screen, hazard classification, alternatives assessment, controlled-conditions evidence, and final approval.

The Taxonomy Regulation requires undertakings in scope of Article 8 disclosure to report how and to what extent their activities are associated with environmentally sustainable activities. Appendix C evidence should therefore be maintained in a form that supports the broader Taxonomy-alignment and KPI process, without turning an Appendix C page into a KPI calculator.

  • Activity mapping and delegated-act section that triggered Appendix C.
  • Bill of materials, supplier declarations, safety data sheets, or equivalent chemical inventory used for the assessment.
  • Substance classification record showing the REACH Article 57 and Article 59(1) or relevant CLP basis checked.
  • Concentration evidence for the 0.1% weight-by-weight threshold where that threshold is relevant.
  • Alternatives assessment and controlled-conditions evidence for any exception relied on.
  • Approval record that states whether Appendix C is passed, failed, not applicable, or unresolved pending supplier evidence.
Recommended next step

Turn Appendix C into an evidence record

Use this guide to connect the delegated-act trigger, chemical evidence, alternatives assessment, controlled conditions, and approval record before making an EU Taxonomy alignment claim.

Section 4

Where do teams usually overstate Appendix C?

The most common overstatement is treating Appendix C as a pass/fail label for the whole company. It is narrower than that: the check belongs to a specific Taxonomy activity and to the substances, mixtures, articles, final products, outputs, market placement, or use covered by the applicable criterion.

Another risk is citing the old essential-use concept without explaining the 2023 amendment. The captured source says that, pending further guidance on horizontal principles for essential use of chemicals, the concept was replaced with criteria intended to be easier to verify: no suitable alternatives on the market and controlled conditions.

  • Do not apply Appendix C to activities whose technical screening criteria do not point to Appendix C.
  • Do not claim alignment from eligibility alone; Appendix C is only one part of the broader alignment chain.
  • Do not publish an exception unless the alternatives assessment and controlled-conditions evidence are both documented.
  • Do not use an Appendix C conclusion from one product, supplier, or activity as evidence for another without checking the actual substances and threshold.
Section 5

What should teams do next?

Create an Appendix C decision record for each activity where the delegated act requires it. Keep the record narrow enough that it can be reviewed: activity, section, assessed item, substances checked, threshold result, exception evidence, owner, approval, and unresolved evidence requests.

If supplier or product evidence is incomplete, mark the Appendix C conclusion as unresolved rather than substituting a policy statement. A narrow unresolved status is more useful than a broad unsupported alignment claim.

  • Name the Taxonomy activity and the delegated-act section before requesting chemical evidence.
  • Ask suppliers for evidence that supports the specific Appendix C threshold and classification questions.
  • Keep exception evidence separate from ordinary screening evidence so reviewers can see why it was used.
  • Review Appendix C records when substance classifications, supplier inputs, product composition, or delegated-act text changes.
Primary sources

References and citations

eur-lex.europa.eu
Referenced sections
  • Official Appendix C amendment source used to define the evidence fields for alternatives and controlled conditions.
"used under controlled conditions"
finance.ec.europa.eu
Referenced sections
  • Commission source describing technical clarifications for generic DNSH criteria and related reporting obligations.
"technical clarifications on the application of the EU taxonomy"
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