REACH SVHC 2026: The Six Documents a Leather Supplier Must Show You
Nov 06 , 2026

Under REACH, an article may not contain a Candidate List substance above 0.1 % by weight. The Candidate List currently holds 253 entries (last updated 4 February 2026), and it changes twice a year. "REACH compliant" is therefore a statement about a list version, not a permanent property of a material — which is why the document set, not the certificate, is what survives an audit.

Every year we see the same sequence: a European buyer approves a supplier on a declaration issued two years earlier, the Candidate List is updated, and the material is suddenly non-compliant without a single change to the formula.Here is the document set that closes that gap.


Why synthetic leather is exposed

Microfiber leather is a composite: non-woven microfiber base, PU impregnation, top coat, sometimes a flame-retardant package and a colour layer. Each layer is a place where a restricted substance can enter.

Layer Likely substance group Why it is there
PU resin / coating Residual solvents (DMF, toluene), isocyanates, organotin catalysts Polymerisation and film formation
Plasticised layers Phthalates (DEHP, DBP, BBP, DINP, DIBP…) Softness, hand feel
Flame retardants Chlorinated paraffins (SCCP/MCCP), brominated compounds UN R118, EN 45545-2 compliance
Pigments / colour Azo dyes, lead and cadmium pigments, PAHs from carbon black Colour matching
Backing / finishing Formaldehyde-based crosslinkers, PFAS for water repellency Anti-wrinkle, water resistance

A material can pass every physical test and still fail on document review at one of these layers.


The six documents that actually matter

① Full material decomposition (layer by layer). Not "PU + microfiber". Each layer, each additive, each supplier of each additive. If a flame-retardant package is sub-contracted, its composition must be declared too. Without this, no lab can design the right test panel.

② SVHC screening report from an accredited laboratory. Method matters: GC-MS and LC-MS for organics, ICP-OES/ICP-MS for metals, ion chromatography for the inorganic salts. The report must list detection limits — a result of "not detected" with no stated limit is not evidence of anything.

③ The list version the report was tested against. A report tested against the 2024 list does not cover the 253 entries current since 4 February 2026. The correct wording is explicit: "screened against the Candidate List as updated on 4 February 2026 (253 entries)". This single sentence is the difference between a document and a defence.

④ A signed Declaration of Conformity referencing that same version. Signed, dated, on company letterhead, naming the product code and the batch range it covers. A generic PDF titled "REACH Certificate" is not a DoC.

⑤ Annex XVII compliance statement. Separate from SVHC. Annex XVII restricts substances outright — azo colourants, formaldehyde in textiles, certain phthalates, cadmium. A material can be SVHC-clean and still breach an Annex XVII limit.

⑥ SCIP notification reference (if you sell into the EU). Where an article contains a Candidate List substance above 0.1 % w/w, the EU supplier must submit it to ECHA's SCIP database. Ask for the SCIP number; if the supplier is outside the EU, your own notification obligation depends on your role in the chain.

For automotive interiors, add three more: VDA 270 (odour), VDA 278 (VOC/VOCct), and VDA 275 (formaldehyde release). These are not REACH obligations, but they are the tests that decide whether an OEM accepts the part.


Four red flags that predict a failed audit

Red flag 1 — "REACH compliant" with no list version. The phrase alone is meaningless. Ask which version, on what date, for which batch.

Red flag 2 — XRF screening presented as a full test. XRF is a fast screen for heavy metals only. It says nothing about phthalates, azo dyes or PFAS. A report that is 90 % XRF and 10 % conclusion has not tested the material.

Red flag 3 — no detection limits. "ND" is only meaningful next to a limit of detection. A limit of 1,000 ppm cannot support a 0.1 % claim in any useful way.

Red flag 4 — a declaration older than the latest Candidate List update. Since the list changes twice a year (typically January/February and June), a declaration over six months old is already stale by design.


PVC-free is a separate question from SVHC-free

These two get conflated constantly.

  • PVC-free means the polymer system contains no polyvinyl chloride — which removes the phthalate plasticiser package and the dioxin risk at end-of-life. It says nothing about other SVHCs.
  • SVHC-free means no Candidate List substance above 0.1 % w/w — which can be true of a PVC material and false of a "green" one.

A serious supplier states both, separately, with the test evidence for each. If a supplier answers "we are eco-friendly" to a REACH question, you have learned nothing.

Low-VOC: the requirement that arrives after REACH

For interior applications, compliance has moved from "no restricted substances" to "no emissions". Two different questions:

Question Test What it protects
Is a restricted substance present? SVHC screening, Annex XVII Market access, customs
Does the finished part emit? VDA 278 (VOC), VDA 270 (odour) Cabin air quality, OEM approval

A material can be fully SVHC-clean and still fail an interior odour panel — usually because of residual solvent in the PU or an amine-based catalyst. Water-based PU systems exist precisely to close that gap, at a higher unit cost.


The one-page checklist to send your supplier

  1. Layer-by-layer material decomposition
  2. Accredited-lab SVHC report with detection limits
  3. Explicit statement of the Candidate List version tested (253 entries, 4 Feb 2026)
  4. Signed DoC on letterhead, batch-referenced
  5. Annex XVII statement (azo, formaldehyde, phthalates, cadmium)
  6. SCIP reference where applicable
  7. For interiors: VDA 270 / 278 / 275 results
  8. Change-control commitment: any formulation change triggers a full re-test

If a supplier can return all eight within a week, you are dealing with a manufacturer. If they return two and a logo, you are dealing with a trader.


 If your current material fails the check

Discovery is usually late: the goods are made, the container is booked, and the lab report says one substance is over the line. There are three routes, in order of cost:

① Re-test before you panic. An exceedance in a screening test is not an exceedance in the article. Confirm with a quantitative method on the finished component, at the concentration it exists in the product — not on the raw resin. A plasticiser measured at 0.3 % in the resin may sit far below 0.1 % in the finished coated fabric once the resin is only part of the mass. Get the number right before making a decision.

② Change the layer, not the material. Most failures sit in one layer: the flame-retardant package, the pigment, or the plasticiser. A supplier who can substitute one additive and re-certify the full article keeps your physical properties intact; a supplier who asks you to change the whole material resets every other approval you hold.

③ Declare and continue, where the law allows. Above 0.1 % w/w, the obligation is information transfer, not prohibition — unless the substance is also restricted under Annex XVII. In that case there is no route: the material must change. Knowing which of the two situations you are in is the whole decision.

What you should not do is accept a supplier's reassurance without a batch-referenced report. The audit does not care about intent; it asks for a document.


Need the document set for a European submission? We issue batch-referenced SVHC reports, Annex XVII statements and VDA results with every eco-series order, and we will send the current pack with your samples.

Request the compliance pack and samples →

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