Digital Product Passport for chemical products: deadlines, requirements and preparation
15/02/2026 | By Ivan Milenković
The European Union has adopted a new regulation that changes the rules of the game.
The Digital Product Passport (DPP) is becoming mandatory for all products on the EU market – including chemicals.
Many domestic companies are not aware of all the requirements and obligations related to the DPP. And the compliance deadline is 2028-2030.
In this article you will learn:
- What the “Digital Product Passport” is and how it works
- Specific deadlines for the chemical industry
- Which data you already have (80% in the SDS!)
- How to prepare in 5 steps
What is the Digital Product Passport?
The DPP is a set of structured digital data about a product – from composition and safety to environmental characteristics.
That data is accessed via a QR code (or an NFC tag) on the product label.
You scan the QR code → you get the data relevant to you:
If you are a consumer:
- Basic safety information
- Hazard pictograms
- How to dispose of the product
If you are a B2B customer:
- The complete SDS
- REACH registration number
- Transport documentation
- Certificate of analysis
If you are a regulator:
- The full compliance dossier
- Change history (audit trail)
- Supply chain transparency
The key point: One QR code, different content for different users.
This is possible through “resolver” logic – the system detects who is scanning and shows the appropriate data.
Why does the DPP matter? (And why now?)
The EU adopted the ESPR Regulation (EU 2024/1781) in July 2024.
The goal: a circular economy – products must be designed for:
- Longer use (durability)
- Easier repair (reparability)
- Better recycling (recyclability)
The DPP is the tool for this – it provides transparency on materials, composition and carbon footprint.
Without a DPP = you will not be able to sell the product on the EU market. Simple as that.
Deadlines: when does the DPP become mandatory?
The ESPR is in force. Implementation is phased – different products get different deadlines.
Confirmed dates:
📅 February 2027 – DPP MANDATORY for batteries
- EV batteries
- Industrial batteries >2kWh
- Light means of transport batteries
📅 2027-2028 – Priority products
- Textiles
- Detergents
- Construction materials
- Furniture and mattresses
Why are chemicals later?
The European Commission postponed chemicals because of:
- Overlap with REACH/CLP (avoiding duplication)
- Trade secrets (protecting competitive formulations)
- A lack of sustainability standards
Projection for chemicals:
📅 End of 2025 – EU study (which chemicals come under the DPP)
📅 2027-2028 – Delegated acts for paints, lubricants, chemicals
📅 2029-2030 – Compliance deadline (12-18 months after the act)
This means: you have 24-36 months to prepare.
The question is not “whether” – but “how and when”.
You already HAVE 80% of the data (in the SDS!)
The good news: you already have most of the data for the DPP in the SDS.
What exists in the SDS:
✅ Product identification (Section 1)
✅ Hazard identification (Section 2)
✅ Composition/information on ingredients (Section 3)
✅ First aid measures (Section 4)
✅ Handling and storage (Section 7)
✅ Exposure controls/personal protection (Section 8)
✅ Ecotoxicological information (Section 12)
✅ Disposal (Section 13)
✅ Transport information (Section 14)
What is NEW for the DPP:
❌ Carbon footprint – kg CO₂ per kg of product
❌ Recycled content – % of recycled materials
❌ Water footprint – m³ of water per kg
❌ Packaging recyclability – whether it can be recycled
❌ Production location – where it is produced
❌ Batch traceability – from raw material to product
The gap = 20% – but it can be filled step by step.
Sources for this data:
- Carbon footprint → LCA study or the TfS PCF guideline
- Recycled content → Supplier declarations
- Production location → Company data
Substances of Concern – a broader definition
The DPP requires information on Substances of Concern (SoC).
This is not just the SVHC list from REACH – it covers more:
What counts as SoC:
CMR substances (carcinogenic, mutagenic and toxic to reproduction)
- Categories 1A/1B
- Threshold ≥0.1% w/w
PBT/vPvB (Persistent, Bioaccumulative, Toxic)
- Do not degrade in nature
- Accumulate in organisms
Endocrine disruptors (ED)
- New CLP hazard classes
- Affect the hormonal system
Respiratory/skin sensitisation
- Categories 1, 1A, 1B
- Relevant for worker protection
The key difference: impact on recycling
The DPP does not only ask “is it dangerous to people” but also “does it hinder recycling?”.
Example: Brominated flame retardants may not be CMR, but they prevent plastic recycling.
The DPP must flag this as “incompatible with recycling”.
That is why DPP = a tool for the circular economy, not only for safety.
The technology behind the DPP
The DPP uses the GS1 Digital Link standard – the same system as barcodes in supermarkets.
How it works:
- You get a GTIN (Global Trade Item Number) – a unique product number
- You generate a QR code that contains the GTIN + a link to the data
- Whoever scans the QR – gets data tailored to them
In practice:
- QR code on the label
- Behind the QR – all the data (SDS, PCF, instructions)
- A different view for the consumer, B2B and the regulator
We will leave the details of the GS1 technical implementation for the next blog post.
What the industry is asking of the EU
In December 2025, the chemical industry (Cefic + FECC) organised a workshop and published recommendations.
Top 3 requests:
1. Realistic preparation time
- 18-24 months after the delegated act
- Gradual implementation (not all at once)
- Additional time for small and medium-sized enterprises (+6-12 months)
2. Tools adapted to small businesses
- Simple interfaces
- Template-based systems
- Affordable SaaS models (not €50K+ software)
3. Smart verification
- Checking the methodology (HOW the data was obtained)
- Sample checks (not 100% coverage)
- Self-declaration + on-site checks
The industry’s message: “Gradual implementation – NOT a ‘big bang’ that chokes small and medium-sized enterprises.”
How to prepare: 5 steps
Don’t wait for the delegated act. The infrastructure is being built NOW.
STEP 1: Data check (1 month)
Map what you have:
- ✅ SDS for all products?
- ✅ REACH registrations up to date?
- ❌ Carbon footprint data?
- ❌ Recycled content %?
Make a list of gaps – that is your roadmap.
STEP 2: Pilot project (2-3 months)
Choose 2-3 products:
- A simple product (one substance)
- A complex mixture (10+ substances)
- A hazardous product (CMR or SVHC)
Create a DPP manually (Excel/Word).
Goal: Understand the process before automating it.
STEP 3: Supplier engagement (ongoing)
Ask your suppliers for:
- Substance composition (CAS numbers, %)
- Carbon footprint (PCF) – if they have it
- Recycled content %
- Certificates (ISO 14001)
Reality: 80% will not have a PCF.
That is OK – document what you have requested. Regulators look for “demonstrated good faith”.
STEP 4: Choosing the technology (3-6 months)
Three options:
A) Manual (Excel + QR generator)
- Free
- Slow, error-prone
- OK for <20 products
B) SaaS platform (€100-400/month)
- Automatic SDS → DPP mapping
- QR code generation
- Version control
- OK for small and medium-sized enterprises (20-500 products)
C) Enterprise software (€50K+ licence)
- Full ERP integration
- Multi-site implementation
- For 1000+ products
Advice for small businesses: Start with B (SaaS).
STEP 5: Monitoring the regulations (ongoing)
Stay up to date:
- ECHA newsletter (sign up at echa.europa.eu)
- EU Official Journal (weekly checks)
- Industry events (Cefic, associations)
Key date: End of 2025 – the EU study on chemicals.
Once the delegated act is published (2027?) → you have 12-18 months.
But preparation starts today.
Conclusion: first or last-minute?
The Digital Product Passport is coming. The question is not IF – but WHEN.
Summary:
- ✅ ESPR adopted (July 2024)
- ✅ Battery passport mandatory (Feb 2027)
- ✅ Chemicals on the list (2028-2030)
- ✅ 80% of the data in the SDS
- ⚠️ 20% new (sustainability)
Two scenarios:
Scenario A – Early adopter:
- Preparation in 2026-2027
- Ready 12-18 months BEFORE the deadline
- Advantages: Competitive edge, smooth implementation, no panic
Scenario B – Last minute:
- Waiting for the delegated act
- Implementing a system 6 months before the deadline
- Advantages: None
The choice is yours.
Next steps
- Data check – SDS → DPP mapping (1 week)
- Pilot – 2-3 products manually (1 month)
- Suppliers – request PCF data (now)
- Technology – Research SaaS platforms (1-2 months)
- Monitoring – ECHA newsletter (ongoing)
The compliance deadline is coming faster than you think.
Start today.
Follow the series
This is the introductory post. Upcoming topics:
- GS1 Digital Link – a step-by-step technical guide
- A Substances of Concern checklist for your products
- Carbon footprint – practical examples
- Collecting data from suppliers – templates
Follow the blog or sign up for the newsletter.
Have questions?
Contact us for a free consultation.
We will analyse your products and give recommendations for DPP preparation.
References:
This blog post is for informational purposes only and does not constitute legal advice. For specific situations, consult a licensed chemical adviser or a lawyer specialising in chemical regulation.
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