Mironova Labs

DMTMM for DEL / On-DNA Chemistry

Higher on-DNA conversion than HATU in published comparisons

For DEL chemists building DNA-encoded libraries with maximum building-block diversity

Supported by peer-reviewed research≥99% purity (HPLC)US-manufactured (Fairfield, NJ)Published DEL data (2024)Peer-reviewed evidence

Your Challenge. Our Answer.

We understand the specific problems you face — and we built solutions for each one.

The Problem

HATU delivers limited conversion with sterically hindered building blocks, restricting accessible chemical space in DEL libraries

Mironova’s Answer

DMTMM·PF₆ achieved higher on-DNA amidation conversion than HATU, especially with hindered partners (Hosozawa et al., 2024)

The Problem

Reagent stability in aqueous-organic DEL conditions is unpredictable, causing batch-to-batch variability in library quality

Mironova’s Answer

PF₆ counterion provides enhanced stability in polar aprotic solvents used in DEL workflows — predictable activation kinetics

The Problem

Building-block scope is limited by reagent compatibility, reducing the pharmacological diversity of screening libraries

Mironova’s Answer

Expanded scope for sterically demanding acids and amines means richer libraries and more diverse hit chemotypes

Published Evidence

Key findings from peer-reviewed literature relevant to your application.

Higher Conversion than HATU

DMTMM·PF₆ achieved higher on-DNA amidation conversion than HATU or DMTMM·Cl, particularly with sterically hindered building blocks.

Hosozawa et al., Bioorg. Med. Chem. Lett. 2024

Triazine Activation Mechanism

DMTMM forms a stable acyloxytriazine active ester that resists hydrolysis in aqueous-organic conditions typical of DEL synthesis.

Kunishima et al., Tetrahedron 1999

No Guanidinylation Side Products

Unlike uronium reagents, DMTMM cannot produce guanidino byproducts that contaminate DNA-conjugated intermediates.

Vrettos et al., RSC Advances 2017

On-DNA Amidation Conditions

  • Solvent: DMF/water mixtures or DMA/borate buffer
  • Equivalents: 20–50 eq in optimized protocols
  • Temperature: RT to 40 °C
  • Time: 2–16 h
  • Base: NMM or DIPEA

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Request DEL Evaluation Kit

Receive PF₆ samples with on-DNA protocol guidance and certificate of analysis. Typical lead time: 4 weeks.

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Related Resources

Technical data, product specifications, and application guidance.