DMTMM
DMTMM (CAS No.: 3945-69-5) is a widely utilized coupling reagent in biochemical and biomaterials research, characterized by its ability to efficiently activate carboxyl groups and facilitate amide bond formation under mild aqueous conditions. As a synthetic small-molecule reagent, it is primarily employed in organic and bioorganic chemistry workflows to enable the conjugation and modification of biomacromolecules, including proteins, peptides, and polysaccharides, thereby supporting studies in bioconjugation, polymer functionalization, and macromolecular engineering. Mechanistically, DMTMM promotes the formation of reactive intermediates that enhance nucleophilic substitution by amines, allowing for selective and high-yield coupling reactions with reduced side-product formation compared to traditional carbodiimide-based systems. Although not associated with a specific biological target or signaling pathway, its functional role in modifying biomolecular structures makes it an important tool in the preparation of functionalized materials for applications such as tissue engineering scaffolds, hydrogel systems, and surface immobilization strategies. In vitro applications commonly involve its use in buffer systems compatible with biological macromolecules, with effective concentrations typically optimized within low millimolar ranges depending on substrate reactivity and experimental design. DMTMM is therefore a valuable reagent in life sciences research and early-stage drug discovery workflows, particularly in the development of biomaterials, conjugated therapeutics research tools, and chemically modified biological systems for mechanistic and screening studies.
| Physical Appearance | A solid |
| Storage | 4°C, sealed storage, away from moisture |
| M.Wt | 276.72 |
| Cas No. | 3945-69-5 |
| Formula | C10H17ClN4O3 |
| Synonyms | DMTMM, 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride |
| Solubility | ≥12.08 mg/mL in DMSO; ≥46.7 mg/mL in EtOH; ≥49.9 mg/mL in H2O |
| Chemical Name | 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium chloride |
| Canonical SMILES | COC1=NC(OC)=NC([N+]2(C)CCOCC2)=N1.[Cl-] |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |







