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TriLink BioTechnologies

mRNA capping, oligonucleotide, and nucleotide CDMO with proprietary CleanCap® technology.

TriLink manufactures mRNA, oligonucleotides, and modified nucleotides with proprietary CleanCap® capping technology achieving >95% Cap1 efficiency, supported by in-house analytical method development and a 118,000 sq ft GMP-capable facility.

Modalities

Development & manufacturing

Structured CDMO capabilities from verified public sources.

Manufacturing (M)

Biologics / bioreactor infrastructure

Expression systems
Cell-Free

Synthetic chemistry infrastructure

Max chemical scale
Pilot (10 kg – 100 kg)

Regulatory clearances

Services

About this organization

TriLink BioTechnologies is a specialized CDMO focused on nucleic acid manufacturing and mRNA technologies. The company offers:

mRNA Manufacturing & Capping:

  • Proprietary CleanScript™ in vitro transcription method optimized to reduce dsRNA
  • CleanCap® one-pot capping solutions generating Cap1 structure with >95% efficiency
  • mRNA synthesis scales from milligram to multi-gram quantities
  • Construct lengths from hundreds of nucleotides to over 14 kilobases

Oligonucleotide Synthesis:

  • DNA and RNA oligonucleotides at scales up to multiple grams
  • Specialized synthesis of challenging constructs including gRNA, siRNA, microRNA, and aptamers
  • Extensive modification options: backbone modifications, dye labels, biotin conjugation, linkers, and spacers
  • Industry-leading quality control via PAGE, HPLC, and MS

Custom Nucleotides:

  • Synthesis of ultrapure novel nucleotides and modified amidites
  • Over 150 modified nucleoside triphosphates (NTPs) in portfolio
  • Custom chemistry from discovery phase through multi-kilogram scale-up
  • Specialty modified nucleotides including 5'-3' bisphosphates, monophosphates, and alpha-thiol NTPs

Analytical & QC Services:

  • In-house method development and analytical testing capabilities
  • Identity, characterization, purity, and impurity analysis
  • Safety testing including contaminating nuclease detection for GMP products
  • Construct-specific assays and QC support across all product lines

Infrastructure:

  • 118,000 sq ft facility with multiple specialized manufacturing suites and support labs
  • Scalable processes designed to maintain timelines and accommodate demand surges
  • GMP-grade manufacturing capabilities

Locations

  • Headquarters

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