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Synthesis Analytics

About us

The peak you cannot explain is our starting point.

Synthesis Analytics is a research-driven chemistry company. We make the compounds that let analytical teams put a name to every peak in a chromatogram — and the documentation that lets them defend it.

Who we are

A chemistry company, not a catalogue reseller.

Impurity standards sit at an awkward point in pharmaceutical development. They are needed in milligram quantities, at high purity, with complete structural proof — and usually at short notice, because nobody plans for the peak that appears at month three of a stability study.

Synthesis Analytics exists for exactly that moment. We synthesise, isolate and characterise API impurities, degradation products, process intermediates and pharmacopoeial reference standards, and we supply them with the analytical package a filing actually needs: assigned potency, NMR, mass spectrometry, chromatographic purity and the method conditions behind each number.

Our catalogue currently runs to 912 compounds across 12 therapeutic areas — statins and sartans, macrolides and cephalosporins, gliflozins and gliptins, antipsychotics, antiretrovirals and the long tail of isomers, N-oxides and dimers that never make it onto a monograph but always make it onto a chromatogram.

Everything else is made to order. If the compound does not exist yet, our chemists will propose a route, tell you honestly what the risks are, and commit to a date before starting.

Our mission

To make well-characterised impurity standards ordinary rather than exceptional — available quickly, documented completely, and priced so that good analytical practice is never the expensive option.

Our vision

A reference library deep enough that no analytical chemist in the region has to abandon an investigation because the standard could not be sourced in time.

Gloved hands handling sample vials during preparation

“Give us the retention time, the mass and the conditions. That is usually enough to start proposing structures.”

— How most of our projects begin

Racks of capped sample tubes in a laboratory
Catalogued compounds
912+
Parent drug molecules
141+
Therapeutic areas
12
Years of combined experience
35+

How we work

Four things we refuse to compromise on.

Identity before quantity

A number on a certificate means nothing without the spectra that justify it. Structure comes first, potency second, paperwork third — in that order, every time.

Built for the auditor

We assume every batch we release will one day be defended in front of a regulator, and we prepare the documentation accordingly.

Dates we can keep

We would rather quote an honest twelve weeks than an optimistic six. A committed date is agreed before any chemistry starts.

Chemists answer the phone

Technical enquiries reach the people who ran the reaction, not a sales desk reading from a datasheet.

Capability

What sits behind the catalogue.

Synthesis, purification and characterisation under one roof, so a compound never has to leave the building between being made and being proven.

Synthetic chemistry

  • Multi-step organic synthesis
  • Air- and moisture-sensitive handling
  • Milligram to multi-gram scale
  • Route scouting and optimisation

Purification

  • Preparative HPLC
  • Column and flash chromatography
  • Recrystallisation and trituration
  • Chiral separation

Characterisation

  • NMR — ¹H, ¹³C and 2D
  • LC-MS and HRMS
  • HPLC / UPLC and GC
  • FT-IR and melting point

Documentation

  • Characterisation protocols
  • Certificates of Analysis
  • GHS-format safety data sheets
  • Regulatory query support
Rows of stoppered glass tubes under warm light

Next step

Can’t find the impurity you need?

Send us the compound name, the CAS number, or simply the chromatogram you are trying to explain. Our chemists will come back with availability, scale and a realistic timeline.