Modules · not projects

Synthesis, assembled from modules.

Preclinical peptides, oligonucleotides, silicones, degraders and conjugates — specified like a plan, delivered like a part. You define the target, the scale, and the difficulty; we build the module.

Assemble a request.

This is how you work with us: build a request like blocks. Pick a capability, a target, a scale, a difficulty tier — and watch the specification, literature precedent, and an indicative price and lead time assemble in real time. Stack several targets into a list and submit them together.

Modules

Assembly

Start with a capability
Specification builds as you assemble
Can't find your target molecule in the modules above? Draw your own structure →

Precedent

Choose a target to see literature precedent.

Literature landscape

via Crossref · broad keyword match, not synthesis-specific

Indicative estimate

optional — refines the estimate
Select a capability, tier and scale.
Placeholder values · non-binding · replace with your economics

Modular by design.

The whole program is built the way the request is — from modules. Make the molecule, prove what you made, and move it downstream when it advances. Step by step, type by type: priced per synthetic step, scoped by capability type and difficulty tier. Take one module on its own, or stack them.

Synthesis

Make the molecule. Nine capability lines, priced by the step and scoped by difficulty tier — a single target or a whole library.

9 lines · step-based · tier A–C

Analysis

Prove what you made. Purity, identity, and full characterization with a certificate of analysis — bolted onto any synthesis, or run on its own.

HPLC · MS · NMR · COA

Downstream

When it advances. Scale-up and a clean handoff into partner development and GMP manufacturing — the same molecule, one step further.

scale-up · GMP handoff

Take any module on its own — but a program is only whole when all three are in place.

Every module, its specialist.

Modular work has a quiet advantage: each module goes to the person who does it best. A silicone-systems specialist, a metal-catalysis chemist, a purification lead — matched to the part they own, not one generalist stretched across all of it. Best part, best hands.

Silicone systems

Vinyl & crosslinker systems, cure chemistry, functional PDMS.

Metal catalysis

Pd / Ni cross-couplings, hydrogenation, C–H functionalization.

Macrocyclization

Ring-closure screening, stapling, the cyclizations others avoid.

Modified oligonucleotides

Phosphorothioate, modified bases & sugars, conjugation handles.

Conjugation chemistry

PDC / POC, GalNAc, ADC linker-payload, click handles.

Purification & isolation

Prep-HPLC, chiral separation, difficult isolations.

Route design

Retrosynthesis, feasibility, starting-material sourcing.

Scale-up & handoff

Gram-to-preclinical scale, clean handoff to development.

Priced by the step, not the mole.

Every route is a stack of synthetic steps. Each step gets a difficulty tier, and the tier sets its per-step rate. Your quote is the sum of the steps — so a long route of routine steps can cost less than a short route of hard ones.

A Routine step

Precedented transformation; conditions transfer directly. Fixed rate per step.

B Screening step

Selectivity or functional-group conflicts; needs a condition / ligand screen. Rate plus screening.

C Development step

No precedent, or purification is the bottleneck. Milestone-based, quoted case by case.

steps × per-step rate (by tier) × scale → estimate. Try a live estimate in the configurator →

Our lines, one bench.

Each line is deep by design. We work at research and preclinical scale — the range where speed, judgement, and clean characterization matter more than plant capacity.

ASHLAR

Products.

The catalog — nucleosides & nucleotides, oligonucleotides, protected nucleosides, and peptide APIs — from stock or made to order. Browse the full catalog →

Analytical & characterization.

The analysis module. Every deliverable ships with data — standard methods for this work, trimmed to what you actually run.

Purity & identity

  • HPLC / UPLC purity
  • LC-MS, high-res MS
  • UV / concentration

Peptides

  • MS/MS sequencing
  • Amino acid analysis
  • Chiral / enantiomeric analysis

Oligonucleotides

  • ESI LC-MS, intact mass
  • IEX / RP purity
  • UV quantitation

Structure

  • ¹H / ¹³C NMR
  • 2D-NMR
  • IR / UV

Content & impurities

  • Residual solvents (GC)
  • Water (Karl Fischer)
  • Counterion / salt content

Documentation

  • Certificate of Analysis
  • Full data package
  • Method summary

Selected work.

A few representative problems — including targets other suppliers had turned down. Illustrative placeholders; replace with your real projects.

Peptide

A macrocycle others declined

A 14-residue head-to-tail macrocycle with two non-natural residues. We screened closure conditions and delivered on the second attempt.

Tier B · 2 g · >95% purity
Oligonucleotide

Modified backbone with a click handle

A phosphorothioate sequence carrying a non-standard base and a terminal azide for downstream conjugation.

Tier B→C · milestone delivery
Molecular & route design

A target with no route

The client had a structure in mind but no way to make it. We designed a 4-step sequence, confirmed feasibility and starting-material availability, then ran it.

Route + feasibility → synthesis

Have a target but no route? We can design it →

Why Ashlar.

Not the biggest bench — the one you call for the targets that are hard to make and easy to get wrong.

Deep, not broad

We take the hard end of each line — macrocycles, modified oligos, difficult conjugates — the work most catalogs decline.

Judgement is the product

A shop can run the reaction. We tell you whether your step is routine or a development problem — before you commit.

Built for preclinical speed

Research and preclinical scale, where flexibility and turnaround matter more than plant capacity.

Bilingual, compliance-handled

A clear interface for Western and Chinese partners, with export classification and dangerous-goods handling built into delivery.

Need GMP production? Talk with our teams →

Ways to work with us.

Match the engagement to the program.

Per project

Defined target, defined scope, fixed quote. Best for one-off molecules and building blocks.

Fee-for-service

Dedicated FTE

A chemist reserved for your program, billed by the month. Best for ongoing or multi-target work.

Full-time equivalent

Library / analogs

A batch of related analogs run together — one scope, shared method development, lower cost per compound.

Batch pricing

How it works.

From first message to material in hand — a short, predictable path.

1

Send your request

Target, scale, and timeline — or a structure you drew. Attach sequences, structures, or specs.

Any time
2

Tier assessment & quote

We classify each step's difficulty, confirm feasibility, and send a quote with scope and timeline.

~1 working day
3

Agreement & PO

Scope, price, and timeline confirmed. NDA in place first if you need one.

Your pace
4

Synthesis & analytics

We make it and characterize it. You get progress updates on longer routes.

Per quote
5

Delivery

Material plus its data package, shipped with export and DG handling. Support continues after.

Per quote

Questions.

The things people ask before the first project. Replace or extend with your own.

What scale do you work at?

Milligram to kilogram. Our focus is the research and preclinical range; kilogram requests are quoted separately.

Is this GMP?

No. Everything here is research-use and preclinical, made non-GMP. If you need GMP production, tell us — we can point you to the right team.

How does pricing work?

By the step. Each synthetic step carries a difficulty tier that sets its rate; your quote is the sum of the steps, adjusted for scale. Development-stage steps and kilogram scale are quoted case by case.

How fast will I get a quote?

Typically within one working day of receiving a defined target and scale.

Can you take a target other suppliers declined?

Often, yes — the hard end of each line is where we focus. Send the structure and we'll give an honest read on feasibility.

What if I have a target but no route?

We design the route and confirm feasibility before committing to synthesis. Share the structure and what you know about it.

How do you handle confidentiality?

We'll sign an NDA before you share sensitive structures. Your targets, sequences, and data remain yours.

Who owns the intellectual property?

You do. Any IP generated for your project — routes, methods, and results — belongs to the customer, as set out in your agreement. We don't retain rights to your molecules or data.

Do you ship internationally?

Yes, with export classification and dangerous-goods handling managed as part of delivery.

Start a conversation.

Send the module you built, or just describe what you need. We reply with a tier assessment and a quote — typically within one working day. Or email us directly at info@ashlar-chem.com.

Or email us directly at info@ashlar-chem.com