10⁶⁰

Now in design-partner pilots · Battery, polymer, pharma

SOLVOLYTE

From years of bench screening to a shortlist in weeks. Physics-constrained AI for the chemistry of liquid mixtures.

100k

training datapoints

0.83

R² out-of-distribution

10⁵

Na-ion screened

Trusted in pilots by

Battery cell manufacturerTier-1 OEM, Asia · Under NDA
Polymer R&D groupSpecialty chemicals, EU · Under NDA
National labEnergy storage division, US · Under NDA
Academic groupTop-10 chemistry program, US · Under NDA
What changes

Two years of screening, in a sprint.

01 · Today

12–24 months on the bench.

A new electrolyte program runs months of formulation, cell builds, and cycling. Most candidates fail by week 6.

02 · With Solvolyte

A ranked shortlist in weeks.

We take your target chemistry, screen 10⁵ candidates against ionic conductivity, viscosity, and electrochemical stability — return the top 50 with confidence intervals.

03 · Why it works

3D physics, not 2D fingerprints.

Mixtures aren't the sum of their parts. Our Set-SE(3) equivariant model learns shape-aware solvation — the part 2D GNNs throw away.

Where it ships

Industries we're building for.

Energy storage

Batteries.

10⁶⁰ candidate mixtures. Most are dead. The sweet spot is rare. We find it before the bench does.

Drag to rotate
Loop time
Bench
~6 wks
per cycle
GeoSolv
0 s
per inference
Throughput0 / hr
Polymer engineering

Polymer blends.

Tg, miscibility and modulus are exquisitely sensitive to composition and processing. Blind blend screens cost months on the rheometer.

  • Phase behavior depends on chain conformations, not just monomers
  • Industrial blend datasets are sparse and proprietary
  • Failure mode: phase separation, brittleness, processing window
  • → PolySolv learns conformer-ensemble representations, fine-tuned on your in-house blend data
↑ TEMPERATURE
COMPOSITION φ →
MisciblePhase-separated
PHASE LANDSCAPE
Pharma & formulation

Drug delivery.

The same API can be inert or therapeutic depending on the co-solvent matrix. Solubility and crystallization are entangled and hard to optimize.

  • Co-solvent ratios shift solubility curves non-monotonically
  • Crystalline polymorphs threaten shelf life
  • Excipient screening is high-dimensional and bench-bound
  • → PharmaSolv predicts non-monotonic solubility curves and ranks polymorph stability before bench
↑ CO-SOLVENT B
CO-SOLVENT A →
Height = log S
SOLUBILITY TOPOGRAPHY
How a pilot runs

Eight weeks. Fixed scope.

We engage as a paid 8-week design partnership. You bring the chemistry; we return a ranked, physics-validated shortlist plus the fine-tuned model head. IP on derived predictions stays with you.

  1. Week 0

    Scoping call.

    30 minutes. We confirm fit, target property, and what data you can share.

  2. Week 1–2

    Data ingest + baseline.

    Your private dataset lands in an isolated namespace. We fit a baseline head and report held-out R² on your data.

  3. Week 3–6

    Domain-tuned screen.

    We screen 10⁵ candidates with the tuned model and rank by your composite objective.

  4. Week 7–8

    Validated shortlist.

    Top 50 with confidence intervals, MD-grounded sanity checks, and synthesis notes for each candidate.

Get started

Into your screening loop.