io.github.JonasRackl/labmate-mcp
81 chemistry tools — literature, calculations, retrosynthesis
Open source Open in the app JSON README (API)
About
81 chemistry tools — literature, calculations, retrosynthesis
Details
- Kind
- MCP servers
- Topic
- No topic detected
- Publisher
- jonasrackl
- Origin
- official
- Category
- ferramentas
- Transport
- local
- Version
- 7.3.1
- Stars
- 2
- Last push
- 2026-02-03T07:25:24Z
- Repository state
- ativo
- Language
- Python
- License
- MIT
- Added
- 2026-08-29 03:01:59
- Updated
- 2026-08-29 03:01:59
- Origin id
io.github.JonasRackl/labmate-mcp
README
<div align="center">
<br>
# 🧪 labmate-mcp
**Your AI lab companion — from literature search to benchwork to publication.**
<br>
[](https://pypi.org/project/labmate-mcp/)
[](https://pypi.org/project/labmate-mcp/)
[](https://python.org)
[](LICENSE)
<br>
**81 tools** · **25+ scientific APIs** · **202 named reactions** · **zero config required**
<br>
[**Quick Start ↓**](#-quick-start) • [What Can I Do?](#-what-can-i-do-with-this) • [All 81 Tools](#-tool-reference) • [Configuration](#%EF%B8%8F-configuration) • [Examples](#-examples)
<br>
</div>
---
labmate-mcp is an [MCP server](https://modelcontextprotocol.io) that connects Claude to scientific databases, computational chemistry tools, bench references, and writing utilities. **One install covers the entire research workflow.**
<div align="center">
<br>
<table>
<tr>
<td align="center" width="20%"><b>📚 Literature</b><br>15 tools</td>
<td align="center" width="20%"><b>⚗️ Synthesis</b><br>11 tools</td>
<td align="center" width="20%"><b>🧪 Bench</b><br>30 tools</td>
<td align="center" width="20%"><b>📊 Analysis</b><br>15 tools</td>
<td align="center" width="20%"><b>✍️ Publication</b><br>10 tools</td>
</tr>
<tr>
<td align="center">Search papers<br>Citation graphs<br>Author profiles<br>Preprints<br>Open access PDFs</td>
<td align="center">Retrosynthesis<br>Forward prediction<br>Atom mapping<br>pKa / ADMET<br>NMR prediction</td>
<td align="center">Named reactions<br>Reagent calculator<br>Protecting groups<br>Solvent reference<br>Rxn dev checklist</td>
<td align="center">Isotope patterns<br>Mass spectra<br>Binding data<br>Crystal structures<br>Safety data</td>
<td align="center">Format citations<br>Build bibliography<br>Experimental templates<br>Journal guides<br>SI checklist</td>
</tr>
</table>
<br>
</div>
## 🚀 Quick Start
```bash
pip install labmate-mcp
```
Then add this to your Claude config:
<details>
<summary><b>Claude Desktop</b> → <code>claude_desktop_config.json</code></summary>
<br>
On macOS: `~/Library/Application Support/Claude/claude_desktop_config.json`
On Windows: `%APPDATA%\Claude\claude_desktop_config.json`
```json
{
"mcpServers": {
"labmate": {
"command": "labmate-mcp"
}
}
}
```
</details>
<details>
<summary><b>Claude Code</b> → <code>.mcp.json</code> in your project root</summary>
<br>
```json
{
"mcpServers": {
"labmate": {
"command": "labmate-mcp"
}
}
}
```
</details>
<details>
<summary><b>Docker</b></summary>
<br>
```bash
docker build -t labmate-mcp .
docker run -it labmate-mcp
```
</details>
<br>
Restart Claude. **61 of 81 tools work out of the box** — no API keys needed.
> [!TIP]
> Want retrosynthesis, pKa prediction, or NMR shifts? Run `labmate-mcp --setup` to add free API keys.
---
## 💬 What Can I Do With This?
Just talk to Claude naturally:
<table>
<tr><td>
> **"Find the most cited papers on copper-catalyzed C–H activation from the last 5 years"**
Searches across multiple databases, ranks by citations, and gives you abstracts and AI-generated summaries.
</td></tr>
<tr><td>
> **"Suzuki coupling, 150 mg aryl bromide (MW 261), 5 mol% Pd(PPh₃)₄, 1.3 eq boronic acid, 2.5 eq K₂CO₃ — how much of everything?"**
Calculates exact masses for each reagent with your substrate as the limiting reagent.
</td></tr>
<tr><td>
> **"I'm developing a new reaction. What should I be thinking about?"**
Walks you through a structured [reaction development checklist](https://doi.org/10.1039/D4CS01046A) — covering everything from initial mechanistic hypotheses to scope exploration and scale-up.
</td></tr>
<tr><td>
> **"I need to protect a primary amine — stable to acid, cleavable by hydrogenation"**
Compares protecting groups against a stability matrix and suggests the best match (here: Cbz).
</td></tr>
<tr><td>
> **"Format these DOIs as an ACS bibliography, then give me an experimental template for a Buchwald–Hartwig"**
Generates a numbered reference list and a fill-in-the-blank procedure with suggested workup and safety notes.
</td></tr>
</table>
<details>
<summary><b>More things you can ask</b></summary>
<br>
| Ask Claude… | What happens |
|:---|:---|
| "What are the NMR solvent peaks for DMSO-d₆?" | Residual ¹H: 2.50 ppm (quintet), ¹³C: 39.52 ppm, water: 3.33 ppm |
| "Generate 20 cyclic pentapeptides with some D-amino acids" | Returns SMILES with MW, logP, and TPSA for each |
| "I want to submit to JACS — what do I need to know?" | Word limits, abstract length, citation format, graphical abstract specs |
| "Retrosynthesis of ibuprofen" | Multi-step route back to commercial starting materials |
| "pKa of 4-nitrophenol?" | Quantum-chemistry prediction via Rowan Science |
| "Cooling bath for −42 °C?" | MeCN / dry ice, or chlorobenzene / dry ice |
</details>
---
## 🔧 Tool Reference
### 📚 Literature & Discovery — 15 tools
Search papers across multiple databases, explore citation graphs, find open access PDFs, and track research trends.
<details>
<summary>Show all 15 tools</summary>
| Tool | Source | What it does |
|:-----|:-------|:-------------|
| `search_papers` | Crossref + OpenAlex + S2 | Multi-source paper search with metadata fusion |
| `get_paper_details` | Crossref + OpenAlex + S2 | Full metadata: abstract, authors, citations, references |
| `find_similar_papers` | Semantic Scholar | Content-based paper recommendations |
| `get_paper_citations` | Semantic Scholar | Forward citation graph + context snippets |
| `get_paper_references` | Semantic Scholar | Backward citation graph (bibliography) |
| `get_author_profile` | OpenAlex + S2 | h-index, publications, co-authors, topics |
| `analyze_research_topic` | OpenAlex | Publication volume trends over time |
| `find_open_access_pdf` | Unpaywall | Legal open access PDF URLs |
| `search_chemrxiv` | Crossref + OpenAlex | Chemistry preprint search |
| `get_chemrxiv_categories` | — | List ChemRxiv subject categories |
| `search_web_of_science` | Web of Science | WoS search *(requires API key)* |
| `generate_bibtex` | Crossref | DOI → BibTeX (single or batch) |
| `get_journal_metrics` | OpenAlex | Impact metrics, open access %, policy |
| `search_protein_structures` | RCSB PDB | Search PDB by keyword, organism, method |
| `get_protein_structure` | RCSB PDB | Full PDB entry: resolution, ligands, sequence |
</details>
### 🔬 Compound Data & Safety — 12 tools
Look up any compound by name, SMILES, or formula. Get safety data, binding affinities, crystal structures, and more.
<details>
<summary>Show all 12 tools</summary>
| Tool | Source | What it does |
|:-----|:-------|:-------------|
| `search_compound` | PubChem | Name/SMILES/formula → compound data |
| `get_compound_properties` | PubChem | MW, SMILES, InChI, formula, XLogP, TPSA |
| `profile_compound` | Multiple | Comprehensive profile combining several databases |
| `get_safety_data` | PubChem GHS | GHS pictograms, H-statements, P-statements |
| `translate_compound_ids` | UniChem | Convert PubChem ↔ ChEMBL ↔ DrugBank ↔ ChEBI |
| `search_crystal_structures` | COD | Crystallography Open Database search |
| `search_materials_project` | Materials Project | Band gaps, formation energies *(requires key)* |
| `search_nist_webbook` | NIST | ΔHf, Cp, phase transitions, IR spectra |
| `search_mass_spectra` | MassBank | Mass spectrum search by exact mass or name |
| `search_binding_data` | BindingDB | IC₅₀, Ki, Kd binding affinities |
| `search_toxicity` | EPA CompTox | Toxicity endpoints *(requires key)* |
| `classify_natural_product` | GNPS | NP superclass / class / pathway |
</details>
### ⚗️ Computational Chemistry — 11 tools
AI-powered retrosynthesis, forward reaction prediction, pKa, solubility, ADMET, and NMR shift prediction.
<details>
<summary>Show all 11 tools</summary>
| Tool | Source | What it does |
|:-----|:-------|:-------------|
| `predict_retrosynthesis` | IBM RXN | Multi-step retrosynthetic analysis |
| `plan_synthesis` | IBM RXN | Forward synthesis route planning |
| `predict_product` | IBM RXN | Predict products from reactants + reagents |
| `predict_atom_mapping` | IBM RXN | Atom-by-atom mapping for mechanisms |
| `text_to_procedure` | IBM RXN | Natural language → structured procedure |
| `predict_pka` | Rowan Science | pKa values (any functional group, aqueous) |
| `predict_solubility` | Rowan Science | Aqueous solubility prediction |
| `predict_admet` | Rowan Science | Absorption, metabolism, toxicity prediction |
| `search_tautomers` | Rowan Science | Enumerate tautomeric forms |
| `compute_descriptors` | Rowan Science | Molecular descriptors from SMILES |
| `predict_nmr` | Rowan Science | ¹H and ¹³C chemical shift prediction |
*IBM RXN and Rowan tools require free API keys. See [Configuration](#%EF%B8%8F-configuration).*
</details>
### 🧬 Peptide Chemistry — 10 tools
Sequence-to-SMILES conversion with 450+ amino acids, cyclization, library generation, pI calculation, and MS/MS interpretation.
<details>
<summary>Show all 10 tools</summary>
| Tool | Source | What it does |
|:-----|:-------|:-------------|
| `peptide_to_smiles` | p2smi | Sequence → SMILES (450+ AAs, 5 cyclization types) |
| `peptide_cyclization_options` | p2smi | Which cyclizations does a sequence support? |
| `generate_peptide_library` | p2smi | Random peptide generation with NCAAs, D-stereo |
| `peptide_properties` | p2smi + RDKit | MW, logP, TPSA, HBD/HBA, Lipinski |
| `check_peptide_synthesis` | p2smi | SPPS feasibility: difficult motifs, aggregation |
| `modify_peptide` | p2smi | Apply N-methylation, PEGylation |
| `calculate_peptide_pi` | pichemist | Isoelectric point (8 pKa reference sets) |
| `calculate_peptide_extinction` | pep-calc.com | ε₂₈₀ (Trp/Tyr/Cys contributions) |
| `get_peptide_ion_series` | pep-calc.com | b/y/a/c/z ion ladders for MS/MS |
| `assign_peptide_ms_peaks` | pep-calc.com | Match m/z values to fragments |
</details>
### 🧪 Bench Chemistry — 18 tools
Everyday lab calculators and a reference library covering named reactions, protecting groups, solvents, workup protocols, and more.
<details>
<summary>Show all 5 calculators</summary>
| Tool | What it does |
|:-----|:-------------|
| `calculate_molarity` | Solve for any unknown: mass, moles, volume, or MW |
| `calculate_dilution` | C₁V₁ = C₂V₂ with automatic unit handling |
| `calculate_reaction_mass` | Multi-reagent mass calc from equivalents |
| `calculate_yield` | Percent yield from actual / theoretical |
| `calculate_concentration` | M ↔ mM ↔ mg/mL ↔ %w/v ↔ ppm ↔ ppb |
</details>
<details>
<summary>Show all 13 reference tools</summary>
| Tool | Coverage |
|:-----|:---------|
| `lookup_named_reaction` | **202 named reactions** — conditions, mechanism, scope, limitations |
| `lookup_rxn_dev_checklist` | Structured checklist for reaction development — [Kerr *et al.*, *Chem. Soc. Rev.* 2025](https://doi.org/10.1039/D4CS01046A) |
| `lookup_protecting_group` | **30 PGs** for OH, NH, C=O, COOH with stability / lability matrix |
| `lookup_workup_procedure` | Step-by-step protocols: LAH quench, aqueous extraction, etc. |
| `lookup_solvent_properties` | **32 solvents** — bp, density, polarity index, dielectric, miscibility |
| `lookup_cooling_bath` | **24 recipes** from −196 °C (lN₂) to +100 °C |
| `lookup_tlc_stain` | **13 stains** organized by functional group selectivity |
| `lookup_column_chromatography` | Solvent selection, Rf rules, loading, troubleshooting |
| `lookup_buffer_recipe` | **20+ buffers** — PBS, Tris, HEPES, TAE, TBE, RIPA, citrate… |
| `lookup_amino_acid_properties` | **20 canonical AAs** — MW, pKa, pI, hydropathy |
| `lookup_nmr_solvent` | **12 solvents** — residual ¹H/¹³C shifts, water peak, multiplicity |
| `lookup_lab_tips` | **35 practical tips** across 9 categories |
| `lookup_safety_card` | **9 safety cards** for hazardous reagents (*n*-BuLi, NaH, LAH…) |
</details>
### 🔧 Chemistry Utilities — 5 tools
<details>
<summary>Show all 5 tools</summary>
| Tool | What it does |
|:-----|:-------------|
| `calculate_isotope_pattern` | Isotope distribution from formula/SMILES (Cl, Br, S patterns) |
| `validate_cas_number` | CAS registry check-digit validation |
| `convert_units` | Mass, volume, energy, pressure, temperature, length, amount |
| `lookup_periodic_table` | Z, mass, electron config, electronegativity, radius, group |
| `calculate_buffer_ph` | Henderson-Hasselbalch solver with built-in pKa database |
</details>
### ✍️ Writing & Publication — 10 tools
Format citations, build bibliographies, generate experimental section templates, check journal requirements, and prepare your SI — all from within Claude.
<details>
<summary>Show all 10 tools</summary>
| Tool | Source | What it does |
|:-----|:-------|:-------------|
| `format_citation` | Crossref | DOI → formatted reference in **20+ styles** (ACS, RSC, Nature, Angew, APA…) |
| `build_bibliography` | Crossref | Batch DOIs → numbered, styled reference list |
| `lookup_iupac_name` | PubChem | SMILES → IUPAC systematic name |
| `name_to_smiles` | PubChem | Common name → SMILES + InChI + InChIKey + MW |
| `format_molecular_formula` | Local | C6H12O6 → C₆H₁₂O₆ (Unicode) / `\ce{C6H12O6}` (LaTeX) / `<sub>` (HTML) |
| `lookup_experimental_template` | Local | **18 reaction templates** with fill-in fields and safety notes |
| `lookup_journal_guide` | Local | Submission requirements for **12 top chemistry journals** |
| `generate_si_checklist` | Local | SI checklist tailored to compound type |
| `lookup_abbreviation` | Local | **193 standard abbreviations** (solvents, reagents, spectroscopy) |
| `get_thesis_guide` | Local | Section-by-section writing guide: abstract → SI |
</details>
---
## 📖 Examples
### Literature workflow
```
You: "Find the 5 most cited papers on photoredox catalysis from 2020–2024"
Claude: [returns papers ranked by citations with abstracts and TLDRs]
You: "Who cited paper #2? What topics did they focus on?"
Claude: [shows forward citation graph with context snippets]
You: "Is there a free PDF for paper #3?"
Claude: [finds a legal open access link via Unpaywall]
You: "Generate BibTeX for all 5"
Claude: [outputs formatted BibTeX entries]
```
### Synthesis planning
```
You: "I want to make 4-methoxybiphenyl from 4-bromoanisole"
Claude: [suggests Suzuki coupling, gives conditions and literature precedent]
You: "Calculate amounts for a 200 mg scale, 5 mol% catalyst"
Claude: [returns exact mg for every reagent and solvent volume]
You: "What's a good workup?"
Claude: [aqueous workup protocol with solvent, drying agent, and column conditions]
```
### Reaction development
```
You: "I have a new C–H activation — how do I figure out the mechanism?"
Claude: [suggests KIE, radical clocks, Hammett, Stern–Volmer, and computational approaches]
You: "Walk me through optimisation"
Claude: [covers DoE vs one-variable-at-a-time, green metrics, solvent screening]
You: "How do I prove this is catalytic, not stoichiometric?"
Claude: [mercury drop test, hot filtration, TON benchmarks, nonlinear effects]
```
### Writing a paper
```
You: "Format these 12 DOIs as an ACS bibliography"
Claude: [numbered reference list in ACS style]
You: "Give me an experimental template for a Sonogashira"
Claude: [fill-in-the-blank procedure with safety notes]
You: "What SI do I need for a small molecule paper?"
Claude: [checklist with ¹H/¹³C NMR, HRMS, mp, HPLC, formatting tips]
You: "I'm submitting to Angew — what are the requirements?"
Claude: [word limits, abstract format, citation style, graphical abstract specs]
```
---
## ⚙️ Configuration
The easiest way to add API keys:
```bash
labmate-mcp --setup
```
This walks you through each key and saves them to `~/.labmate-mcp.env`. They're loaded automatically whenever you use labmate.
**All keys are optional.** 61 of 81 tools work without any configuration.
<details>
<summary><b>Available API keys</b></summary>
<br>
| Variable | Service | Free? | What it unlocks |
|:---------|:--------|:-----:|:----------------|
| `RXN_API_KEY` | [IBM RXN](https://rxn.res.ibm.com) | ✅ | Retrosynthesis, product prediction, atom mapping |
| `ROWAN_API_KEY` | [Rowan Science](https://rowan.ai) | ✅ | pKa, solubility, ADMET, tautomers, NMR prediction |
| `SEMANTIC_SCHOLAR_API_KEY` | [Semantic Scholar](https://www.semanticscholar.org/product/api#api-key) | ✅ | Higher rate limits for citations & recommendations |
| `UNPAYWALL_EMAIL` | [Unpaywall](https://unpaywall.org/) | ✅ | Open access PDF discovery |
| `MATERIALS_PROJECT_API_KEY` | [Materials Project](https://materialsproject.org) | ✅ | Crystal structures, band gaps, formation energies |
| `WOS_API_KEY` | [Web of Science](https://developer.clarivate.com) | 🏛️ | Web of Science search (institutional) |
| `COMPTOX_API_KEY` | [EPA CompTox](mailto:ccte_api@epa.gov) | ✅ | Toxicity & environmental data |
**Aliases:** `S2_API_KEY`, `MP_API_KEY`, `RXN4CHEMISTRY_API_KEY` also work.
</details>
<details>
<summary><b>Manual configuration</b></summary>
<br>
If you prefer to configure keys manually, add them to your Claude config:
```json
{
"mcpServers": {
"labmate": {
"command": "labmate-mcp",
"env": {
"RXN_API_KEY": "your-rxn-key",
"ROWAN_API_KEY": "your-rowan-key",
"UNPAYWALL_EMAIL": "you@university.edu"
}
}
}
}
```
Or create `~/.labmate-mcp.env` directly:
```bash
RXN_API_KEY=your-rxn-key
ROWAN_API_KEY=your-rowan-key
```
</details>
---
## 🗄️ Built-in Databases
Everything below ships with labmate — no API calls, no internet required.
<div align="center">
| | Database | Entries | What's inside |
|:--|:---------|-------:|:--------------|
| ⚗️ | Named reactions | **202** | Conditions, mechanism type, scope, limitations |
| 📋 | Rxn dev checklist | **30** questions | Kinetics, mechanism, DoE, catalysis, scope, scale-up |
| 🛡️ | Protecting groups | **30** | OH / NH / C=O / COOH, stability matrix |
| 🧴 | Solvents | **32** | bp, density, polarity index, dielectric, miscibility |
| ❄️ | Cooling baths | **24** | Recipes from −196 °C to +100 °C |
| 🎨 | TLC stains | **13** | Selectivity by functional group, recipe, procedure |
| 🧫 | Buffer recipes | **20+** | Preparation at specific pH, temperature correction |
| 🧬 | Amino acids | **20** | pKa, pI, MW, hydropathy, special notes |
| 📻 | NMR solvents | **12** | Residual ¹H, ¹³C, water peak, multiplicity |
| 📝 | Experimental templates | **18** | Fill-in-the-blank for common reaction types |
| 📰 | Journal guides | **12** | JACS, Angew, Nature Chem, JOC, Org Lett… |
| 🔤 | Abbreviations | **193** | Standard abbreviations across 7 categories |
| 💡 | Lab tips | **35** | Practical tips in 9 categories |
| ☣️ | Safety cards | **9** | Hazardous reagent protocols |
| 📄 | SI requirements | **18** | Per-technique formatting and common mistakes |
| 🎓 | Thesis writing | **6** | Section-by-section guidance |
</div>
<details>
<summary><b>All 202 named reactions</b></summary>
Alder-Ene · Aldol · Appel · Arbuzov · Arndt-Eistert · Baeyer-Villiger · Balz-Schiemann · Bamford-Stevens · Barton Decarboxylation · Barton-McCombie · Baylis-Hillman · Beckmann · Biginelli · Birch · Bischler-Napieralski · Blanc Chloromethylation · Bouveault-Blanc · Brown Hydroboration · Buchner Ring Expansion · Buchwald-Hartwig (C–N) · Buchwald-Hartwig (C–O) · Burgess Dehydration · Cadiot-Chodkiewicz · Cannizzaro · Carroll · Catellani · CBS · Chan-Lam · Chichibabin · Claisen Condensation · Claisen Rearrangement · Clemmensen · Click (CuAAC) · Comins · Cope Elimination · Cope Rearrangement · Corey-Bakshi-Shibata · Corey-Chaykovsky · Corey-Fuchs · Corey-Kim · Corey-Nicolaou · Corey-Winter · Cross-Metathesis · Curtius · Dakin · Darzens · Dess-Martin · Dieckmann · Diels-Alder · Doering-LaFlamme · Enders SAMP/RAMP · Eschenmoser-Claisen · Eschenmoser-Tanabe Fragmentation · Eschweiler-Clarke · Evans Aldol · Favorskii · Ferrier · Finkelstein · Fischer Esterification · Fischer Indole · Fleming-Tamao · Friedel-Crafts Acylation · Friedel-Crafts Alkylation · Fries · Fukuyama · Gabriel · Gewald · Glaser · Grignard · Grubbs Metathesis · Hantzsch Pyridine · Heck · Henry · Hiyama · Hiyama-Denmark · Hofmann · Horner · Horner-Wadsworth-Emmons · IBX · Ireland-Claisen · Jacobsen Epoxidation · Jones · Julia-Lythgoe · Kharasch · Knoevenagel · Knorr Pyrrole · Koenigs-Knorr · Kolbe · Kulinkovich · Kumada · Lawesson · Lemieux-Johnson · Ley · Liebeskind-Srogl · Lossen · Luche · Malaprade · Mander Methylenation · Mannich · Matteson · Meerwein Arylation · Meerwein Reduction · Meerwein-Ponndorf-Verley · Meinwald · Michael · Midland · Minisci · Mitsunobu · Modified Julia · Mukaiyama Aldol · Myers · Negishi · Noyori · Nozaki-Hiyama-Kishi · Ohira-Bestmann · Olefin Metathesis · Oppenauer · Oppolzer Sultam · Overman · Oxy-Cope · Ozonolysis · Paal-Knorr · Parikh-Doering · Passerini · Paternò-Büchi · Pauson-Khand · Petasis · Peterson · Pfitzner-Moffatt · Piancatelli · Pictet-Spengler · Pinner · Pinnick · Polonovski · Prevost · Prins · Ramberg-Bäcklund · Reductive Amination · Reformatsky · Rieche · Riley · Ring-Closing Metathesis · Ritter · Robinson Annulation · Roskamp · Roush · Rubottom · Saegusa-Ito · Sakurai-Hosomi · Sandmeyer · Schmidt · Shapiro · Sharpless AD · Sharpless AE · Shi Epoxidation · Shiina · Simmons-Smith · Skraup · Sonogashira · Staudinger Ligation · Staudinger Reduction · Steglich · Stetter · Still-Gennari · Stille · Stork Enamine · Strecker · Suzuki · Suzuki-Miyaura · Swern · Takai · Tebbe · TEMPO · Tiffeneau-Demjanov · Transfer Hydrogenation · Trost AAA · Tsuji-Trost · Ugi · Ullmann · Upjohn · Van Leusen · Vilsmeier-Haack · Wacker · Weinreb Amide · Wharton · Williamson · Wittig · Wittig Rearrangement · Wohl-Ziegler · Wolff · Wolff-Kishner · Yamaguchi · Zincke Aldehyde
</details>
<details>
<summary><b>Reaction development checklist — 7 sections</b></summary>
Based on Kerr, Jenkinson, Sheridan & Sparr, "Reaction Development: A Student's Checklist", [*Chem. Soc. Rev.* 2025, DOI: 10.1039/D4CS01046A](https://doi.org/10.1039/D4CS01046A). Each section contains guiding questions, specific checks to perform, and practical tips.
| Section | Questions |
|:--------|----------:|
| 🔍 Take Stock | 5 |
| 📈 Kinetics & Thermodynamics | 6 |
| ⚙️ Mechanism | 4 |
| 📊 Optimisation | 3 |
| 🔄 Catalysis | 4 |
| 🎯 Scope | 3 |
| 🚀 Applications | 5 |
| **Total** | **30** |
</details>
---
## 🏗️ Architecture
```
labmate_mcp/
├── server.py 5,248 lines 81 MCP tool definitions + response formatting
├── bench.py 4,714 lines Calculators + reference databases
├── apis.py 1,744 lines HTTP clients for 25+ scientific APIs
├── writing.py 1,488 lines Citations, templates, journal guides, SI, thesis
├── chemistry.py 572 lines Isotope patterns, CAS, units, periodic table, pH
├── peptide.py 384 lines p2smi + pichemist + pep-calc.com integration
└── __init__.py 4 lines Version
──────────────
14,154 lines
```
---
## 🤝 Contributing
Contributions are welcome! See [CONTRIBUTING.md](CONTRIBUTING.md) for details.
High-impact areas: more named reactions, more experimental templates, more journal guides, tests, and bug reports.
---
## 📄 License
[MIT](LICENSE) — use freely in academia and industry.
---
<div align="center">
## 📚 Cite
If labmate-mcp is useful in your research, please cite the tools it builds on:
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- **Reaction development checklist** — Kerr, M. A.; Jenkinson, M. A.; Sheridan, H.; Sparr, C. *Chem. Soc. Rev.* **2025**. [doi:10.1039/D4CS01046A](https://doi.org/10.1039/D4CS01046A)
- **p2smi** — Feller, A. *JOSS* **2025**, *10*, 8319. [doi:10.21105/joss.08319](https://doi.org/10.21105/joss.08319)
- **pichemist** — Trastoy, B. *et al.* *J. Chem. Inf. Model.* **2023**. [AstraZeneca/peptide-tools](https://github.com/AstraZeneca/peptide-tools)
- **OpenAlex** — Priem, J.; Piwowar, H.; Orr, R. [arXiv:2205.01833](https://arxiv.org/abs/2205.01833) (2022)
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Made with 🧪 for chemists who'd rather be in the lab than Googling.
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