# MolSketchGo

> Molecule Editor

Canonical page: [https://chrome-stats.com/d/com.japality.molsketch](https://chrome-stats.com/d/com.japality.molsketch)

## Overview

- **ID:** `com.japality.molsketch`
- **Platform:** Android
- **Type:** Android app
- **Status:** Available
- **Publisher:** Japality Limited
- **Category:** EDUCATION
- **Downloads:** 1,227
- **Version:** 0.0.5
- **Last updated:** 2026-03-27
- **First published:** 2025-12-15
- **Publisher country:** HK
- **Size:** 23 MB
- **Data as of:** 2026-09-14
- **Store listing:** [Google Play Store](https://play.google.com/store/apps/details?id=com.japality.molsketch)
- **Website:** [https://app.japality.com/molsketch/a/marketing/](https://app.japality.com/molsketch/a/marketing/)
- **Privacy policy:** [https://app.japality.com/molsketch/a/privacy\_policy/](https://app.japality.com/molsketch/a/privacy_policy/)

## Description

MolSketchGo is a mobile molecular structure editor designed for chemistry students, educators, and researchers. Sketch 2D chemical structures with an intuitive touch-based editor, then instantly convert them to interactive 3D models.<br><br>KEY FEATURES<br>• Intuitive 2D Editor — Draw atoms and bonds with simple tap and drag gestures. Supports single, double, triple, wedge, and dash bonds.<br>• Element Palette — Quickly switch between C, N, O, S, P, F, Cl, Br, I, B, and H.<br>• Ring Templates — Place benzene, cyclohexane, and cyclopentane rings with one tap.<br>• 3D Viewer — Convert your 2D sketches into rotatable, zoomable 3D models with ball-and-stick, space-filling, and stick representations.<br>• PubChem Integration — Search compounds by name, CID, or SMILES. View compound data including molecular formula, weight, exact mass, IUPAC name, and synonyms. Load 2D structures or view 3D conformers directly from PubChem.<br>• Import &amp; Export — Import and export SMILES strings, MOL files, and SDF files. Export structures as PNG images or SVG vectors. Generate IUPAC names via PubChem.<br>• Molecule Info — View molecular formula, molecular weight, exact mass, degree of unsaturation (DBE), atom counts, and aromaticity analysis.<br>• Save &amp; Organize — Save drawings locally with search. Backup and restore your library as JSON. Selective export and import with conflict resolution.<br>• Atom Properties — Set formal charge, isotope, explicit hydrogens, and aromatic flags on individual atoms.<br>• Undo &amp; Redo — Full history support for confident editing.<br>• Clean Structure — Auto-optimize molecular geometry with force-directed layout.<br>• Customizable — Adjust bond length, toggle skeletal mode, snap-to-grid, implicit hydrogen display, and per-element color themes.<br><br>IUPAC naming is powered by PubChem (NCBI) and provided for informational purposes only.

## Rankings

- #1,093,761 — Overall

## Permissions and access

### Permissions

- `android.permission.ACCESS_ADSERVICES_AD_ID`
- `android.permission.ACCESS_ADSERVICES_ATTRIBUTION`
- `android.permission.ACCESS_ADSERVICES_TOPICS`
- `android.permission.ACCESS_NETWORK_STATE`
- `android.permission.FOREGROUND_SERVICE`
- `android.permission.INTERNET`
- `android.permission.WAKE_LOCK`
- `com.android.vending.CHECK_LICENSE`
- `com.google.android.gms.permission.AD_ID`
- `com.japality.molsketch.DYNAMIC_RECEIVER_NOT_EXPORTED_PERMISSION`

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Source: [Chrome-Stats](https://chrome-stats.com/d/com.japality.molsketch)