Skip to main content

Indium(III) Chloride

InCl3 salt

Properties

StateSolid (anhydrous is hygroscopic; tetrahydrate is common commercial form)
ColorWhite to pale yellow
SolubilityVery soluble in water (1950 g/L as tetrahydrate); soluble in ethanol and ether
Melting Point586 °C (anhydrous)
Boiling Point800 °C (sublimes)

About Indium(III) Chloride

Indium(III) chloride is the workhorse soluble In(III) source — a hygroscopic white salt that you almost always handle as the tetrahydrate InCl3·4H2O because the anhydrous form pulls water out of room air fast enough to liquefy on the bench. The anhydrous solid has a layered YCl3-type structure with octahedrally coordinated In(III); dissolve it in water and you get [In(H2O)6]^3+ at low chloride, sliding to [InCl4]- as you add Cl-. Its synthetic niche comes from where it sits on the Lewis-acid hardness scale: harder than the late transition metals and softer than Al(III) or Ti(IV), and water-tolerant where most strong Lewis acids are not. Strong classical Lewis acids (AlCl3, BF3, TiCl4) hydrolyze the moment they see a hydroxyl, which kills any chemistry in protic solvents. InCl3 keeps catalyzing through aqueous and wet-organic conditions, which has made it the go-to catalyst for green-chemistry versions of the Mukaiyama aldol, Sakurai allylation, Mannich reaction, Friedel-Crafts acylation of activated arenes, Markovnikov alkyne hydration, and acetal protection/deprotection. Beyond catalysis, InCl3 is the standard In(III) feedstock for solution-phase nanocrystal syntheses of InP, InAs, and CuInS2 quantum dots, and it shows up as the indium source in electroplating baths and as a dopant precursor for indium-doped phosphors and glasses.

Where you'll encounter it

If you've ever run an indium-mediated Barbier allylation in water at room temperature instead of fighting an anhydrous Grignard setup — or pulled red InP quantum dots out of an octadecene flask at 300 °C for a Cd-free LED — InCl3 was the indium source you weighed out. In a Mukaiyama aldol screen, a few mol% of InCl3·4H2O in wet THF will activate the silyl enol ether without the moisture-exclusion ritual that AlCl3 demands. In an indium-electroplating bath formulating bearing surfaces for aerospace bushings, InCl3 plus boric acid plus a brightener is the classical sulfate-free recipe. And if your nano-lab sintered an InP/ZnS core-shell QD batch for a QLED prototype tube, the InCl3 you started with traced through every step of the synthesis.

Common Uses

  • Water-tolerant Lewis-acid catalyst for Mukaiyama aldol, Sakurai allylation, and Mannich reactions
  • In(III) precursor for InP, InAs, and CuInS2 colloidal quantum-dot synthesis
  • Indium source for In-doped phosphors and high-refractive-index optical glasses
  • Electrolyte component in indium electroplating baths for bearing surfaces and solder finishes
  • Indium reagent for Barbier-type allylations in aqueous media (organoindium chemistry)

Safety Information

GHS: Skin Corr. 1B, Eye Dam. 1, STOT-RE Cat 1 (respiratory tract). OSHA PEL 0.1 mg/m³ as In. Indium compounds cause 'indium lung' (pulmonary alveolar proteinosis with interstitial fibrosis) on chronic dust inhalation — first reported in ITO production workers and now established across all soluble In compounds. Use a fume hood with HEPA-filtered exhaust for any dry powder handling, and wear nitrile gloves and safety goggles for solutions. Hydrolyzes vigorously in moist air, releasing HCl gas; store in a desiccator under N2 or Ar.

This safety summary is for educational reference only and may not be complete. It is not a substitute for Safety Data Sheets (SDS), medical advice, or professional chemical safety guidance. Always consult appropriate SDS and qualified professionals before handling chemicals.

Constituent Elements

Frequently Asked Questions

What is the molar mass of indium(III) chloride?
Anhydrous InCl3 is 221.168 g/mol — 114.818 (In) + 3(35.45) (Cl). The commercial tetrahydrate InCl3·4H2O is 293.23 g/mol; remember to scale your weigh-out by 1.326 if your procedure calls for the anhydrous mass and you're using the hydrate, which you almost always are.
Why is InCl3 so useful as a Lewis acid in wet conditions?
Most strong Lewis acids you learn in undergrad (AlCl3, BF3·Et2O, TiCl4) are useless in water — they hydrolyze instantly to hydroxides and HCl/HF. InCl3 has intermediate Lewis acidity that's strong enough to activate carbonyl substrates and silyl enol ethers but stable enough in water to survive aqueous reaction conditions. This opened up a whole class of 'green' Mukaiyama aldol, Mannich, and allylation reactions you can run in water or wet THF without an anhydrous setup. Yamamoto, Loh, and Chandrasekhar have all published extensively on InCl3 catalysis with this rationale.
How are InP quantum dots synthesized from InCl3?
The standard hot-injection recipe dissolves InCl3 in octadecene with myristic acid or oleic acid as a coordinating ligand, heats it to 280–320 °C under inert atmosphere, then injects tris(trimethylsilyl)phosphine — P(SiMe3)3 — as the phosphide source. The Si-P bonds break, In-P bonds form, and the dots nucleate and grow over minutes. You can tune sizes from 2 to 7 nm (corresponding to bandgap emission from 1.9 down to 1.35 eV, roughly red through near-IR), and the resulting cores are the basis of every Cd-free QLED display marketed today by Samsung and Nanosys.