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Copper(I) Iodide | CAS 7681-65-4 | ≥99%

Copper(I) Iodide | CAS 7681-65-4 | ≥99%

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Technical Specifications

CAS Number 7681-65-4
EC / EINECS Number 231-674-6
MDL Number MFCD00010978
SMILES [Cu+].[I-]
InChI InChI=1S/Cu.HI/h;1H/q+1;/p-1
InChIKey LSXDOTMGLUJQCM-UHFFFAOYSA-M
PubChem CID 6432705
Molecular Formula CuI
Molecular Weight 190.45 g/mol
Melting Point 605 °C
Solubility Practically insoluble in water, slightly soluble in acetonitrile and DMSO
Purity ≥99%
Physical Form Brown solid
HS Code 2827.60
Shelf Life Retest period: 36 months from date of manufacture
Storage Conditions Store in a cool, dry place in a tightly sealed container, protected from light

Product Description & Scientific Applications

Copper(I) iodide (cuprous iodide, CuI) is a widely used soft Cu(I) source in synthesis and a well-studied p-type semiconductor. It adopts the zincblende (γ) structure at room temperature, converting to wurtzite (β) and rock-salt (α) phases on heating. Essentially insoluble in water, it dissolves in concentrated iodide solutions through iodocuprate formation and is soluble in ammonia and selected donor solvents such as acetonitrile. Commercial material is commonly supplied as white to off-white powder; slight cream or tan colouration can arise from trace iodine impurities.

Applications in synthesis

  • Sonogashira co-catalysis: a classical Cu(I) co-catalyst alongside palladium in the coupling of aryl, heteroaryl and vinyl halides with terminal alkynes; Cu(I) forms a copper acetylide that transmetalates to palladium, accelerating the coupling under amine bases.
  • Ullmann-type C–N, C–O and C–S coupling: a Cu(I) source for ligand-accelerated coupling chemistry — including diamine-, amino-acid- and 1,3-diketone-supported variants — used for arylation of amines, amides, phenols, azoles and related heteroatom nucleophiles.
  • Azide–alkyne cycloaddition (CuAAC): Cu(I) source for copper-catalysed click reactions between organic azides and terminal alkynes, giving 1,4-disubstituted 1,2,3-triazoles through copper-acetylide chemistry.
  • Aromatic Finkelstein reaction: catalyst for halide exchange that converts aryl, heteroaryl and vinyl bromides into the corresponding iodides, typically with sodium iodide and a diamine ligand in dioxane.
  • Organocuprate generation: precursor to Gilman-type cuprates (R2CuLi) and related organocopper reagents for conjugate (1,4-) addition and substitution chemistry.

Beyond synthesis

  • Coordination chemistry and luminescent clusters: a soft Cu(I) building block for complexes with N-heterocyclic carbene, phosphine and pyridyl ligands, and for [Cu4I4] cubane and stair-step clusters whose Cu–Cu interactions give temperature-dependent (thermochromic) photoluminescence.
  • p-Type semiconductor and transparent conductor: γ-CuI is a wide-direct-bandgap p-type semiconductor (~3.1 eV) with high hole mobility, studied as a hole-transport layer in thin-film photovoltaics and in transparent electronics.

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Safety Information

GHS Pictograms
GHS05 Corrosive GHS07 Harmful/Irritant GHS08 Health Hazard GHS09 Environment
Signal Word Danger
Hazard Class DG, UN 3077, Class 9, PG III
Transport Category Class 9, PG III (ADR/IATA/IMDG)
H-Statements H302 - H315 - H317 - H318 - H372 - H410
P-Statements P260 - P264 - P270 - P273 - P280 - P301+P312 - P302+P352 - P305+P351+P338 - P310 - P330 - P333+P313 - P362+P364 - P391 - P501
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