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298212

Sigma-Aldrich

Copper(I) thiocyanate

99%

Synonym(s):

Cuprous thiocyanate

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About This Item

Linear Formula:
CuSCN
CAS Number:
Molecular Weight:
121.63
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

Assay

99%

form

powder

application(s)

battery manufacturing

SMILES string

[Cu]SC#N

InChI

1S/CHNS.Cu/c2-1-3;/h3H;/q;+1/p-1

InChI key

PDZKZMQQDCHTNF-UHFFFAOYSA-M

General description

The crystal belongs to the orthorhombic system, space group: Pbca,a=10.994(9)Å, b=7.224(3)Å,c=6.662(2)Å.

Application

The product can be prepared from Cu(CH3COO)2·H2O, AgNO3, NH4NCS and im(im = imidazole). The structure and optical properties were reported. It is an air- and light-stable source of Cu(I).

Pictograms

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Supplementary Hazards

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis, structure and non-linear optical property of a copper(II) thiocyanate three-dimensional supramolecular compound
Bie HY, et al.
Journal of Molecular Structure, 660, 107-112 (2003)
Graham A Bowmaker et al.
Dalton transactions (Cambridge, England : 2003), (39)(39), 5290-5292 (2008-10-02)
The role of short-range diffusion in solvent-assisted mechanochemical synthesis is demonstrated in studies of a polymorphic transition and a ligand dissociation reaction involving copper(I) thiocyanate complexes.
S Bacon
Journal of human nutrition, 34(6), 445-449 (1980-12-01)
The advantages and disadvantages of faecal markers that are available in the UK are discussed. Opinions and comments from units using them are included.
Graham A Bowmaker et al.
Dalton transactions (Cambridge, England : 2003), 41(25), 7513-7525 (2012-05-24)
A number of adducts of copper(I) thiocyanate with bulky tertiary phosphine ligands, and some nitrogen-base solvates, were synthesized and structurally and spectroscopically characterised. CuSCN:PCy3 (1:2), as crystallized from pyridine, is shown by a single crystal X-ray study to be a
The crystal structure of copper(I) thiocyanate and its relation to the crystal structure of copper(II) diammine dithiocyanate complex
Kabesova M, et al.
Inorgorganica Chimica Acta, 17, 161-165 (1976)

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