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Copper(II) sulfide, with the chemical formula CuS, is a black, crystalline solid that is typically formed as a byproduct in the mining industry through the reaction between copper and sulfur. It is insoluble in most acids but can dissolve in nitric acid. Copper(II) sulfide is known for its stability under normal conditions, although it can release toxic fumes of sulfur oxide and copper oxide when heated to decomposition, necessitating careful handling.

1317-40-4

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1317-40-4 Usage

Uses

Used in Copper Manufacturing:
Copper(II) sulfide is used as a raw material in the production of various copper components, contributing to the manufacturing process of copper-based products.
Used in Laboratory Applications:
In the laboratory, Copper(II) sulfide serves as a precursor for the production of pure copper, facilitating research and development in the field of metallurgy and material science.
Used in Mining Industry:
As a common byproduct in the mining industry, Copper(II) sulfide is utilized in the extraction and processing of copper, playing a role in the overall mining operations.

Check Digit Verification of cas no

The CAS Registry Mumber 1317-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,1 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1317-40:
(6*1)+(5*3)+(4*1)+(3*7)+(2*4)+(1*0)=54
54 % 10 = 4
So 1317-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H10N2O2.Cu/c19-15-9-5-1-3-7-11(9)17-13(15)14-16(20)10-6-2-4-8-12(10)18-14;/h1-8,17-18H;/q;+2/b14-13+;

1317-40-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (14300)  Copper(II) sulfide, ultra dry, 99.98% (metals basis)   

  • 1317-40-4

  • 10g

  • 2052.0CNY

  • Detail
  • Alfa Aesar

  • (14300)  Copper(II) sulfide, ultra dry, 99.98% (metals basis)   

  • 1317-40-4

  • 50g

  • 5649.0CNY

  • Detail
  • Alfa Aesar

  • (42925)  Copper(II) sulfide, 99.8% (metals basis)   

  • 1317-40-4

  • 50g

  • 617.0CNY

  • Detail
  • Alfa Aesar

  • (42925)  Copper(II) sulfide, 99.8% (metals basis)   

  • 1317-40-4

  • 250g

  • 1777.0CNY

  • Detail
  • Alfa Aesar

  • (42925)  Copper(II) sulfide, 99.8% (metals basis)   

  • 1317-40-4

  • 1kg

  • 6454.0CNY

  • Detail
  • Aldrich

  • (450820)  Copper(II)sulfide  powder, 99.99% trace metals basis

  • 1317-40-4

  • 450820-10G

  • 1,437.93CNY

  • Detail
  • Aldrich

  • (342467)  Copper(II)sulfide  powder, −100 mesh, ≥99% trace metals basis

  • 1317-40-4

  • 342467-100G

  • 943.02CNY

  • Detail
  • Aldrich

  • (342467)  Copper(II)sulfide  powder, −100 mesh, ≥99% trace metals basis

  • 1317-40-4

  • 342467-500G

  • 3,729.96CNY

  • Detail

1317-40-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name copper(II) sulfide

1.2 Other means of identification

Product number -
Other names C.I. Pigment Blue 34

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1317-40-4 SDS

1317-40-4Downstream Products

1317-40-4Relevant academic research and scientific papers

Transition metal sulfide studies: The pure rotational spectrum of the CuS radical (X2Πi)

Thompsen,Ziurys

, p. 75 - 84 (2001)

The pure rotational spectrum of CuS in its X2Πi ground state has been recorded using direct absorption techniques in the range 140-540 GHz. This radical was produced by the reaction of copper vapour with CS2. Both the v=0

Aminoglycoside antibiotic compounds

-

, (2008/06/13)

Selective blocking of some amino groups in a polyamino organic compound having at least one pair of available neighboring hydroxyl and amino groups is effected by first preparing in situ transition metal salt complexes of available neighboring amino and hydroxyl group pairs in said polyamino organic compound, followed by introduction of blocking groups on the non-complexed amino groups and, finally, removing the transition metal cations from the selectively N-blocked polyamino organic compound complex to obtain a polyamino organic compound having selectively blocked amino groups. This process is particularly valuable when carrying out aminocyclitol-aminoglycoside transformations utilizing transition metal salt complexes of cupric acetate, nickel (II) acetate, cobalt (II) acetate or mixtures thereof.

Process of selectively blocking amino functions in aminoglycosides using transition metal salts and intermediates used thereby

-

, (2008/06/13)

Selective blocking of some amino groups in a polyamino organic compound having at least one pair of available neighboring hydroxyl and amino groups is effected by first preparing in situ transition metal salt complexes of available neighboring amino and hydroxyl group pairs in said polyamino organic compound, followed by introduction of blocking groups on the non-complexed amino groups and, finally, removing the transition metal cations from the selectively N-blocked polyamino organic compound complex to obtain a polyamino organic compound having selectively blocked amino groups. This process is particularly valuable when carrying out aminocyclitol-aminoglycoside transformations utilizing transition metal salt complexes of cupric acetate, nickel (II) acetate, cobalt (II) acetate or mixtures thereof.

Protected amino acids or peptides

-

, (2008/06/13)

In an amino acid having ω-amino group protected with a protective group or a peptide having the residue of such a protected amino acid, the improvement according to which the protective group is p-methylbenzylsulfonyl group. The ω-amino acids protected with p-methylbenzylsulfonyl or the peptides having residues of such protected amino acids are useful for production of various peptides by liquid phase method as well as by solid-phase method, because the protective group has specific selectivity of remaining stable under the conditions commonly employed in the removal of α-aminoprotecting group but is cleaved smoothly in a good yield by hydrogen fluoride without exerting untoward unfluences upon peptides.

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