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Ammonium thiocyanate (CAS 1762-95-4)

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Alternate Names:
Ammonium rhodanide
Application:
Ammonium thiocyanate is an agent for the degradation of peptides
CAS Number:
1762-95-4
Purity:
≥98%
Molecular Weight:
76.12
Molecular Formula:
CH4N2S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ammonium thiocyanate, with the chemical formula NH4SCN, is a colorless crystalline salt renowned for its versatility in analytical chemistry and materials science research. It is extensively employed in titrations to determine the concentration of various metal ions, notably iron and silver, through the formation of visibly distinct complexes. The thiocyanate ion acts as a ligand, coordinating with metal ions to produce colored complexes, such as the red complexes with iron, which are crucial for accurate endpoint detection in colorimetric assays. This property is not only pivotal for analytical purposes but also facilitates the exploration of thiocyanate complexes in research focused on developing novel materials with unique magnetic and electronic properties. Furthermore, ammonium thiocyanate serves as a precursor in synthesizing other thiocyanate compounds, which are investigated for their potential in producing new herbicides, fungicides, and dyes. Its role in forming bridges between metal centers also opens avenues for studying advanced molecular architectures, contributing substantially to advancements in conductive materials and industrial chemistry applications.


Ammonium thiocyanate (CAS 1762-95-4) References

  1. Ammonium thiocyanate for detaching antibodies from histological specimens.  |  Iturriza, FC., et al. 1991. Biotech Histochem. 66: 239-41. PMID: 1790238
  2. Study of the interactions of sodium thiocyanate, potassium thiocyanate and ammonium thiocyanate in water+N,N-dimethylformamide mixtures by Raman spectroscopy.  |  Molinou, IE. and Tsierkezos, NG. 2008. Spectrochim Acta A Mol Biomol Spectrosc. 71: 954-8. PMID: 18420453
  3. Extraction of high-quality epidermal RNA after ammonium thiocyanate-induced dermo-epidermal separation of 4 mm human skin biopsies.  |  Clemmensen, A., et al. 2009. Exp Dermatol. 18: 979-84. PMID: 19645824
  4. Multicomponent reactions of ammonium thiocyanate, acyl chlorides, alkyl bromides, and enaminones: a facile one-pot synthesis of thiophenes.  |  Hossaini, Z., et al. 2011. Mol Divers. 15: 911-6. PMID: 21695452
  5. Phytotoxicity of thiocyanate to rice seedlings.  |  Yu, XZ., et al. 2012. Bull Environ Contam Toxicol. 88: 703-6. PMID: 22310846
  6. Thiocyanate radical mediated dehydration of aldoximes with visible light and air.  |  Ban, YL., et al. 2019. Chem Commun (Camb). 55: 9701-9704. PMID: 31348482
  7. Electrochemical synthesis of versatile ammonium oxides under metal catalyst-, exogenous-oxidant-, and exogenous-electrolyte-free conditions.  |  Yuan, Y., et al. 2021. Chem Commun (Camb). 57: 2768-2771. PMID: 33596296
  8. Thiocyanate-Passivated Diaminonaphthalene-Incorporated Dion-Jacobson Perovskite for Highly Efficient and Stable Solar Cells.  |  Yukta, ., et al. 2022. ACS Appl Mater Interfaces. 14: 850-860. PMID: 34978806
  9. Thermal batteries based on inverse barocaloric effects.  |  Zhang, Z., et al. 2023. Sci Adv. 9: eadd0374. PMID: 36800425
  10. Copper-catalyzed thiocyanation of cyclobutanone oxime esters using ammonium thiocyanate.  |  Zhao, X., et al. 2024. Org Biomol Chem. 22: 1466-1474. PMID: 38284473

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ammonium thiocyanate, 100 g

sc-202950
100 g
$46.00

Ammonium thiocyanate, 500 g

sc-202950A
500 g
$110.00