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V900111

Sigma-Aldrich

Potassium cyanate

Vetec, reagent grade, 96%

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About This Item

Linear Formula:
KOCN
CAS Number:
Molecular Weight:
81.12
Beilstein:
3594798
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
Assay:
96%
grade:
reagent grade
form:
powder, crystals or chunks
Pricing and availability is not currently available.

grade

reagent grade

product line

Vetec

Assay

96%

form

powder, crystals or chunks

density

2.056 g/mL at 25 °C (lit.)

SMILES string

[K+].[O-]C#N

InChI

1S/CHNO.K/c2-1-3;/h3H;/q;+1/p-1

InChI key

GKKCIDNWFBPDBW-UHFFFAOYSA-M

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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Jeroen N Stoop et al.
PloS one, 9(7), e102163-e102163 (2014-07-16)
The immune response to post-translationally modified antigens is a key characteristic of rheumatoid arthritis. Carbamylation is such a posttranslational modification. Recently, we demonstrated that autoantibodies recognizing carbamylated proteins are present in sera of rheumatoid arthritis. The molecular mechanisms underlying the
E S Roberts et al.
Inhalation toxicology, 18(3), 159-167 (2006-01-10)
Hydrogen sulfide (H(2)S) is a naturally occurring gas that is also associated with several industries. The potential for widespread human inhalation exposure to this toxic gas is recognized as a public health concern. The nasal epithelium is particularly susceptible to
Jirí Verner et al.
Molecules (Basel, Switzerland), 11(1), 34-42 (2007-10-27)
The reactivity of alicyclic ketazines in criss-cross cycloadditions was investigated. They react with potassium cyanate and ammonium thiocyanate in the presence of acetic acid to form spirocyclic perhydro[1,2,4]triazolo[1,2-alpha][1,2,4]triazole-1,5-diones and perhydro[1,2,4]triazolo[1,2-alpha][1,2,4]triazole-1,5-dithiones, respectively, in relatively high yields.
Grégoire Danger et al.
Amino acids, 42(6), 2331-2341 (2011-07-20)
The reaction of cyanate with C-terminal carboxyl groups of peptides in aqueous solution was considered as a potential pathway for the abiotic formation of peptide bonds under the condition of the primitive Earth. The catalytic effect of dicarboxylic acids on
R M Satpute et al.
Neurotoxicology, 29(1), 170-178 (2007-12-15)
Cyanide is a rapidly acting neurotoxin that inhibits cellular respiration and energy metabolism leading to histotoxic hypoxia. This results in the dissipation of mitochondrial membrane potential (MMP) accompanied by decreased cellular ATP content which in turn is responsible for increased

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