609358
Potassium cyanate-15N
≥98 atom % 15N, ≥95% (CP)
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About This Item
Linear Formula:
KOC15N
CAS Number:
Molecular Weight:
82.11
MDL number:
UNSPSC Code:
12352118
PubChem Substance ID:
Note: This product can be packaged on demand. For information on pricing, availability and packaging of custom sizes, please contact Stable Isotopes Customer Service
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isotopic purity
≥98 atom % 15N
Assay
≥95% (CP)
form
solid
mass shift
M+1
SMILES string
[K+].[O-]C#[15N]
InChI
1S/CHNO.K/c2-1-3;/h3H;/q;+1/p-1/i2+1;
InChI key
GKKCIDNWFBPDBW-CGOMOMTCSA-M
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Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
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
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J Zambonin et al.
Journal of neuroscience methods, 192(1), 115-120 (2010-07-28)
Mitochondrial defects have been implicated in the degeneration of axons in a number of CNS disorders, including multiple sclerosis. Uniquely, mitochondria harbor the only non-nuclear DNA (mitochondrial DNA or mtDNA), which encodes functionally important subunits of the respiratory chain. The
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
LAIS Allergoid.
G Mistrello
International journal of immunopathology and pharmacology, 18(4 Suppl), 21-24 (2007-12-06)
Małgorzata Iciek et al.
Human & experimental toxicology, 30(10), 1601-1608 (2010-12-24)
Cyanate and its active form isocyanate are formed mainly in the process of nonenzymatic urea biodegradation. Cyanate is capable of protein S- and N-carbamoylation, which can affect their activity. The present studies aimed to demonstrate the effect of cyanate on
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