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609358

Sigma-Aldrich

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

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

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.

Pictograms

Exclamation mark

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

609358-VAR:
609358-BULK:


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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
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
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
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.
George S Espie et al.
Journal of bacteriology, 189(3), 1013-1024 (2006-11-24)
The cyanobacteria Synechococcus elongatus strain PCC7942 and Synechococcus sp. strain UTEX625 decomposed exogenously supplied cyanate (NCO-) to CO2 and NH3 through the action of a cytosolic cyanase which required HCO3- as a second substrate. The ability to metabolize NCO- relied

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