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185086

Sigma-Aldrich

Sodium cyanate

96%

Synonym(s):

Sodium isocyanate, Zassol

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About This Item

Linear Formula:
NaOCN
CAS Number:
917-61-3
Molecular Weight:
65.01
Beilstein:
3655041
EC Number:
213-030-6
MDL number:
MFCD00011121
UNSPSC Code:
12161600
eCl@ss:
38060512
PubChem Substance ID:
24850666
NACRES:
NA.22

Quality Level

100

Assay

96%

reaction suitability

core: sodium
reagent type: catalyst

SMILES string

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

InChI

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

InChI key

ZVCDLGYNFYZZOK-UHFFFAOYSA-M

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK3488
STBJ8198
STBJ8197
STBG4161V
STBC6440V

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Jay K Herman et al.
Respiratory physiology & neurobiology, 136(1), 1-12 (2003-06-18)
The purpose of the present study was to use chemoafferent recordings from the goat carotid body (CB) to pharmacologically identify the putative low affinity excitatory receptor for dopamine (DA). Close arterial injections of DA (1-50 microg kg(-1)) induced a dose-dependent
M Shaykh et al.
The Journal of laboratory and clinical medicine, 133(3), 302-308 (1999-03-11)
Carbamylated proteins formed in renal insufficiency from the spontaneous decomposition of urea exert a variety of metabolic effects. Here we examined the effects of carbamylated proteins on glomerular mesangial cells to determine whether urea retention in early renal insufficiency may
Ekaterina V Vinogradova et al.
Organic letters, 15(6), 1394-1397 (2013-02-28)
An efficient synthesis of aryl carbamates was achieved by introducing alcohols into the reaction of palladium-catalyzed cross-coupling of ArX (X = Cl, OTf) with sodium cyanate. The use of aryl triflates as electrophilic components in this transformation allowed for an
I Koshiishi et al.
Biochimica et biophysica acta, 1336(3), 566-574 (1997-11-21)
Ascorbate-dehydroascorbate redox cycle plays a key role in protecting organisms from an excess of oxidants. Recently, we found a novel reaction of dehydroascorbate with cyanate under the conditions of neutral pH and ordinary temperature. In this report, we demonstrated that
C Geers et al.
Comparative biochemistry and physiology. Part A, Physiology, 112(1), 111-117 (1995-09-01)
In isolated rat soleus and extensor digitorum longus (EDL) muscles, the effects of carbonic anhydrase inhibitors were studied on oxygen consumption as well as lactate release and accumulation after incubation in inhibitors lasting long enough to produce marked changes in
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