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Merck

431354

Supelco

Ammonium thiocyanate

99.99% trace metals basis

Sinónimos:

Ammonium rhodanide

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About This Item

Fórmula lineal:
NH4SCN
Número de CAS:
Peso molecular:
76.12
Beilstein/REAXYS Number:
3595135
EC Number:
MDL number:
UNSPSC Code:
12352300
eCl@ss:
38060604
PubChem Substance ID:
NACRES:
NA.55

grade

for inorganic trace analysis

assay

99.99% trace metals basis

form

crystals

impurities

≤0.004 meq/g I2 consumers
≤0.005% insolubles

ign. residue

≤0.025%

pH

4.5-6.0

mp

152-154 °C (lit.)

solubility

water: 76.1 g/L at 20 °C

anion traces

chloride (Cl-): ≤0.005%
sulfate (SO42-): ≤0.005%

cation traces

Fe: ≤3 ppm
heavy metals: ≤5 ppm

SMILES string

N.SC#N

InChI

1S/CHNS.H3N/c2-1-3;/h3H;1H3

InChI key

SOIFLUNRINLCBN-UHFFFAOYSA-N

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General description

Ammonium thiocyanate is an ammonium salt commonly used for thiocyanation reaction of organic compounds.

Application

Ammonium thiocyanate (ATC) may be used the synthesis of the following:
  • Graphitic carbon nitride.
  • Three-dimensional nitrogen and sulfur co-doped graphene frameworks (N/S-GFs).
  • Substituted 2-aminothiazole derivatives by reacting with α-halo ketone carbonyls in the presence of N-methylimidazole.
  • Thiiranes from corresponding oxiranes in the presence of LiBF4.
  • 1,2,4-triazole-3-thiones by a multi-component reaction with benzohydrazide acid and acid chloride in the absence of solvent.
Applied in the formation of novel two-dimensional Cd-SCN coordination solids with unusual and tailorable, checkerboard- or herringbone-patterned structures these structures are important steps toward technologically useful materials.

Features and Benefits

Meets ACS reagent specifications.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1

supp_hazards

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Low-temperature synthesis of nitrogen/sulfur co-doped three-dimensional graphene frameworks as efficient metal-free electrocatalyst for oxygen reduction reaction.
Su Y, et al.
Carbon, 62, 296-301 (2013)
Three-component reaction between benzohydrazide acid, ammonium thiocyanate and acid chlorides under solvent-free conditions.
Hassanabadi A, et al.
Journal of Sulfur Chemistry, 32(4), 355-359 (2011)
Hong Zhang et al.
Inorganic chemistry, 38(5), 886-892 (2001-10-24)
This paper reports the syntheses, characterization, and structures of two new two-dimensional cadmium-thiocyanate coordination solids [(12C4)(2)Cd][Cd(2)(SCN)(6)] (1) and [(12C4)(2)Cd][Cd(3)(SCN)(8)] (2), where 12C4 denotes 12-crown-4, C(8)H(16)O(4). 1 crystallizes in a monoclinic unit cell, space group C2/c with lattice parameters a =
Synthesis of bulk and nanoporous carbon nitride polymers from ammonium thiocyanate for photocatalytic hydrogen evolution.
Cui Y, et al
Journal of Materials Chemistry, 21(34), 13032-13039 (2011)
Efficient conversion of oxiranes to thiiranes with ammonium thiocyanate catalysed with LiBF4.
Kazemi F, et al.
J. Chem. Res. (M), 2002(4), 176-177 (2002)

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