모든 사진(4)
About This Item
Linear Formula:
KSCN
CAS Number:
Molecular Weight:
97.18
Beilstein:
3594799
EC Number:
MDL number:
UNSPSC 코드:
12352302
PubChem Substance ID:
분석:
99%
Grade:
ACS reagent
양식:
crystalline powder
추천 제품
Grade
ACS reagent
Quality Level
분석
99%
양식
crystalline powder
불순물
Iodine consuming substances, passes test
≤0.005% insol. water
색상
colorless to white
pH
5.3-8.7 (25 °C, 5%)
mp
173 °C (lit.)
음이온 미량물
chloride (Cl-): ≤0.005%
sulfate (SO42-): ≤0.005%
양이온 미량물
Fe: ≤2 ppm
NH4+: ≤0.003%
Na: ≤0.005%
heavy metals (as Pb): ≤5 ppm
SMILES string
[K]SC#N
InChI
1S/CHNS.K/c2-1-3;/h3H;/q;+1/p-1
InChI key
ZNNZYHKDIALBAK-UHFFFAOYSA-M
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Potassium thiocyanate is an inorganic potassium salt. Phase transitions in potassium thiocyanate (KSCN) have been investigated by X-ray diffraction studies. The order-disorder type transition with respect to the orientation of the thiocyanate ions was identified. Its polarized infrared spectrum has been reported. It participates in the ring-opening of aziridines. The reaction was carried out in the presence of sulfated zirconia to afford the corresponding β-aminothiocyanates.
애플리케이션
Potassium thiocyanate (KSCN) may be used for the colorimetric quantification of intracellular iron content of the superparamagnetic iron oxide (SPIO) nanoparticles.
Potassium thiocyanate may be used in the synthesis of the following:
- α-Amino nitriles from tertiary amines.
- Polysubstituted 2-aminothiazoles from vinyl azides.
- Benzisothiazol-3(2H)-one derivatives from o-bromobenzamides.
- Diaryl thioethers from aryl halides.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1
보충제 위험성
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
Synthesis of diaryl thioethers from aryl halides and potassium thiocyanate.
Hajipour AR, et al.
Applied Organometallic Chemistry, 28(12), 879-879 (2014)
Potassium Thiocyanate as Source of Cyanide for the Oxidative α-Cyanation of Tertiary Amines.
Wagner A and Ofial AR.
The Journal of Organic Chemistry, 80(5), 2848-2854 (2015)
Iron (II)-Promoted Synthesis of 2-Aminothiazoles via C=N Bond Formation from Vinyl Azides and Potassium Thiocyanate.
Zhang G, et al.
Advanced Synthesis & Catalysis, 357(5), 1065-1069 (2015)
Regioselective ring-opening of aziridines with potassium thiocyanate and thiols using sulfated zirconia as a heterogeneous recyclable catalyst.
Das B, et al.
Tetrahedron Letters, 47(5), 779-782 (2006)
Bowmaker, G.A. et al.
Inorganic Chemistry, 37, 1734-1734 (1998)
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