Sodium Thiocyanate

FORMULA : NaSCN
ORIGIN : China
PACKING : 25kg/bag
APPLICATION : Used in construction, food industry...

Short description

Chemical name: Sodium thiocyanate Other names: Sodium thiocyanate, Sodium sulfoxate, Sodium rhodanite, Sodium rhodanate, Sodium rhodanide, Sodium sulfocyanate, Sodium rhodanate, Thiocyanic acid, sodium salt Formula: NaSCN CAS number: 540-72-7 Appearance: colorless crystals, rotting Packing: 25kg / bag Origin: China Molecular weight: 81,072 g / mol Density: 1.74 g / cm³ CID PubChem: 516871 Sodium thiocyanate is employed to convert alkyl halides into the corresponding alkylthiocyanates. Closely related reagents include ammonium thiocyanate and potassium thiocyanate, which has twice the solubility in water. Silver thiocyanate may be used as well; the precipitation of insoluble silver halides help simplify workup. Treatment of isopropyl bromide with sodium thiocyanate in a hot ethanolic solution affords isopropyl thiocyanate.[4] Protonation of sodium thiocyanate affords isothiocyanic acid, S=C=NH (pKa = −1.28).[5] This species is generated in situ from sodium thiocyanate; it adds to organic amines to afford derivatives of thiourea.
Description
Sodium thiocyanate (sometimes called sodium sulphocyanide) is the chemical compound with the formula NaSCN.
Technical Data

Chemical name: Sodium thiocyanate

Other names: Sodium thiocyanate, Sodium sulfoxate, Sodium rhodanite, Sodium rhodanate, Sodium rhodanide, Sodium sulfocyanate, Sodium rhodanate, Thiocyanic acid, sodium salt

Formula: NaSCN

CAS number: 540-72-7

Appearance: colorless crystals, rotting

Packing: 25kg / bag

Origin: China

Molecular weight: 81,072 g / mol

Density: 1.74 g / cm³

CID PubChem: 516871

Sodium thiocyanate (sometimes called sodium sulphocyanide) is the chemical compound with the formula NaSCN. This colorless deliquescent salt is one of the main sources of the thiocyanate anion. As such, it is used as a precursor for the synthesis of pharmaceuticals and other specialty chemicals.[2] Thiocyanate salts are typically prepared by the reaction of cyanide with elemental sulfur:

8 NaCN + S8 → 8 NaSCN

Sodium thiocyanate crystallizes in an orthorhombic cell. Each Na+ center is surrounded by three sulfur and three nitrogen ligands provided by the triatomic thiocyanate anion.[3] It is commonly used in the laboratory as a test for the presence of Fe3+ ions.

Applications:

Sodium thiocyanate is employed to convert alkyl halides into the corresponding alkylthiocyanates. Closely related reagents include ammonium thiocyanate and potassium thiocyanate, which has twice the solubility in water. Silver thiocyanate may be used as well; the precipitation of insoluble silver halides help simplify workup. Treatment of isopropyl bromide with sodium thiocyanate in a hot ethanolic solution affords isopropyl thiocyanate.[4] Protonation of sodium thiocyanate affords isothiocyanic acid, S=C=NH (pKa = −1.28).[5] This species is generated in situ from sodium thiocyanate; it adds to organic amines to afford derivatives of thiourea.

 

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                    Giấy phép kinh doanh số : 0304920055 cấp ngày : 05/04/2007 bởi Sở Kế Hoạch và Đầu Tư TP.Hồ Chí Minh

                    Người đại diện : ông Phạm Đình Chung