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89050

Sigma-Aldrich

Thiosemicarbazide

puriss. p.a., 98%

Sinonimo/i:

Thiocarbamoyl hydrazide

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About This Item

Formula condensata:
NH2CSNHNH2
Numero CAS:
79-19-6
Peso molecolare:
91.14
Beilstein:
506320
Numero CE:
201-184-7
Numero MDL:
MFCD00007620
Codice UNSPSC:
12352100
ID PubChem:
329769689
NACRES:
NA.22

Grado

puriss. p.a.

Livello qualitativo

100

Saggio

98%

Forma fisica

crystals

Residuo alla calcinazione

≤0.08% (as SO4)

Punto di fusione

180-183 °C (dec.) (lit.)

Anioni in tracce

sulfate (SO42-): ≤100 mg/kg

Cationi in tracce

Ca: ≤50 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

Stringa SMILE

NNC(N)=S

InChI

1S/CH5N3S/c2-1(5)4-3/h3H2,(H3,2,4,5)
BRWIZMBXBAOCCF-UHFFFAOYSA-N

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Descrizione generale

Thiosemicarbazide is an environmentally toxic compound, which is usually derived from thiourea. Its ability to chelate trace metals promotes its biological activity against certain tumors, protozoa, influenza, pesticides, and fungicides. It is widely used as a metal complexing agent in various fields involving the characterization of aliphatic or aromatic aldehydes, ketones, and polysaccharides.

Applicazioni

Thiosemicarbazide has been used as an analytical reagent for the measurement of urea net high-affinity uptake in roots of intact maize plants using colorimetric assay.

Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H300 - H412

Classi di pericolo

Acute Tox. 2 Oral - Aquatic Chronic 3

Codice della classe di stoccaggio

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
BCBS7883V
BCBT8461
BCBT7029
BCBT4808
BCBQ8169V

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Electrochemical determination of thiosemicarbazide using the glassy carbon electrode modified with multi-walled carbon nanotubes
Faizbakhsh N and Safari Z
Advances in Nanochemistry, 1(2), 52-55 (2019)
Hong-Jia Zhang et al.
European journal of medicinal chemistry, 46(9), 4702-4708 (2011-08-06)
A series of novel chalcone thiosemicarbazide derivatives (4a-4x) have been designed, synthesized, structurally determined, and their biological activities were also evaluated as potential EGFR kinase inhibitors. All the synthesized compounds are first reported. Among the compounds, compound 4r showed the
José Ruiz et al.
Inorganic chemistry, 52(2), 974-982 (2013-01-11)
A series of new organoiridium(III) complexes [Ir(N-C)(2)(N-S)]Cl (HN-C = 2-phenylpyridine (Hppy), N-S = methyl thiosemicarbazide (1), phenyl thiosemicarbazide (2) and naphtyl thiosemicarbazide (3)) have been synthesized and characterized. The crystal structure of (1) has been established by X-ray diffraction, showing
Pedro I da S Maia et al.
Inorganic chemistry, 51(3), 1604-1613 (2012-01-12)
Na[AuCl(4)]·2H(2)O reacts with tridentate thiosemicarbazide ligands, H(2)L1, derived from N-[N',N'-dialkylamino(thiocarbonyl)]benzimidoyl chloride and thiosemicarbazides under formation of air-stable, green [AuCl(L1)] complexes. The organic ligands coordinate in a planar SNS coordination mode. Small amounts of gold(I) complexes of the composition [AuCl(L3)] are
Juan Liu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 93, 245-249 (2012-04-10)
A simple and highly selective colorimetric sensor (L1) bearing thiosemicarbazide moiety as binding site and nitrophenyl moiety as signal group were synthesized. Sensor L1 showed great colorimetric single selectivity and high sensitivity for mercury cation in DMSO and DMSO/H(2)O binary
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