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89050

Sigma-Aldrich

Thiosemicarbazide

puriss. p.a., 98%

Sinônimo(s):

Thiocarbamoyl hydrazide

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About This Item

Fórmula linear:
NH2CSNHNH2
Número CAS:
79-19-6
Peso molecular:
91.14
Beilstein:
506320
Número CE:
201-184-7
Número MDL:
MFCD00007620
Código UNSPSC:
12352100
ID de substância PubChem:
329769689
NACRES:
NA.22

grau

puriss. p.a.

Nível de qualidade

100

Ensaio

98%

forma

crystals

resíduo de ignição

≤0.08% (as SO4)

pf

180-183 °C (dec.) (lit.)

traços de ânion

sulfate (SO42-): ≤100 mg/kg

traços de cátion

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

cadeia de caracteres SMILES

NNC(N)=S

InChI

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

chave InChI

BRWIZMBXBAOCCF-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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.

Pictogramas

Skull and crossbones
GHS06

Palavra indicadora

Danger

Frases de perigo

H300,H412

Classificações de perigo

Acute Tox. 2 Oral - Aquatic Chronic 3

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

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Certificados de análise (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)
Measurement of net high-affinity urea uptake in maize plants
Zanin L, et al.
Bio-protocol, 5 (2015)
Ming Xue Li et al.
European journal of medicinal chemistry, 46(9), 4383-4390 (2011-07-26)
4-Cyclohexyl-1-(1-(pyrazin-2-yl)ethylidene)thiosemicarbazide (HL) and its transition metal complexes formulated as [Mn(L)(2)] (1) and [Ni(L)(2)] (2) have been prepared in 55-75% yield and characterized by elemental analysis, IR, MS, NMR and single-crystal X-ray diffraction studies. Biological activities of the synthesized compounds have
Agata Siwek et al.
Journal of molecular modeling, 18(9), 4159-4170 (2012-04-27)
The in vitro antifungal potency of six series of 4-arylthiosemicarbazides was evaluated. Two isoquinoline derivatives with an ortho-methoxy or ortho-methyl group at the phenyl ring were the most potent antifungal agents. Molecular modeling studies and docking of all 4-arylthiosemicarbazides into
Junbo He et al.
European journal of medicinal chemistry, 54, 925-930 (2012-07-04)
Series of novel derivatives of quinazoline containing thiosemicarbazide moiety 5 and 9 have been synthesized and tested for their antitumor activities in vitro against a panel of five human cancer cell lines. Bioassay results indicated that most of the prepared
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