等级
puriss. p.a.
质量水平
方案
98%
表单
crystals
灼烧残渣
≤0.08% (as SO4)
mp
180-183 °C (dec.) (lit.)
痕量阴离子
sulfate (SO42-): ≤100 mg/kg
痕量阳离子
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
官能团
amine
hydrazine
thiourea
SMILES字符串
NNC(N)=S
InChI
1S/CH5N3S/c2-1(5)4-3/h3H2,(H3,2,4,5)
InChI key
BRWIZMBXBAOCCF-UHFFFAOYSA-N
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一般描述
硫代氨基脲是一种对环境有毒的化合物，通常来源于硫脲。螯合微量金属的能力提高了它对某些肿瘤、原生动物、流行性感冒、杀虫剂和杀真菌剂的生物活性。它是一种使用广泛的金属络合剂，用于涉及脂肪族或芳香族醛、酮和多糖表征的各个领域。
应用
硫代氨基脲已被用作分析试剂，用于通过比色法测量完整玉米植株根系中尿素的净高亲和力吸收。
警示用语：
Danger
危险声明
危险分类
Acute Tox. 2 Oral - Aquatic Chronic 3
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
农药列管产品
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)
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Bio-protocol, 5 (2015)
Moamen S Refat et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 92, 336-346 (2012-03-27)
Two derivatives of thiosemicarbazide were prepared. Their complexes were prepared using Mn(II) and Cu(II) salts. All the isolated complexes are characterized using the following spectra: IR, UV-Vis, Mass, (1)H NMR and X-ray diffraction. Magnetic measurements and thermal analysis are the
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
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