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Merck
CN

89050

Sigma-Aldrich

硫代氨基脲

puriss. p.a., 98%

别名:

肼基碳硫酰胺

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About This Item

线性分子式:
NH2CSNHNH2
CAS号:
分子量:
91.14
Beilstein:
506320
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

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。

象形图

Skull and crossbones

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

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Zanin L, et al.
Bio-protocol, 5 (2015)
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)
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
Mohamed A Riswan Ahamed et al.
Journal of hazardous materials, 248-249, 59-68 (2013-01-29)
2-Amino-6-nitro-benzothiazole and thiosemicarbazide with formaldehyde (BTF) terpolymer was synthesized by the condensation polymerization technique. The elemental analysis and physico-chemical parameters of the terpolymer were measured. This chelation terpolymer was characterized by infrared, electronic and nuclear magnetic resonance ((1)H &(13)C NMR)
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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