T8656
硫脲
ACS reagent grade, ≥99.0%
别名:
Sulfourea, 硫代尿素
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关于此项目
线性分子式:
NH2CSNH2
化学文摘社编号:
分子量:
76.12
Beilstein:
605327
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.21
产品名称
硫脲, ACS reagent, ≥99.0%
等级
ACS reagent
质量水平
方案
≥99.0%
灼烧残渣
≤0.1% (as SO4)
缺失
≤0.5% loss on drying, 105°C, 2h
mp
170-176 °C (lit.)
174-177 °C
溶解性
H2O: passes test
官能团
amine
thiourea
SMILES字符串
NC(N)=S
InChI
1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)
InChI key
UMGDCJDMYOKAJW-UHFFFAOYSA-N
基因信息
mouse ... Ephx2(13850)
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一般描述
硫脲是含尿素硫的类似物。
应用
硫脲已用于：
- 用作肝组织匀浆的裂解缓冲液组分
- 二维凝胶蛋白酪氨酸磷酸酶（PTP）测定所用的二维样品缓冲液
- 蛋白质提取补液缓冲液
离液剂；强变性剂。增加蛋白质的溶解性和回收率
生化/生理作用
硫脲是过氧化物自由基的自由基清除剂。其表现出了抑制脂质过氧化和紫外线(UV)诱导胶原交联的作用。硫脲可用作生长刺激剂，抑制植物芽休眠。目前确知其可用于治疗甲状腺功能亢进症。
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Repr. 2
储存分类代码
11 - Combustible Solids
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
危险化学品
此项目有
Effect of copper nanoparticles exposure in the physiology of the common carp (Cyprinus carpio): Biochemical, histological and proteomic approaches
Gupta YR, et al.
Aquaculture and Fisheries, 1(2), 15-23 (2016)
Investigation of protein-tyrosine phosphatases by in-gel assays.
Markova B, et al.
Methods, 35(1), 22-27 (2005)
Mechanism of the reduction of methylene blue by thiourea in aqueous acidic medium
Osunlaja AA
International Journal of ChemTech Research, 4(2), 609-617 (2012)
Shrinivas Venkataraman et al.
Macromolecular rapid communications, 34(8), 652-658 (2013-03-14)
Readily water-soluble PEGylated amphiphiles containing bis-thiourea-based molecular recognition units at the interface of hydrophobic and hydrophilic blocks are developed. Self-assembly of these amphiphiles is found to be dependent on the exact chemical composition of the hydrophobic component. Elongated, spherical, and
Mireille Vonlanthen et al.
The Journal of organic chemistry, 78(8), 3980-3988 (2013-03-09)
Proof that sulfur is a viable reporting element for the development of fluorescent chemosensors for metal ions is presented. To date, the majority of metal-responsive fluorescent chemosensors have relied on metal-nitrogen coordination to provide a fluorescence response, most commonly by
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