蒸汽压
100 mmHg ( 26.7 °C)
质量水平
检测方案
99%
形式
powder or chunks
expl. lim.
2 %
储存温度
2-8°C
SMILES字符串
[H]N([H])[H].NC(O)=O
InChI
1S/CH3NO2.H3N/c2-1(3)4;/h2H2,(H,3,4);1H3
InChI key
BVCZEBOGSOYJJT-UHFFFAOYSA-N
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应用
- 二胺附加镁-奥萨拉嗪框架的协同二氧化碳捕集:本文讨论了一种利用二胺附加框架捕获二氧化碳的新方法,其中氨基甲酸铵用作关键的化学中间体。该研究强调了在碳捕获技术中使用氨基甲酸铵的环境效益,有助于减缓气候变化(Zhu et al., 2023)。
警示用语:
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
Chembiochem : a European journal of chemical biology, 18(19), 1903-1909 (2017-08-06)
Although widely occurring lipid oxidation, which is triggered by reactive oxygen species (ROS), produces a variety of oxidized lipids, practical methods to efficiently analyze oxidized lipids remain elusive. Herein, it is shown that the glycoblotting platform can be used to
Waste management (New York, N.Y.), 29(11), 2842-2845 (2009-08-18)
The traditional burning process is used to recover copper from scrapped PC board (printed circuit board) but it causes serious environmental problems. In this research a new process was developed which not only prevents pollution problems, but also maximizes the
Analytical chemistry, 82(24), 10021-10029 (2010-11-17)
Glycoblotting, high throughput method for N-glycan enrichment analysis based on the specific chemical ligation between aminooxy/hydrazide-polymers/solids and reducing N-glycans released from whole serum and cellular glycoproteins, was proved to be feasible for selective enrichment analysis of O-glycans of common (mucin)
Organic & biomolecular chemistry, 7(4), 687-694 (2009-02-06)
It was found that N-arylcarbamoyl and N-(phenylsulfonyl)carbamoyl (psc) groups could be effectively introduced onto the amino groups of deoxycytidine and deoxyadenosine derivatives and could be removed thermolytically. We succeeded in synthesizing DNA probes incorporating these thermo-removable protecting groups and developed
The Journal of organic chemistry, 71(7), 2811-2819 (2006-03-25)
We present a convenient synthesis of novel heteroaryl-fused 3-oxo-1,4-thiazepine-5-carboxamides and 5-oxo-1,4-thiazepine-3-carboxamides using a modification of four-component Ugi condensation. We demonstrate the usefulness and versatility of the developed approach for the synthesis of variously substituted compounds and discuss the scope and
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