N,O-Di(2-hydroxyethyl)-2-amino-5-nitrophenol丨CAS 59820-43-8

N,O-Di(2-hydroxyethyl)-2-amino-5-nitrophenol丨CAS 59820-43-8
Product Introduction:
Catalog No.: SS129929
CAS No.: 59820-43-8
Purity(HPLC): 98% min
Product Name: N,O-Di(2-hydroxyethyl)-2-amino-5-nitrophenol
Molecular Formula: C10H14N2O5
Molecular Weight: 242.23
Synonym(s): 2-(3-Nitro-6-(beta-hydroxyethylamino)phenoxy)ethanol; 2-((2-(2-Hydroxyethoxy)-4-nitrophenyl)amino)ethanol; HC Yellow 4
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of n,o-di(2-hydroxyethyl)-2-amino-5-nitrophenol丨cas 59820-43-8 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance: Yellow-brown crystal powder
Purity (HPLC): 98% min
Loss on drying: 1.0% max
Ash: 1.0% max
Fe: 50 ppm max

 

 

 

Applications

 

N,O-Di(2-hydroxyethyl)-2-amino-5-nitrophenol is a multifunctional chemical widely used in pharmaceuticals, dye chemistry, and biochemical research. It serves as a key intermediate in the synthesis of nitrophenol derivatives, which are used in drug development, enzyme inhibition studies, and as building blocks for bioactive molecules. In dye and pigment industries, it can be incorporated into functionalized colorants and fluorescent compounds due to its nitrophenol structure, which allows electron-rich interactions and tunable optical properties. Additionally, it is utilized in chemical research to study amino- and hydroxy-functionalized aromatic compounds, enabling the development of novel synthetic methodologies and structure-activity relationship studies.

 

Benefits

 

The compound offers several advantages due to its multifunctional groups – amino, nitro, and hydroxyethyl moieties – which provide high reactivity and versatility in chemical transformations. Its hydroxyethyl groups improve solubility in polar solvents and enable selective derivatization, while the nitrophenol moiety allows electron-withdrawing effects that are useful in tuning chemical and optical properties. The compound is chemically stable under proper storage conditions and compatible with a variety of reaction conditions, making it convenient for both laboratory research and industrial applications. These features allow efficient synthesis of derivatives with applications in pharmaceuticals, dyes, and biochemical studies.

 

Conclusion

 

N,O-Di(2-hydroxyethyl)-2-amino-5-nitrophenol is a versatile intermediate with significant applications in drug development, dye chemistry, and chemical research. Its multifunctional structure provides chemical reactivity, solubility, and tunable properties, supporting the synthesis of bioactive molecules, functional colorants, and novel aromatic derivatives. The compound continues to be valuable in developing advanced materials and bioactive compounds.

 

 

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