• Product NameSodium 2-nitrophenoxide
  • CasNo. 824-39-5
  • MFC6H4NNaO3
  • MW161.092
  • Purity
  • Appearancedark red acicular crystals
  • Packing
  • Contact usInquiry

Product Details

CasNo: 824-39-5

MF: C6H4NNaO3

Appearance: dark red acicular crystals

Factory Sells Best Quality Sodium 2-nitrophenoxide 824-39-5 with steady supply

  • Molecular Formula:C6H4NNaO3
  • Molecular Weight:161.092
  • Appearance/Colour:dark red acicular crystals 
  • Vapor Pressure:0.0987mmHg at 25°C 
  • Melting Point:215-218°C 
  • Boiling Point:215.8 °C at 760 mmHg 
  • Flash Point:97.1 °C 
  • PSA:68.88000 
  • Density:1.301 
  • LogP:2.26180 

Sodium 2-nitrophenoxide(Cas 824-39-5) Usage

General Description

Sodium 2-nitrophenoxide, also known as sodium o-nitrophenolate, is an organic compound primarily used as a plant growth regulator. Chemically, it's a sodium salt of 2-nitrophenol, created through the process of nitration of phenol. Its structural formula is C6H4NO3Na. Sodium 2-nitrophenoxide helps stimulate the growth of crops by enhancing the rate of photosynthesis, promoting the absorption of nutrients and improving resistance to pests and diseases. It's generally used in the agriculture industry for crops like wheat, cotton, and fruit trees. Moreover, due to its nitro group, it can also act as a strong reducing agent. Overexposure can potentially cause harm to the environment or human health.

InChI:InChI=1/C6H5NO3.Na/c8-6-4-2-1-3-5(6)7(9)10;/h1-4,8H;/q;+1/p-1

824-39-5 Relevant articles

Catalytic applications of β-cyclodextrin/palladium nanoparticle thin film obtained from oil/water interface in the reduction of toxic nitrophenol compounds and the degradation of azo dyes

Zare Asadabadi, Azam,Hoseini, S. Jafar,Bahrami, Mehrangiz,Nabavizadeh, S. Masoud

, p. 6513 - 6522 (2019/05/10)

A supramolecular catalyst of Pd/β-cyclod...

Synthesis and isolation of non-chromophore cage-rearranged silsesquioxanes from base-catalyzed reactions

Hanprasit, Sasikarn,Tungkijanansin, Nuttanee,Prompawilai, Arisa,Eangpayung, Supattra,Ervithayasuporn, Vuthichai

supporting information, p. 16117 - 16120 (2016/10/31)

The nucleophilicity of both ortho- and m...

A process for the preparation of ortho-aminophenol

-

Paragraph 0043; 0044, (2017/04/08)

The invention belongs to the technical f...

SYNTHESIS OF BAPTA-AM ANALOGUES CAPABLE OF ENHANCING THE VASCULAR PRODUCTION OF PROSTACYCLIN

Heilporn, S.,Broeders, F.,Daloze, D.,Braekman, J. C.,Boeynaems, J. M.

, p. 309 - 320 (2007/10/02)

About 30 analogues of BAPTA-AM, a potent...

824-39-5 Process route

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

sodium o-nitrophenate
824-39-5

sodium o-nitrophenate

Conditions
Conditions Yield
With sodium hydroxide; at 160 - 175 ℃; for 4.5h; under 51005.1 - 54005.4 Torr; Large scale;
1.2 t
2-hydroxynitrobenzene
88-75-5,78813-12-4

2-hydroxynitrobenzene

sodium o-nitrophenate
824-39-5

sodium o-nitrophenate

Conditions
Conditions Yield
With sodium hydroxide; In ethanol;
With sodium hydroxide; In water; at 20 ℃; for 1h;
With sodium tetrahydroborate; In water;

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