Basic information Safety Supplier Related

1,2-DIAMINO-4,5-DIMETHOXYBENZENE

Basic information Safety Supplier Related

1,2-DIAMINO-4,5-DIMETHOXYBENZENE Basic information

Product Name:
1,2-DIAMINO-4,5-DIMETHOXYBENZENE
Synonyms:
  • 1,2-DIAMINO-4,5-DIMETHOXYBENZENE
  • 4,5-Dimethoxy-1,2-benzenediamine
  • 4,5-Dimethoxy-1,2-diaminobenzene
  • 4,5-Dimethoxy-1,2-phenylenediamine
  • 4,5-Dimethoxy-o-phenylenediamine
  • 4,5-diMethoxybenzene-1,2-diaMine
  • 1,2-Diamino-4,5-methoxybenzene
  • 2-Amino-4,5-dimethoxyaniline
CAS:
27841-33-4
MF:
C8H12N2O2
MW:
168.19
Product Categories:
  • Aromatic Hydrocarbons (substituted) & Derivatives
Mol File:
27841-33-4.mol
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1,2-DIAMINO-4,5-DIMETHOXYBENZENE Chemical Properties

Melting point:
134-135℃
Boiling point:
329.0±37.0 °C(Predicted)
Density 
1.184
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka
4?+-.0.10(Predicted)
form 
Solid
color 
Brown to black
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
2922290090
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1,2-DIAMINO-4,5-DIMETHOXYBENZENE Usage And Synthesis

Uses

1,2-Diamino-4,5-dimethoxybenzene reacts with aldehydes to produce highly fluorescent benzimidazole derivatives. It can be used for the detection of aromatic aldehydes as well as DTAN.

Synthesis

3395-03-7

27841-33-4

1,2-Dimethoxy-4,5-dinitrobenzene (5 g, 21.9 mmol) was used as starting material and dissolved in methanol (147 ml). Subsequently, 10% Pd/C catalyst (639 mg) was added to the solution. The reaction was stirred for 6 h at room temperature under hydrogen atmosphere. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated under reduced pressure. The resulting residue gave 4,5-dimethoxy-1,2-phenylenediamine (compound 28) directly without further purification.

References

[1] Patent: KR101840674, 2018, B1. Location in patent: Paragraph 0684-0686
[2] RSC Advances, 2016, vol. 6, # 30, p. 25203 - 25214
[3] Journal of Medicinal Chemistry, 1993, vol. 36, # 3, p. 331 - 342
[4] European Journal of Organic Chemistry, 2011, # 28, p. 5427 - 5440
[5] Chemistry - A European Journal, 2017, vol. 23, # 41, p. 9888 - 9896

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