2-Amino-4-nitro anisidine
98%
- Product Code: 135268
Alias:
Big red group R; 2-amino-4-nitroanisole; 5-nitroo-methoxyaniline; crude chromo-R; o-amino-p-nitroanisole
CAS:
99-59-2
| Molecular Weight: | 168.15 g./mol | Molecular Formula: | C₇H₈N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00007261 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed |
Product Description:
Used primarily in the synthesis of azo dyes and pigments, this compound serves as a key intermediate in the textile and printing industries. Its structure allows for diazotization and coupling reactions, making it valuable for producing colored compounds with good light and wash fastness. It is also employed in the manufacture of specialty dyes for inkjet printing and optical sensors due to its distinct electron-donating and accepting groups. Additionally, it finds use in research settings for developing new aromatic amines and nitro-substituted compounds with potential biological activity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light Orange to Brown Powder or Crystals or Solid |
| Purity | 97.5-100 (%) |
| Melting Point | 117-120 Degree Celsius |
| Infrared Spectrum | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | Ft6,096.05 |
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| 25.000 | 10-20 days | Ft18,708.57 |
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| 100.000 | 10-20 days | Ft67,266.78 |
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2-Amino-4-nitro anisidine
Used primarily in the synthesis of azo dyes and pigments, this compound serves as a key intermediate in the textile and printing industries. Its structure allows for diazotization and coupling reactions, making it valuable for producing colored compounds with good light and wash fastness. It is also employed in the manufacture of specialty dyes for inkjet printing and optical sensors due to its distinct electron-donating and accepting groups. Additionally, it finds use in research settings for developing new aromatic amines and nitro-substituted compounds with potential biological activity.
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| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
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