| 2-Methoxy-4-nitroaniline Basic information |
| Product Name: | 2-Methoxy-4-nitroaniline |
| Synonyms: | redbasecibav;redbaseirgav;METHOXY-4-NITROANILINE;Brilliant Red Developing Base 4B;4-NITRO-ORTHO-ANISIDINE;-Amino-5-nitrophenyl methyl ether;RED B ASE;RED B BASE |
| CAS: | 97-52-9 |
| MF: | C7H8N2O3 |
| MW: | 168.15 |
| EINECS: | 202-588-6 |
| Product Categories: | Intermediates of Dyes and Pigments;Dyes and Pigments;Anilines, Amides & Amines;Anisoles, Alkyloxy Compounds & Phenylacetates;Nitro Compounds |
| Mol File: | 97-52-9.mol |
| 2-Methoxy-4-nitroaniline Chemical Properties |
| Melting point | 140-142 °C(lit.) |
| Boiling point | 337.07°C (rough estimate) |
| density | 1,211 g/cm3 |
| refractive index | 1.6010 (estimate) |
| storage temp. | Store below +30°C. |
| solubility | 0.2g/l |
| form | Crystalline Powder |
| pka | 1.02±0.10(Predicted) |
| color | Yellow to orange |
| PH | 6.2 (0.2g/l, H2O, 20℃) |
| Water Solubility | slightly soluble |
| BRN | 879619 |
| InChIKey | GVBHRNIWBGTNQA-UHFFFAOYSA-N |
| CAS DataBase Reference | 97-52-9(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzenamine, 2-methoxy-4-nitro-(97-52-9) |
| EPA Substance Registry System | 2-Methoxy-4-nitroaniline (97-52-9) |
| Safety Information |
| Hazard Codes | Xn,Xi |
| Risk Statements | 22-36/37/38-20/21/22 |
| Safety Statements | 26-37/39-36/37 |
| RIDADR | UN 3077 9 / PGIII |
| WGK Germany | 2 |
| RTECS | BZ7170000 |
| Hazard Note | Irritant |
| TSCA | Yes |
| HS Code | 29222900 |
| MSDS Information |
| Provider | Language |
|---|---|
| 2-Methoxy-4-nitroaniline | English |
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| 2-Methoxy-4-nitroaniline Usage And Synthesis |
| Chemical Properties | yellow to orange crystalline powder |
| Uses | 2-Methoxy-4-nitroaniline is used as a photometric reagent for the determination of ethinylestradiol (ETE), a semi-synthetic estrogen that is widely used in oral contraceptives. |
| General Description | 2-Methoxy-4-nitroaniline is an important inducer of CYP1A2 owing to its small molecular size. |
| Flammability and Explosibility | Nonflammable |
| Biochem/physiol Actions | The metabolism of 2-methoxy-4-nitroaniline (MNA) occurs via the hydroxylation of the phenyl ring to form 6-hydroxy MNA in Harlan Sprague Dawley rats and B6C3F(1)/N mice. |
| 2-Methoxy-4-nitroaniline Preparation Products And Raw materials |
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