| CAS: | 95-55-6 |
| MF: | C6H7NO |
| MW: | 109.13 |
| EINECS: | 202-431-1 |
| Product Categories: | A;A-BAlphabetic;Alpha sort;AM to AQChemical Class;Amines;Aromatics;Intermediates of Dyes and Pigments;Aromatic Phenols;Phenoles and thiophenoles;Organic Building Blocks;Oxygen Compounds;Phenols;Pesticides&Metabolites;dye intermediates;Amine |
| Mol File: | 95-55-6.mol |
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| 2-Aminophenol Chemical Properties |
| Melting point | 172 °C |
| Boiling point | 164 °C (11.2515 mmHg) |
| density | 1.328 |
| vapor pressure | 14 hPa (153 °C) |
| refractive index | 1.5444 (estimate) |
| Fp | 168 °C |
| storage temp. | Store below +30°C. |
| solubility | 17 g/L (20°C) |
| form | Powder |
| pka | 4.78, 9.97(at 20℃) |
| Colour Index | 76520 |
| color | White to brown |
| PH | 6.5-7.5 (10g/l, H2O, 20℃) |
| PH Range | 6.5 - 7.5 at 10 g/l at 20 °C |
| Water Solubility | 17 g/L (20 ºC) |
| Merck | 14,461 |
| BRN | 606075 |
| Stability: | Stable, but may be air or light sensitive. Incompatible with strong oxidizing agents. |
| LogP | 0.620 |
| CAS DataBase Reference | 95-55-6(CAS DataBase Reference) |
| NIST Chemistry Reference | Phenol, 2-amino-(95-55-6) |
| EPA Substance Registry System | o-Aminophenol (95-55-6) |
| 2-Aminophenol Usage And Synthesis |
| Chemical Properties | 2-aminophenol appears as colorless needles or as white crystalline substance turning tan to brown on exposure to air. It forms white orthorhombic bipyramidal needles when crystallized from water or benzene. The crystals have eight molecules to the elementary cell. Insoluble in benzene, soluble in ethanol and water. o-aminophenol is contained in hair dyes and can cause contact dermatitis in hairdressers. |
| Uses | 2-Aminophenol is an isomer of 4-Aminophenol and is used as a reagent for the synthesis of heterocyclic compounds and dyes. It is also used to make dyes and pharmaceuticals. |
| Definition | ChEBI: 2-aminophenol is the aminophenol which has the single amino substituent located ortho to the phenolic -OH group. It has a role as a bacterial metabolite. |
| Preparation | 2-Aminophenol is obtained by reduction of o-nitrophenol with sodium sulfide or hydrogen gas. |
| Synthesis Reference(s) | Synthetic Communications, 13, p. 495, 1983 DOI: 10.1080/00397918308081828 |
| General Description | Off-white crystals or beige powder. |
Packing &shipping&Payment
Packing:25kg/drum
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
| Quantity(Kilograms) | 1 - 10000 | >10000 |
| Est. Time(days) | 5 | To be negotiated |
Company information
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.
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