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Alfa Aesar
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| Products Intro: |
Product Name:N-Phenyl-1-naphthylaMine hydrobroMide, 97%
CAS:205526-65-4
Package:5g Remarks:H27615
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N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE manufacturers
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| | N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE Basic information |
| Product Name: | N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE | | Synonyms: | N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE, 98;1;2,3-trimethoxy benzene;N-Benzyl Albuterol-d9;α1-[(Benzyl-tert-(butyl-d9)aMino)Methyl]-4-hydroxy-M-xylene-α,α'-diol;α1-[[(1,1-DiMethylethyl-d9)(phenylMethyl)aMino]Methyl]-4-hydroxy-1,3-benzenediMethanol;α1-Benzyl-tert-(butyl-aMino)aMinoMethyl-4-hydroxy-M-xylene-α1,α3-diol;6-N-acetylglucosaminyltransferase 6 | | CAS: | 205526-65-4 | | MF: | C16H13N.BrH | | MW: | 300.2 | | EINECS: | | | Product Categories: | | | Mol File: | 205526-65-4.mol |  |
| | N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE Chemical Properties |
| Melting point | 221-229℃ | | storage temp. | -20°C | | form | buffered aqueous solution | | biological source | rabbit | | CAS DataBase Reference | 205526-65-4 |
| WGK Germany | WGK 1 | | HazardClass | 9 | | Storage Class | 10 - Combustible liquids |
| | N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE Usage And Synthesis |
| Chemical Properties | light purple crystalline powder | | Uses | Labelled N-Benzyl Albuterol (B224760). N-Benzyl Albuterol is an impurity of Albuterol sulfate (A514500) (Salbutamol sulfate) bulk drug. | | Biological Activity | This enzyme catalyzes O-glycan branch synthesis of the core 2 and core 4 type in mucins and controls expression of core 2 branched oligosaccharides and I antigens on the cell surface.This enzyme catalyzes O-glycan branch synthesis of the core 2 and core 4 type in mucins and controls expression of core 2 branched oligosaccharides and I antigens on the cell surface. | | Synthesis | 1-Naphthylamine was added to the reactor and melted by heating, then dehydrated at 110??C-180??C for 2-3 hours. Add aniline and p-aminobenzenesulfonic acid, stir well, then slowly raise the temperature to 230??-240?? in 25 hours for condensation reaction. The ammonia released in the reaction is absorbed with water and sulfuric acid to produce ammonia and ammonium sulfate by-products. When the amount of ammonia released in the reaction is very small, the reaction is stopped, neutralized to neutral by adding soda ash, and fractionated in high vacuum. Recover unreacted aniline and naphthylamine, and vaporize the product. After cooling, slicing and packing, it is N-phenyl-1-naphthylamine hydrobromide. |
| | N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE Preparation Products And Raw materials |
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