| Identification | Back Directory | [Name]
N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE, 98 | [CAS]
205526-65-4 | [Synonyms]
Core 2/core 4 β-1
N-Benzyl Albuterol-d9
2,3-trimethoxy benzene
6-N-acetylglucosaminyltransferase
6-N-acetylglucosaminyltransferase 3
6-N-acetylglucosaminyltransferase 6
Anti-GCNT6 antibody produced in rabbit
Anti-GCNT3 antibody produced in rabbit
3-galactosyl-O-glycosyl-glycoprotein β-1
N-PHENYL-1-NAPHTHYLAMINE HYDROBROMIDE, 98
α1-[(Benzyl-tert-(butyl-d9)aMino)Methyl]-4-hydroxy-M-xylene-α,α'-diol
α1-Benzyl-tert-(butyl-aMino)aMinoMethyl-4-hydroxy-M-xylene-α1,α3-diol
Anti-Glucosaminyl(N-acetyl) transferase 3, mucin type antibody produced in rabbit
α1-[[(1,1-DiMethylethyl-d9)(phenylMethyl)aMino]Methyl]-4-hydroxy-1,3-benzenediMethanol | [Molecular Formula]
C16H13N.BrH | [MDL Number]
MFCD00044801 | [MOL File]
205526-65-4.mol | [Molecular Weight]
300.2 |
| Hazard Information | Back Directory | [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 |
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Alfa Aesar
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Merck KGaA
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