26271-75-0

Basic information

• Product Name: 3,5-dichloro-1,4-aminophenol
• Synonyms: 3,5-dichloro-1,4-aminophenol;4-Amino-3,5-dichlorophenol
• CAS NO: 26271-75-0
• Molecular Formula: C₆H₅Cl₂NO
• Molecular Weight: 178.02
• Mol File: 26271-75-0.mol

Chemical Properties

• Boiling Point: 294°Cat760mmHg
• Flash Point: 131.6°C
• Appearance: /
• Density: 1.56g/cm³
• Vapor Pressure: 0.00095mmHg at 25°C
• Refractive Index: 1.661
• CAS DataBase Reference: 3,5-dichloro-1,4-aminophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dichloro-1,4-aminophenol(26271-75-0)
• EPA Substance Registry System: 3,5-dichloro-1,4-aminophenol(26271-75-0)

Safety Data

• Hazardous Substances Data: 26271-75-0(Hazardous Substances Data)

Usage

Uses

4-Amino-3,5-dichlorophenol is a useful research chemical compound.

InChI:InChI=1/C6H5Cl2NO/c7-4-1-3(10)2-5(8)6(4)9/h1-2,10H,9H2

Upstream product

• 51225-20-8 1,3-dichloro-5-ethoxy-2-aminobenzene 
• 10034-85-2 hydrogen iodide 
• 15307-86-5 [2-(2,6-dichloroanilino)phenyl]acetic acid 
• 591-35-5 3,5-dichlorophenol 
• 60144-85-6 4'-acetoxy-2'-chloroacetanilide 
• 2623-33-8 4-acetoxyacetanilide 
• 7647-01-0 hydrogenchloride 
• 60-29-7 diethyl ether 
• 637-62-7 p-benzoquinone oxime 
• 857623-82-6 5-acetoxy-2-acetylamino-1,3-dichloro-benzene 
• 50590-08-4 3,5-dichloro-4-nitrophenol 

Downstream Products

• 609-19-8 3,4,5-trichlorophenol 
• 3336-19-4 2,6-dichloro-4-hydroxy-benzonitrile 
• 697-91-6 2,6-dichloro-1,4-benzoquinone 
• 1092065-44-5 C₂₆H₂₆Cl₂N₄O₄ 
• 213747-80-9 N-(3,5-dichloro-4-hydroxyphenyl)-4-(3,5-dimethylphenylsulphanyl)-2-pyrimidineamine 
• 500878-30-8 3,4,5-trichloro-2,6-bis-hydroxymethyl-phenol 
• 303049-41-4 N-Tosyl-3,5-dichloro-1,4-benzoquinonemonoimine 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 5335-87-5 4,4'-dimethoxyphenyl disulfide 
• 103-19-5 di(p-tolyl) disulfide 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 5147-73-9 N-[(4-nitrophenyl)thio]-2,6-dichloro-1,4-benzoquinone imine 

Relevant articles and documents

TiO2-modified MALDI target for in vitro modeling of the oxidative biotransformation of diclofenac

The UV-induced photocatalytic oxidation in the presence of TiO2 nanoparticles (UV/TiO2-PCO) is a more adequate approach than electrochemical oxidation to simulate the oxidative metabolism of diclofenac based on the comparative analysis of oxidation products using high-resolution tandem mass spectrometry. A simple and fast high-throughput technique is proposed for modeling the oxidative metabolism, which involves UV/TiO2-PCO performed directly on a MALDI target and subsequent analysis by matrix-assisted laser desorption/ionization mass spectrometry. The ranges and yields of diclofenac oxidation products obtained by the conventional bulk UV/TiO2-PCO and the proposed on-target version are in excellent agreement.

Biobased Poly(ethylene furanoate) Polyester/TiO2 Supported Nanocomposites as Effective Photocatalysts for Anti-inflammatory/Analgesic Drugs

In the present study, polymer supported nanocomposites, consisting of bio-based poly(ethylene furanoate) polyester and TiO2 nanoparticles, were prepared and evaluated as effective photocatalysts for anti-inflammatory/analgesic drug removal. Nanocomposites were prepared by the solvent eVaporation method containing 5, 10, 15, and 20 wt% TiO2 and characterized using Fourier Transform Infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). Thin films of them have been prepared by the melt press and optimization of the photocatalytic procedure was conducted for the most efficient synthesized photocatalyst. Finally, mineralization was evaluated by means of Total organic carbon (TOC) reduction and ion release, while the transformation products (TPs) generated during the photocatalytic procedure were identified by high-resolution mass spectrometry.