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HYDROXYDICHLORODIPHENYL ETHER

  • Product Name HYDROXYDICHLORODIPHENYL ETHER
  • cas 3380-30-1
  • purity 99%
Inquiry

Manufacturer supply high quality HYDROXYDICHLORODIPHENYL ETHER 3380-30-1 with GMP standards

  • Molecular Formula: C12H8Cl2O2
  • Molecular Weight: 255.1
  • Vapor Pressure: 7.23E-05mmHg at 25°C 
  • Melting Point: 78-79 °C 
  • Boiling Point: 333.1°Cat760mmHg 
  • PKA: 8.07±0.35(Predicted) 
  • Flash Point: 155.2°C 
  • PSA: 29.46000 
  • Density: 1.398g/cm3 
  • LogP: 4.49130 

HYDROXYDICHLORODIPHENYL ETHER(Cas 3380-30-1) Usage

General Description

Hydroxydichlorodiphenyl ether, also known as OH-PCB, is a chemical compound that belongs to the group of polychlorinated biphenyls (PCBs). It is a byproduct of the metabolism of PCBs in the environment and has been found to have toxic effects on both humans and wildlife. OH-PCB has been shown to interfere with hormone signaling and disrupt normal endocrine function, leading to a range of health problems such as reproductive and developmental issues, immune system suppression, and increased risk of cancer. Due to its persistence in the environment and potential for bioaccumulation, OH-PCB poses a significant threat to ecosystems and human health, and measures to reduce its exposure and production are necessary to mitigate its harmful effects.

InChI:InChI=1/C12H8Cl2O2/c13-8-1-4-10(5-2-8)16-12-6-3-9(14)7-11(12)15/h1-7,15H

3380-30-1 Relevant articles

Method for preparing diclosan through Baeyer-Villiger oxidation

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Paragraph 0010; 0037-0051, (2021/07/01)

The invention provides a method for prep...

Preparation method of active bactericide 4,4'-dichloro-2-hydroxyl diphenyl ether

-

Paragraph 0032; 0033; 0034; 0037; 0038, (2017/12/09)

The invention discloses a preparation me...

Process for the preparation of halogenated hydroxydiphenyl compounds

-

, (2008/06/13)

There is described a process for the pre...

Process for the preparation of halogenated hydroxydiphenyl compounds

-

, (2008/06/13)

A process for the preparation of halohyd...

3380-30-1 Process route

C<sub>12</sub>H<sub>8</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>5</sub>S

C12 H8 Cl2 N2 O5 S

5-chloro-2-(4-chlorophenoxy)phenol
3380-30-1

5-chloro-2-(4-chlorophenoxy)phenol

Conditions
Conditions Yield
With sulfuric acid; at 165 ℃; for 1h; Temperature; Large scale;
616 kg
Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester
3380-53-8

Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester

5-chloro-2-(4-chlorophenoxy)phenol
3380-30-1

5-chloro-2-(4-chlorophenoxy)phenol

Conditions
Conditions Yield
With toluene; sodium hydroxide; for 2h; Reflux;
1.58 g

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    Thiocarbonic acid O-[5-chloro-2-(4-chloro-phenoxy)-phenyl] ester O-(4-octyl-phenyl) ester

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