Monobenzone

Basic information

  • Product Name:Monobenzone
  • CasNo.:103-16-2
  • MF:C13H12O2

Physical and Chemical Properties

  • Purity:99%
  • Melting Point:119-120 °C(lit.)
  • Appearance:cream to beige-light brownish crystals
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Product Details

CasNo: 103-16-2

MF: C13H12O2

Appearance: cream to beige-light brownish crystals

99% Purity Commercial production Monobenzone 103-16-2 with Cheapest Price

  • Molecular Formula:C13H12O2
  • Molecular Weight:200.237
  • Appearance/Colour:cream to beige-light brownish crystals 
  • Melting Point:119-120 °C(lit.) 
  • Refractive Index:1.5906 (estimate) 
  • Boiling Point:359.1 °C at 760 mmHg 
  • PKA:10.29±0.15(Predicted) 
  • Flash Point:213.4 °C 
  • PSA:29.46000 
  • Density:1.16 g/cm3 
  • LogP:2.97120 

Monobenzone(Cas 103-16-2) Usage

Monobenzone is a depigmenting agent. It is commonly used to treat skin hyperpigmentation conditions such as vitiligo. It achieves the depigmentation effect by destroying melanocytes and reducing the production of melanin in the skin. The use of monobenzone requires strict adherence to doctor's orders and specific usage methods, as improper use may lead to uneven depigmentation or other skin problems. It usually comes in the form of a cream or ointment and should be used with caution under the guidance of a doctor. For example, for some severe pigmentation diseases, monobenzone may be an effective treatment option, but the skin's reaction needs to be closely observed during use.

 

InChI:InChI=1/C14H14O.C6H6O2/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14;7-5-1-2-6(8)4-3-5/h1-10H,11-12H2;1-4,7-8H

103-16-2 Relevant articles

Expedient and simple method for regeneration of alcohols from toluenesulfonates using Mg-MeOH

Sridhar, Madabhushi,Kumar, B. Ashok,Narender

, p. 2847 - 2850 (1998)

Efficient conversion of toluenesulfonate...

Anti-Melanoma immunity and local regression of cutaneous metastases in melanoma patients treated with monobenzone and imiquimod; a phase 2 a trial

Hansje-Eva Teulings,Esther P. M. Tjin,Karina J. Willemsen,Stephanie van der Kleij,Sylvia ter Meulen,E. Helen Kemp,Gabrielle Krebbers,Carel J. M. van Noesel,Cornelis L. M. C. Franken,Jan W. Drijfhout,Cornelis J. M. Melief,Ludmila Nieuweboer-Krobotova,Omgo E. Nieweg,Jos A. van der Hage,J. P. Wietze van der Veen,Germaine N. RelyveldORCID Icon &Rosalie M. LuitenDept. of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands Correspondence r.m.luiten@amc.uva.nl View further author information

, OncoImmunology Volume 7, 2018 - Issue 4

We investigated a novel immunotherapeutic approach of the skin-depigmenting compound monobenzone synergizing with imiquimod in inducing antimelanoma immunity and melanoma regression. Stage III-IV melanoma patients with non-resectable cutaneous melanoma metastases were treated with monobenzone and imiquimod (MI) therapy applied locally to cutaneous metastases and adjacent skin during 12 weeks, or longer.

Baeyer-Villiger oxidation of β-aryl substituted unsaturated carbonyl compounds with hydrogen peroxide and catalytic selenium dioxide

Guzman,Mendoza,Garcia,Garibay,Oliveras,Maldonado

, p. 2121 - 2133 (1995)

A simple and cheap oxidative procedure u...

103-16-2 Process route

4-(benzyloxy)-4-methoxy-2,5-cyclohexadien-1-one
73010-55-6

4-(benzyloxy)-4-methoxy-2,5-cyclohexadien-1-one

4-Benzyloxyphenol
103-16-2

4-Benzyloxyphenol

benzaldehyde
100-52-7

benzaldehyde

4-methoxy-phenol
150-76-5

4-methoxy-phenol

Conditions
Conditions Yield
In tetrahydrofuran; at 180 ℃; for 4.5h;
 
benzyl chloride
100-44-7

benzyl chloride

hydroquinone
123-31-9,8027-02-9

hydroquinone

4-Benzyloxyphenol
103-16-2

4-Benzyloxyphenol

1,4-dibenzyloxybenzene
621-91-0

1,4-dibenzyloxybenzene

Conditions
Conditions Yield
With xylene;
 
With potassium carbonate; acetone;
 
With ethanol; sodium ethanolate;
 
With ethanol; anion-exchanger;
 

103-16-2 Upstream products

  • 100-39-0
    100-39-0

    benzyl bromide

  • 123-31-9
    123-31-9

    hydroquinone

  • 100-44-7
    100-44-7

    benzyl chloride

  • 6630-18-8
    6630-18-8

    4-methoxyphenyl benzyl ether

103-16-2 Downstream products

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    119-98-2

    (2RS,4'R,8'R)-Tocol

  • 625851-45-8
    625851-45-8

    4-benzyloxy-[1,2]benzoquinone

  • 102079-74-3
    102079-74-3

    4-(4-benzyloxy-phenoxy)-2,6-dimethyl-3,5-dinitro-pyridine

  • 101936-55-4
    101936-55-4

    1-benzyloxy-4-(2,4-dinitro-phenoxy)-benzene