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136-36-7

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136-36-7 Usage

Chemical Properties

white fine crystalline powder

Uses

Different sources of media describe the Uses of 136-36-7 differently. You can refer to the following data:
1. Noncoloring UV inhibitor for various plastics, color stabilizer in cosmetic compositions.
2. Resorcinol monobenzoate is used as an ultraviolet stabilizer in certain types of plastic films.
3. Resorcinol monobenzoate is used as UV-light absorber added mainly to outdoor plastics; additive in spectacle frames.

Synthesis Reference(s)

The Journal of Organic Chemistry, 41, p. 3419, 1976 DOI: 10.1021/jo00883a020

Check Digit Verification of cas no

The CAS Registry Mumber 136-36-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136-36:
(5*1)+(4*3)+(3*6)+(2*3)+(1*6)=47
47 % 10 = 7
So 136-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O3/c14-11-7-4-8-12(9-11)16-13(15)10-5-2-1-3-6-10/h1-9,14H

136-36-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (A19150)  Resorcinol monobenzoate, 94%   

  • 136-36-7

  • 100g

  • 251.0CNY

  • Detail
  • Alfa Aesar

  • (A19150)  Resorcinol monobenzoate, 94%   

  • 136-36-7

  • 500g

  • 871.0CNY

  • Detail

136-36-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name RESORCINOL MONOBENZOATE

1.2 Other means of identification

Product number -
Other names 1,3-Benzenediol, monobenzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:136-36-7 SDS

136-36-7Relevant articles and documents

Zaugg

, p. 3419 (1976)

Method for synthesizing ultraviolet ray absorber UV-0 through solid acid catalysis

-

Paragraph 0021; 0023, (2018/11/10)

The invention provides a method for synthesizing an ultraviolet ray absorber UV-0 through solid acid catalysis. The method comprises the following steps that benzoic acid, resorcinol and phosphotungstic acid are added into a container, heating is conducted in an oil bath to 110-140 DEG C, stirring is conducted for a reaction for 5-24 hours, it is monitored that the reaction is completed through thin layer chromatography, after cooling, toluene is added for dissolving the product, and solid catalyst phosphotungstic acid is subjected to suction filtration and recycled; a residue obtained throughevaporation of a filtrate is recrystallized with methanol/water to obtain pale yellow solid, namely the ultraviolet ray absorber UV-0. By means of the process, the yield of the UV-0 is greater than 96%.

Synthesis of industrially important aromatic and heterocyclic ketones using hierarchical ZSM-5 and Beta zeolites

Kore, Rajkumar,Srivastava, Rajendra,Satpati, Biswarup

, p. 129 - 141 (2015/09/28)

Hierarchical ZSM-5 and Beta zeolites were investigated in the synthesis of wide range of industrially important aromatic/heterocyclic ketones by Friedel-Crafts acylation and benzoylation reactions. For comparative study, conventional ZSM-5 and Beta, and amorphous mesoporous Al-MCM-41 were investigated. Hierarchical zeolites were prepared by multi-ammonium structure directing agents whereas conventional zeolites were prepared by mono-ammonium structure directing agents. Among the catalysts investigated in this study, hierarchical Beta exhibited the highest reactant conversion in the acylation and benzoylation reactions. In this study, the systematic assessment of the catalytic activity of acid catalysts for wide range of aromatic and heterocyclic compounds is shown under one umbrella. To the best of our knowledge, these reactions over hierarchical zeolites (ZSM-5 and Beta) are reported here for the first time. Structure activity relationship is explained based on the physico-chemical properties, molecular size, reactivity of reactants, and reaction mechanism. Catalysts can be easily recovered and reused with negligible loss in the catalytic activity.

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