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3386-32-1

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3386-32-1 Usage

Description

P-Toluenesulfonic acid N-octadecyl ester, also known as octadecyl p-toluenesulfonate, is a long-chain alkyl ester of p-toluene-sulfonic acid. It is a white to off-white solid that is soluble in organic solvents and exhibits a wide range of applications in the chemical industry due to its surfactant and solubility properties.

Uses

Used in Pharmaceutical Synthesis:
P-Toluenesulfonic acid N-octadecyl ester is used as an intermediate in the synthesis of pharmaceuticals for its ability to facilitate chemical reactions and improve the solubility of active ingredients.
Used in Agrochemical Production:
In the agrochemical industry, P-Toluenesulfonic acid N-octadecyl ester serves as an intermediate, aiding in the production of various agrochemicals by enhancing the reactivity and solubility of key components.
Used as an Ion-Pairing Reagent in HPLC Analysis:
P-Toluenesulfonic acid N-octadecyl ester is used as an ion-pairing reagent for the high-performance liquid chromatography (HPLC) analysis of polar compounds, improving the separation and detection of these compounds in analytical processes.
Used as a Phase Transfer Catalyst in Organic Reactions:
This chemical acts as a phase transfer catalyst, facilitating reactions between organic and inorganic compounds, which is particularly useful in the synthesis of complex organic molecules.
Used as an Emulsifier and Wetting Agent in Industrial Processes:
P-Toluenesulfonic acid N-octadecyl ester is utilized as an emulsifier and wetting agent in various industrial processes and formulations, enhancing the stability and performance of emulsions and improving the wetting properties of surfaces.
Used as a Corrosion Inhibitor in Metalworking Fluids:
In metalworking applications, P-Toluenesulfonic acid N-octadecyl ester functions as a corrosion inhibitor, protecting metal surfaces from degradation and extending the life of machinery and tools.
Used as a Detergent in Cleaning Products:
This chemical is also used as a detergent in cleaning products, contributing to the removal of dirt and stains from various surfaces due to its surfactant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 3386-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3386-32:
(6*3)+(5*3)+(4*8)+(3*6)+(2*3)+(1*2)=91
91 % 10 = 1
So 3386-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C25H44O3S/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-23-28-29(26,27)25-21-19-24(2)20-22-25/h19-22H,3-18,23H2,1-2H3

3386-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name octadecyl 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names Octadecyl p-Toluenesulfonate

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:3386-32-1 SDS

3386-32-1Relevant articles and documents

Keana,Ertle

, p. 402,404 (1976)

Solvent-free and selective tosylation of alcohols and phenols with p-toluenesulfonyl chloride by heteropolyacids as highly efficient catalysts

Fazaeli, Razieh,Tangestaninejad, Shahram,Aliyan, Hamid

, p. 812 - 818 (2007/10/03)

Tosylation of some alcohols and phenols has been directly carried out with p-toluenesulfonyl chloride using heterodoxy acids (H3PW 12O40, H3PMo12O40, A 3PW12O40, and AlPMo12O40) as catalysts in the absence of solvent. We found that heteropoly acids AlPW12O40 and AlPMo 12O40 were effective catalysts for the tosylation of alcohols and phenols. In the case of aliphatic alcohols, secondary alcohols undergo tosylation chemoselectively in the presence of primary hydroxyl groups. This new method consistently has the advantage of excellent yields and short reaction time.

An efficient and selective tosylation of alcohols with p-toluenesulfonic acid

Das, Biswanath,Reddy, V. Saidi,Reddy, M. Ravinder

, p. 6717 - 6719 (2007/10/03)

Silica chloride has been found to be an efficient catalyst for facile tosylation of alcohols directly with p-toluenesulfonic acid in methylene chloride under reflux. The process is associated with selective tosylation of secondary alcohols over primary al

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