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Benzenesulfonic acid, hexyl ester, also known as hexyl benzenesulfonate, is an organic compound with the chemical formula C12H18O3S. It is a colorless liquid that is soluble in water and has a slight odor. This ester is formed by the reaction of benzenesulfonic acid with hexanol, and it is commonly used as a surfactant, detergent, and emulsifier in various industrial applications, including the production of personal care products, cleaning agents, and textile processing. Due to its amphiphilic nature, it can lower the surface tension of water, making it an effective wetting agent and foaming agent. Additionally, it is known for its biodegradability and low toxicity, which makes it a preferred choice in environmentally friendly formulations.

781-07-7

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781-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 781-07-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 781-07:
(5*7)+(4*8)+(3*1)+(2*0)+(1*7)=77
77 % 10 = 7
So 781-07-7 is a valid CAS Registry Number.

781-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name hexyl benzenesulfonate

1.2 Other means of identification

Product number -
Other names Benzolsulfonsaeure-hexylester

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:781-07-7 SDS

781-07-7Relevant academic research and scientific papers

Electrochemical cross-coupling reactions of sodium arenesulfinates with thiophenols and phenols

Ma, Jinfeng,Xu, Pan,Zhong, Zijian,Zhou, Aihua

, (2021)

A green electrochemical oxidative cross-coupling protocol for the generation of thiosulfonates and sulfonate esters using sodium arenesulfinates and thiophenols/phenols is disclosed. The protocol involves using inorganic and non-toxic NaI as both redox catalyst and supporting electrolyte at room temperature without oxidant and base. The reactions provide good yields of products and tolerate broad substrate scope. The mechanistic studies revealed that the reactions proceed via a radical pathway for the formation of SO2–S and SO2–O bonds.

Process for preparation of oxyglutaric acid ester derivatives

-

, (2008/06/13)

A process for preparing an oxyglutaric acid ester derivative of the formula: STR1 in which each of R1 and R2 is C1-5 alkoxy, C1-7 aralkyloxy, C7-9 halogenated aralkyloxy or phenyl, R4 is a hydroxyl-protecting group, and R5 is C1-10 alkyl which may have a substituent, comprises the steps of reacting a methyl phosphonate derivative or methyl phosphine oxide derivative with an oxyglutaric acid mono-ester to give a reaction product which comprises an oxyglutaric acid derivative having a phosphorus-containing group and a pentenedioic acid mono-ester (by-product), removing the pendenedioic acid mono-ester from the reaction product to isolate the oxyglutaric acid derivative, and converting the isolated oxyglutaric acid derivative into the oxyglutaric acid ester derivative. A process for obtaining an optically active oxyglutaric acid ester derivative is also disclosed.

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