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2-(hexadecylsulfonyl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24475-69-2

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24475-69-2 Usage

Type of compound

Anionic surfactant and sulfonic acid derivative

Common uses

Detergent, emulsifying agent in industrial and household products

Surface tension reduction

Enhances wetting and dispersing properties of formulations

Applications

Personal care products, cleaners, and industrial applications

Safety concerns

Skin and eye irritation, harmful if ingested or inhaled

Check Digit Verification of cas no

The CAS Registry Mumber 24475-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,7 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24475-69:
(7*2)+(6*4)+(5*4)+(4*7)+(3*5)+(2*6)+(1*9)=122
122 % 10 = 2
So 24475-69-2 is a valid CAS Registry Number.

24475-69-2SDS

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 2-hexadecylsulfonylethanol

1.2 Other means of identification

Product number -
Other names -

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:24475-69-2 SDS

24475-69-2Downstream Products

24475-69-2Relevant academic research and scientific papers

On the Use of Hydrophobic Probes in the Chromatographic Purification of Solid-phase-synthesized Peptides

Garcia-Echeverria, Carlos

, p. 779 - 780 (2007/10/02)

A strategy for the reversed-phase chromatographic purification of solid-phase-synthesized peptides is described and illustrated by the synthesis of a 23-mer model peptide; the target peptide is distinguished from terminated by-products by the attachment of a hydrophobic probe to the resin-bound peptide.

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