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10147-40-7

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10147-40-7 Usage

General Description

1-Dodecanesulfonyl chloride, also known as lauryl sulfonyl chloride, is an organic chemical compound that is commonly used as a sulfonating and chlorinating agent. It is derived from dodecane, a straight-chain alkane with 12 carbon atoms, and is functionalized with a sulfonyl chloride group. 1-Dodecanesulfonyl chloride is a versatile intermediate in the synthesis of various organic compounds, including surfactants, detergents, and pharmaceuticals. It is known for its ability to introduce the sulfonyl group into organic molecules, which can enhance their chemical and physical properties. 1-Dodecanesulfonyl chloride is typically handled and stored under controlled conditions due to its corrosive and toxic nature, and it is important to use proper safety precautions when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 10147-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,4 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10147-40:
(7*1)+(6*0)+(5*1)+(4*4)+(3*7)+(2*4)+(1*0)=57
57 % 10 = 7
So 10147-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H25ClO2S/c1-2-3-4-5-6-7-8-9-10-11-12-16(13,14)15/h2-12H2,1H3

10147-40-7 Well-known Company Product Price

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  • Alfa Aesar

  • (L01224)  1-Dodecanesulfonyl chloride, 98+%   

  • 10147-40-7

  • 5g

  • 713.0CNY

  • Detail
  • Alfa Aesar

  • (L01224)  1-Dodecanesulfonyl chloride, 98+%   

  • 10147-40-7

  • 25g

  • 2748.0CNY

  • Detail

10147-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecane-1-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names dodecylsulfonic acid chloride

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:10147-40-7 SDS

10147-40-7Relevant articles and documents

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Klamann,Drahowzal

, p. 463,468,469 (1952)

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A new application of S,S-dialkyl dithiocarbonates. A convenient synthesis of alkanesulfonyl chlorides

Barbero,Cadamuro,Degani,Fochi,Regondi

, p. 957 - 958 (1989)

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Synthesis and some surface properties of glycine-based surfactants

Mousli, Radia,Tazerouti, Amel

, p. 65 - 72 (2011)

A new group of anionic surfactants, namely sodium salts of secondary alkanesulfonamidoacetic acid, were synthesized using n-alkanesulfonyl chlorides as starting materials. These surfactants, having the formula: R-SO 2-NH-CH2-COONa, with R = C12, C14, C16 and C18, were obtained in a simple way with quantitative yields. Different chain lengths and positional isomers of this new type of surfactants are expected to present differences in surface properties and foamability. The surface properties including critical micelle concentrations and minimal surface tensions γmin were determined for each prepared surfactant using surface tension measurements with a Wilhelmy plate. Surface excess and minimum area per molecule at the air-water interface were determined for different concentrations at 25 and 50 °C using the Gibbs equation. The foaming power was also determined by the Bartsch method, and the results obtained were compared to those of a commercial surfactant, the linear alkylbenzenesulfonate. The stability of the foam formed was also evaluated. As expected, these surfactants exhibit good surface properties and show good foaming power.

HORMONE RECEPTOR MODULATORS FOR TREATING METABOLIC CONDITIONS AND DISORDERS

-

, (2018/03/25)

The invention relates to activators of FXR useful in the treatment of autoimmune disorders, liver disease, intestinal disease, kidney disease, cancer, and other diseases in which FXR plays a role, having the Formula (I): (I), wherein L1, A, X1, X2, R1, R2, and R3 are described herein.

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