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2-Pentanesulfonic acid, also known as 2-amylsulfonic acid or pentane-2-sulfonic acid, is an organic compound with the chemical formula C5H12SO3. It is a colorless, water-soluble solid that is widely used as a surfactant, detergent, and wetting agent in various industrial applications. 2-pentanesulfonic acid is derived from the sulfonation of 2-pentanol, a process that involves the introduction of a sulfonic acid group (-SO3H) to the molecule. 2-Pentanesulfonic acid exhibits strong acidic properties and is known for its ability to form salts with various metal ions, which further enhances its utility in different chemical processes and formulations.

7433-51-4

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7433-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7433-51-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7433-51:
(6*7)+(5*4)+(4*3)+(3*3)+(2*5)+(1*1)=94
94 % 10 = 4
So 7433-51-4 is a valid CAS Registry Number.

7433-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name pentane-2-sulfonic acid

1.2 Other means of identification

Product number -
Other names Pentansulfonsaeure-2

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:7433-51-4 SDS

7433-51-4Downstream Products

7433-51-4Relevant academic research and scientific papers

Cyclohexenone derivatives

-

, (2008/06/13)

Cyclohexenone derivatives I STR1 The cyclohexenone derivatives I are suitable as herbicides and for regulating plant growth.

Mercury-Photosensitized Sulfination, Hydrosulfination, and Carbonylation of Hydrocarbons: Alkane and Alkene Conversion to Sulfonic Acids, Ketones, and Aldehydes

Ferguson, Richard R.,Crabtree, Robert H.

, p. 5503 - 5510 (2007/10/02)

Mercury-photosensitized sulfination of alkanes, RH, with SO2 forms sulfinic acids (RSOOH) and sulfinate esters (RSOOR) in high conversion and yield; oxidation of the mixture produces RSO2OH in high yield.Mercury-photosensitized hydrosulfination of alkenes with H2 and SO2 gives RSO2OH after oxidative workup.Mercury-photosensitized carbonylation of alkanes with CO gives RCHO and R2CO.

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