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35452-30-3

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35452-30-3 Usage

General Description

1-Pentanesulfonicsalt, also known as sodium 1-pentanesulfonate, is a straight-chain alkyl sulfonate that is commonly used as an ion-pairing reagent in chromatography and as a counterion for cationic surfactants. It is a white, crystalline powder that is highly soluble in water and has a bitter taste. 1-Pentanesulfonicsalt is used in various industries, including pharmaceuticals, cosmetics, and agriculture, as a stabilizer, emulsifier, and dispersing agent. It has also been used as a corrosion inhibitor in oil fields and as a preservative in chemical synthesis. Additionally, it is considered to be relatively safe and non-toxic, making it suitable for use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 35452-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,5 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35452-30:
(7*3)+(6*5)+(5*4)+(4*5)+(3*2)+(2*3)+(1*0)=103
103 % 10 = 3
So 35452-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H12O3S/c1-2-3-4-5-9(6,7)8/h2-5H2,1H3,(H,6,7,8)

35452-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name pentane-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names 1-Pentanesulfonic acid

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:35452-30-3 SDS

35452-30-3Relevant articles and documents

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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