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35192-74-6

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  • Sodium 1-nonanesulfonate CAS 35192-74-6 1-Nonanesulfonic acid sodium salt CAS no 35192-74-6 sodium nonane-1-sulfonate

    Cas No: 35192-74-6

  • USD $ 3.5-5.0 / Kiloliter

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35192-74-6 Usage

Description

1-NONANESULFONIC ACID SODIUM SALT, also known as Sodium 1-Nonanesulfonate, is a white fine powder with ionic surfactant properties. It is commonly utilized in various scientific and industrial applications due to its unique chemical characteristics.

Uses

Used in Chemical Research:
1-NONANESULFONIC ACID SODIUM SALT is used as a research compound for studying the kinetics of micellization through ultrasonic relaxation studies. This application is crucial in understanding the behavior of surfactants and their interactions in different environments.
Used in Pharmaceutical Industry:
1-NONANESULFONIC ACID SODIUM SALT is used as an excipient in the pharmaceutical industry for the formulation of various drugs. Its surfactant properties aid in enhancing the solubility, stability, and bioavailability of active pharmaceutical ingredients.
Used in Cosmetics Industry:
In the cosmetics industry, 1-NONANESULFONIC ACID SODIUM SALT is used as an ingredient in personal care products. It serves as a surfactant, emulsifier, or stabilizer, improving the texture, consistency, and effectiveness of the final product.
Used in Environmental Science:
1-NONANESULFONIC ACID SODIUM SALT is used as a component in the development of advanced water treatment technologies. Its surfactant properties help in the removal of contaminants and pollutants from water, contributing to a cleaner and safer environment.
Used in Analytical Chemistry:
1-NONANESULFONIC ACID SODIUM SALT is used as a reagent in various analytical chemistry techniques. It aids in the separation, identification, and quantification of different chemical compounds, enhancing the accuracy and reliability of experimental results.

Check Digit Verification of cas no

The CAS Registry Mumber 35192-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,9 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35192-74:
(7*3)+(6*5)+(5*1)+(4*9)+(3*2)+(2*7)+(1*4)=116
116 % 10 = 6
So 35192-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O3S.Na/c1-2-3-4-5-6-7-8-9-13(10,11)12;/h2-9H2,1H3,(H,10,11,12);/q;+1/p-1

35192-74-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L06407)  Sodium 1-nonanesulfonate, 98+%   

  • 35192-74-6

  • 5g

  • 349.0CNY

  • Detail
  • Alfa Aesar

  • (L06407)  Sodium 1-nonanesulfonate, 98+%   

  • 35192-74-6

  • 25g

  • 1363.0CNY

  • Detail
  • Sigma-Aldrich

  • (74316)  Sodium1-nonanesulfonate  for ion pair chromatography, ≥99.0% (T)

  • 35192-74-6

  • 74316-10G-F

  • 1,614.60CNY

  • Detail

35192-74-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,nonane-1-sulfonate

1.2 Other means of identification

Product number -
Other names nonane-1-sulfonic acid,sodium-salt

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:35192-74-6 SDS

35192-74-6Upstream product

35192-74-6Downstream Products

35192-74-6Relevant articles and documents

N-Sulfonyl homoserine lactones as antagonists of bacterial quorum sensing

Castang, Sandra,Chantegrel, Bernard,Deshayes, Christian,Dolmazon, René,Gouet, Patrice,Haser, Richard,Reverchon, Sylvie,Nasser, William,Hugouvieux-Cotte-Pattat, Nicole,Doutheau, Alain

, p. 5145 - 5149 (2007/10/03)

A series of 11 N-sulfonyl homoserine lactones has been synthesised. Some of them were found to competitively inhibit the action of 3-oxohexanoyl-L- homoserine lactone, the natural inducer of bioluminescence in the bacterium Vibrio fischeri. Molecular modeling suggests a possible explanation based on the prevention of structural rearrangements necessary for the formation of the active dimer of LuxR.

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