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2386-53-0

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2386-53-0 Usage

Description

1-DODECANESULFONIC ACID SODIUM SALT, also known as Sodium 1-dodecanesulfonate, is a white to light cream powder with surfactant properties. It functions as an ion-pairing reagent and is commonly used in various chemical reactions and applications due to its ability to increase the retention of certain compounds during analysis.

Uses

Used in Suzuki Reaction:
1-DODECANESULFONIC ACID SODIUM SALT is used as a catalyst in the Suzuki reaction for facilitating the formation of carbon-carbon bonds between an organoboron compound and an organic halide or triflate, which is crucial in the synthesis of various organic compounds.
Used in Synthesis of Metal Oxide-Graphene Nanocomposites:
1-DODECANESULFONIC ACID SODIUM SALT is used as a surfactant in the synthesis of metal oxide-graphene nanocomposites for enhancing the dispersion and stability of the nanocomposites, which are essential in various applications such as energy storage, catalysis, and electronics.
Used in High-Performance Liquid Chromatography (HPLC):
1-DODECANESULFONIC ACID SODIUM SALT is used as an ion-pairing reagent for increasing the retention of thiabendazole on the HPLC column during the determination of thiabendazole in citrus fruit and banana, which is important for ensuring accurate and reliable analytical results.
Used in Surfactant Standard:
1-DODECANESULFONIC ACID SODIUM SALT is used as a surfactant standard for evaluating the performance of other surfactants and for quality control purposes in various industries, including pharmaceuticals, cosmetics, and cleaning products.

Purification Methods

Recrystallise it twice from EtOH and dry it in an oven at 105o for 2hours. It picks up moisture to form the 3.5H2O. Its hydrate crystallises in several phases. [Tartar & Wright J Am Chem Soc 61 543 1939, Reed & Tartar J Am Chem Soc I 57 571 1935, Beilstein 4 III 27, 4 IV 64.]

Check Digit Verification of cas no

The CAS Registry Mumber 2386-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2386-53:
(6*2)+(5*3)+(4*8)+(3*6)+(2*5)+(1*3)=90
90 % 10 = 0
So 2386-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H26O3S.Na/c1-2-3-4-5-6-7-8-9-10-11-12-16(13,14)15;/h2-12H2,1H3,(H,13,14,15);/q;+1/p-1

2386-53-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A12829)  Sodium 1-dodecanesulfonate, 99%   

  • 2386-53-0

  • 1g

  • 335.0CNY

  • Detail
  • Alfa Aesar

  • (A12829)  Sodium 1-dodecanesulfonate, 99%   

  • 2386-53-0

  • 10g

  • 1555.0CNY

  • Detail
  • Alfa Aesar

  • (A12829)  Sodium 1-dodecanesulfonate, 99%   

  • 2386-53-0

  • 25g

  • 3490.0CNY

  • Detail
  • Vetec

  • (V900633)  Sodium1-dodecanesulfonate  Vetec reagent grade

  • 2386-53-0

  • V900633-250G

  • 239.85CNY

  • Detail
  • Aldrich

  • (106437)  Sodium1-dodecanesulfonate  ReagentPlus®, ≥99%

  • 2386-53-0

  • 106437-1G

  • 961.74CNY

  • Detail

2386-53-0SDS

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 1-DODECANESULFONIC ACID SODIUM SALT

1.2 Other means of identification

Product number -
Other names sodium dodecanesulphonate

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:2386-53-0 SDS

2386-53-0Relevant articles and documents

Reed, R. M.,Tartar, H. V.

, p. 570 - 571 (1935)

HORMONE RECEPTOR MODULATORS FOR TREATING METABOLIC CONDITIONS AND DISORDERS

-

Page/Page column 366, (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.

Method for virus inactivation in the presence of polyalkylene glycol as well as the pharmaceutical preparation obtained therewith

-

, (2008/06/13)

The invention relates to a pharmaceutical preparation comprising a plasma protein wherein said preparation is free of infectious agents as well as essentially free of denaturation products and is obtainable by a method that encompasses the following steps: a) addition of a polyether and a chaotropic agent to a solution comprising the plasma protein, optional lyophilization of the solution; b) inactivation of infectious agents in the presence of the polyether by a physio-chemical or chemical treatment, and c) removal of the polyether and the chaotropic agent.

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