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2530-33-8

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2530-33-8 Usage

Description

2-Decylsuccinic acid, also known as DSA, is a versatile chemical compound derived from succinic acid. It features a long hydrophobic tail that contributes to its unique properties, such as reducing surface tension and increasing the solubility of water-insoluble compounds. DSA is commonly used as an intermediate in the production of various products, including surfactants, detergents, and corrosion inhibitors. Furthermore, it serves as a building block in the synthesis of biodegradable polymers and functions as a chelating agent in metal extraction processes. The pharmaceutical industry also recognizes DSA's potential, particularly in the development of new drug delivery systems and as an ingredient in topical formulations for skin care products.

Uses

Used in Surfactant and Detergent Production:
2-Decylsuccinic acid is used as an intermediate in the production of surfactants and detergents due to its ability to reduce surface tension and increase the solubility of water-insoluble compounds. This makes it an essential component in creating effective cleaning agents.
Used in Corrosion Inhibitor Formulation:
DSA is utilized in the formulation of corrosion inhibitors, where its chemical properties help protect materials from corrosion, extending their lifespan and maintaining their integrity.
Used in Biodegradable Polymer Synthesis:
2-Decylsuccinic acid serves as a building block in the synthesis of biodegradable polymers, contributing to the development of environmentally friendly materials that can break down naturally over time.
Used in Metal Extraction Processes:
As a chelating agent, DSA is used in metal extraction processes to bind and separate metal ions, facilitating the efficient extraction and purification of metals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Decylsuccinic acid has potential applications in the development of new drug delivery systems, enhancing the efficacy and targeted delivery of pharmaceutical agents.
Used in Skin Care Product Formulation:
DSA is also used as an ingredient in topical formulations for skin care products, where its properties can contribute to improved skin hydration, texture, and overall health.

Check Digit Verification of cas no

The CAS Registry Mumber 2530-33-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2530-33:
(6*2)+(5*5)+(4*3)+(3*0)+(2*3)+(1*3)=58
58 % 10 = 8
So 2530-33-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O4/c1-2-3-4-5-6-7-8-9-12-18-14(17)11-10-13(15)16/h2-12H2,1H3,(H,15,16)

2530-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-decylbutanedioic acid

1.2 Other means of identification

Product number -
Other names n-Decylbernsteinsaeure

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:2530-33-8 SDS

2530-33-8Downstream Products

2530-33-8Relevant articles and documents

Intramolecular Cooperative Reactions of 1,2-Bis(diazoketone)s. The First Syntheses of trans-Hydro-1H-2-inden-1-ones

Nakatani, Kazuhiko,Takada, Kazunori,Isoe, Sachihiko

, p. 2466 - 2473 (2007/10/02)

The intramolecular cooperative reactions of 1,2-bis(diazoketone)s initiated by the Wolff rearrangement of α-diazoketones have been investigated.Under thermal conditions, 1,2-bis(diazoketone)s are efficiently transformed into 2-cyclopenten-1-one derivatives with complete stereospecificity.Thus, a most extraordinary result is reported, that trans-hydro-2-inden-1-ones (1-3) were synthesized for the first time from trans-1,2-bis(diazoketone)s (5, 11, and 12), respectively.The unprecedented trans-hydroindenone structure was confirmed by X-ray analysis of 3 as well as 1H NMR analysis and was supported by ab initio molecular orbital calculations.The same reactions were also carried out under photochemical conditions and were applied to 1,3-bis(diazoketone)s, giving 2-cyclohexen-1-one derivatives.

Potential antitubercular drugs: II. Synthesis of some mono-N-arylamides of alkylsuccinic acids

Nargund,Prasad,Thakur

, p. 479 - 482 (2007/10/08)

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