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4372-29-6

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4372-29-6 Usage

General Description

Decylmalonic acid is a long-chain dicarboxylic acid with the chemical formula C11H20O4. It is a derivative of malonic acid, with a decyl group attached to one of the carboxyl groups. Decylmalonic acid is commonly used in the production of polymers and resins, as well as in the synthesis of other organic compounds. It has also been studied for its potential applications in medicinal and cosmetic products due to its antimicrobial and antioxidant properties. Decylmalonic acid is a versatile chemical with various industrial and potential biomedical uses.

Check Digit Verification of cas no

The CAS Registry Mumber 4372-29-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4372-29:
(6*4)+(5*3)+(4*7)+(3*2)+(2*2)+(1*9)=86
86 % 10 = 6
So 4372-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O4/c1-2-3-4-5-6-7-8-9-10-11(12(14)15)13(16)17/h11H,2-10H2,1H3,(H,14,15)(H,16,17)

4372-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-decylpropanedioic acid

1.2 Other means of identification

Product number -
Other names 2-decylmalonic 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:4372-29-6 SDS

4372-29-6Relevant articles and documents

Counterion-Dependent Access to Low-Symmetry Lyotropic Sphere Packings of Ionic Surfactant Micelles

Jayaraman, Ashish,Mahanthappa, Mahesh K.

, p. 2290 - 2301 (2018)

The water-driven self-assembly of homologous dianionic surfactants into lyotropic liquid crystals (LLCs) is investigated, with a focus on understanding how surfactant headgroup and counterion identities guide supramolecular spherical mesophase selection. Using temperature-dependent small-angle X-ray scattering (SAXS), we demonstrate that 2-alkylmalonate surfactants (CnMal-M2) with n = 8 (octyl) or 10 (decyl) and M = K+, Cs+, or (CH3)4N+ form both simple and complex micelle packings. Observed spherical morphologies include body-centered cubic (BCC), hexagonally closest-packed (HCP), and tetrahedrally closest-packed Frank-Kasper (FK) A15 and σ phases (Pm3(-)n and P42/mnm symmetries, respectively). Previously observed in only one other minimally hydrated surfactant, the σ phase is a rare LLC morphology comprising a low-symmetry unit cell containing 30 sub-2-nm quasispherical micelles, each of which belongs to one of five symmetry-equivalent classes with discrete aggregation numbers. Temperature versus water concentration phase maps for CnMal-M2 LLCs reveal that σ-phase formation depends sensitively on the size and polarizability of the surfactant counterion and the length of the surfactant alkyl tail. These observations are rationalized in terms of a delicate interplay between global packing symmetry and local particle symmetry, and the extent to which counterion-headgroup correlations enforce the latter structures in these LLC phases.

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