• 1. Aggregation-induced emission of luminol: a novel strategy for fluorescence ratiometric detection of ALP and As(v) with high sensitivity and selectivity?
  Yuan-Jun Tong,Lu-Dan Yu,Lu-Lu Wu,Shu-Ping Cao,Ru-Ping Liang,Li Zhang,Xing-Hua Xia,Jian-Ding Qiu Chem. Commun., 2018,54, 7487-7490
• 2. An integrated cathode and solid electrolyte via in situ polymerization with significantly reduced interface resistance?
  Jialiang Yuan,Ran Dong,Yuan Li,Yang Liu,Zhuo Zheng,Yuxia Liu,Yan Sun,Benhe Zhong,Zhenguo Wu,Xiaodong Guo Chem. Commun., 2021,57, 13004-13007
• 3. An atlas of endohedral Sc2S cluster fullerenes?
  Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
• 4. An automated computational approach to kinetic model discrimination and parameter estimation?
  Connor J. Taylor,Hikaru Seki,Friederike M. Dannheim,Mark J. Willis,Graeme Clemens,Brian A. Taylor,Thomas W. Chamberlain,Richard A. Bourne React. Chem. Eng., 2021,6, 1404-1411
• 5. An aquatic host–guest complex between a supramolecular G-quadruplex and the anticancer drug doxorubicin?
  José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565

• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Glycerolipids Diradylglycerols Diacylglycerols

Heptadecanoic Acid, 2-Hydroxy-1,3-Propanediyl Ester: A Comprehensive Overview

CAS No. 71431-35-1, commonly referred to as Heptadecanoic acid, 2-hydroxy-1,3-propanediyl ester, is a compound of significant interest in various scientific and industrial domains. This compound is a derivative of heptadecanoic acid, which is a saturated fatty acid with a 17-carbon chain. The ester functional group in this compound adds unique properties that make it valuable in applications ranging from pharmaceuticals to cosmetics and materials science.

The chemical structure of Heptadecanoic acid, 2-hydroxy-1,3-propanediyl ester consists of a long hydrocarbon chain (heptadecanoic acid) linked to a propanediyl group with a hydroxyl functional group. This structure contributes to its amphiphilic nature, allowing it to interact with both polar and non-polar substances. Recent studies have highlighted its potential as a surfactant in drug delivery systems due to its ability to form micelles and enhance the solubility of hydrophobic drugs.

In the field of materials science, CAS No. 71431-35-1 has been explored for its role in the development of biodegradable polymers. Researchers have found that this compound can be used as a building block for synthesizing polyesters with controlled degradation rates, which are highly desirable for applications in packaging and agriculture.

The synthesis of Heptadecanoic acid, 2-hydroxy-1,3-propanediyl ester typically involves esterification reactions between heptadecanoic acid and propane diol under specific conditions. Recent advancements in catalytic methods have improved the efficiency and yield of this process, making it more viable for large-scale production.

In the cosmetics industry, this compound has gained attention for its emollient properties. Its ability to form stable emulsions makes it an effective ingredient in creams and lotions, providing enhanced moisturizing effects without leaving a greasy residue on the skin.

Recent research has also explored the use of CAS No. 71431-35-1 in bio-based lubricants. Its high viscosity index and thermal stability make it a promising alternative to traditional petroleum-based lubricants, contributing to the development of more sustainable industrial practices.

In summary, Heptadecanoic acid, 2-hydroxy-1,3-propanediyl ester (CAS No. 71431-35-1) is a versatile compound with a wide range of applications across multiple industries. Its unique chemical properties and recent advancements in its synthesis and application continue to expand its potential in both scientific research and industrial production.

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