• 1. Distinction of trans–cis photoisomers with comparable optical properties in multiple-state photochromic systems – examining a molecule with three azobenzenes via in situ irradiation NMR spectroscopy?
  Jonas Kind,Lukas Kaltschnee,Martin Leyendecker,Christina M. Thiele Chem. Commun., 2016,52, 12506-12509
• 2. Emerging investigator series: first-principles and thermodynamics comparison of compositionally-tuned delafossites: cation release from the (001) surface of complex metal oxides?
  Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
• 3. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 4. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 5. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
  Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745

• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty alcohols

Professional Introduction to Isooctyl Alcohol (CAS No: 26952-21-6)

Isooctyl Alcohol, with the chemical name 2-methylbutyl alcohol, is a significant compound in the field of chemical and pharmaceutical applications. Its CAS number, 26952-21-6, uniquely identifies it as a specific isomer within the alcohol family. This compound has garnered considerable attention due to its versatile properties and its role in various industrial and scientific domains.

The molecular structure of Isooctyl Alcohol consists of an eight-carbon chain with a branched structure, making it an isomer of octanol. This particular configuration imparts unique solvency characteristics, making it an effective solvent in numerous applications. The compound’s ability to dissolve both polar and non-polar substances has made it invaluable in formulating personal care products, cosmetics, and pharmaceutical intermediates.

In recent years, Isooctyl Alcohol has been extensively studied for its potential in drug delivery systems. Its lipophilic nature allows it to enhance the bioavailability of active pharmaceutical ingredients (APIs), particularly in topical formulations. Research has demonstrated that incorporating Isooctyl Alcohol into transdermal patches can significantly improve the penetration of therapeutic agents through the skin barrier. This has opened new avenues for developing more efficient and targeted treatments for various skin conditions.

The compound’s role in nanotechnology has also been a focal point of recent studies. Scientists have explored the use of Isooctyl Alcohol as a stabilizing agent in the synthesis of nanoparticles. Its ability to prevent aggregation and stabilize colloidal dispersions makes it an excellent candidate for drug delivery systems that rely on nanoparticle technology. For instance, studies have shown that nanoparticles formulated with Isooctyl Alcohol exhibit improved stability and controlled release profiles, which are critical for therapeutic efficacy.

CAS No: 26952-21-6 is not only significant for its chemical properties but also for its regulatory compliance. As a compound that does not fall under hazardous or controlled substance classifications, it can be handled and transported more freely, making it highly practical for industrial use. This regulatory advantage has facilitated its adoption in a wide range of applications without stringent restrictions.

The pharmaceutical industry has also leveraged the properties of IsoOctyl Alcohol in the development of novel drug formulations. Its use as a co-solvent in liquid chromatography (LC) has improved the separation efficiency of complex mixtures, aiding in the purification and characterization of APIs. Additionally, its role as a surfactant in emulsion formulations has enhanced the stability and texture of liquid medications, improving patient compliance.

In environmental science, the biodegradability of IsoOctyl Alcohol has been a subject of interest. Unlike some synthetic solvents that persist in the environment, studies have shown that IsoOctyl Alcohol undergoes biodegradation relatively quickly under aerobic conditions. This characteristic makes it a more environmentally friendly option compared to alternatives with higher persistence profiles.

The cosmetic industry has similarly benefited from the inclusion of IsoOctyl Alcohol in various formulations. Its emollient properties make it effective in skincare products, where it helps to soften and smooth the skin. Furthermore, its ability to enhance the penetration of other active ingredients means that cosmeceutical products containing this compound can deliver more potent effects.

The future prospects for IsoOctyl Alcohol are promising, with ongoing research exploring new applications across multiple sectors. As advancements continue in drug delivery systems and nanotechnology, the demand for this versatile compound is expected to grow. Its compatibility with various chemical processes and regulatory advantages position it as a key component in innovative formulations.

• 74650-55-8(1,4-BUTANEDIOL, 2-ETHYL-, (R)-)
• 91241-30-4(1,6-HEXANEDIOL, 2,5-DIETHYL-)
• 90951-76-1(1,4-BUTANEDIOL, 2-METHYL-3-PROPYL-)
• 187728-12-7(1,6-HEXANEDIOL, 2,4-DIMETHYL-)
• 90951-74-9(1,4-BUTANEDIOL, 2-(1-METHYLPROPYL)-)
• 90192-55-5(1,4-BUTANEDIOL, 2-ETHYL-3-METHYL-, (R*,R*)-)
• 55232-18-3(1,4-BUTANEDIOL, 2-PROPYL-, (2R)-)
• 75924-60-6(1,6-HEXANEDIOL, 2,5-DIMETHYL-, (R*,S*)-)
• 61244-59-5(1,5-CYCLONONANEDIMETHANOL, (1R*,5S*)-)
• 61154-08-3(1,2-CYCLOHEPTANEDIMETHANOL, TRANS-)