• 1. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 2. Evolution of cellulose into flexible conductive green electronics: a smart strategy to fabricate sustainable electrodes for supercapacitors
  Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
• 3. Fe3O4/Au/Fe3O4 nanoflowers exhibiting tunable saturation magnetization and enhanced bioconjugation
  Feng Shi,Kunping Yan,Mingli Peng,Xiao Cheng,Yanling Luo,Xuemei Chen,V. A. L. Roy,Zuankai Wang Nanoscale, 2012,4, 747-751
• 4. Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
  Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
• 5. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid esters
• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid derivatives Carboxylic acid esters

Methyl 2-Mercapto-2-methylpropionate: Properties, Applications, and Industry Insights

Methyl 2-Mercapto-2-methylpropionate (CAS No. 87123-08-8) is a sulfur-containing ester compound with significant industrial relevance. This organosulfur compound features a unique molecular structure combining a thiol group with an ester functionality, making it valuable for various chemical applications. The compound's systematic name reflects its structure: methyl ester of 2-mercapto-2-methylpropionic acid.

Chemically, Methyl 2-Mercapto-2-methylpropionate demonstrates interesting properties due to its thioester functionality. The compound typically appears as a colorless to pale yellow liquid with a characteristic sulfurous odor. Its molecular formula is C₅H₁₀O₂S, and it has a molecular weight of 134.19 g/mol. The presence of both the mercapto group and ester group in the same molecule creates unique reactivity patterns that are exploited in synthetic chemistry.

One of the primary applications of Methyl 2-Mercapto-2-methylpropionate is in the flavor and fragrance industry. The compound contributes to the creation of complex aroma profiles, particularly in fruit flavors where sulfur notes are desired. Recent trends in natural flavor alternatives have increased interest in such sulfur-containing compounds that can replicate natural flavor molecules.

In pharmaceutical research, this compound serves as a valuable building block for drug synthesis. The thiol group can participate in various chemical reactions, making it useful for creating sulfur-containing drug candidates. With the growing focus on targeted drug delivery and personalized medicine, compounds like Methyl 2-Mercapto-2-methylpropionate are gaining attention for their potential in developing novel therapeutic agents.

The material science field also utilizes this compound in polymer modification. Its ability to act as a chain transfer agent in radical polymerization processes makes it valuable for controlling polymer molecular weight. This application aligns with current industry demands for precisely engineered polymers with tailored properties for specific applications.

From an environmental perspective, research continues on the biodegradation pathways of sulfur-containing compounds like Methyl 2-Mercapto-2-methylpropionate. As sustainability becomes a key concern across industries, understanding the environmental fate of such chemicals is crucial. Recent studies have explored its behavior in various ecosystems, contributing to better green chemistry practices.

The global market for specialty chemicals including Methyl 2-Mercapto-2-methylpropionate has shown steady growth, driven by demand from end-use industries. Market analysts note particular expansion in the Asia-Pacific region, where pharmaceutical and flavor industries are rapidly developing. Quality standards and regulatory compliance remain key considerations for manufacturers and users of this compound.

Handling Methyl 2-Mercapto-2-methylpropionate requires standard laboratory precautions due to its thiol content. Proper ventilation and personal protective equipment are recommended when working with this compound. Storage typically involves keeping it in tightly sealed containers under inert atmosphere to prevent oxidation of the thiol group.

Recent advancements in analytical techniques have improved the detection and quantification of Methyl 2-Mercapto-2-methylpropionate in various matrices. Gas chromatography-mass spectrometry (GC-MS) methods have been refined to achieve lower detection limits, important for quality control in industrial applications and environmental monitoring.

Looking forward, research continues into novel applications of Methyl 2-Mercapto-2-methylpropionate, particularly in green chemistry initiatives and sustainable manufacturing processes. Its potential as a bio-based chemical intermediate is being explored, aligning with global trends toward renewable resources and circular economy principles in chemical production.

For researchers and industry professionals seeking information about CAS 87123-08-8, it's important to consult up-to-date technical literature and safety data sheets. The compound's unique properties continue to make it a subject of interest across multiple scientific disciplines, from organic synthesis to materials engineering and beyond.

• 19788-50-2(PROPYL2-MERCAPTOPROPIONATE)
• 33441-51-9(Propanoic acid, 2-(ethylthio)-2-methyl-, ethyl ester)
• 103616-07-5((R)-Ethyl alpha-methylthioglycolate)
• 33441-50-8(Ethyl 2-Mercapto-2-methylpropionate (>90%))
• 53907-46-3(2-Mercaptopropionic Acid Methyl Ester)
• 132958-63-5(Propanoic acid, 2-mercapto-, methyl ester, (S)- (9CI))
• 66707-26-4(Ethyl 2-sulfanylpropanoate)
• 4695-31-2(2-Mercaptoisobutyric Acid, 90%)
• 49773-24-2(Ethyl 2-methyl-2-(methylthio)propionate)
• 19788-49-9(Ethyl 2-mercaptopropionate)