• 1. KI-catalyzed arylation of benzothiazoles from the coupling of aryl aldehydes with benzothiazoles in neat water
  Yuyu Gao,Qiuling Song,Guolin Cheng,Xiuling Cui Org. Biomol. Chem. 2014 12 1044
• 2. NaI/KI/NH4I and TBHP as powerful oxidation systems: use in the formation of various chemical bonds
  Prasanjit Ghosh,Bhaskar Ganguly,Sajal Das Org. Biomol. Chem. 2021 19 2146
• 3. Iodine-mediated arylation of benzoxazoles with aldehydes
  Yew Chin Teo,Siti Nurhanna Riduan,Yugen Zhang Green Chem. 2013 15 2365
• 4. Structures of the ring-opened oxidation products from meso-tetraphenylporphyrin
  Jose A. S. Cavaleiro,Michael J. E. Hewlins,Anthony H. Jackson,G. P. Maria,S. Neves J. Chem. Soc. Chem. Commun. 1986 142

• Natural Products and Extracts Plant Extracts Plant based Decalepis hamiltonii

Benzaldehyde-(carbonyl-13C): A Comprehensive Guide to Its Properties and Applications

Benzaldehyde-(carbonyl-13C) (CAS No. 10383-90-1) is a stable isotope-labeled derivative of benzaldehyde, where the carbonyl carbon is replaced with the carbon-13 isotope. This compound is widely used in research, pharmaceuticals, and analytical chemistry due to its unique isotopic properties. The 13C-labeled benzaldehyde is particularly valuable in NMR spectroscopy and mass spectrometry, where it serves as a tracer or internal standard.

The chemical formula of Benzaldehyde-(carbonyl-13C) is C₇H₆¹³CO, and it retains the characteristic almond-like odor of natural benzaldehyde. However, its isotopic enrichment makes it indispensable in metabolic studies and drug development. Researchers often use this compound to track reaction pathways or investigate biochemical mechanisms with high precision.

One of the most common applications of Benzaldehyde-(carbonyl-13C) is in isotope dilution mass spectrometry (IDMS), a technique used for accurate quantification of analytes in complex matrices. The 13C label ensures minimal interference with natural isotopes, improving measurement accuracy. Additionally, this compound is employed in flavor and fragrance research, where isotopic labeling helps distinguish synthetic from natural sources.

Recent advancements in green chemistry have increased the demand for isotopically labeled compounds like Benzaldehyde-(carbonyl-13C). Scientists are exploring its use in sustainable synthesis and catalysis, where it aids in optimizing reaction efficiency. Furthermore, the rise of personalized medicine has spurred interest in 13C-labeled tracers for diagnostic and therapeutic applications.

From a market perspective, Benzaldehyde-(carbonyl-13C) is gaining traction due to its role in pharmaceutical innovation and environmental analysis. Companies specializing in isotope-labeled chemicals are expanding their production capacities to meet growing demand. Researchers frequently search for "buy Benzaldehyde-(carbonyl-13C)" or "13C-labeled benzaldehyde suppliers," highlighting its commercial relevance.

In summary, Benzaldehyde-(carbonyl-13C) (CAS No. 10383-90-1) is a versatile tool in modern science, bridging gaps between analytical chemistry, life sciences, and industrial applications. Its unique properties ensure continued relevance in cutting-edge research and technology.

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