29809-11-8

Basic information

• Product Name: PHENOL (1-13C)
• Synonyms: PHENOL (1-13C);PHENOL-1-13C 99%
• CAS NO: 29809-11-8
• Molecular Formula: C₆H₆O
• Molecular Weight: 95.12
• Product Categories: Alphabetical Listings;P;Stable Isotopes
• Mol File: 29809-11-8.mol
• Article Data: 4

Chemical Properties

• Melting Point: 40-42 °C(lit.)
• Boiling Point: 182 °C(lit.)
• Appearance: /
• Density: 1.082 g/mL at 25 °C
• Storage Temp.: -20°C
• CAS DataBase Reference: PHENOL (1-13C)(CAS DataBase Reference)
• NIST Chemistry Reference: PHENOL (1-13C)(29809-11-8)
• EPA Substance Registry System: PHENOL (1-13C)(29809-11-8)

Safety Data

• Hazard Codes: T,C
• Statements: 23/24/25-34-48/20/21/22-68
• Safety Statements: 24/25-26-28-36/37/39-45
• RIDADR: UN 1671 6.1/PG 2
• WGK Germany: 2
• Hazardous Substances Data: 29809-11-8(Hazardous Substances Data)

Usage

General Description

PHENOL (1-13C) is a stable isotope of phenol, a chemical compound that is commonly used in products such as disinfectants, antiseptics, and industrial processes. The 1-13C labeling indicates that one of the carbon atoms in the phenol molecule has been replaced by a stable carbon-13 isotope, which can be used for research purposes such as nuclear magnetic resonance (NMR) spectroscopy to study the chemical structure and behavior of phenol. This labeling allows for the tracking and analysis of the carbon atom in phenol, providing valuable insights into its interactions and reactions in various applications and processes.

Upstream product

• 100790-30-5 C₅⁽¹³⁾CH₇NO*ClH 
• 3881-08-1 [1-¹³C]₄-aminophenol 
• 3881-07-0 <1-13C>-p-nitro-phenol 

Downstream Products

• 120666-19-5 2-(Phenoxy-1-⁽¹³⁾C)ethanol 
• 81201-90-3 L-<4'-13C>tyrosine 
• 6998-50-1 benzene-⁽¹³⁾C 
• 100790-35-0 L-<4'-13C>tyrosine benzyl ester p-toluenesulfonate 

Relevant articles and documents

Unraveling the Dynamic Network in the Reactions of an Alkyl Aryl Ether Catalyzed by Ni/γ-Al2O3 in 2-Propanol

The reductive cleavage of aryl ether linkages is a key step in the disassembly of lignin to its monolignol components, where selectivity is determined by the kinetics of multiple parallel and consecutive liquid-phase reactions. Triphasic hydrogenolysis of

Synthesis and NMR spectroscopy of stable isotope-labelled phenols and L-tyrosines

The syntheses of (17O)phenol from (17O)water, (18O)phenol from (18O)water, (1-13C)-phenol and (4-13C)phenol from (2-13C)acetone and (2-13C)phenol and (3-13C)phenol from (1-13C)acetone with high isotopic enrichment are described.The labelled phenols are converted into their corresponding L-tyrosines by the bacterium Erwinia herbicola.A full analysis of the 1H and 13C NMR spectra of phenol and L-tyrosine is reported.