Oxygen Compounds
Items 1 to 10 of 43 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Hydrogen Peroxide | 7722-84-1 | sc-203336 sc-203336A sc-203336B | 100 ml 500 ml 3.8 L | $30.00 $60.00 $93.00 | 27 | |
Hydrogen peroxide is a unique oxygen compound characterized by its ability to act as both an oxidizing and reducing agent, facilitating diverse redox reactions. Its molecular structure allows for the formation of reactive hydroxyl radicals, which play a crucial role in various chemical pathways. The compound exhibits interesting kinetics, particularly in decomposition reactions, where it breaks down into water and oxygen, releasing energy. This property underpins its role in various environmental and industrial processes, showcasing its dynamic behavior in chemical systems. | ||||||
1,2-Hexadecanediol | 6920-24-7 | sc-251560 | 50 g | $387.00 | ||
1,2-Hexadecanediol is a versatile oxygen compound notable for its dual hydroxyl groups, which enable strong hydrogen bonding and enhance its solubility in polar solvents. This structure facilitates unique molecular interactions, allowing it to participate in esterification and etherification reactions. Its long hydrocarbon chain contributes to its hydrophobic characteristics, influencing its behavior in surfactant applications and enhancing its stability in various chemical environments. | ||||||
Ruthenium red | 11103-72-3 | sc-202328 sc-202328A | 500 mg 1 g | $184.00 $245.00 | 13 | |
Ruthenium red is a distinctive oxygen compound characterized by its ability to form strong coordination complexes with metal ions, particularly in redox reactions. Its unique structure allows for selective binding, influencing electron transfer kinetics and enhancing catalytic activity. The compound exhibits notable stability under varying pH conditions, which can affect its solubility and reactivity. Additionally, its colorimetric properties make it useful in visualizing specific molecular interactions in complex systems. | ||||||
Cyclohexanone dimethyl ketal | 933-40-4 | sc-234451 | 50 ml | $88.00 | ||
Cyclohexanone dimethyl ketal is an intriguing oxygen compound characterized by its unique structural arrangement, which allows for effective intramolecular hydrogen bonding. This feature enhances its stability and influences its reactivity in nucleophilic addition reactions. The compound exhibits distinct pathways in photochemical processes, where it can undergo fragmentation to yield reactive intermediates. Its moderate polarity contributes to selective solubility, facilitating interactions in various organic synthesis applications. | ||||||
PTIO | 18390-00-6 | sc-202782 sc-202782A | 25 mg 100 mg | $56.00 $158.00 | 6 | |
PTIO is a unique oxygen compound known for its role as a stable radical, exhibiting distinctive electron paramagnetic resonance properties. It engages in specific molecular interactions that facilitate the modulation of oxidative stress pathways. The compound's reactivity is influenced by its ability to participate in one-electron transfer processes, which can alter reaction kinetics. Its solubility in various solvents further enhances its versatility in diverse chemical environments. | ||||||
5-Amino-1-naphthol | 83-55-6 | sc-233217 sc-233217A | 25 g 100 g | $94.00 $306.00 | ||
5-Amino-1-naphthol is a notable oxygen compound distinguished by its ability to form strong hydrogen bonds due to the presence of both amino and hydroxyl functional groups. This dual functionality enhances its reactivity in electrophilic aromatic substitution reactions, allowing it to act as a versatile building block in organic synthesis. Its planar structure promotes π-π stacking interactions, influencing its solubility and reactivity in various organic solvents. | ||||||
α,α,α′,α′-Tetramethyl-1,3-benzenedimethanol | 1999-85-5 | sc-227177 | 25 g | $61.00 | ||
α,α,α',α'-Tetramethyl-1,3-benzenedimethanol is an intriguing oxygen compound characterized by its bulky tert-butyl groups, which significantly influence steric hindrance and molecular interactions. This unique structure enhances its solubility in nonpolar solvents while limiting its reactivity in certain nucleophilic substitution pathways. The compound's ability to engage in intramolecular hydrogen bonding can stabilize conformations, affecting its overall reactivity and physical properties in various chemical environments. | ||||||
DMPO | 3317-61-1 | sc-202587 sc-202587A | 500 mg 1 g | $210.00 $312.00 | 6 | |
DMPO, a notable oxygen compound, is recognized for its ability to stabilize radical species through spin trapping, forming stable adducts that can be analyzed via electron paramagnetic resonance (EPR) spectroscopy. This compound exhibits unique reactivity patterns, particularly in oxidative environments, where it participates in electron transfer processes. Its distinctive molecular interactions enhance its role in studying reaction kinetics and mechanistic pathways in radical chemistry. | ||||||
3,3′,5,5′-Tetrabromobisphenol A | 79-94-7 | sc-238640 sc-238640A | 100 g 500 g | $80.00 $190.00 | 2 | |
3,3',5,5'-Tetrabromobisphenol A is a halogenated compound characterized by its tetrabrominated structure, which significantly enhances its hydrophobicity and thermal stability. The presence of bromine atoms alters electron density, facilitating unique interactions with various substrates. This compound exhibits notable reactivity in electrophilic aromatic substitution reactions, where its bromine substituents can influence reaction rates and selectivity, making it a key player in polymer chemistry and flame retardant applications. | ||||||
3-Bromo-1-propanol | 627-18-9 | sc-256461 sc-256461A | 5 g 25 g | $36.00 $87.00 | ||
3-Bromo-1-propanol is an intriguing oxygen compound characterized by its ability to engage in nucleophilic substitution reactions due to the presence of the bromine atom. This halogen enhances its reactivity, allowing it to participate in various coupling reactions and form diverse derivatives. The compound's polar nature facilitates hydrogen bonding, influencing solubility and reactivity in different solvents. Its unique structural features make it a valuable intermediate in organic synthesis, particularly in the formation of alcohols and ethers. | ||||||