Non Polar Solvents
Non-polar solvents are a class of solvents that dissolve non-polar compounds due to their low dielectric constants and lack of significant partial charges. They are widely used in various chemical processes and applications, including organic synthesis, extractions, and chromatography. Common non-polar solvents include substances with 6-membered rings and building blocks such as hexane and toluene, which are crucial for dissolving hydrophobic compounds. These solvents play an essential role in the preparation of active pharmaceutical ingredients (APIs) and related research compounds. Additionally, non-polar solvents are utilized in NMR spectroscopy, where they help dissolve non-polar analytes without interfering with the spectral analysis. They are also important in processes involving amino acids, organic chlorinated compounds, and various building blocks. Their effectiveness in dissolving organic compounds makes non-polar solvents indispensable in both laboratory and industrial settings.
Found 188 products for "Non Polar Solvents".
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(E)-5-(-But-1-en-1-yl)benzene-1,3-diol
CAS:(E)-5-(-But-1-en-1-yl)benzene-1,3-diol is a chemical building block that reacts readily with a variety of reagents. It is also a versatile intermediate and has been used as a building block in the synthesis of complex compounds. (E)-5-(-But-1-en-1-yl)benzene-1,3-diol has been shown to be an important component in the synthesis of peptides, amines, and other organic compounds. This compound is also useful for research purposes and as a speciality chemical or fine chemical.Formula:C10H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:164.2 g/mol4-(Dimethylamino)phenol
CAS:4-(Dimethylamino)phenol is a reactive molecule that can react with sodium carbonate to form a fluorescent product. The reaction mechanism has been elucidated by fluorescence spectroscopy and linear calibration curves. 4-DMA(OH)P reacts with sodium carbonate in water at physiological levels, producing p-hydroxybenzoic acid and 4-dimethylaminobenzoic acid. These compounds are also found in the matrix of bacterial cells and may serve as markers for the identification of bacterial metabolism. The reaction between 4DMA(OH)P and sodium carbonate was examined by X-ray crystal structures, which revealed that the reactive site is located on the phenolic hydroxyl group of 4DMA(OH)P. This study showed that the reactive site is localized on the phenolic hydroxy group of 4DMA(OH)P, which makes this molecule useful for identification of bacterial metabolism by means of matrix effect.Formula:C8H11NOPurity:Min. 95%Molecular weight:137.18 g/mol2,4,6-Triisopropylbenzenesulfonyl chloride
CAS:2,4,6-Triisopropylbenzenesulfonyl chloride is a molecule that belongs to the class of ethylene diamine. It has been shown to inhibit the replication of herpes simplex virus in cell culture. This compound has an intramolecular hydrogen and steric interactions with a hydroxyl group. The analog of this molecule is 2,4,6-triisopropylbenzenesulfonic acid. 2,4,6-Triisopropylbenzenesulfonyl chloride can be used as a sulfonation agent and is known for its ability to react with nitrogen nucleophiles such as amines or ammonia.Formula:C15H23SO2ClPurity:Min. 95%Molecular weight:302.86 g/mol4-Methoxybenzenediazonium tetrafluoroborate
CAS:4-Methoxybenzenediazonium tetrafluoroborate (MBD) is a synthetic molecule that can be prepared by the reaction of sodium hydrogen with UV irradiation. MBD has been shown to have a pharmacokinetic profile similar to methyl cinnamate and is used in the treatment of hyperpigmentation, such as melasma and post-inflammatory hyperpigmentation. MBD interacts with the amino acid tyrosine at its 4-hydroxyl group, cleaving the C-O bond and forming an intramolecular hydrogen bond with the oxygen atom. This results in the formation of diazonium salt which reacts with tyrosinase and inhibits its activity.Formula:C7H7BF4N2OPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:221.95 g/mol4-Amino-N-(2-phenylethyl)benzenesulfonamide
CAS:4-Amino-N-(2-phenylethyl)benzenesulfonamide (4APBS) is a histone deacetylase inhibitor. It has been shown to inhibit the histone methyltransferase activity of EZH2, which is important for regulating gene expression, in cells treated with 4APBS. This inhibition leads to increased levels of the transcriptional coactivator β-catenin and reduced levels of tumor suppressor genes. These changes ultimately lead to an increase in cancer cell proliferation and decreased apoptosis. 4APBS also interacts with hormone receptors that are found on the surface of cells and can regulate cellular functions such as proliferation, differentiation, or apoptosis.Formula:C14H16N2O2SPurity:Min. 95%Color and Shape:Off-White PowderMolecular weight:276.36 g/mol4-Dodecylbenzenesulfonic acid - mixture of C10-C13 isomers
CAS:4-Dodecylbenzenesulfonic acid is a mixture of C10-C13 isomers. It is used as an additive to biodiesel or petroleum diesel fuel to reduce the corrosivity of the fuel and protect the engine. 4-Dodecylbenzenesulfonic acid can be synthesized by reacting hydrochloric acid with a fatty acid. The product is then purified by hydrophilic interaction chromatography and sodium carbonate. 4-Dodecylbenzenesulfonic acid has been shown to have synergistic effects when combined with other compounds, such as boron nitride, in treating breast cancer cells. This compound has also been shown to have antimicrobial properties against bacteria, fungi, and protozoa through its hydroxide solution reaction with nitrogen atoms on the surface of multi-walled carbon nanotubes. 4-Dodecylbenzenesulfonic acid is a white solid that can be crystallized at roomFormula:C18H30O3SPurity:Min. 95%Color and Shape:Brown Clear LiquidMolecular weight:326.5 g/mol1,3-Diisopropenylbenzene - stabilized with TBC
CAS:1,3-Diisopropenylbenzene is a hydrocarbon solvent with thermal expansion properties. It has been shown to be an effective cross-linking agent for cationic polymerization and is used as a surfactant for the production of polyurethanes. 1,3-Diisopropenylbenzene is also used as a chemical intermediate in the production of higher molecular weight polymers and plastics. The ester linkages in 1,3-diisopropenylbenzene are susceptible to hydrolysis and oxidation, which can lead to degradation. 1,3-diisopropenylbenzene is stabilized with TBC by forming an ether linkage with the terminal hydroxyl group on TBC.Formula:C12H14Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:158.24 g/mol3,4-Dimethoxytoluene
CAS:3,4-Dimethoxytoluene is a methoxylated aromatic hydrocarbon. It has the chemical formula CH3OCH2C6H4CH3. 3,4-Dimethoxytoluene is used as an intermediate in the synthesis of a variety of organic compounds including olefins, polymers, and pharmaceuticals. It can also be used to extract fatty acids from plant oils and animal fats. The extraction yield increases when using this compound as an extraction solvent. 3,4-Dimethoxytoluene is synthesized by reacting benzene with formaldehyde in the presence of a Friedel-Crafts catalyst such as aluminum chloride or zinc chloride. END>>Formula:C9H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:152.19 g/mol1-(2-Bromoethoxy)-4-chloro-benzene
CAS:1-(2-Bromoethoxy)-4-chloro-benzene is a monomer that is soluble in organic solvents and has been shown to be an electron donor. The reaction mechanism of the bromination of 1-(2-bromoethoxy)-4-chlorobenzene involves the formation and subsequent decomposition of a radical anion, which is stabilized by the solvent acetonitrile. This monomer can also be used as a sensitizer for polymerization reactions. The yield of this product has been found to increase with increasing amounts of ethanol in the solution. 1-(2-Bromoethoxy)-4-chlorobenzene can also undergo an intramolecular cyclization to form a five membered ring with two stereogenic centers. 1-(2-Bromoethoxy)-4-chlorobenzene yields optical rotation values that are dependent on the concentration of water in the solution and it has beenFormula:C8H8BrClOPurity:Min. 95%Color and Shape:Off-White PowderMolecular weight:235.51 g/mol2-Toluenesulfonyl isocyanate
CAS:2-Toluenesulfonyl isocyanate (2TSIC) is a reactive compound that belongs to the group of polyols. It has high resistance to water and other solvents, which makes it an excellent sealant. 2TSIC reacts with hydroxy groups on polymers and monomers to form hydrogen bonds. This reaction can be used in radiation curing of sealants. 2TSIC also interacts with m1 receptors, which are proteins found in the brain and spinal cord that regulate neurotransmitter release.
Formula:C8H7NO3SPurity:Min. 95%Color and Shape:Colourless liquid.Molecular weight:197.21 g/mol(S)-4-Methylbenzenesulfinamide
CAS:(S)-4-Methylbenzenesulfinamide is a synthetic β-amino acid that has been used for the synthesis of various heterocycles. It has been shown to be a selective inhibitor of the enzyme carboxypeptidase B (CPB) in vitro, which is involved in the degradation of β-amino acids. The stereoselective synthesis of (S)-4-methylbenzenesulfinamide has been achieved through the use of hydrophobic phenylphosphinate as a chiral ligand and an azetidine as a starting material. The reaction time was found to be 20 minutes at room temperature with ethyl phenylphosphinate.Formula:C7H9NOSPurity:Min. 95%Color and Shape:White PowderMolecular weight:155.22 g/molIsopropyl benzenesulfonate
CAS:Isopropyl benzenesulfonate is an ester compound that reacts with the chlorine atom to produce a sulfonic acid. It has antimicrobial properties and is used in the production of quinoline derivatives, which are aliphatic hydrocarbons that have been found to be effective in the treatment of cancer. Isopropyl benzenesulfonate also has potential as a cross-linking agent for ester compounds, due to its ability to react with both aromatic hydrocarbons and radiation. It can be synthesized by reacting a phase liquid chromatography solution with hydroxyl group or patterning with a solid catalyst. Isopropyl benzenesulfonate has carbonyl groups that are reactive with other chemicals and may be used as a reagent for storing reactive substances.Formula:C9H12O3SPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:200.26 g/mol2-Iodobenzenesulfonic acid
CAS:2-Iodobenzenesulfonic acid is a synthetic molecule with a molecular weight of 169.27 g/mol. It is an acidic salt that reacts with nucleophilic substitutions, such as hydroxyl groups and heterocycles. 2-Iodobenzenesulfonic acid has been studied using molecular modeling techniques to identify its pharmacophore and the key features that may be important for binding to the active site of the enzyme. The results of these studies show that the most important features are a sulfonyl group, two hydroxyl groups, and an aromatic ring.
Formula:C6H5IO3SPurity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:284.07 g/molTrimethyl 1,3,5-benzene tricarboxylate
CAS:Trimethyl 1,3,5-benzene tricarboxylate is a chemical compound that belongs to the group of polycarboxylic acids. It is used as a polymerization agent in the manufacture of ionic polymers. The first step in this process is cationic polymerization, which involves the reaction between trimethyl 1,3,5-benzene tricarboxylate and sodium citrate to form an ion pair. This process can be followed by hydrolysis with hydrochloric acid and sodium carbonate to release the carboxylate anion from the polymer chain and regenerate trimethyl 1,3,5-benzene tricarboxylate. Trimethyl 1,3,5-benzene tricarboxylate has been shown to have optical properties that depend on its molecular weight and metal surface interactions. It can also be used as a chelating agent for zinc diethyld
Formula:C12H12O6Purity:Min. 95%Color and Shape:White PowderMolecular weight:252.22 g/mol3,5-Dibromo-4-hydroxytoluene
CAS:3,5-Dibromo-4-hydroxytoluene (DBHT) is a brominated aromatic hydrocarbon. It has been shown to be an efficient debrominating agent for bromophenols and chloride, which are two major environmental pollutants. DBHT can also catalyze the conversion of styrene to benzene and acetic acid in the presence of hydrogen, as well as methylating styrene. This chemical is an effective catalyst for the formation of metabolic intermediates and crystal x-ray diffraction studies have shown that DBHT is a good substrate for enzyme activity.Formula:C7H6Br2OPurity:Min. 95%Color and Shape:White To Yellow To Light Brown SolidMolecular weight:265.93 g/mol1,2-Dimethoxy-4,5-dinitrobenzene
CAS:1,2-Dimethoxy-4,5-dinitrobenzene is a fluorescent compound that can be used as a probe to study the response elements in DNA. It has been shown to inhibit HDAC activity and induce nuclear translocation of Nrf2 in wild-type mice. 1,2-Dimethoxy-4,5-dinitrobenzene has also been shown to decrease the level of plasma protein carbonyls in cancer patients. This molecule has analytical applications for determining the presence of it's target compounds in biological samples.Formula:C8H8N2O6Purity:Min. 95%Color and Shape:PowderMolecular weight:228.16 g/molPyridinium p-Toluenesulfonate
CAS:Pyridinium p-toluenesulfonate is a reagent that can be used in the reduction of chloride to produce chloride ions. This process is called desulfurization. Pyridinium p-toluenesulfonate also reacts with cyclodepsipeptides, and can be used to recrystallize them. The main use for this reagent is in organic synthesis, where it can be used as an acid catalyst to synthesize polyene compounds or as a stereoselective agent for the preparation of dye cations.Formula:C7H8O3S·C5H5NPurity:Min. 95%Color and Shape:White PowderMolecular weight:251.3 g/mol3,5-Dihydroxytoluene
CAS:3,5-Dihydroxytoluene is a natural compound that is structurally related to p-hydroxybenzoic acid. It has been shown to be an efficient fluorescent probe for the detection of quillaja saponaria in wastewater treatment plants. 3,5-Dihydroxytoluene also reacts with orcinol to produce a disulfide bond and can undergo polymerization reactions with nucleophiles such as amines and thiols. It is not active against aerobacter aerogenes, but has been shown to have high values against carcinoma cell lines.Formula:C7H8O2Purity:Min. 97.5 Area-%Color and Shape:White Off-White PowderMolecular weight:124.14 g/mol1-Iodo-4-nitrobenzene
CAS:1-Iodo-4-nitrobenzene is an insecticide with a nitro group. It is synthesized by the asymmetric synthesis of diazonium salt and hydroxyl group in the presence of a solid catalyst, such as palladium. 1-Iodo-4-nitrobenzene can be used as a coupling reagent for Suzuki coupling reactions, halide transfer reactions, and other multi-walled carbon transfer reactions. It has also been reported to have neuroprotective effects against Parkinson's disease in levopimaric acid model system. 1-Iodo-4-nitrobenzene has also been shown to inhibit the proliferation of neuro2a cells.Formula:C6H4INO2Purity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:249.01 g/mol4-Methoxybenzenesulfonyl chloride
CAS:4-Methoxybenzenesulfonyl chloride is a water-soluble and colorless solid that is used in the treatment of wastewater. It binds to hydroxyl groups and copper complexes, which are present in high concentrations in wastewater. 4-Methoxybenzenesulfonyl chloride can be used as an analytical reagent for determining binding constants, as well as for the separation of amyloid proteins. This compound has been shown to have anti-inflammatory properties by inhibiting the production of pro-inflammatory cytokines such as tumor necrosis factor (TNF) and interleukin (IL)-1β. 4-Methoxybenzenesulfonyl chloride also has activity against certain cancers such as L1210 leukemia cells in mice and diphenyl ethers.Formula:C7H7ClO3SPurity:Min. 97 Area-%Color and Shape:Brown Off-White PowderMolecular weight:206.65 g/mol
