
Benzoic Acids
Found 5475 products of "Benzoic Acids"
Gentisic acid sodium salt hydrate
CAS:Gentisic acid sodium salt hydrate is a benzoate that is used as a diagnostic agent in the study of inflammatory bowel disease. Gentisic acid sodium salt hydrate is a sodium salt of gentisic acid and has been shown to have anti-inflammatory properties. It is used as a stabilizer for solid dispersions, such as capsules, tablets, and granules. Gentisic acid sodium salt hydrate also has the ability to prevent degradation of certain drugs by hydrolysis or oxidation. Gentisic acid sodium salt hydrate can be synthesized from 2,6-dihydroxybenzoic acid (2,6-DHB) and hippuric acid.Formula:C7H5NaO4·xH2OPurity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:176.1 g/mol2,4-Diaminobenzoic acid dihydrochloride
CAS:2,4-Diaminobenzoic acid dihydrochloride is a versatile building block for complex compounds. This compound can be used as a research chemical and is also a reagent and speciality chemical. 2,4-Diaminobenzoic acid dihydrochloride has been used in the synthesis of many useful compounds, including pharmaceuticals and agrochemicals. It is also an intermediate in the synthesis of some pharmaceuticals and agrochemicals. 2,4-Diaminobenzoic acid dihydrochloride can be used as a scaffold to produce new molecules that are potentially useful as drugs or other chemicals.Formula:C7H8N2O2•(HCL)2Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:225.07 g/mol2,4,6-Trihydroxybenzoic acid methyl ester
CAS:2,4,6-Trihydroxybenzoic acid methyl ester is a synthetic compound that has been used in animal studies to investigate the inflammatory effects of substances. It has been shown to have anti-inflammatory properties in vitro and in vivo. Furthermore, 2,4,6-Trihydroxybenzoic acid methyl ester has been shown to inhibit the production of tumour necrosis factor-α (TNF-α) and other cytokines. This drug also has anti-fungal activity against Candida albicans and Aspergillus fumigatus. 2,4,6-Trihydroxybenzoic acid methyl ester is biodegradable.
Formula:C8H8O5Purity:Min. 95%Color and Shape:PowderMolecular weight:184.15 g/mol3,6-Dichloro-2-hydroxy benzoic acid
CAS:3,6-Dichloro-2-hydroxy benzoic acid is a reactive compound that is used as an intermediate in the synthesis of organic compounds. It reacts with the chlorine atom to form a diazonium salt. The diazonium salt then undergoes demethylation, which allows it to be converted into various products such as 3,5-dichloro-2-hydroxybenzoic acid or 2,4-dichloro-3,5-dimethoxybenzoic acid. 3,6-Dichloro-2-hydroxy benzoic acid is a strong base and can react with any acidic compounds present in the reaction vessel. This product has been shown to be effective for wastewater treatment by converting organic compounds into less harmful compounds.Formula:C7H4Cl2O3Purity:Min. 95%Color and Shape:PowderMolecular weight:207.01 g/mol5-Bromosalicylic acid
CAS:5-Bromosalicylic acid is a derivative of p-hydroxybenzoic acid that is used in wastewater treatment. The reaction of 5-bromosalicylic acid with the 1,3-benzodioxole-5-carboxylic acid leads to the formation of a new compound, which can be used as an intermediate in organic synthesis. 5-Bromosalicylic acid has been shown to inhibit the growth of hepg2 cells and K562 cells by damaging DNA. It also inhibits the suzuki coupling reaction by acting as a hydrogen sink and stabilizing the transition state through intramolecular hydrogen bonding interactions. A possible mechanism for this inhibition is that 5-bromosalicylic acid reacts with hydroxide ions to form bromohydroxylated products, which then react with amine compounds to produce carboxylates that can hydrogen bond with other molecules.Formula:C7H5BrO3Purity:Min. 95%Color and Shape:White PowderMolecular weight:217.02 g/molBis(2-ethylbutyl)phthalate
CAS:Bis(2-ethylbutyl)phthalate (BEBP) is a chemical that has been used in the production of polyvinyl chloride (PVC) plastics, and as a stabilizer for PVC resins. BEBP is found in low levels in human tissue samples and sediments. Levels of BEBP have been measured through gas chromatography-mass spectrometry and liquid chromatography-mass spectroscopy methods. The environmental concentrations of BEBP can be calculated using the linear regression equation. Biota are also exposed to this chemical, which may be due to its use as an additive in certain food packaging materials.Formula:C20H30O4Purity:Min. 95%Color and Shape:Colourless To Pale Yellow LiquidMolecular weight:334.45 g/mol2,4-Dihydroxy-6-pentylbenzoic acid
CAS:An intermediate in the phytocannabinoid biosynthetic pathway.Formula:C12H16O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:224.25 g/mol3,5-Dihydroxybenzoic acid methyl ester
CAS:3,5-Dihydroxybenzoic acid methyl ester is a potent tyrosinase inhibitor that has been shown to be effective in inhibiting the production of melanin. 3,5-Dihydroxybenzoic acid methyl ester is an active ingredient in skin lightening products and has been shown to be more potent than kojic acid, arbutin and ascorbic acid. The reaction mechanism of 3,5-Dihydroxybenzoic acid methyl ester is stepwise with hydroxybenzoic acid (HBA) being the first substrate. HBA reacts with iron oxides to form a ferric hydroxide intermediate that undergoes gelation reactions with chloride ions. This results in a molecule containing three ether linkages, which are responsible for its inhibitory activity on the enzyme tyrosinase.
Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/mol2,3-Diaminobenzoic acid methyl ester
CAS:2,3-Diaminobenzoic acid methyl ester is a redox potential catalyst that has been shown to have anticancer activity in vitro and in vivo. It is a 5-ht4 receptor agonist, which causes an increase in the intracellular concentration of cAMP. The anticancer effect of this compound may be due to its ability to inhibit the growth of cancer cells by blocking DNA synthesis and cell division. The biological properties of this drug are not well understood, but it has been shown to have antioxidant effects, as well as proton-reducing and electron-accepting properties. This compound has also been studied electrochemically.Formula:C8H10N2O2Purity:95%NmrColor and Shape:PowderMolecular weight:166.18 g/molMethyl 4-amino-2-methyl benzoate
CAS:Methyl 4-amino-2-methyl benzoate is a fine chemical that can be used as a building block for research chemicals, pharmaceuticals, and speciality chemicals. Methyl 4-amino-2-methyl benzoate is a versatile building block in organic synthesis because it can be used as a reaction component and intermediate to synthesize other compounds. This compound is also an excellent scaffold for the synthesis of complex compounds, making it a useful intermediate for organic chemistry. Methyl 4-amino-2-methyl benzoate has CAS No. 6933-47-7 and is soluble in organic solvents such as dichloromethane, chloroform, ether, or acetone.Formula:C9H11NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:165.19 g/mol3-Methyl-2-nitrobenzoic acid
CAS:3-Methyl-2-nitrobenzoic acid is a chemical that can be used for wastewater treatment. It has been shown to be effective against chlorantraniliprole, a pesticide that is often found in wastewater. 3-Methyl-2-nitrobenzoic acid also has the ability to reduce chloride levels by oxidizing it to produce chloride ions and nitrogen gas. This chemical can be used as an oxidation catalyst in wastewater treatment. 3-Methyl-2-nitrobenzoic acid has been shown to have photocatalytic activity with titanium dioxide and copper sulfate (CuSO4) under visible light illumination conditions.Formula:C8H7NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:181.15 g/mol2,6-Dimethoxybenzoic acid
CAS:2,6-Dimethoxybenzoic acid is a chemical compound with the molecular formula of C9H8O4. It belongs to the group of sesquiterpene lactones and has been shown to have anti-inflammatory properties. 2,6-Dimethoxybenzoic acid exhibits a carboxylate reaction mechanism that can be activated by an enzyme, curculigoside, which hydrolyzes the ester bond in 2,6-dimethoxybenzoic acid. The reaction mechanism involves the group p2 (COOH) on 2,6-dimethoxybenzoic acid reacting with an alcohol on curculigoside to form an ester and protocatechuic acid. The dianthus caryophyllus plant produces 2,6-dimethoxybenzoic acid as a byproduct of its synthesis of protocatechuic acid. This compound is chemically studied using solid phase microextractionFormula:C9H10O4Purity:Min. 95%Color and Shape:PowderMolecular weight:182.17 g/mol2-Hydroxy-3-methoxybenzoic acid
CAS:2-Hydroxy-3-methoxybenzoic acid is a chemical compound that has been studied for its potential use in the treatment of prostate cancer. It is a coordination complex that binds to DNA and inhibits the process of transcription. This compound also possesses anti-inflammatory properties, which are related to its ability to inhibit prostaglandin synthesis. 2-Hydroxy-3-methoxybenzoic acid has been shown to have an effect on human HL60 cells, which may be due to its ability to induce apoptosis. This compound has also been shown to have a high degree of metabolic stability and is not toxic to normal cells at doses up to 100 μM.Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/mol4-Amino-3,5-diiodobenzoic acid
CAS:4-Amino-3,5-diiodobenzoic acid is a conjugate of the amino acid histidine with two iodine atoms. It is used as a radiopaque contrast agent for X-ray imaging and has been shown to be useful in distinguishing between normal tissue and cancerous lesions. The molecule can be modified to contain various functional groups that allow it to bind to other molecules such as proteins or DNA, which can alter its properties. 4-Amino-3,5-diiodobenzoic acid is also known as diaminobenzene diiodide and is soluble in water.Formula:C7H5I2NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:388.93 g/molMethyl 4-(N-methylamino)benzoate
CAS:Methyl 4-(N-methylamino)benzoate is a substance that inhibits the enzyme DPP-4, which is involved in blood glucose regulation. It has been shown to be effective against certain types of cancer and impurities that may be present in the drug. Methyl 4-(N-methylamino)benzoate is an acidic compound with molecular descriptors that include acidic and amines. This compound also has genotoxic impurities, such as benzofurans, which may affect its efficacy.Formula:C9H11NO2Purity:90%Color and Shape:PowderMolecular weight:165.19 g/mol4-Acetylbenzoic acid
CAS:4-Acetylbenzoic acid is a reactive functional group that is used to synthesize esters and amides. It has been shown to have anticancer activity in vitro, which may be due to the disruption of basic cellular proteins involved in DNA replication. 4-Acetylbenzoic acid is soluble in neutral pH and reacts with nucleophiles such as hydroxide ions or alcohols, forming alcohols or acetates respectively. The reaction mechanism for this compound is nucleophilic attack on the carbonyl carbon, followed by loss of water from the leaving group. Significant cytotoxicity has been observed in vitro at concentrations of 2mM and higher. This effect was particularly pronounced for cells exposed to radiation or treated with 4-acetylbenzoic acid before being exposed to radiation.
Formula:C9H8O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:164.16 g/mol5-Amino-2-nitrobenzoic acid
CAS:5-Amino-2-nitrobenzoic acid is an organic compound that belongs to the class of versatile building block. It is a white solid that has been used as a research chemical, reagent, and specialty chemical for the synthesis of complex compounds and pharmaceuticals. 5-Amino-2-nitrobenzoic acid is also known as 2-amino-5-chlorobenzoic acid (ACBA). It is soluble in water, but insoluble in ethanol. The CAS number for this chemical is 13280-60-9.
Formula:C7H6N2O4Molecular weight:182.14 g/molRef: 3D-A-6802
1kgTo inquire100gTo inquire250gTo inquire500gTo inquire2500gTo inquire-Unit-ggTo inquireMethyl 3-amino-4-chlorobenzoate
CAS:Methyl 3-amino-4-chlorobenzoate is an analog of 3-amino-4-chlorobenzoic acid. It is a multidrug that can cross the blood brain barrier and has been shown to have cytotoxic activity in vitro. Methyl 3-amino-4-chlorobenzoate has been postulated as a possible organometallic compound and may be synthesized through a chemical diversity approach. The chloride ion, which is present in methyl 3-amino-4-chlorobenzoate, has been shown to decrease the toxicity of nitrobenzoic acid, making this compound resistant to nitrosation reactions.Formula:C8H8ClNO2Purity:Min. 95%Color and Shape:PowderMolecular weight:185.61 g/mol3,5-Diiodo-4-hydroxybenzoic acid
CAS:3,5-Diiodo-4-hydroxybenzoic acid (3,5 DIBA) is an aminotriazole that inhibits the growth of a wide range of bacteria. 3,5 DIBA inhibits the transport of catechol and 2,6-dichlorobenzoic acid into cells. This inhibition leads to decreased levels of catechol-O-methyltransferase activity and increased levels of lysine decarboxylase activity. The combination of these two reactions causes a decrease in lysine production. Lysine is important for cell division and protein synthesis in bacteria. 3,5 DIBA also inhibits root formation in plants and has been shown to inhibit the uptake of nutrients by plant roots. Also known as: Dibenzoylmethane; 1,2-Benzenediamine, 3-[(2,6-dichlorophenyl)imino]-, diiodide;Formula:C7H4I2O3Purity:Min 97%Color and Shape:PowderMolecular weight:389.91 g/mol3,4-Dihydroxybenzoic acid
CAS:Dietary polyphenolFormula:C7H6O4Purity:Min. 95%Color and Shape:PowderMolecular weight:154.12 g/mol
