Alcoholes

Pigment Yellow 138 is a polycarboxylic acid with the chemical formula C8H6Cl4O2. Pigment Yellow 138 has a molecular weight of 434.07 and can be used as a yellow pigment in paint, plastics, and textiles. Pigment Yellow 138 has an acidic pH and can be prepared by reacting phthalic anhydride with sodium hydroxide in aqueous solution to produce the sodium salt of pigment yellow 138. Pigment Yellow 138 is also soluble in hydroxide solutions, which makes it an excellent cross-linking agent for polymers. The color of pigments depends on the size of their particles; pigments with larger particle sizes are more opaque than those with smaller particle sizes.

Codlemone is a pheromone that is secreted by the female codling moth (Cydia pomonella) to attract males for mating. This compound has been shown to have pesticidal activity against various insect species, including codling moths, fruit flies, and aphids. Codlemone is an odorant that binds to olfactory receptors in insects and mammals. It has been shown to bind to the OR1 receptor in mammalian cells and may be involved in physiological functions such as reproduction, stress response, and sexual behavior. The biosynthesis of codlemone starts with the conversion of fatty acid into fatty acid esters by means of transfer reactions with alcohols or alkyl halides. These esters are then converted into dienols by the action of aldehyde oxidase. The dienols are then converted into the final product by means of a palladium-catalyzed coupling reaction with acetaldehyde.

Please enquire for more information about 2,6-Difluoro-4-methoxyphenol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Triglycerol monolaurate (GLA) is a fatty acid that can be synthesized by reacting glycerol with lauric acid. It has been shown to have antimicrobial properties, inhibiting the growth of fungi such as flavus and staphylococcus. GLA also inhibits the production of lipase and protease, enzymes that are required for the digestion of dietary fats. GLA has been used in infant formulas to inhibit the growth of bacteria, such as p. aeruginosa, which may cause infantile diarrhea. Triglycerol monolaurate is also used as dietary supplement to treat eczema due to its inhibitory effect on inflammatory cytokines such as tumor necrosis factor-α (TNF-α).

Please enquire for more information about (4S)-3,4-Dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazin-4-ol 1,1-dioxide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Xylenol orange tetrasodium salt is a fluorescent dye that can be used to measure the degree of mineralization in animal tissue. The dye is composed of xylenol, which is a fatty acid, and sodium chloride. Xylenol orange tetrasodium salt is used for measuring the rate of enzyme reactions by incubating it with the enzyme and measuring the formation rate. It has been shown to have damaging effects on mitochondria and tissues when exposed to an acidic environment. Xylenol orange tetrasodium salt binds to the membrane potential of cells in order to measure reactive oxygen species (ROS) production. This dye can also be used as a marker for autofluorescence of mitochondria and lipase activity.

4-Butoxybenzyl alcohol is a primary alcohol that is used as a solvent and reagent. It has been shown to disrupt the architecture of bacterial cell walls by destabilizing the molybdenum cofactor, which is essential for the enzyme xylose reductase. The destabilization of this cofactor leads to inhibition of cell wall synthesis and subsequent death of bacteria. 4-Butoxybenzyl alcohol also has antibacterial properties and can be used to inhibit the growth of Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis. This compound may also act by inhibiting amide formation or by binding to magnesium, aluminium, or amides in the bacterial cell wall.

2,5-Dimethylresorcinol is a natural organic compound that has been shown to have the ability to inhibit the formation of reactive oxygen species. It is used in wastewater treatment and as an antioxidant. 2,5-Dimethylresorcinol has been shown to exhibit an inhibitory effect on lipid hydroperoxides and hydroxyl group binding. This compound can also be used as a substrate or product in catalytic domains. 2,5-Dimethylresorcinol is found in the form of usnic acid and orsellinic acid. The use of this compound as a catalyst for oxidation reactions has been studied extensively. It has also been shown to be an effective inhibitor for catalytic domains with a range of different metal ions.

Senkyunolide A is a bioactive compound, which is a type of phthalide derived from the roots of Ligusticum chuanxiong, a plant commonly used in traditional Chinese medicine. This compound is notable for its antioxidant and anti-inflammatory properties, which are believed to arise from its ability to scavenge free radicals and modulate inflammatory pathways.

4-Phenylazophenol is an organic azobenzene that has a specific treatment for the degradation of amines and mineralization. It has been shown to reduce the levels of phenols, fatty acids, and amines in wastewater. 4-Phenylazophenol is also used as an enzyme inhibitor in reactions with hydrogen bond formation and as a receptor α ligand. The natural compounds found in 4-phenylazophenol have borohydride reduction properties.

3-Nitrophenol is an organic compound that is used in wastewater treatment, specifically to remove nitrogenous compounds from the water. It reacts with a hydroxyl group and a nitro group to form a molecule with three nitro groups. The presence of this molecule in wastewater can lead to population growth, which may be reduced by thermal expansion. 3-Nitrophenol is also used as an electrode for gravimetric analysis of metals and as a reagent for the detection of sodium ions. This compound has been shown to have a ph optimum of 7.5, but will react with hydrogen bonds at any ph value.

4,5-Dimethylresorcinol is a decarboxylated form of resorcinol that has been extracted from the acetate extract of an endophytic fungus. It has been shown to have anti-inflammatory properties and can be used for the treatment of symptoms such as diarrhea. 4,5-Dimethylresorcinol is produced by a series of enzymatic reactions in which resorcinol is first decarboxylated and then hydroxylated to produce 4,5-dimethylresorcinol. There are two isomers of this compound: the alpha-isomer and beta-isomer. The alpha-isomer has been shown to have more potent anti-inflammatory activity than the beta-isomer. 4,5-Dimethylresorcinol has also been found to be effective in treating intestinal disorders such as Crohn's disease and ulcerative colitis in clinical trials.

Amodiaquine is a drug that belongs to the class of antimalarial agents. It is used for the treatment and prevention of malaria caused by erythrocytic forms of Plasmodium falciparum. Amodiaquine has shown synergistic effects with other drugs, such as sulfadoxine and pyrimethamine, for the treatment of malaria due to P. falciparum. The mechanism of action of amodiaquine is not well understood, but it may involve inhibition of the Toll-like receptor. Amodiaquine has been shown to inhibit polymerase chain reaction in a concentration-dependent manner and also inhibits polymorphonuclear leucocytes, which are important in innate immunity. In addition, amodiaquine is a hypoglycemic agent and can be used for the treatment of bowel disease.

5-Nitroisoquinoline is a nitro compound that has been shown to be a potential biomarker for liver disease. 5-Nitroisoquinoline is synthesized from the reaction of hydroxylamine, sodium carbonate, and nitric acid. This chemical can also be found in human liver tissue. The titration calorimetry experiments performed on 5-nitroisoquinoline showed that the compound has a high heat of formation (194.1 kJ/mol) and low enthalpy of formation (-19.6 kJ/mol). Vibrational analysis revealed that there are four nitrogens in the molecule and two nitrogen atoms per molecule. X-ray crystal structures were obtained for 5-nitroisoquinoline with different solvents and hydrogen bonding was observed in all cases. Molecular modeling showed that there are five nitro groups, which would explain the name "5-nitro." The five nitrogen atoms coordinate to form a trigonal bip

Heptadecafluoro-1-decanol is a chemical substance that has been used in wastewater treatment and as an odorant. It is also found naturally in human liver, heart tissue, and adrenocortical carcinoma. Heptadecafluoro-1-decanol can be chemically synthesized by the reaction of 1H,1H,2H,2H-heptadecafluorodecane with hydrogen fluoride. This chemical substance is known for its ability to bind to fatty acids and other organic compounds on the surface of water droplets. The hydroxyl groups on this molecule are able to form hydrogen bonds with water molecules, which may lead to increased surface tension. Heptadecafluoro-1-decanol has been shown to have anti-inflammatory properties in humans.

5-Thiazolemethanol is a synthetic compound that is used as an antimicrobial agent. It inhibits bacterial growth by disrupting the cell membrane and interfering with protein synthesis. 5-Thiazolemethanol has been shown to be effective against Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa, Staphylococcus aureus, and other bacteria. 5-Thiazolemethanol is not toxic to humans and does not cause irritation or sensitization. The material has been classified as a low level of toxicity in animal studies. This chemical has also been found to have no mutagenic effects on human erythrocytes.

3-Chloro-4-methylbenzyl alcohol is a building block chemical that is used in the synthesis of a variety of organic compounds. It is a versatile chemical that can be used as a reagent, reaction component, and intermediate. 3-Chloro-4-methylbenzyl alcohol has been found to be useful in the synthesis of complex compounds, such as 4-chloromethoxybenzoic acid and 3-(3,5-dimethoxyphenyl)acetic acid. This chemical can also be used to produce speciality chemicals, such as 3-(2-(2,4-dichlorophenoxy)ethyl)benzonitrile.

Allylestrenol is a synthetic steroid hormone that is used as a contraceptive. It works by preventing ovulation and thickening the cervical mucus to prevent sperm from reaching the egg. Allylestrenol has been shown to have a statistically significant effect on infectious diseases of the ovary, such as endometritis, pelvic inflammatory disease, and salpingitis. Allylestrenol also inhibits ovarian enzyme activity, which may lead to autoimmune diseases. This drug has not been studied for its toxicity or pharmacokinetics in humans, but it has been found to be highly toxic in animals with levels of allylestrenol that are 100 times higher than those found in humans. A polymer composition was developed to control the release of allylestrenol in vivo.

7-Chloro-4-hydroxyquinoline-3-carboxylic acid is a chemical compound that has antioxidative activity and is used in the production of various organic substances. It is synthesized by reacting ammonium nitrate with a hydroxy group, an organic solvent, and phenoxy. The resulting product can be heated to form 7-chloro-4-hydroxyquinoline, which undergoes a series of reactions to produce 7-chloro-4-(2,2,2,-trichloroethoxy)quinoline. This reaction system produces a quinoline derivative that has been shown to be expressed at high levels in phosphatidylcholine (PC) and alpha-tocopherol (a vitamin E derivative). The final product is then purified by triethyl orthoformate (TEO), which removes the sulfoxide group.

4-(Phenylthio)benzyl alcohol is a versatile building block used in the synthesis of complex compounds. It has been shown to be an effective reagent for the synthesis of polymers and other organic molecules. 4-(Phenylthio)benzyl alcohol is also a useful intermediate for the preparation of chemical compounds with high quality, such as fine chemicals, speciality chemicals, and research chemicals. This compound can be used as a reaction component in the synthesis of valuable scaffolds.

6-Aminopyrimidin-4-ol is an intermediate in the synthesis of orotic acid. It is also a precursor to 6-chloropurine, which is used in the manufacture of orotic acid and 6-aminopurine. 6-Aminopyrimidin-4-ol can be prepared by benzannulation of phosphorus oxychloride with orotic acid or by hydrolysis of 6-chloropurine with thiourea. The latter method is preferred because it results in less waste.
6-Aminopyrimidin-4-ol is labile and must be stored under an inert gas at low temperature to prevent decomposition. It undergoes inactivating reactions with strong oxidizing agents, such as chlorine dioxide, peracetic acid, hydrogen peroxide, and potassium permanganate.
It also reacts with nucleophiles such as ammonia or amines to form stable taut

Mycophenolic acid is a guanosine monophosphate synthesis pathway blocker. It selectively inhibits inosine monophosphate dehydrogenase (IMPDH) which blocks the conversion of inosine-5-phosphate and xanthine-5-phosphate to guanosine-5-phosphate. This drug inhibits de novo purine biosynthesis. Mycophenolic acid is an immunosuppressant metabolite present in drug formulations that are used to prevent rejections after organ transplants. It has also shown to have antibacterial and antifungal properties.

4-Hydroxy-3-nitrophenylacetic acid (4ONPA) is an organic compound that is the product of the reaction between hydroxylamine and nitrobenzaldehyde. It has been shown to have cytotoxicity in breast cancer cells and has been used as a probe for optical imaging studies. 4ONPA has also been shown to be able to inhibit the activity of enzymes such as catalase, peroxidase, and lipoxygenase. The uptake of 4ONPA into cells is dependent on its concentration and the cell type. This drug can be useful for treating degenerative diseases because it inhibits microglia activation by blocking the enzyme phospholipase A2. Clinical trials are currently being conducted for 4ONPA’s potential use in treating herpes simplex virus infections and cancerous lesions associated with Alzheimer's disease.

(R)-(+)-3-Butyn-2-ol is a chiral alcohol that can be used as a substrate for the synthesis of antibiotics. It has been shown to inhibit phosphatases in vivo and can be used as an inhibitor for phosphatases. (R)-(+)-3-Butyn-2-ol can also be used to synthesize glyoxylate, which is an intermediate for the production of antibiotics. This compound has been shown to have optical activity and stereoselectivity. The synthesis of (R)-(+)-3-butyn-2-ol starts with the alkylation reaction between acetylene and formaldehyde, followed by a cross-coupling reaction with bromoethane and lithium aluminum hydride. The final step is the hydrolysis of furfural using water or lipase, yielding (R)-(+)-3-butyn-2-ol.

2,6-Dimethoxybenzyl alcohol is a synthetic compound that is a peroxidase substrate. It is used as an alternative for papaverine in the synthesis of penicillin and cephalosporin antibiotics. 2,6-Dimethoxybenzyl alcohol reacts with Mn2+ ions to form hydronium and hydrogen peroxide. This reaction has been shown to be more efficient than the decomposition of hydrogen peroxide by catalases or superoxide dismutases. 2,6-Dimethoxybenzyl alcohol also forms a reactive congener with erythrocytes and plasma proteins that can cause vasoconstriction in the blood vessels. The dimethoxybenzyl group (DMB) is a monosubstituted phenol group that binds to the active site of enzymes such as cytochrome P450s and glutathione reductase.

1,7-Heptanediol is a fatty acid that is used as a solvent and coating agent. It has been shown to inhibit leukemia cells in vitro. 1,7-Heptanediol has been shown to bind to the dna binding domains of transcription factors in vitro and may act as an anticancer agent by inhibiting the synthesis of proteins involved in biochemical pathways. 1,7-Heptanediol also inhibits tumor xenografts in vivo and induces apoptosis through hydrogen bond formation with DNA. It has been demonstrated to have detergent properties and can be used for biochemical reactions, such as the synthesis of chemical substances.

Phenol red is a pH indicator that finds broad applications from chemistry to microbiology. Colour varies from yellow at pH<6.8 (lmax 443nm) through to light red/pink at 6.8<pH<8.2 (lmax 570 nm) to vivid purple/red at pH>8.2. It is widely used in cell culture to monitor pH and for colorimetric titration. For example, phenol red can be used to quantify Br- content in sea or fresh water. It is added to VTM as pH indicator, at the concentration of 10mg/ml, maintaining a pink colour at neutral pH.

2,4,6-Tribromo-3-methoxyphenol is a high quality reagent that is used as an intermediate in the production of many fine chemicals. It is also a useful building block for the synthesis of speciality chemicals and research chemicals. This chemical can be used as a versatile building block for reactions with other compounds. 2,4,6-Tribromo-3-methoxyphenol has CAS number 24967-79-1 and can be found at Chemical & Laboratory Equipment.

2,4,5-Trimethoxybenzyl alcohol is a metabolite that is produced by the p. pastoris strain. It has been shown to be active against the enzyme glyceraldehyde-3-phosphate dehydrogenase and has been expressed heterologously in yeast. 2,4,5-Trimethoxybenzyl alcohol also has been shown to inhibit peroxidases and may have biochemical applications in pharmaceuticals as an inhibitor of lipid peroxidation.

4-Bromo-2,6-difluorobenzyl alcohol (4BDFA) is a molecule that has been shown to be able to produce magnetic resonance images. It can be used in tumor diagnosis as well as in the imaging of tumors. 4BDFA is synthesized by coupling 2,6-difluoroaniline with bromoacetaldehyde diethyl acetal. The syntheses are carried out under phase transfer catalysis conditions and the reaction is monitored by thin layer chromatography.
The synthesis of 4BDFA starts with the preparation of 2,6-difluoroaniline via a Grignard reaction between aniline and magnesium metal. The Grignard reagent is then added to bromoacetaldehyde diethyl acetal in dichloromethane followed by addition of triethylamine dropwise to maintain pH neutrality. The product is then extracted from the organic solution using ethyl ether

1-Benzyl-4-piperidyl)methanol is a linker molecule that can be used to connect a variety of heterocycles with the ability to modulate their biological activities. This molecule has been shown to be a potent inhibitor of 5-HT receptor activity and has been used in molecular modeling studies. 1-Benzyl-4-piperidyl)methanol also has the potential for use as an environmental pollutant, which may be due to its reactivity with naphthalene compounds. The modifications that are possible on this molecule include introducing substituents on the benzene ring or amide groups, which can provide potent inhibitory activity.