Ácidos graxos

<p>Applications Benzenebutanoic Acid Ethyl Ester is used in the synthesis of thiazolium salts with potent antimalarial activity. Also used in the preparation of novel lactate dehydrogenase A inhibitors. This compound is suitable for lactate dehydrogenase (LDH) related research.<br>References Hamze, A. et al.: J. Med. Chem., 48, 3639 (2005); Ward, R. et al.: J. Med. Chem., 55, 3285 (2012);<br></p>

<p>Applications 2-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]butyric Acid Ethyl Ester-d5 is labelled 2-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]butyric Acid Ethyl Ester (T302660) which is used as a reagent to prepare N-heterocyclylcarbamates and biphenylisoxazoles as lysophosphatidic acid (LPA) receptor antagonists.<br>References Buckman, B., et al.: PCT Int. Appl., WO 2013025733 A1 20130221 (2013)<br></p>

<p>Applications Propargyl Alcohol-13C3 is labelled Propargyl Alcohol (P762550) which is used as a corrosion inhibitor, a metal complex solution, a solvent stabilizer and an electroplating brightener additive. It is also used as an intermediate in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Zhang, T., et al.: Res. Chem. Interm. (2013); Choudhary, Y., et al.: SPE Product. Operat., 28, 268 (2013); Hed, Y., et al.: J. Mater. Chem. Mater. Bio. Med., 1, 6015 (2013)<br></p>

<p>Applications Glyceryl Tri(hexadecanoate-16,16,16-d3) (CAS# 285979-78-4) is a useful isotopically labeled research compound.<br></p>

<p>Applications Ethyl Propargylate is used in the synthesis of substituted anthraquinones. Also used in the preparation of inhibitory pyrazolo[1,5-a]pyridines for anti-inflammatory activity.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Chang, M. et al: Synth. Comm., 43, 3363 (2013); Kojima, A. et al.: Bioorg. Med. Chem. Lett., 23, 5311 (2013);<br></p>

<p>Applications 2-Formyl-3-oxopropanoic Acid Ethyl Ester is used cyclocondensation reactions for the preparation of heterocyclic compounds such as polyfunctionally substituted pyridines.<br>References Torii, S. et al.: Synthesis, 5, 400 (1986); Schenone, P. et al.: J. Heterocyc. Chem., 27, 295 (1990);<br></p>

<p>Applications Glyceryl Tri(hexadecanoate-2,2-d2) (CAS# 241157-06-2) is a useful isotopically labeled research compound.<br></p>

<p>Applications Used in the preparation of cosmetic and pharamceutical products.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications Pregabalin intermediate.<br>References Decicco, C., et al.: Bioorg. Med. Chem. Lett., 7, 2331 (1997),<br></p>

<p>Applications Hexadecanoic-3,3-d2 Acid (CAS# 83293-32-7) is a useful isotopically labeled research compound.<br></p>

<p>Applications 1,4-Phenylenediacetic Acid Eethyl Ester is an arendiacetic ester used in the preparation of potent β-3 receptor agonist.<br>References Badland, M. et al.: Green Chem., 13, 2888 (2011)<br></p>

<p>Applications 3,4-Dihydro-4-hydroxy-1(2H)-pyridinecarboxylic Acid Ethyl Ester is a synthetic intermediate/reactant in the synthesis of streptazolin.<br>References Kozikowski, A., Park, P.: J. Org. Chem., 55, 4668 (1990);<br></p>

<p>Applications Hexadecanoic-9,9-d2 Acid (CAS# 272442-14-5) is a useful isotopically labeled research compound.<br></p>

<p>Applications 1-Bromohexadecane-d33 (CAS# 284474-41-5) is a useful isotopically labeled research compound.<br></p>

<p>Rac-1,2-Bis-palmitoyl-3-chloropropanediol (rac1,2BPC) is a dispersive compound that has been used in the experimental phase of extraction. It has been shown to be efficient in the quantification and screening of fatty acids. Rac1,2BPC has also been used as a spiking agent for food samples to identify contaminants. The recoveries have been validated and linearity has been demonstrated. Rac1,2BPC is an anion that can be quantified by liquid chromatography with wavelength detection at 202 nm.</p>

<p>Ethyl palmitate is a glycol ether that belongs to the group of esters. It has been shown to have biochemical properties and natural compounds such as caproic acid and ethyl palmitate. The liquid form of ethyl palmitate is clear, colorless, and odorless with a density of 1.065 g/mL at 20°C. Ethyl palmitate is soluble in ethanol, diethylether, benzene, chloroform, carbon tetrachloride, acetic acid ethyl ester, acetone, ethyl acetate, dichloromethane, and methanol. Ethyl palmitate can be used as a model system or analytical method for the identification of other lipids in biological samples.</p>

<p>Glycidyl palmitate is a synthetic fatty acid ester that has reactive hydroxyl groups. It is used in the production of polylactic acid, a biodegradable polymer. Glycidyl palmitate can be prepared by reacting a fatty acid with glycerol and an epichlorohydrin. The elimination rate of glycidyl palmitate from the body has been shown to be activated by surface methodology such as chemical ionization mass spectrometry. Glycidyl palmitate can also be analyzed using gas chromatography with flame ionization detection (GC-FID) or gas chromatography-mass spectrometry (GC-MS). A sample preparation technique for glycidyl palmitate is to dissolve it in sodium salts and use filtration as the final step before analysis. The most common fatty acids present in glycidyl palmitate are oleic acid and linoleic acid.</p>

<p>4-Oxo-1-piperidinecarboxylic acid ethyl ester is an antimicrobial agent that belongs to the group of unsaturated ketones. It has been shown to have clinical activity against gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis and Streptococcus pneumoniae, as well as Candida albicans. It also exhibits significant antiinflammatory activity in mice with chronic inflammation induced by carrageenan or LPS. 4-Oxo-1-piperidinecarboxylic acid ethyl ester inhibits the enzyme dpp-4, which is involved in the production of amyloid beta peptides and type II diabetes. This compound was also shown to possess anticholinesterase activity in vitro.</p>

<p>1,2-Dilinoleoyl-3-palmitoyl-rac-glycerol (DLPG) is a lipid molecule that is structurally similar to the sphingolipid ceramide. It has been shown to be an inhibitor of cellular uptake and growth rate and also has long-term toxicity effects. DLPG has been shown to inhibit the signal transduction pathway by binding to microprocessors in the cell membrane and changing their frequency. DLPG also has a profile that can be used as an analog for dextran sulfate, which is a chemical compound that inhibits the uptake of glucose in mammalian cells. The uptake of DLPG can be decoupled from its signaling activity by using constant magnetic fields, which can be generated with superparamagnetic iron oxides or iron particles.</p>

<p>Please enquire for more information about (2S,3S,5S)-5-[(N-Formyl-L-leucyl)oxy]-2-hexyl-3-hydroxyhexadecanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Rac-1,2-bis-palmitoyl-3-chloropropanediol is a dispersive molecule that is composed of a fatty acid and a chlorinated derivative of palmitic acid. It is used to calibrate the mass spectrometer and as an internal standard in quantitative analysis. Rac-1,2-bis-palmitoyl-3-chloropropanediol reacts with electrospray ionization with a dose-dependent response. It has been shown to be toxic to kidney cells at high doses but not at low doses. This chemical has been detected in food samples after being absorbed from the gastrointestinal tract. Rac 1,2-bis-palmitoyl 3 chloropropanediol can be found in the dipalmitate form or as formic acid.</p>

<p>Dipalmitoylglycerol is a fatty acid that is naturally found in catfish. The optimal conditions for the synthesis of dipalmitoylglycerol from tripalmitin have been determined by surface methodology to be at pH 5 and at 0°C. Dipalmitoylglycerol has been shown to bind to the enzyme acetyl-CoA carboxylase, which is involved in the synthesis of fatty acids, and prevent its activation. As a result, there is no production of malonyl CoA, which is an important precursor in the synthesis of fatty acids. This may be beneficial for infants because it prevents them from developing allergies and asthma.</p>

<p>3-Bromo-4-oxo-piperidine-1-carboxylic acid ethyl ester is a monoclinic crystal of the salt of 3-bromo-4-oxo-piperidine and 1,2-ethanediol. It is used as an intermediate in the synthesis of cisapride, a medication that regulates gastrointestinal motility. 3BOCEP has been shown to hydrolyze in the stomach with a rate constant of 2 x 10 M s. The bromination product is cisapride, which has been shown to regulate gastrointestinal motility by stimulating GI smooth muscle contractions.</p>

<p>Please enquire for more information about Boc-HomoGly(Propargyl)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about rac 2-palmitoyl-3-chloropropanediol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-Oxopyrrolidine-3-carboxylic acid ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about rac-3-hexadecanamido-2-methoxypropan-1-ol phosphocholine monohydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl palmitate is a chemical compound that belongs to the group of esters. It is a colorless liquid with a melting point of -17 °C, boiling point of 113 °C, and density of 0.834 g/mL. Methyl palmitate has shown genotoxic activity in a water vapor-resistant strain of Salmonella typhimurium TA100 and in the Ames assay. This chemical also has metabolic response properties, which may be due to its ability to induce prostaglandin J2 production and inhibit cyclic AMP accumulation in cells. Methyl palmitate is used as an additive for cosmetics, such as skin care products, perfumes, and hair dyes. It can also be found in food products such as margarine and coffee creamer.</p>

<p>Propargylaldehyde diethyl acetal is a chemical compound that is used as an intermediate in the synthesis of other compounds. It is a white crystal or crystalline powder that is soluble in organic solvents such as ether, alcohols, and benzene. Propargylaldehyde diethyl acetal has been shown to be potent inhibitors of HSV-1, HSV-2, and HCMV. Furthermore, it has been reported that propargylaldehyde diethyl acetal inhibits the growth of cancer cells in vitro. In addition, propargylaldehyde diethyl acetal has been shown to inhibit the production of autoimmune diseases such as rheumatoid arthritis and multiple sclerosis.</p>

<p>3,7,11,15-Tetramethyl-1,2,3-hexadecane-triol is a fatty alcohol that is used in detergent compositions. It has been shown to be biocompatible with human skin cells and does not show any carcinogenic potential. 3,7,11,15-Tetramethyl-1,2,3-hexadecane-triol is chemically stable and can be used for sample preparation and light exposure. The particle size of this compound is about 1 micrometer. This substance does not have any toxic effects on skin cells or other cells when it is exposed to light.</p>

<p>Ternary mixtures of hexadecafluoro(1,3-dimethylcyclohexane) with fluorine and hydrogen fluoride are stable compounds. The proton is a constant, which is the only variable in the equation. The analytical method for determining the amount of hexadecafluoro(1,3-dimethylcyclohexane) in a mixture can be found in reference 1. This reference also discusses the matrix effect on this compound's stability and optical properties. Reference 2 discusses transfer reactions that are present when hexadecafluoro(1,3-dimethylcyclohexane) is heated to temperatures of 400°C or above. Reference 3 discusses how polymer films can be formed by heating hexadecafluoro(1,3-dimethylcyclohexane) with a solvent such as pentane. Reference 4 discusses how covid-19 pandemic has been shown to be effective against the H2 strain of subt</p>

<p>Boc-L-Propargylglycine is an antibacterial agent that can be used for the treatment of cancer. It has been shown to have specificities against cancer cells, as well as a high potency and low toxicity. Boc-L-Propargylglycine may be useful in biochemistry experiments because it can form conjugates with amines, hydroxyl groups, and amino acids. This drug also binds to DNA by forming triplexes and high-potency complexes with guanine residues. Boc-L-propargylglycine has been shown to inhibit the growth of cancer cells in vitro. It is orally bioactive, which means that it is absorbed and distributed throughout the body when taken by mouth.</p>

<p>2,3-Dipalmitoyl-sn-glycero-1-phosphocholine is a synthetic lipid that is used as a surfactant in biological research. It is a proton donor that destabilizes membranes and interacts with phosphatidylcholine. The deformation of the lipid bilayer may be due to its protonation state. This synthetic lipid has been shown to increase fluidity of the membrane by changing the acyl chain composition and surfactant properties. 2,3-Dipalmitoyl-sn-glycero-1-phosphocholine also increases membrane transport by interacting with the bilayer and forming lamellar structures. The enantiomeric form of this lipid has been found to be more effective than its racemic mixture in the inhibition of cholesterol biosynthesis.</p>

<p>Palmitoyl chloride is a chemical compound that has the chemical formula CH3(CH2)16COCl. It is an ester of palmitic acid and chloroform. Palmitoyl chloride has a phase transition temperature of 39°C, giving it high resistance to heat. It can be used as a model system for studying the interactions between hydroxyl groups and chloride ions in water. This compound also has high water permeability and water vapor permeability, making it useful in the treatment of infectious diseases such as malaria. Palmitoyl chloride can be synthesized by reacting sodium carbonate with trifluoroacetic acid, which generates sodium trifluoroacetate. The sodium trifluoroacetate can react with 4-chlorobutyl alcohol to form 4-chlorobutylchloroformate, which reacts with palmitic acid to form palmitoyl chloride.</p>