Organic Halides

<p>1,6-Diaminohexane dihydrochloride is a chemical that is used in the analytical method for the determination of p-hydroxybenzoic acid. It has also been used to measure fatty acids and anhydrous sodium. The sample preparation required for this chemical includes mixing with water and adding hydroxyl groups. A toxicological study on 1,6-diaminohexane dihydrochloride shows that it has no acute toxicity in rats. However, it does show some signs of toxicity in rabbits and dogs at high doses. Amine compounds are usually very reactive due to the presence of a lone electron pair on nitrogen.</p>

<p>Sodium fluoroacetate is a salt that is synthesized by the reaction of methyl ethyl and sodium trifluoroacetate. It has been used as an insecticide, but also has been used to treat metabolic disorders such as bowel disease and eye disorders. Sodium fluoroacetate also has been used in natural products for the treatment of autoimmune diseases. The toxicological studies of sodium fluoroacetate have shown that it can cause eye disorders and x-ray crystal structures have revealed its mechanism of action.</p>

<p>Please enquire for more information about (3,5-Dibromo-Tyr1)-Leu-Enkephalin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2'-Bromoacetophenone is a chemical compound that is used in the synthesis of unsaturated ketones. It reacts with terminal alkynes to form 2-bromo-2-methylpropene, which can subsequently be converted into unsaturated ketones such as methyl vinyl ketone. The reaction time for this process is less than five minutes and no catalyst is required. This chemical has been shown to have anticancer activity and may act as a biomimetic. 2'-Bromoacetophenone also has been shown to react with hydroxyl groups in the presence of copper salts and hydrochloric acid to form an unsaturated ketone with a terminal alkene.</p>

<p>DABCYL-Tyr-Val-Ala-Asp-Ala-Pro-Val-EDANS trifluoroacetate salt is a reactive dye that has been shown to bind to the granule neurons of the cerebellum in HL60 cells. It is used as an indicator of protease activity, as it undergoes hydrolysis by serine proteases. DABCYL-Tyr-Val-Ala-Asp-Ala-Pro-Val-EDANS trifluoroacetate salt has also been shown to activate caspase 1 and cause neuronal death in a number of experimental models. This molecule is used for fluorescent labeling and detection of protein synthesis, as well as for visualization of the termini of proteins and other molecules. DABCYL Tyr Val Ala Asp Ala Pro Val EDANS trifluoroacetate salt is also known to be an antiinflammatory agent that may be effective against infectious diseases such as HIV,</p>

<p>Please enquire for more information about H-Trp-Phe-Tyr-Ser(PO3H2)-Pro-Arg-pNA trifluoroacetate salt 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 (Deamino-Cys3, Nle 4,Arg5,D-2-Nal 7,Cys11)-a-MSH (3-11) amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Chlorimuron-ethyl is a herbicide belonging to the class of pyrazole compounds. It inhibits plant growth by interfering with photosynthesis and chlorophyll synthesis. Chlorimuron-ethyl can be used in wastewater treatment, as well as applications to grow crops such as soybeans. The compound has been shown to have a sublethal effect on myeloma cells in vitro and has been shown to be an effective antimetastatic agent in vivo.</p>

<p>Please enquire for more information about 2-Bromobenzo[d]thiazol-6-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-2'-chlorophenyl acetic acid methyl ester is a synthetic chemical that can be used as a pharmaceutical intermediate. It is prepared by the reaction of bromine with 2-chloroacetic acid and magnesium, which yields the desired product. The catalytic effect of this chemical is due to its ability to act as a catalyst for many reactions, such as the synthesis of clopidogrel. This chemical also has an industrial application in the production of other medicines, such as aspirin.</p>

<p>Prifiniumbromide is an analog of GABA, which is a neurotransmitter found in the brain. It has been shown to be effective in patients with diabetic neuropathy and geriatric patients with constipation. Prifiniumbromide has also been used to treat inflammatory bowel disease and bladder disorders, such as detrusor muscle dysfunction. In addition, it has been shown to increase urinary output in patients with metabolic disorders.</p>

<p>H-Ala-Ala-Pro-Val-chloromethylketone is a hydrogen peroxide prodrug that is activated by the enzyme chloromethyl ketone. This drug has been shown to be active against schistosoma and pancreatic cancer cells, as well as in activating peroxide. HAPV may also have an effect on immunity and leukocytes, which could be due to its ability to sensitize these cells to damage caused by other agents, or through the hydrolytic enzymes it generates.</p>

<p>(3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone is an organic compound that belongs to the class of carbonyl reductase. It is used as a catalyst for the transformation of secondary alcohols to ketones or aldehydes, including isopropyl alcohol. The reaction proceeds via an intermediate carboxylic acid. The enzyme has been found in various microorganisms, and can be purified from Bacillus megaterium and Streptomyces lividans. The enzyme’s activity can be inhibited by steric effects, metal ions, or other compounds. (3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone crystallizes in two forms: one with the chiral center at the 3 position and one with it at the 4 position.</p>

<p>5-Bromo-2-hydroxybenzaldehyde (5BHB) is an organic compound that has been shown to have a coordination geometry of group p2. This compound binds to DNA and RNA, inhibiting the transcription process. 5BHB also has the ability to form a copper complex with malonic acid. This redox potential is reduced by one electron when copper is added in order to form the copper complex, which allows for the reactivity of 5BHB to be increased. 5BHB binds to nucleic acids through hydrogen bonding interactions with nitrogen atoms and lone pairs on oxygen atoms. The reaction mechanism for 5BHB involves intramolecular hydrogen transfer from one molecule of 5BHB to another, forming an intermediate that then reacts with nucleic acid.</p>

<p>Aminoguanidine hydrochloride is a basic compound that can be used as an anti-inflammatory drug. It has been shown to have a hypoglycemic effect, which may be due to its ability to increase the activity of glutathione peroxidase and glutathione reductase in experimental models. Aminoguanidine hydrochloride also inhibits the production of inflammatory cytokines such as TNF-α, IL-1β and IL-6. Experiments with transfected cells have shown that aminoguanidine hydrochloride induces neuronal death, which may be due to its ability to inhibit protein synthesis by interfering with ribosomal function.</p>

<p>Please enquire for more information about Amyloid P Component (33-38) amide trifluoroacetate salt 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 TGF alpha (1-50) (rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trichlorobenzoic acid is a chemical compound that is found in plants, such as Trifolium pratense L. and other legumes. It has been shown to inhibit the growth of bacteria by competitive inhibition of the enzyme ribonucleotide reductase, which catalyzes the conversion of ribonucleotides to deoxyribonucleotides. This prevents the production of RNA, which is necessary for protein synthesis and cell division. Inhibition of this enzyme can be achieved by either conjugating trichlorobenzoic acid with a sugar or using ion-exchange resins to remove it from water. The concentration required for this type of inhibition varies depending on the type of organism, but generally ranges between 5-10 ppm.END&gt;</p>

<p>Please enquire for more information about H-Arg-4MbetaNA hydrochloride salt 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 Dnp-(Leu421)-Collagen Type VIII a1 Chain (419-426) amide (human, mouse) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Chloro-6-methoxyquinoline is an inhibitor of bacterial DNA gyrase. It has antibacterial activity against Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Pseudomonas aeruginosa. 4-Chloro-6-methoxyquinoline is a synthetic compound that was reinvestigated for its antibacterial activity. It has been shown to be effective in the treatment of Staphylococcal infections. The mechanism of action may involve inhibition of topoisomerase II or interference with the synthesis of DNA by binding to the enzyme bacterial DNA gyrase. Quinidine and cinchonidine are quinine derivatives that have been found to inhibit bacterial DNA gyrase. These compounds are found in the bark of Cinchona species, which includes Cinchona ledgeriana, Cinchona officinalis, and Cinchona succirub</p>

<p>Please enquire for more information about (D-Trp12,Tyr34)-pTH (7-34) amide (bovine) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Chloro-4-fluorobenzoyl chloride is a chlorinating agent that is used as a fungicide, phytotoxin, and an insecticide. It is an effective pesticide against many fungal diseases that affect plants. 3-Chloro-4-fluorobenzoyl chloride has been shown to be effective in the treatment of cervical cancer and other cancers. It also has photochromic properties, which make it useful for detecting skin cancer. 3-Chloro-4-fluorobenzoyl chloride is synthesized by reacting chlorine with 4-fluorobenzoyl chloride in the presence of a base such as sodium hydroxide or potassium hydroxide. This reaction can be carried out in either liquid or gaseous phases. The product can be purified by vacuum distillation or crystallization. 3-Chloro-4-fluorobenzoyl chloride is primarily used as a fungicide</p>

<p>Decamethonium bromide is a potent and selective antagonist of nicotinic acetylcholine receptors. It is used in the treatment of autoimmune diseases, such as myasthenia gravis, Lambert-Eaton syndrome, and Guillain-Barre syndrome. Decamethonium bromide has been shown to inhibit the enzyme activity of acetylcholinesterase, which leads to an accumulation of acetylcholine at neuromuscular junctions. This causes muscle paralysis and increased bronchoconstriction in humans. In animal models, decamethonium bromide has been shown to be a potent inhibitor of receptor activity in the muscle tissue.</p>

<p>Please enquire for more information about H-Glu(EDANS)-Lys-Pro-Ala-Lys-Phe-Phe-Arg-Leu-Lys(DABCYL)-NH2 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trifluoroacetate salt</p>

<p>3,3'-Dichlorobenzidine dihydrochloride is a chemical compound that is used in the manufacture of industrial chemicals. 3,3'-Dichlorobenzidine dihydrochloride is also used as a biochemical to detect copper and chloride ions in urine samples. This chemical has shown binding activities with receptor α, which is responsible for the transmission of nerve impulses. 3,3'-Dichlorobenzidine dihydrochloride has been shown to have a high affinity for receptor α and can be used as an antagonist for this receptor in binding studies.</p>

<p>Please enquire for more information about Amyloid beta-Protein (1-40) (scrambled) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trifluoroacetate salt</p>

<p>Please enquire for more information about H-D-His(1-Me)-OH hydrochloride salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Endothelin-1 (11-21) trifluoroacetate salt H-Cys-Val-Tyr-Phe-Cys-His-Leu-Asp-Ile-Ile-Trp is a peptide that is derived from endothelin. It has been shown to have an inhibitory effect on insulin stimulated glucose uptake in Sprague Dawley rats. This peptide has also been shown to bind to the endothelin receptor and act as a nonselective agonist. Endothelin 1 (11–21) trifluoroacetate salt H-Cys Val Tyr Phe Cys His Leu Asp Ile Ile Trp, when incubated with cells, had a maximal response at micron concentrations.</p>

<p>Trifluoroacetate salt</p>

<p>3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid is a synthetic chemical that is used as a pesticide. This chemical has been found to be more effective than other pesticides because it can inhibit the synthesis of fatty acids, which are necessary for the growth of insect larvae. 3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid is synthesized by reacting sodium hydroxide solution with triethyl orthoformate in the presence of hexamethylenetetramine. This reaction produces a mixture of diethyl ester and carboxylate esters, which are then separated from each other. The resulting carboxylate ester is then oxidized to produce 3-(difluoromethyl)-1-methyl-1H pyrazole 4 carboxylic acid.</p>

<p>Copeptin (rat) trifluoroacetate salt is a peptide that belongs to the group of protein inhibitors. It can inhibit the activity of the acetylcholine receptor, which leads to an increase in muscle tone and rigidity. Copeptin is also used as a research tool for studying protein interactions, antibody-antigen reactions, cell biology, ligand-receptor binding, pharmacology and life sciences. Copeptin has been shown to inhibit ion channels such as nicotinic receptors and potassium channels. The CAS number for copeptin (rat) trifluoroacetate salt is 86280-64-0.</p>

<p>5-Bromo-2-methoxyphenyl)acetic acid (BMPEA) is a hydroxylated derivative of aspartic acid. It has been shown to induce apoptotic cell death in various cell lines, including human lung cells and rat hippocampal cells. BMPEA is synthesized by the solid-phase method and is characterized by a constant structure. It can be used to treat degenerative diseases and other conditions where apoptosis is desirable, such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, and Duchenne muscular dystrophy.</p>

<p>Please enquire for more information about (1S,4S)-2-Oxa-5-azabicyclo[2.2.1]heptane hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Chloro-2-formylpyridine is a peroxide that reacts with pyridine rings to form epoxides. It has been shown to be a potent oxidant and is used in the synthesis of epoxides. 5-Chloro-2-formylpyridine can also react with imidazoles and form tetradentate ligands, which are compounds that bind to metals. This chemical has selectivity for carboxylic acid groups, hydrogen peroxide, alkene, and piperazine. Irradiation of 5-chloro-2-formylpyridine yields an epoxide group on the pyridine ring.</p>

<p>Please enquire for more information about 1-(Chloroacetyl)-2-(trifluoroacetyl)hydrazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5'-Bromo-2'-hydroxypropiophenone is a synthetic compound that inhibits the dimerization of survivin, which is a protein involved in cancer pathways. This compound has been shown to inhibit the growth of cells in culture and can be used as an inhibitor for assays. 5'-Bromo-2'-hydroxypropiophenone has also been shown to integrate into DNA, which may lead to chromosomal rearrangements and mutations. It also binds with high affinity to the family of modifications borealin, which are implicated in cellular processes such as cell differentiation and proliferation.</p>

<p>Chloramine T trihydrate is a water-soluble and biodegradable chemical that is used in wastewater treatment. It reacts with chloramines to produce chloramine, which has a higher disinfectant potential than chlorine. Chloramine T trihydrate also has antimicrobial properties and can be used to control microbial growth in biological samples. In addition, it can inhibit the activity of certain enzymes, such as aziridination, which is involved in the production of nitrosamines and nitric oxide. The matrix effect for chloramine-t may be different from other antimicrobial agents because it does not have a high affinity for proteins. It was found that benzalkonium chloride had an inhibitory effect on chloramine-t activity.<br>MECHANISM OF ACTION: Chloramine T trihydrate is an oxidizing agent that reacts with organic matter to form chloramines and other oxidized products. When these reactions occur in the presence of water or organic material,</p>

<p>2-Chloro-5-iodopyridine is a synthetic compound that binds to nicotinic acetylcholine receptors, and is an agonist of these receptors. It has been shown to bind selectively to the alpha4beta2 subtype of these receptors. 2-Chloro-5-iodopyridine binds to the receptor by means of hydrogen bonding and chelation, which results in the activation of the receptor. This process leads to increased levels of catecholamines and other neurotransmitters, which causes changes in the heart rate and blood pressure. 2-Chloro-5-iodopyridine is a halogenated organic molecule that can be synthesized from sodium trifluoroacetate in two steps: first with chlorination followed by iodination. The synthesis can be carried out using copper (II) chloride as a catalyst or copper (I) iodide as an oxidant, followed by reduction with sodium borohydride.</p>

<p>4-Chlorobenzophenone is an aryl halide with a molecular weight of 198.4 g/mol, nitrogen atoms, and glycol ester. It has the chemical formula C6H5ClO2 and a melting point of -25°C. 4-Chlorobenzophenone is also known as p-chlorophenyl methyl ketone. This compound is used in particle synthesis, which occurs by reacting sodium carbonate with hydrochloric acid to form particles. Sodium citrate can be added to the reaction mixture to increase the yield of particles. The particle size is determined by the time of reaction and concentration of reactants. In addition, 4-chlorobenzophenone reacts with sodium carbonate in water to form allyl carbonate, which can be used for synthesizing styrene derivatives.</p>

<p>4(5)-Iodoimidazole is a chemical compound that is used in the synthesis of other compounds. It can be synthesized by cross-coupling reactions with 4-iodoaniline and 4-bromoimidazole. The reaction yields are high, and this method has been shown to be an efficient method for the synthesis of 4(5)-iodoimidazole. This compound has antibacterial activity against bacterial strains such as Escherichia coli and methicillin-resistant Staphylococcus aureus.</p>

<p>Please enquire for more information about H-Val-AMC trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Leu-Arg-Leu-OH is a synthetic, basic tripeptide with the sequence H-Leu-Arg-Leu. It has been shown to have physiological properties in an electrophoresis experiment, as well as being synthesized in a laboratory.</p>

<p>Please enquire for more information about Adrenomedullin (porcine) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Fluoro-6-methoxybenzonitrile (2FMN) is a compound that is used as a starting material for the synthesis of other pharmaceuticals. It has been shown to bind to the acetylcholine receptor by using vibrational spectroscopy and functional theory. It also has been shown to be an effective chemokine inhibitor. Computational methods were used to optimize 2FMN's binding affinity for the acetylcholine receptor, and it was found that 2FMN binds with a dipole orientation in order to increase its binding affinity.</p>

<p>Please enquire for more information about 2,3,6-Trifluorophenylacetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Intermediate in the synthesis of dapagliflozin</p>

<p>Please enquire for more information about H-Pro-2-chlorotrityl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>