Amines

<p>Applications O-(Tetrahydro-2H-pyran-2-yl)hydroxylamine can be used to treat fibrotic and inflammatory diseases.<br>References Gomer, R.H., et.al., PCT Int. Appl., 167, (2020);<br></p>

<p>Applications (Z)-2-(2-Aminothiazol-4-yl)-2-(hydroxyimino)acetic Acid can be used to synthesize cephalosporin derivatives and β-lactam antibiotics.<br>References Lee, H., et al.: Synth. Comm. 28, 1339 (1998); Bucourt, R., et al.: Tetrahedron 34, 2233 (1978); Borowwicz, P., et al.: PL 154681 B1 19910930 (1992); Hecker, S., et al.: US 5756493 A 19980526 (1998)<br></p>

<p>Applications 4-​(Dimethyloxidoamino)​butanoic Acid Hydrochloride, is a metabolite of Lauramine Oxide (L178530), which is a frequently used amine oxide surfactant. It is strongly hydrophilic , and it forms normal micelles and normal liquid crystalline phases.<br>References Kocherbitov, v., et al.: J. Molec. Struct.: Theochem., 808, 111 (2007); Kocherbitov, v., et al.: J. Phys. Chem. B., 110 (27), 13649 (2006); Turan, T.S., et al.: Xenobiotica, 11, 447 (1981)<br></p>

<p>Applications Cyclopent-3-enamine hydrochloride (cas# 91469-55-5) is a useful research chemical.<br></p>

<p>Applications It can be used in the preparation of sanitizer for use in factories.<br>References Yuan, H., et al.: Sanitizer used in factory and preparation method thereof, CN 106038470 (2016)<br></p>

<p>Applications 1,2,4-Triazin-3-amine can be used as integrade inhibiting antiviral agents.<br>References Kiyama, R., et.al.: PCT Int. Appl.WO 2003016275 A1, 663, (2003);<br></p>

<p>Applications Ethylammonium Thiocyanate is used in the study of protic ionic liquid nanostructure.<br>References Hayes, R., et al.: Angewandte Chemie, International Edition, 52, 4623 (2013); Murphy, T., et al.: J. Phys. Chem., 118, 12017 (2014)<br></p>

<p>Applications 7-Azaindole derivative<br>References Showell, G., et al.: Bioorg. Med. Chem., 6, 1 (1998), Huang, Y., et al.: Bioorg. Med. Chem. Lett., 11, 1375 (2001),<br></p>

<p>Applications (±)-trans-1,2-Diaminocyclohexane is a reagent used in the thyroid receptor agonists for treatment of androgenetic alopecia.<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 Li, J. J., et al.: Bioorg. Med. Chem. Lett., 20, 306 (2010)<br></p>

<p>Applications Used in the synthesis of novel phosphorothioates and phosphorodithioates as cholinesterase inhibitor.<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 Millard, C., et al.: J. Neurochem., 64, 1909 (1995), Nicolet, Y., et al.: J. Biol. Chem., 278, 41141 (2003), Casida, J., et al.: Chem. Res. Toxicol., 17, 983 (2004),<br></p>

<p>Stability Hygroscopic<br>Applications N-Benzyl-bis(2-chloroethyl)amine hydrochloride (cas# 10429-82-0) is a useful research chemical.<br></p>

<p>Applications 4-Azidobutylamine is weakly or non-mutagenic to Salmonella typhimurium.<br>References Owais, W.M., et. al.: Mutat. Res. Genetic Toxicol. Testing, 118, 229 (1983)<br></p>

<p>Stability Hygroscopic<br>Applications [3-(3,4-dimethoxyphenyl)propyl](methyl)amine hydrochloride (cas# 83979-31-1) is a useful research chemical.<br></p>

<p>Applications N-[3-(4-Aminophenyl)propyl]-N,N-dimethylamine<br></p>

<p>Applications 2-[6-(Acetylphenylamino)-1,3,5-hexatrienyl]-1,1-dimethyl-3-sulfobutyl-1H=-benz[e]indolium Inner Salt is a reactant used in the preparation of indocyanine green as an infrared probe.<br>References Suganami, A. et al.: Bioorg. Med. Chem. Lett., 22, 7481 (2012); Doi, T. et al.: Synlett., 23, 306 (2012);<br></p>

<p>Stability Store in freezer at -20°C<br>Applications A synthetic intermediate<br></p>

<p>Applications Methyl 2-Aminothiazole-5-carboxylate (cas# 6633-61-0) is a compound useful in organic synthesis.<br></p>

<p>Applications Di(3,5,5-trimethylhexyl)amine Hydrochloride is used in the preparation of N-nitrosoamines series.<br>References Wang, J., et al.: Huaxue Shiji, 31, 658 (2009)<br></p>

<p>Applications (1S,3R,4S)-Ethyl 4-Amino-3-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate Oxalate has been used as a reactant for the preparation of oxadiazole compounds containing cyclohexanediamine moiety.<br></p>

<p>Applications N-aminomorpholine-4-carbothioamide (cas# 6499-15-6) is a useful research chemical.<br></p>

<p>Applications Used for induction of nitrilase activity in Arthrobacter. Used as radioprotective agent.<br>References Houseman, A., et al.: Biochem. 32, 4430 (1993),<br></p>

<p>Applications Extremely hindered tertiary amine.<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 Burdick, J., et al.: Biomaterials, 22, 1779 (2001), Liu, V., et al.: Biomed. Microdev., 4, 257 (2002),<br></p>

<p>Stability Volatile<br>Applications 2-Furfurylamine is used in the synthesis of 2-Amino-N-(2-furylmethyl)propanamide, as a novel alanylglycine equivalent synthesized by bacilysin synthetase.<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 Mah, R., et al.: Appl. Microbiol., 15, 866 (1967), Faber, K., et al.: Pure Appl. Chem., 69, 1613 (1997), Marahiel, M., et al.: Chem. Biol. 4, 561 (1997),<br></p>

<p>Applications Methyl 5-Chloro-2-[(4-ethoxy-4-oxobutyl)amino]benzoate is a reactant in the synthesis of 7-chloro-5-oxo-2,3,4,5-tetrahydro-1H-1-benzoazepin, an intermediate in synthesis of Tolvaptan (T536650).<br>References Liu, Dengke, et al.: Tianjin Institute of Pharmaceutical Research, CN 103012265 A 20130403(2013);<br></p>

<p>Applications A polyethyleneglycol (PEG) derivative used in the preparation of single cell optical biosensors.<br>References Kilian, K. et al.: Nano Lett., 9, 2021 (2009); Kilian, K. et al.: Proc. SPIE, 7397, 739703 (2009);<br></p>

<p>Stability Air Sensitive<br>Applications Can be used as a building block for chiral ligands.<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 Amino(3-​chlorophenyl)​acetic Acid functions as intermediate useful in the preparation of synthetic penicillins, also used in the structure-activity relationship examination of several drugs containing the benzyl moiety, their roles in biochemical and pharmacological processes.<br>References Hansch, C., et al.: J. Med. Chem., 13, 957 (1970); Holdrege, C. T., et al.: Can. (1975), CA 966853 A2 19750429;<br></p>

<p>Applications 2-Aminomethyl-1,4-benzodioxane is used in the synthesis of N-substituted (dihydrobenzodioxinyl)methylamine derivatives as D2 antagonists/5-HT1A partial agonists with potential as atypical antipsychotic agents in relation to affinity for α1 adrenoceptors.<br>References Birch, A. M., et al.: J. Med. Chem., 42, 3342 (1999);<br></p>

<p>Applications TERT-BUTYL N-(DIAMINOMETHYLIDENE)CARBAMATE (cas# 219511-71-4) is a useful research chemical.<br></p>

<p>Applications [4-(Trimethylammonium)benzyl] Alcohol Bromide is a compound useful in organic synthesis.<br></p>

<p>Stability Volatile<br>Applications rac 1,2-Diaminopropane is used as model precursor in the electron induced deposition of amorphous carbon nitride films. It is also used to synthesize cage peroxide, 1,6-diaza-3,4,8,9-tetraoxa-11-methylbicyclo[4.4.2]dodecane.<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 Wnuk, J., et al.: J. Phys. Chem., 113, 12345 (2009); Edward, J., et al.: Can. J. Chem., 77, 1057 (1999)<br></p>

<p>Please enquire for more information about (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-3-bromoisoquinoline is an isocyanide that reacts with nucleophilic heteroatoms such as the amino group. It also reacts with bromine to form a bromopyridine. The nitrile group of 4-amino-3-bromoisoquinoline can be reduced with sodium borohydride to produce 4-aminoquinoline. This compound has shown potential for use in chemotherapy and treating bacterial infections.</p>

<p>Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid is a synthetic amino acid that has been shown in vitro to inhibit the growth of prostate cancer cells. It is an analog of butyric acid, a naturally occurring fatty acid. Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid has been synthesized by solid phase methods and labeled with radiotracers such as indium 111 or technetium 99m. The use of Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid in vivo is limited by its short circulating half life, rapid metabolism, and high toxicity.</p>

<p>Hydroxylamine HCl is a chemical compound that has been shown to exhibit anti-inflammatory properties. It is a nitrosobenzene derivative with the molecular formula NH2OH, and it is also known as hydroxylamine salt or hydroxylamine sulfate. Hydroxylamine HCl has been used in pharmaceutical preparations for the treatment of inflammatory bowel diseases such as ulcerative colitis and Crohn's disease. This drug inhibits the production of inflammatory cytokines by binding to the receptor sites on cells in the body. Hydroxylamine HCl binds to the herpes simplex virus (HSV) and inhibits viral replication, which may be due to its ability to inhibit protein synthesis at an early stage of HSV infection. This drug also binds to CD-1 mouse liver cells and blocks cellular respiration, leading to cell death.</p>

<p>2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine is a versatile chemical substance that has various applications in different industries. It can be used as a dianhydride to create high-performance polymers or as an electrode material for batteries and fuel cells. This compound is also used in the production of lacosamide, a medication used to treat epilepsy. In addition to its industrial uses, 2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine is also utilized in research laboratories as a reagent or marker. It is commonly used in aerosol compositions for testing purposes and in the analysis of toxicological samples. Researchers also rely on this compound for dispersive solid-phase extraction techniques and for studying photodegradation processes. Furthermore, 2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine has shown potential in the development of polymeric compositions with</p>

<p>(1R,2R)-Boc-aminocyclopentane carboxylic acid (BCPC) is a high quality, reagent, and useful intermediate. It is a versatile building block that can be used as a speciality chemical or research chemical. BCPC has been shown to react with amines to form ureas, with nitriles to form oxazolidines, and with epoxides to form aziridinones.</p>

<p>Please enquire for more information about 2-(Benzylmethylamino)-3',4'-dihydroxyacetophenone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Amino-5-methoxybenzoic acid is a macrocyclist, which means that it can switch between two different forms. When the temperature is below 27 degrees Celsius, it exists as a mesomorphic phase and when the temperature increases above 27 degrees Celsius, it exists as an isotropic phase. 3-Amino-5-methoxybenzoic acid also has homologues that are also mesomorphic or isotropic depending on their temperatures. The chemoenzymatic parameters of the two phases are different and so are their lamellar morphologies. The fluorine atom in 3-amino-5-methoxybenzoic acid makes it act like a Lewis acid, decreasing its melting point and increasing its vapor pressure. There are two isomers of 3-amino-5-methoxybenzoic acid: dodecyl and octadecyl 3--amino--5--methoxyben</p>

<p>3-Aminopropyltrimethoxysilane is a chemical that belongs to the group of aminopropyltriethoxysilanes. It is a reactive substance and is commonly used as an additive in adhesives and sealants. 3-Aminopropyltrimethoxysilane has been shown to be an efficient coupling agent for the formation of hydroxyl groups on nanoparticles, which are then used as drug carriers. The optimum concentration of 3-aminopropyltrimethoxysilane lies between 0.01 and 0.1 M, with a pH range of 6 and 8. This chemical can react with hydrochloric acid, resulting in the production of hydrogen gas; with cervical cancer cells in culture, leading to cell death; or with skin cells, causing damage to their transport properties.</p>

<p>Please enquire for more information about Benzyl N-(2-aminoethyl)carbamate hydrochloride 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-(Trifluoroacetamido)Ethylamine Hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid is a synthetic amide that is used as an intermediate in the synthesis of peptides. It has a conformational structure and can be labeled with dyes to study the structures of proteins or peptides. Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid has been used as an immunogen in the preparation of monoclonal antibodies. It also can be conjugated to drugs or other compounds for use as bioconjugates. This compound has been shown to have enzymatic activity and can be used as a substrate for enzyme linked immunosorbent assays (ELISA). Trifluoroacetic acid is commonly used in the synthesis of this compound.</p>

<p>Dihydroergotamine mesylate is a medication that is used in the treatment of migraines. It belongs to the group of drugs called ergot alkaloids and has been shown to have high values in cerebral metabolism. Dihydroergotamine mesylate has also been shown to have an effect on dopamine levels in human serum, which may be due to its ability to inhibit neuronal death. Dihydroergotamine mesylate is administered intravenously, orally or intramuscularly for the treatment of acute migraine attacks. The drug can also be given rectally for the prevention of chronic migraine episodes. This drug may cause side effects such as nausea, vomiting and dizziness.</p>

<p>Pyridin-4-ylmethanamine is a chemical compound that contains a pyridine ring and an amine (-NH2) group. It is usually used as a building block for the synthesis of other compounds. Pyridin-4-ylmethanamine can be synthesized from picolinic acid, which is obtained through a reaction with sodium hydrochloride in an alkaline solution. This reaction proceeds via two steps: first, the formation of a pyridinecarboxylic acid ester and then the addition of ammonia to form pyridin-4-ylmethanamine. The transfer reactions that occur during this process are highly dependent on temperature and pH. The frequency shift effect can be observed when pyridin-4-ylmethanamine interacts with amines, which changes its absorption spectrum.</p>

<p>Please enquire for more information about 5-Bromo-N1-methylbenzene-1,2-diamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(2-Methoxyphenoxy)ethylamine base is an inorganic base with a hydroxyl group. It is soluble in organic solvents and has been used as a coumarin derivative. 2-(2-Methoxyphenoxy)ethylamine base has shown potential use as an antifungal agent, which may be due to its ability to cause lysis in fungi cells. This compound has also shown in vitro activity against bacteria and viruses, including herpes simplex virus type 1 and HIV-1. The 2-(2-methoxyphenoxy)ethylamine base can be sulfonated or acid catalyzed to produce other derivatives that have potential use as anti-inflammatory or analgesic agents.</p>

<p>4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is a chemical compound that inhibits the growth of cancer cells by binding to the active site of b-raf and blocking its activity. It has been shown in a pharmacokinetics study that 4-(4-aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is absorbed rapidly through the oral administration, excreted in urine, and eliminated rapidly from the body. The optimal reaction for this drug was found to be at pH 7.0 with an ionic strength of 0.1 M (sodium chloride). This drug also has significant inhibitory activities against human cervical carcinoma and breast cancer cell lines (MDA-MB-231).</p>

<p>Please enquire for more information about [(6-Chloro-1-isopropyl-1H-benzimidazol-2-yl)methyl]amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2-Diaminocyclohexane is a chiral compound with a cyclohexane ring. It is reactive and has been shown to be carcinogenic. It is used in the preparation of other compounds, such as amino acid derivatives and dyes. 1,2-Diaminocyclohexane can also be used as an intermediate for the synthesis of various drugs. This compound has been shown to inhibit transcriptional regulation and to have biochemical properties that are related to cancer. 1,2-Diaminocyclohexane reacts with copper to form a coordination geometry complex with six nitrogen atoms. The reaction mechanism involves the formation of a copper complex that bears an electron-deficient carbon atom in its structure.</p>

<p>Please enquire for more information about Demethyl benzydamine hydrochloride 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 [1-Methyl-2-(7-methyl-1H-indol-3-yl)ethyl]amine hydrochloride 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-(5-Fluoro-1-methyl-1H-indol-3-yl)ethyl]amine hydrochloride 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 8-[(2-Hydroxyethyl)(methyl)amino]-1,3,9-trimethyl-3,9-dihydro-1H-purine-2,6-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Dimethylamino)ethanol is a colorless liquid that has a molecular weight of 78.1 g/mol and a boiling point of 176.1 °C. It can be found in many household products as well as cosmetics, pharmaceuticals, and chemical manufacturing. 2-(Dimethylamino)ethanol is a precursor to acetaldehyde and acetic acid, which are important intermediates in the production of polymers such as nylon. It can also be used to synthesize other chemicals such as dimethylformamide, ethylene glycol, and methyl methacrylate. This chemical reacts with calcium to form insoluble calcium 2-(dimethylamino)ethanolate (Ca(DMAE)). This reaction is reversible and the equilibrium can be shifted by changing the pH or adding another reactant such as hydrogen peroxide or hydroxide ions.</p>

<p>Please enquire for more information about 4-Benzyloxy-3-methoxy-N-methylphenethylamine hydrochloride 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-{2-[2-(2-Aminoethyl)-4,5-dimethoxybenzyl]-4,5-dimethoxyphenyl}ethyl)amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Diethylamino)ethyl acrylate is a reactive, film-forming polymer that can be used as a cross-linking agent or additive to coat surfaces and films. It is used in the production of cellulose films and as a protective coating for paper and textile fabrics. 2-(Diethylamino)ethyl acrylate is also used in the manufacture of reactive functional groups by reacting with hydrochloric acid to form diethyl chloroacetate. This chemical is used to make particle films for cell culture. The optimum concentration for 2-(diethylamino)ethyl acrylate is between 0.1% and 1%.</p>

<p>2-(2-Aminoethoxy)ethanol (2-AE) is a natural compound that has been synthesized from ethanol and 2-aminoethanol. It has been shown to react with sodium carbonate to form stable complexes that are resistant to hydrolysis by amines. The stability of the complex is attributed to the formation of an intermolecular hydrogen bond between the hydroxyl group on the 2-AE molecule and the carboxylate group on the sodium carbonate molecule. 2-AE reacts with benzalkonium chloride, a quaternary ammonium salt, in water vapor to produce an alcohol and a fatty acid, which is then hydrolyzed by glycol ethers into glycolates. This mechanism is similar to that of other reactions involving quaternary ammonium salts, such as those in fatty acids or glycol ethers.</p>

<p>Ammonium carbonate is an inorganic salt that consists of ammonium ion and carbonate ion. It is a white crystalline solid with a molecular weight of about 166.4 g/mol. Ammonium carbonate is soluble in water, alcohol, acetone, and other organic solvents. It has been used as a buffer solution for pH adjustment and as a source of ammonium ions in analytical chemistry. Ammonium carbonate can be formed by the reaction of sodium carbonate with ammonia gas or liquid ammonia, or the reaction of sodium bicarbonate with ammonia gas or liquid ammonia. The thermal expansion coefficient of ammonium carbonate is higher than those of sodium salts such as sodium chloride and potassium chloride. Electrochemical impedance spectroscopy (EIS) measurements have shown that the reactivity between ammonium carbonate and plasma mass spectrometry is high due to its high values on the electric spectrum graph at low frequencies (1 kHz).</p>

<p>Didecyl dimethyl ammonium chloride is a quaternary ammonium compound that has been shown to have a broad-spectrum antimicrobial activity. It has been used in disinfectants and as an active ingredient in pharmaceuticals, cosmetics, and foods. The compound is not toxic to humans or animals at concentrations up to 50%. Didecyl dimethyl ammonium chloride has been shown to be effective against infectious diseases caused by bacteria, viruses, fungi, and protozoa. This compound also has an effect on the epithelial-mesenchymal transition (EMT) process. Didecyl dimethyl ammonium chloride can be prepared by titration calorimetry or analytical method. The preparation of didecyl dimethyl ammonium chloride can be done using chloroform and benzalkonium chloride or glycol ether.</p>

<p>2-Chloro-3,4-dimethoxyphenethylamine is an intermediate in the synthesis of zepines. It can be synthesized by reduction of borohydride with 2-chloro-1,2,3,4-tetrahydrobenzaldehyde.</p>

<p>Please enquire for more information about N-(2-Aminoethyl)-4-(1,1-dimethylethyl)-2,6-dimethylbenzeneacetamide 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 1-(4-Chlorophenyl)cyclopropylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methoxybenzylamine is an organic amine that has a redox potential of -0.14 V (vs. SHE) and a pK a of 10.5. It is used in the synthesis of trifluoroacetic acid esters, which are used as pharmaceutical intermediates. 4-Methoxybenzylamine has been shown to be effective in alleviating pain in animal models, and its mechanism of action may be due to inhibition of the enzyme cyclooxygenase. The kinetic data for this reaction were obtained by studying the deuterium isotope effect, which is characterized by a low energy barrier and rapid reaction rate. The hydrolysis step is also important for the reaction mechanism, with protocatechuic acid being an intermediate product. Hydrochloric acid is needed for dehydration of the reactants, while an aryl halide can be used instead in some cases. In these reactions, there are many possible reaction</p>

<p>Please enquire for more information about 2-Methoxy-4-amino-5-ethylthiobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Amino-2,4-imidazolidinedione-13C3 is an antibiotic that belongs to the group of nitrofurans. It is used for the treatment of infections caused by bacteria that are resistant to other antibiotics. The LC-MS/MS analysis showed that 1-aminohydantoin was formed as a degradation product of chloramphenicol and that this metabolite had been detected in urine samples from patients treated with chloramphenicol. Nitrofuran is also a possible degradation product. A reaction monitoring experiment using ionization monitoring and monitoring on the precursor ion at m/z 287 confirmed the presence of 1-aminohydantoin in a sample containing both chloramphenicol and nitrofuran. Quantification was performed using calibration curves obtained from pure standards.</p>

<p>Dioleoyloxypropyl-N,N,N-trimethylammonium methylsulfate (DOTAP) is an antibacterial agent that disrupts the bacterial membrane. It has been shown to inhibit the uptake of chlamydia by inhibiting the binding of chlamydia to cells and enhancing the detection of chlamydia in cells. DOTAP also has pharmacological properties that are related to its ability to interfere with cellular membranes. DOTAP can be used as a strategy for developing antibacterial agents because it inhibits bacterial growth by disrupting their cellular membranes. This results in a decrease in phosphatidylethanolamine levels, leading to increased cell death.</p>