Amino Acids (AA)

<p>N-Methyl-N-phenylazetidin-3-amine hydrochloride is a white solid with a melting point of 175°C. It is soluble in water, ethanol, and ether. N-Methyl-N-phenylazetidin-3-amine hydrochloride is an intermediate for the synthesis of chemical compounds that are used in research and development. This compound can be used as a building block to create complex compounds with biological activity. It can also be used as a scaffold to create novel chemical compounds that have not been observed before. The quality of this chemical is high, making it suitable for research purposes.</p>

<p>Ethyl 2-hydroxy-5-methoxybenzoate (EHMB) is a phenolic compound that belongs to the group of salicylic acid. It is a natural product present in crucifers such as cabbage, broccoli, and cauliflower. EHMB has been shown to induce apoptosis in human leukemia cells through the inhibition of DNA methylation. The results showed that EHMB induces apoptosis in human leukemia cells by targeting the epigenetic regulator protein MLL1, which inhibits DNA methyltransferase 1 activity and leads to decreased levels of 5mC. EHMB also induces apoptosis in lung cancer cells by inhibiting cell proliferation and inducing cell death through the inhibition of GTPase activity, which leads to decreased levels of cyclin D1 and increased levels of p27. EHMB also regulates stem cell function by modulating gene expression; it has been shown that this compound can promote stem cell-like properties in mouse embryonic fibrobl</p>

<p>3-Phenoxybenzaldehyde is a chemical compound that is used as an analytical reagent in the surface methodology. It can be synthesized from 3-phenoxybenzoic acid and phenylmagnesium bromide. The synthesis of 3-phenoxybenzaldehyde was accomplished by the hydrogenation of p-nitrophenyl phosphate, which was catalyzed by rat liver microsomes. The resulting product had a molecular formula of C9H8O2 and a molar mass of 156.2 g/mol. 3-Phenoxybenzaldehyde has been shown to inhibit bacterial growth through the inhibition of fatty acid synthesis, as well as inhibiting fatty acid oxidation in recombinant cytochrome P450 enzymes.</p>

2-Iodo-6-methylbenzoic acid is a chemical used as an additive in the manufacture of plastics, paints and rubber. It is also a ligand for some transition metals. 2-Iodo-6-methylbenzoic acid has been found to be an active natural product that can be synthesized from phthalimides or other amines. 2-Iodo-6-methylbenzoic acid reacts with donepezil to form a multistep reaction intermediate called A, which is then oxidized by a transition metal to form the final product, aricept. The operational mechanism of this reaction is not yet fully understood, but it may involve an alkene intermediate.

<p>5-Bromo-2-methoxyphenyl)acetonitrile is a chemical building block that can be used in the synthesis of complex compounds. It is a versatile intermediate that can be used as a reagent in organic reactions. This compound has been shown to be useful as a reaction component and is a high quality product. 5-Bromo-2-methoxyphenyl)acetonitrile has CAS number 7062-40-0 and is listed on the Chemical Abstracts Service (CAS).</p>

<p>N-Methyl mesoporphyrin IX is a molecule that inhibits the activity of enzymes such as carboxylesterases, proteases, and aminopeptidases. It binds to the active site of these enzymes and blocks the enzyme's activity. N-Methyl mesoporphyrin IX has been shown to inhibit cancer cells in humans and can be used as an adjunct treatment for cancer. This drug also has anti-inflammatory properties due to its ability to inhibit prostaglandins synthesis. N-Methyl mesoporphyrin IX has been shown to have an effect on plant physiology by inhibiting plant growth and photosynthesis. N-Methyl mesoporphyrin IX is also able to enhance hybridization reactions between dsDNA duplexes, which may be useful in research involving DNA sequencing or gene mapping.</p>

<p>4-Methoxybenzoin is a phenolic compound that belongs to the carbinols. It is an aromatic hydrocarbon that can be synthesized by heating benzaldehyde with methanol and sodium carbonate in ethanol. 4-Methoxybenzoin is used as a chemical intermediate for the synthesis of other chemicals, such as quinidine, anisole, thiosemicarbazide and hydrochloric acid. 4-Methoxybenzoin has been shown to react with cellulose acetate to form an acidic photodegradation product. This reaction can be suppressed by adding sulfuric acid or sodium sulfite.</p>

<p>Alpha-methylene-gamma-butyrolactone (AMGBL) is a naturally occurring sesquiterpene lactone. It has been shown to have anticancer effects on solid tumours, such as those of the liver and lung. AMGBL is also used in the treatment of tuliposide-induced skin lesions. The biological activity of AMGBL is due to its ability to inhibit matrix metalloproteinase (MMP)-1 and -2 and to enhance the production of epidermal growth factor receptor (EGFR). AMGBL also binds to DNA at the hydroxyl group and can be used as an anti-aging agent.</p>

<p>2-(2-Butyl)-4-{4-[4-(4-methyloxy-phenyl)-piperazin-1-yl]-phenyl}-2,4-dihydro-[1,2,4]-triazol-3-one (ITZ) is an antifungal drug that inhibits the synthesis of ergosterol. It is used in the treatment of systemic fungal infections such as candidiasis and cryptococcosis. ITZ is a metabolite of itraconazole and fluconazole. The presence of impurities in ITZ can be detected by liquid chromatography with a diode array detector or a fluorescence detector. An antiinfective drug product should be bioequivalent to the reference product and have comparable levels of impurities. Chromatograms are used to identify peaks on a graph and measure their height (area under the curve) to determine how much of each substance is present in the sample.</p>

<p>Macrophage-activating lipopetide-2 (MALP-2) is a TLR2 agonist and activator of  MyD88-dependent signaling pathways. It has potential as a vaccine adjuvant.</p>

<p>Fmoc-Cys(Dpm)-OH is a chemical that belongs to the group of reaction components. It is a high quality reagent for research and development and can be used as a building block in the synthesis of other fine chemicals. Fmoc-Cys(Dpm)-OH is also an intermediate for the synthesis of complex compounds such as peptides, proteins, and antibiotics. This compound has a broad range of applications in biomedicine, organic chemistry, and pharmaceuticals.</p>

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<p>Nalpha,Nalpha-Bis-(carboxymethyl)-L-lysine is a synthetic amino acid that has been used to immobilize proteins and enzymes. It can be used as an inhibitor in cell culture because it binds to the ryanodine receptor, which regulates calcium release from the sarcoplasmic reticulum. This amino acid has also been shown to inhibit kinesin, a protein involved in the movement of organelles along microtubules. In addition, Nalpha,Nalpha-Bis-(carboxymethyl)-L-lysine has been found to be effective against colony-stimulating factor (CSF) and may serve as a model system for enzymatic reactions.</p>

<p>4-Methoxy 17β-estradiol is a synthetic estrogen that is used as a pharmaceutical drug in the treatment of menopausal symptoms and to prevent osteoporosis. It can be taken orally or administered by injection. 4-Methoxy 17β-estradiol has been found to have interactive effects with other drugs, such as fatty acids and catechol-o-methyltransferase (COMT). It also has an effect on body mass index in vivo, which can lead to cancerous cell proliferation. The matrix effect of 4-methoxy 17β-estradiol on tissues depends on the hydrogen bonds it forms with amino acids in the protein matrix. The hydrogen bonds are different for each tissue type and this may contribute to the differences in carcinogenic potential between tissues. This drug is not active against MCF-7 human breast cancer cells, but does inhibit growth of MDA MB 231 human breast cancer cells.</p>

<p>24-Epibrassinolide is a synthetic molecule that has an optical rotation of +19.4° at 20°C. It is also known as H-Leu-Glu-OH and is a product of the reaction between epibatidine and L-glutamic acid. This molecule has been synthesized to study the role of 24-epibrassinolide in photosynthesis, chlorophyll synthesis, and membrane stability. The phosphate group is attached to the amino group on the n-terminal amino acid. 24-Epibrassinolide has an amino acid composition consisting of leucine, glutamate, glutamine, glycine, proline, serine, cysteine, tyrosine, asparagine, histidine and lysine.<br>24-Epibrassinolide was first isolated from chloroplasts using refluxing water with ammonium chloride as a solvent. This molecule can be found in nature as well.</p>

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<p>1,10-Phenanthroline monohydrate is a metal chelate that binds to DNA by hydrogen bonds. It has been shown to have an intramolecular hydrogen and a linear calibration curve with a coefficient of determination (r2) of 0.998. The rate constant for the reaction of 1,10-phenanthroline monohydrate with DNA is 5.00 x 10 M-1 s-1 at 25°C in water and pH 7.4 buffer. The coordination geometry for 1,10-phenanthroline monohydrate is octahedral with the axial ligands occupying the equatorial positions and the equatorial ligands occupying the axial positions. This compound has been shown to be active against HL-60 cells, which causes cancerous transformations in vitro. Fluorescence spectrometry data shows that 1,10-phenanthroline monohydrate can bind to DNA in vitro but not in vivo.</p>

<p>5-Methylcytosine is a nucleic acid that is found in the DNA and RNA of the cell. It is an important component of methylation, which is the process by which a methyl group is added to a molecule. This process can lead to cellular transformation, a process that can cause cancer. 5-Methylcytosine has also been shown as a molecular pathogenesis factor in infectious diseases such as HIV and herpes simplex virus type 1. The presence of 5-methylcytosine in nuclear DNA has been detected by analytical techniques such as gas chromatography/mass spectrometry (GC/MS). There are many analytical methods, including GC/MS, that can be used to detect 5-methylcytosine in cellular nuclei.</p>

<p>Suc-Ala-Ala-Ala-AMC is a fluorogenic substrate that can be used to measure the activity of serine proteases. Suc-Ala-Ala-Ala-AMC has been shown to have high values in mammalian tissue. It also has high activity against many bacteria and fungi, as well as proteolytic enzymes such as collagenase and matrix metalloproteinase. This substrate is activated by phorbol esters and has an optimum pH of 5.5. Suc-Ala-Ala-Ala AMC is a model protein for determining the antibacterial efficacy of various antibiotics.</p>

<p>2-fluoro-5-methoxybenzaldehyde is an asymmetric synthesis that has been shown to inhibit the growth of cancer cells by inhibiting a protein called MT2. 2-Fluoro-5-methoxybenzaldehyde is a nucleophilic compound and reacts with the electrophilic carbon in the enolate to form a sulfoxide, which can be hydrolyzed by acid. This reaction inhibits cancer cell growth as it prevents cellular metabolism and amino acid biosynthesis.</p>

<p>N6-Carbobenzoxy-L-lysine N-carboxyanhydride is a protected form of amino acid L-lysine, where the side chain amine is Z-protected and the α-amine and carboxylic acid groups are linked via a carboxyl. N6-Carbobenzoxy-L-lysine N-carboxyanhydride can undergo a basic polycondensation reaction to afford polylysine, a polymer of α-linked lysine. Polylysine has a range of biological activities, such as, the inhibition of fungal infections (Trichophyton mentagrophytes, T. rubrum, and Candida albicans) in plants. Polylysine is used to coat tissue culture ware, where it enhances cell adherence.</p>

<p>5-Bromo-2-methoxytoluene is a bromoarene that reacts to form aziridines and phosphotungstic acid. It is used in the synthesis of polyaromatic compounds with steric interactions. 5-Bromo-2-methoxytoluene is also a functional group that can be used as an allosteric modulator. This compound also has stereoisomers that are chiral, meaning they have different structures despite being mirror images of each other. The carbonyl group on the 5-bromo compound is polar, which means it has a charge. The hydrogen bonds between this compound and other molecules are nonpolar, which means they do not have a charge and are more likely to form in a nonpolar solvent.</p>

<p>Perfluoro-2-methylbutane is a pharmaceutical dosage form of a perfluorinated liquid. It is used in clinical practice for the treatment of chronic obstructive pulmonary disease (COPD), asthma, or other respiratory disorders. This drug is also used as an inhalation agent in the treatment of adults with acute bronchitis, emphysema, or other airway obstruction. Perfluoro-2-methylbutane has shown resistance to bacteria that are resistant to natural and synthetic polymers. The diameter of Perfluoro-2-methylbutane particles is between 2 and 10 micrometers and it has a viscosity of about 5 centipoise. It has been shown that the reaction time for this drug can be reduced by adding hexamer, which acts as a surfactant for the gas phase. The active substances in Perfluoro-2-methylbutane are unsaturated ketones such as 3-pentanone, 3-hex</p>

<p>Z-Gly-Pro-AMC is a substrate molecule that mimics the natural substrate of dipeptidyl peptidase IV (DPP-IV) and is used in the study of plant physiology. It has been shown to inhibit DPP-IV activity by binding to the enzyme’s active site, preventing it from cleaving biologically active peptides. This drug also has an antidiabetic effect, which may be due to its ability to inhibit α-amylase activity. Z-Gly-Pro-AMC also has been shown to increase locomotor activity and reduce body weight in rats with metabolic disorders. Z-Gly-Pro-AMC inhibits serine proteases, such as trypsin, chymotrypsin, elastase, and cathepsin G, which are involved in tumor progression.</p>

<p>2-Chloro-5-methoxyaniline hydrochloride is an intercalating agent that is used in the treatment of cancer. It binds to DNA and causes a breakage of the hydrogen bonds between the two strands, which leads to cell death. The 2-Chloro-5-methoxyaniline hydrochloride molecule has affinity for lactams, which are sugar molecules found in cell walls of bacteria, fungi, and plants. This compound can be metabolized by lactamase enzymes that are found in cancer cells and other cells. The metabolized products are fluorescent, which allows them to be detected by fluorescence microscopy. 2-Chloro-5-methoxyaniline hydrochloride has been shown to inhibit the growth of lung cancer cells and leukemia cells by interfering with their ability to synthesize DNA and RNA.</p>

<p>3-Methoxyphenylacetonitrile (3MPAN) is a small molecule that has been shown to inhibit the activity of kinases, which are enzymes that transfer phosphate groups from ATP onto other substrates. 3MPAN has been found to be selective for the estrogen receptor alpha (ERα), with little or no effect on ERβ, and shows promise as a potential drug for hormone-dependent breast cancer. It also inhibits fatty acid synthesis and is active against some viruses. 3MPAN binds to the enzyme's ATP binding site and blocks phosphorylation by preventing access of ATP. This prevents DNA synthesis and protein synthesis, leading to cell death.</p>

<p>The 4-Iodo-2-methylaniline is a synthetic molecule that belongs to the group of amines. It has been shown to bind to human protein and can be used for the synthesis of boronic acids and quinoline derivatives. 4-Iodo-2-methylaniline can be synthesized by reacting hydrochloric acid with sodium periodate, followed by addition of an aryl boronic acid. The reaction time is dependent on the nature of the reactant. The pharmacophore consists of a proton and an aryl boronic acid, which is responsible for binding with human protein.</p>

<p>2-Phenylindole-3-carboxaldehyde is an organic compound that belongs to the class of bioactive molecules. It is a nitrogen heterocycle that has been shown to inhibit the growth of cancer cells in culture. 2-Phenylindole-3-carboxaldehyde has also been shown to have anti-inflammatory and antimicrobial properties. This molecule can be used in the treatment of cancer, as it inhibits the growth of tumor cells by inhibiting DNA synthesis, which leads to cell death. The molecular structure can be altered by allylation or replacement with other functional groups. The 2-phenylindole moiety can be modified at its C2 position, altering its pharmacological properties and may lead to new anticancer drugs.</p>

<p>Methylphenidate is a psychostimulant drug used to treat attention deficit hyperactivity disorder (ADHD) and narcolepsy. It is a prodrug of the active compound, 2-phenyl-2-(2-piperidin)acetic acid (Ritalinic acid), which inhibits the reuptake of dopamine and norepinephrine into the presynaptic neuron. Methylphenidate can be detected by LC-MS/MS in wastewater, providing an analytical method for predicting the presence of this substance in wastewater treatment plants. This drug has minimal toxicity in model organisms and can be metabolized by methylation to form a glucuronide conjugate. Methylphenidate has been shown to increase locomotor activity when administered at low doses, but not at high doses. At high doses, it increases locomotor activity up to 3 hours after administration and decreases locomotor activity 1 hour after administration.</p>

<p>Fmoc-Asn(Trt)-OH is a pegylated molecule synthesized by attaching a polyethylene glycol (PEG) to the terminal amino acids. It has been shown that Fmoc-Asn(Trt)-OH inhibits peptide synthesis by inhibiting the formation of an enzyme-substrate complex. This inhibition prevents the transfer of an amino acid from one protein chain to another, preventing the formation of a new chain and subsequent polymerization. Fmoc-Asn(Trt)-OH also has an inhibitory effect on polypeptide synthesis. The molecular weight of this compound is about 535 Daltons.</p>

<p>Please enquire for more information about Fmoc-O-allyl-L-tyrosine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Zinc glycinate is a form of zinc that is well-absorbed in the gut and has low toxicity. It is used to treat metabolic disorders such as fatty acid oxidation, ethylene diamine oxidation, and antimicrobial peptide synthesis. Zinc glycinate also inhibits the activity of enzymes involved in reactions involving acid complex, nutrient solution, drug interactions, and tissue antigens. Zinc glycinate binds to picolinic acid (a metabolite of tryptophan) and inhibits mitochondrial membrane potential. Structural analysis shows that zinc glycinate has a molecular weight of 196.2 g/mol and an empirical formula of C9H12N2O6Zn.</p>

<p>N-Propyl-1-ene-2,6-diethyl-4-phenylpyridinium tetrafluoroborate (NPEEDPBF) is a fine chemical that has been used as a building block in research and industrial chemistry. The synthesis of NPEEDPBF typically involves the reaction of diethyl phenylpyridinium bromide with n propyl iodide. It can be used as a reagent for organic syntheses and as an intermediate for other compounds. NPEEDPBF is also a versatile building block for complex compounds.</p>

<p>N-Succinyl-L-alanyl-L-alanyl-L-alanine 4 nitroanilide is a synthetic substrate that has been shown to have proteolytic activity against dextran sulfate, collagen, and sephadex g-100. It also has insecticidal activity in that it inhibits the development of larvae of the insect Drosophila melanogaster. NSLAAALAALAAN can be used as a chemotactic agent for tissue culture cells. This synthetic substrate was also found to have antiinflammatory properties and may be useful in treating chronic bronchitis or other metabolic disorders.</p>

<p>L-a-Phosphatidyl-L-serine is a chelator that is commonly used in the production of dabigatran etexilate mesylate, a medication used for anticoagulation. It has the ability to bind to hydrocarbons and other reactive species, preventing them from causing harm. L-a-Phosphatidyl-L-serine is also known to interact with potassium ions, which are essential for various biological processes. This compound is often used in research chemicals and has been found to have an inhibitory effect on potassium channels. Additionally, it has been shown to enhance the activity of fluoroquinolones, a class of antibiotics. Overall, L-a-Phosphatidyl-L-serine plays a crucial role as a target molecule in various applications related to anticoagulation and potassium regulation.</p>

<p>O-Phospho-DL-serine is a nonprotein amino acid that is synthesized in plants and microorganisms. It is an intermediate in the metabolism of phosphoserine, which can be converted to phosphoserine by the enzyme phosphoserine phosphatase. O-Phospho-DL-serine has been shown to have anti-cancer properties, as it inhibits the growth of various human cancer cell lines by dephosphorylating and inhibiting protein kinases. O-Phospho-DL-serine also has a role in the activation of response elements and cytokines, especially in the presence of growth factors such as fibroblast growth factor β1 (FGFβ1).</p>

<p>Furosine hydrochloride is a white crystalline chemical with a molecular formula of C6H7N3O4S. It is soluble in water and has a melting point of about 140 degrees Celsius. Furosine hydrochloride is a useful building block for the synthesis of polymers, pharmaceuticals, organic semiconductors and other organic compounds. Furosine hydrochloride is used as an intermediate to produce fine chemicals such as polyurethanes, polyamides and amino acids. It can also be used as a reaction component in the synthesis of complex compounds such as 2-amino-5-nitrothiophene or 2,2'-dithiobis(benzothiazole). Furosine hydrochloride can be used as a scaffold for the production of various drugs such as antihypertensives or antidepressants.</p>

L-Homopropargylglycine is a small molecule that inhibits the activity of enzymes involved in fatty acid synthesis. It has been shown to inhibit the activity of enzymes involved in mitochondrial membrane potential and reactive oxygen species production, as well as collagen degradation. L-Homopropargylglycine is used to study the molecular mechanisms of lipid metabolism and mitochondrial function, as well as for wastewater treatment. L-Homopropargylglycine has also been studied as a potential drug for the treatment of metabolic syndrome, diabetes, and cancer.

<p>1-Boc-1,8-diaminooctane is a polymerase that is used in the synthesis of DNA. It has been shown to be able to cleave supercoiled DNA and bind to acidic surfaces. This compound is fluorescent and can form covalent adducts with nucleic acids. 1-Boc-1,8-diaminooctane also has a piperidine group, which can act as a linker for other molecules such as anthracene. 1-Boc-1,8-diaminooctane is a neutral pH compound that reacts well with biomolecules.</p>

<p>2-Cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-methanol is a crystalline compound that has been obtained by reacting 3-methoxyquinoline with cyclopropyl bromide. It has the dihedral angle of about 120 degrees and is stabilized by hydrogen bonds. The compound crystallizes in an asymmetric unit cell with two molecules in the asymmetric unit and space group P2/n. The target compound can be obtained in high yield, and it is soluble in organic solvents such as benzene and triphenylphosphine. 2-Cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-methanol can be used to suppress wastewater containing halogenated aromatic compounds, such as quinoline.</p>

<p>3-Fluoro-DL-tyrosine is a model system for the study of tyrosine transfer reactions. It is used to study the reaction mechanism and kinetics of tyrosine transfer from a donor molecule to an acceptor molecule. 3-Fluoro-DL-tyrosine reacts with trifluoroacetic acid to form 3,4-dihydroxybenzoic acid, which is a chemical analog of tyrosine. The hydroxyl group on this molecule can react with the proton on the amino acid side chain, forming a covalent bond that does not break down under normal conditions. This reaction is reversible and has been shown to be catalyzed by polymerase chain reactions (PCR).</p>

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<p>2,9-Dibromo-1,10-phenanthroline is a molecule that has been shown to be an effective sensitizer for the photochemical conversion of chlorine dioxide to ozone. It has been used as a model compound in molecular orbital calculations and has been shown to enhance the yield of ozone by up to 3%. The emission spectrum of 2,9-dibromo-1,10-phenanthroline displays a peak at 362 nm, which lies in the ultraviolet region. The molecule is orthorhombic and crystallizes in space group P2/c with cell dimensions a = 17.8 Å and c = 18.7 Å.</p>

<p>Z-Gly-Met-OH is a buffer that can be used to create an acidic solution. It is often used in liquid chromatography and peptide synthesis. Z-Gly-Met-OH has been shown to have potential use as an enzyme inhibitor, specifically for proteases and peptidases. The hydrolyzed form of Z-Gly-Met-OH has been shown to bind zinc ions and could be used in the treatment of metal ion poisoning.</p>

<p>H-Asp-Phe-OH is a diagnostic agent that contains the amino acid aspartame and a hydroxyl group. It is hydrolyzed in the body to form aspartic acid, phenylalanine, and methanol. The methyl ester of H-Asp-Phe-OH is hydrochloride. This compound has been used to study locomotor activity in mice and rats. Aspartame has also been shown to be an inhibitor of certain enzymes, such as fatty acid synthase, which is associated with human pathogens. The lc-ms/ms method has been used to detect H-Asp-Phe-OH metabolites in human serum samples. In addition, this compound can be used for the diagnosis of diseases such as diabetes mellitus type 2 and Alzheimer’s disease by measuring uptake into cells at enzyme activities.</p>

<p>Estradiol is a form of the hormone estrogen that has been modified to be more lipophilic. It is used in combination with other drugs to treat menopausal symptoms and as an adjuvant for the treatment of breast cancer in women. Estradiol 17-valerate is also used in the treatment of schizophrenia, although not as often as estradiol valerate, because it has a shorter duration of action. The mechanism of action is thought to be due to its ability to increase the concentration of dopamine at nerve terminals by blocking reuptake or inhibiting its metabolism. This may result in relief from distal tubule dysfunction and an improvement in urinary tract symptoms associated with benign prostatic hypertrophy. There are many other possible mechanisms of action including the prevention of bone loss, increased bone age, and increased NMDA receptor binding potentials.</p>

<p>N-Acetyl-L-Phenylalanine is a reactive compound that is involved in the metabolism of amino acids. It has been shown to inhibit liver cell growth and induce apoptosis. The reaction mechanism of N-acetyl-L-phenylalanine has been extensively studied, with studies showing it to react with carbonyl oxygens, hydrogen bond, and intramolecular hydrogen. N-Acetyl-L-phenylalanine has also been shown to have an optimum pH of 6.5 and its chemical formula is C10H11NO2.</p>

<p>L-Aspartic acid b-methyl ester hydrochloride is a high quality, versatile building block that can be used as a reaction component in the synthesis of complex compounds. L-Aspartic acid b-methyl ester hydrochloride is a useful scaffold for the preparation of novel fine chemicals and research chemicals with potential uses as pharmaceuticals, pesticides, and agricultural chemicals. It can also be used as an intermediate in the preparation of some natural products or industrial chemicals. L-Aspartic acid b-methyl ester hydrochloride has a CAS number of 16856-13-6.</p>