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1Luminol monosodium salt CAS:20666-12-0
3-Aminophthalhydrazide monosodium salt is a chemical compound that is often used as a reagent in various biochemical and analytical applications. It is a derivative of phthalhydrazide, containing an amino group (NH2) instead of one of the hydrogen atoms on the phthalhydrazide molecule.
This compound is commonly used as a reducing agent or a catalyst in organic synthesis reactions. It can participate in a variety of reactions, including the reduction of carbonyl compounds to their corresponding alcohols, and the conversion of nitro compounds to their corresponding amines.
In addition to its role in organic synthesis, 3-Aminophthalhydrazide monosodium salt also has applications in analytical chemistry. For example, it has been used as a reagent for the determination and quantification of various analytes, such as aldehydes and ketones, through colorimetric or spectrophotometric methods.
Furthermore, this compound can be employed as a probe or indicator in biochemical and molecular biology experiments. It can react selectively with certain functional groups or biomolecules, enabling the detection or labeling of specific targets in biological samples.
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1,8-diazafluoren-9-one CAS:54078-29-4
1,8-Diazafluoran-9-one is an organic compound that belongs to the diazafluoranone family. It is characterized by a fused ring structure containing two nitrogen atoms and a ketone group. This compound has potential applications in various fields, including organic synthesis, medicinal chemistry, and material sciences. Its precise uses and properties may vary depending on the specific context and application.
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N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid sodium salt CAS:66992-27-6
N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid sodium salt, also known as HEPES sodium salt, is a chemical compound commonly used as a pH buffering agent in biological and chemical laboratories. It helps maintain a stable pH range, making it ideal for applications such as cell culture, enzyme assays, protein studies, electrophoresis, and pharmaceutical formulations. HEPES sodium salt ensures optimal conditions for biological processes and enhances the accuracy and reliability of experimental results.
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S-Butyrylthiocholine iodide CAS:1866-16-6
S-Butyrylthiocholine iodide is a chemical compound commonly used in biochemical and enzymatic assays. It is a substrate for the enzyme butyrylcholinesterase (BChE) and is used to measure its activity.
When S-Butyrylthiocholine iodide is hydrolyzed by BChE, it produces thiocholine and butyric acid as products. The release of thiocholine can be measured using a spectrophotometric or fluorometric assay, allowing quantification of BChE activity.
S-Butyrylthiocholine iodide is often used in clinical and research settings to evaluate the activity of BChE in samples such as blood plasma or tissues. It can be used to assess the enzymatic function of BChE and its potential role in various biological processes, as well as in the diagnosis and monitoring of certain medical conditions.
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Heparin sodium CAS:9041-08-1
Heparin sodium is a medication that belongs to the class of anticoagulants or blood thinners. It is derived from the natural compound heparin, which is found in certain tissues in the body, particularly in the liver and lungs.
Heparin sodium is primarily used to prevent and treat blood clotting disorders, such as deep vein thrombosis (DVT), pulmonary embolism (PE), and arterial thromboembolism. It works by inhibiting the production and activity of clotting factors, thus preventing the formation and growth of blood clots.
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D-(+)-Cellobiose CAS:528-50-7
D-(+)-Cellobiose is a disaccharide made up of two glucose units connected by a beta-1,4-glycosidic bond. It is commonly found in cellulose, the main component of plant cell walls. Cellobiose is a colorless, crystalline solid that is soluble in water. It is not digested by most organisms, but can be hydrolyzed by certain enzymes, such as cellobiases, to yield glucose. Cellobiose is an important intermediate in the microbial degradation of cellulose and is used in various biotechnological applications, including the production of biofuels.
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2-Chloroethanesulfonic acid CAS:15484-44-3
2-Chloroethanesulfonic acid, also known as chloroethanesulfonic acid or CES, is an organic compound with the chemical formula C2H5ClSO3H. It is a clear, colorless liquid that is highly soluble in water and polar organic solvents.
CES is widely used as a versatile chemical intermediate in various industries. It is primarily employed in the synthesis of pharmaceuticals, agrochemicals, and organic dyes. Its sulfonic acid group makes it a useful reagent for introducing sulfonic acid functionality into organic molecules, which can enhance their solubility, stability, or bioactivity.
Due to its strong acidity, CES can also be utilized as a catalyst or acidic reagent in organic reactions. Its acidic nature allows it to promote reactions such as esterifications, acylations, and sulfonations. Additionally, it can serve as a pH adjuster, buffering agent, or corrosion inhibitor in industrial processes.
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PIPES monosodium salt CAS:10010-67-0
Sodium hydrogen piperazine-1,4-diethanesulphonate, also known as HEPES-Na, is a commonly used buffering agent in biological and biochemical research. It helps maintain a stable pH range of 6.8 to 8.2 in various applications, including cell culture, enzyme assays, and molecular biology techniques. HEPES-Na is compatible with different biological systems and is stable over a wide temperature range.
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3-NITROPHENYL-BETA-D-GALACTOPYRANOSIDE CAS:3150-25-2
3-Nitrophenyl-beta-D-galactopyranoside (ONPG) is a substrate commonly used in enzymatic assays to detect and measure the activity of beta-galactosidase. When beta-galactosidase is present and active, it hydrolyzes ONPG, releasing a yellow-colored product called 3-nitrophenol. The intensity of the yellow color produced can be measured spectrophotometrically, allowing quantification of beta-galactosidase activity. ONPG is frequently used in molecular biology and microbiology research, as well as in clinical diagnostics, to study gene expression, protein function, bacterial identification, and cell viability.
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3-(cyclohexylamino)-2-hydroxy-1-propanesuhicic acid CAS:73463-39-5
3-(cyclohexylamino)-2-hydroxy-1-propanesuhicic acid is a chemical compound with the molecular formula C12H23NO3S. It belongs to a family of compounds known as sulfonic acids. This particular compound contains a cyclohexylamino group, a hydroxy group, and a propanesuhicic acid moiety. It is used in various industrial applications, including as a building block in organic synthesis and as a reagent in pharmaceutical research. The compound’s unique structure and properties make it suitable for specific chemical reactions and scientific investigations.
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HEIDA CAS:93-62-9 Manufacturer Price
N-(2-Hydroxyethyl)iminodiacetic acid (HEIDA) is a chemical compound with multiple applications in various fields. It is a chelating agent, meaning it has the ability to bind to metal ions and form stable complexes.
In analytical chemistry, HEIDA is often used as a complexing agent in titrations and analytical separations. It can be employed to sequester metal ions, such as calcium, magnesium, and iron, and thereby prevent them from interfering with the accuracy of analytical measurements.
HEIDA also finds application in the pharmaceutical industry, particularly in the formulation of certain medications. It can be used as a stabilizer and solubilizing agent for poorly soluble drugs, helping to improve their bioavailability and efficacy.
Another area of use for HEIDA is in the field of wastewater treatment and environmental remediation. It can be employed as a sequestering agent to remove heavy metal contaminants from water or soil, thereby reducing their toxicity and promoting remediation efforts.
Additionally, HEIDA has been utilized in the synthesis of coordination compounds and metal-organic frameworks (MOFs), which have various applications in catalysis, gas storage, and sensing.
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2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose CAS:14131-84-1
2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose is a compound used in organic synthesis as a protecting group for the hydroxyl groups of mannose. By attaching isopropylidene groups to the hydroxyl groups at positions 2, 3, 5, and 6 of the mannose ring, this compound helps to prevent undesirable reactions from occurring at those sites. This protection allows for selective modifications at other functional groups in the molecule. It is commonly used in the synthesis of complex carbohydrates and glycoconjugates, which play important roles in biological processes and have applications in areas such as drug delivery, diagnostics, and immunology.
