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  • p-Nitrophenyl -a-L-Fucopyranoside CAS:10231-84-2

    p-Nitrophenyl -a-L-Fucopyranoside CAS:10231-84-2

    p-Nitrophenyl-α-L-Fucopyranoside is a chemical compound that belongs to the class of nitrophenyl glycosides. It is commonly used in biochemical research as a substrate for the enzyme α-L-fucosidase, which catalyzes its hydrolysis. This compound is colorless and soluble in organic solvents, making it convenient for enzymatic assays.

  • Heparin lithium salt CAS:9045-22-1

    Heparin lithium salt CAS:9045-22-1

    Heparin lithium is a chemical substance with a white to almost white powder appearance.

     

  • 5-Bromo-6-Chloro-3-Indolyl Acetate CAS:102185-48-8

    5-Bromo-6-Chloro-3-Indolyl Acetate CAS:102185-48-8

    5-Bromo-6-chloro-3-indoxyl-3-acetate is a chemical compound that is commonly used as a substrate in enzymatic assays. It is often employed to detect the presence and activity of certain enzymes, such as esterases and hydrolases.

    When added to a reaction mixture containing the specific enzyme, this compound undergoes enzymatic hydrolysis. As a result, it produces a colored or fluorescent product, allowing researchers to visualize and measure the activity of the enzyme.

    This substrate is widely used in many different fields, including molecular biology, biochemistry, and clinical diagnostics. Its versatility and sensitivity make it a valuable tool for studying enzyme kinetics, activity, and inhibition.

  • b-D-Glucopyranoside,2-chloro-4-nitrophenyl 2-(acetylamino)-2-deoxy- CAS:103614-82-0

    b-D-Glucopyranoside,2-chloro-4-nitrophenyl 2-(acetylamino)-2-deoxy- CAS:103614-82-0

    2-chloro-4-nitrophenyl-N-acetylglucosaminide is a chemical compound that belongs to the family of N-acetylglucosamine derivatives. It is commonly used as a substrate in enzymatic assays to measure the activity of certain enzymes, such as glycosidases and glycosyltransferases.

    The compound has a molecular structure consisting of a N-acetylglucosamine moiety, which is a derivative of glucose, and a 2-chloro-4-nitrophenyl group attached to the sugar molecule. The presence of the 2-chloro-4-nitrophenyl group makes this compound highly sensitive to enzymatic cleavage by glycosidases, resulting in the release of the 2-chloro-4-nitrophenol molecule. The amount of released 2-chloro-4-nitrophenol can be quantified through spectrophotometric measurements, allowing for the determination of enzyme activity.

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  • 3-(1-pyridinio)-1-propanesulfonate CAS:15471-17-7

    3-(1-pyridinio)-1-propanesulfonate CAS:15471-17-7

    3-(1-pyridinio)-1-propanesulfonate (also known as TPPS or TPPS3) is a sulfonated derivative of pyridine. It is a highly water-soluble compound that is commonly used as a fluorescent probe and photosensitizer in various applications, particularly in the field of photodynamic therapy (PDT).

     

     

  • 4-Amino-3-hydrazino-1,2,4-triazol-5-thiol CAS:28836-03-5

    4-Amino-3-hydrazino-1,2,4-triazol-5-thiol CAS:28836-03-5

    4-Amino-3-hydrazino-1,2,4-triazol-5-thiol is a chemical compound with a complex structure consisting of an amino group (NH2), a hydrazino group (NHNH2), and a thiol group (SH) attached to a 1,2,4-triazole ring.

    It is a relatively small molecule with potential use in various applications, including medicinal chemistry and pharmaceutical research. The presence of the amino and hydrazino groups suggests potential reactivity and affinity towards biological targets.

     

  • 1Luminol monosodium salt CAS:20666-12-0

    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.

     

  • 1,8-diazafluoren-9-one CAS:54078-29-4

    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. 

  • N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid sodium salt CAS:66992-27-6

    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.

  • S-Butyrylthiocholine iodide CAS:1866-16-6

    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.

     

  • Heparin sodium CAS:9041-08-1

    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.

     

  • ABTS (2,2′-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) diammonium salt) CAS:30931-67-0

    ABTS (2,2′-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) diammonium salt) CAS:30931-67-0

    Diammonium 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate), often referred to as ABTS, is a commonly used chromogenic substrate in biochemical assays, particularly in the field of enzymology. It is a synthetic compound that is used to measure the activity of various enzymes, including peroxidases and oxidases.

    ABTS is colorless in its oxidized form but turns blue-green when oxidized by an enzyme in the presence of hydrogen peroxide or molecular oxygen. This color change is due to the formation of a radical cation, which absorbs light in the visible spectrum.

    The reaction between ABTS and the enzyme produces a colored product that can be measured spectrophotometrically. The intensity of the color is directly proportional to the enzymatic activity, allowing researchers to quantitatively evaluate enzyme kinetics, enzyme inhibition, or enzyme-substrate interactions.

    ABTS has a broad range of applications in various fields, including clinical diagnostics, pharmaceutical research, and food science. It is highly sensitive and offers a wide dynamic range, making it a popular choice for many biochemical assays.