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  • 2-DIMETHYLAMINOISOPROPYL CHLORIDE HYDROCHLORIDE CAS:4584-49-0

    2-DIMETHYLAMINOISOPROPYL CHLORIDE HYDROCHLORIDE CAS:4584-49-0

    2-Dimethylaminoisopropyl chloride hydrochloride is a chemical compound with the molecular formula C6H15Cl2N. It is commonly abbreviated as DMAIP HCl. This compound is a hydrochloride salt of 2-dimethylaminoisopropyl chloride.

    DMAIP HCl is primarily used as a reagent in organic synthesis, particularly in the synthesis of pharmaceuticals and other organic compounds. It serves as a versatile alkylating agent, contributing to the formation of carbon-carbon and carbon-nitrogen bonds in various reactions.

    Due to its electrophilic nature, DMAIP HCl can react with nucleophiles, such as amines and thiols, to form substituted derivatives. This makes it useful for introducing alkyl or alkyl-aryl functional groups into organic molecules.

    DMAIP HCl is also used in the production of quaternary ammonium compounds, which find applications as surfactants, disinfectants, and catalysts in various industries.

  • TAPSO CAS:68399-81-5 Manufacturer Price

    TAPSO CAS:68399-81-5 Manufacturer Price

    TAPSO (3-[N-tris(hydroxymethyl)methyl]amino]-2-hydroxypropanesulfonic acid) is a zwitterionic buffer commonly used in biological and biochemical research. It is an efficient buffering agent with a pKa close to physiological pH, making it suitable for maintaining a stable pH in biological experiments. TAPSO is often utilized in protein purification, enzyme assays, cell culture, and electrophoresis applications. Its high water solubility and low interference with biological processes make it a popular choice in the scientific community. TAPSO is known for its minimal effect on enzyme activity and is often used as an alternative to other buffering agents like Tris or phosphate buffers.

  • 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.

     

  • 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-Benzylamino-7-nitrobenz-2-oxa-1,3-diazole CAS:18378-20-6

    4-Benzylamino-7-nitrobenz-2-oxa-1,3-diazole CAS:18378-20-6

    4-Benzylamino-7-nitrobenz-2-oxa-1,3-diazole is a chemical compound with a molecular formula C14H11N5O3. It is a heterocyclic compound that contains a diazole ring fused with a benzene ring. This compound is known for its fluorescent properties and is often used as a fluorescent dye in biological research and imaging applications. The benzylamino group attached to the diazole ring enhances its solubility and stability. The nitro group and the oxa atom (oxygen) in the diazole ring contribute to its unique chemical and physical properties. 

  • N-Acetyl-L-cysteine CAS:616-91-1

    N-Acetyl-L-cysteine CAS:616-91-1

    N-Acetyl-L-cysteine (NAC) is a modified form of the amino acid cysteine. It provides a source of cysteine and can be readily converted into the tripeptide glutathione, a powerful antioxidant in the body. NAC is known for its antioxidant and mucolytic properties, making it useful in various health applications.

    As an antioxidant, NAC helps protect cells from damage caused by free radicals, reactive oxygen species, and toxins. It also supports glutathione synthesis, which plays a crucial role in the body’s detoxification processes and maintaining a healthy immune system.

    NAC has been studied for its potential benefits in respiratory health, particularly for individuals with conditions such as chronic bronchitis, COPD, and cystic fibrosis. It is commonly used as an expectorant to help thin and loosen mucus, making it easier to clear the airways.

    Furthermore, NAC has shown promise in supporting liver health by assisting in the removal of toxic substances, such as acetaminophen, a common pain reliever. It may also have protective effects against liver damage caused by alcohol consumption.

    In addition to its antioxidant and respiratory support properties, NAC has been explored for its potential benefits in mental health. Some research suggests that it may have a positive impact on mood disorders, such as depression and obsessive-compulsive disorder (OCD).

  • 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.

     

  • PIPES CAS:5625-37-6 Manufacturer Price

    PIPES CAS:5625-37-6 Manufacturer Price

    PIPES (piperazine-1,4-bisethanesulfonic acid) is a zwitterionic buffering compound commonly used in biological and biochemical research. It is an effective pH buffer with a high capacity for maintaining stable pH conditions in a pH range of 6.1 to 7.5. PIPES has minimal interference with biomolecules and is suitable for temperature-dependent assays. It is often used in gel electrophoresis techniques and pharmaceutical formulation as a stabilizing agent. Overall, PIPES is a versatile and widely used compound in various experimental settings.

  • 2′,6′-DiMethylcarbonylphenyl-10-sulfopropylacridiniuM-9-carboxylate 4′-NHS Ester CAS:194357-64-7

    2′,6′-DiMethylcarbonylphenyl-10-sulfopropylacridiniuM-9-carboxylate 4′-NHS Ester CAS:194357-64-7

    2′,6′-DiMethylcarbonylphenyl-10-sulfopropylacridinium-9-carboxylate 4′-NHS ester is a chemical compound with a complex molecular structure. It contains a sulfopropylacridinium group and a carboxylate ester functional group. The presence of the ester moiety indicates that it is reactive and can be used as a labeling or modifying agent for biomolecules.

    The compound’s sulfopropylacridinium group suggests that it may have potential applications in fluorescence-based assays, where it can be used as a fluorescent probe or dye for detecting and analyzing biomolecules. It may also have relevance in studies of cellular processes, such as intracellular calcium signaling.

    The inclusion of the NHS ester group indicates that it can react with primary amines, such as those found in proteins or peptides, to form stable amide bonds. This reactivity makes it useful for bioconjugation applications, where it can be used to label or modify biomolecules with other functional molecules, such as fluorophores or tags.

  • NBD chloride CAS:10199-89-0

    NBD chloride CAS:10199-89-0

    NBD chloride, also known as 7-chloro-4-nitrobenzo-2-oxa-1,3-diazole, is a fluorescent dye commonly used in chemical and biological applications. It belongs to the class of nitrobenzoxadiazole (NBD) derivatives, which exhibit strong fluorescence properties.

    NBD chloride is characterized by its ability to form covalent bonds with nucleophiles, such as primary amines, thiols, and hydroxyl groups. This property allows it to be used as a labeling agent for biomolecules, including proteins, peptides, nucleic acids, and other small molecules.

    When NBD chloride reacts with a nucleophile, it undergoes a substitution reaction, resulting in the formation of a stable NBD-labeled product. This labeled product exhibits intense fluorescence emission, making it useful for various detection and imaging techniques.

    The fluorescence emission of NBD-labeled molecules can be excited with ultraviolet (UV) light at around 470 nm, and the emitted light is typically detected at around 530 nm. This emission wavelength falls within the green region of the visible spectrum, where detection interference from biological samples is relatively low.

     

     

  • 3′,5′-Dimethoxy-4′-hydroxyacetophenone CAS:2478-38-8

    3′,5′-Dimethoxy-4′-hydroxyacetophenone CAS:2478-38-8

    3′,5′-Dimethoxy-4′-hydroxyacetophenone is a chemical compound with the molecular formula C10H12O4. It belongs to the class of organic compounds known as phenols and is derived from acetophenone. It is characterized by the presence of two methoxy groups (-OCH3) at positions 3′ and 5′ on the phenol ring and a hydroxy group (-OH) at position 4′. This compound is commonly used as an intermediate or building block in organic synthesis, particularly in the production of pharmaceuticals and other biologically active compounds.

  • 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.