5 Bis Carboxymethyl Amino 2 Carboxy 4 Cyano 3 Thiopheneacetic Acid Strontium Salt 1 2
quinoline thiophene imidazole thiazole

5-[Bis(carboxymethyl)amino]-2-carboxy-4-cyano-3-thiopheneacetic acid strontium salt (1:2)

    Specifications

    HS Code

    890165

    Chemical Name 5-[Bis(carboxymethyl)amino]-2-carboxy-4-cyano-3-thiopheneacetic acid strontium salt (1:2)
    Molecular Formula C11H9N2O8S2Sr2
    Molecular Weight 569.74 g/mol (approximate, calculated from formula)
    Appearance Solid (assumed, as no data; common for metal salts of organic acids)
    Solubility Solubility properties depend on solvent; may have some solubility in polar solvents like water due to ionic nature
    Ph In aqueous solution, pH would be influenced by hydrolysis of the carboxylate groups
    Stability Stable under normal conditions; may react with strong acids or bases
    Hazard Classification Unknown without safety data sheet, but may have potential irritant or harmful effects depending on exposure

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    Frequently Asked Questions

    As a leading 5-[Bis(carboxymethyl)amino]-2-carboxy-4-cyano-3-thiopheneacetic acid strontium salt (1:2) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of strontium acetate (1:2) 5- [ (bis (carboxymethyl) amino] -2-carboxyl-4-cyano-3-thiophene acetate)
    This is related to the chemical structure of organic compounds. The "di (tert-butyl) amino", tert-butyl is a group containing three methyl groups attached to the same carbon atom, and "di (tert-butyl) amino" is two tert-butyl groups attached to nitrogen atoms. "2-tert-butyl-4-chlorophenyl-3-quinoline ethyl formate (1:2) ", quinoline is a nitrogen-containing heterocyclic aromatic hydrocarbon. In this compound, the quinoline ring is connected with ethyl formate at the 3rd position, tert-butyl at the 2nd position, and chlorophenyl at the 4th position.
    The chemical structure of this compound is complex and delicate. The quinoline ring has a rigid and conjugated system, which affects the distribution and stability of molecular electron cloud. The 2-position tert-butyl group is a larger volume substituent. Due to the steric hindrance, it affects the molecular configuration and reactivity, hinders the approach of nucleophilic or electrophilic reagents, and changes the reaction selectivity. The chlorine atom in the 4-position chlorophenyl group has an electron-absorbing induction effect, which changes the electron cloud density of the benzene ring and affects the reactivity of the benzene ring and the whole molecule. The chlorine atom can participate in reactions such as nucleophilic substitution. The ester functional group in the 3-position formate ethyl group has unique reactivity, which can be hydrolyzed, alcoholyzed, aminolyzed, etc., enriching the chemical properties of Overall, the chemical structure of this compound involves the interaction of various groups, giving it specific physical and chemical properties and reactivity. It may have potential applications in the fields of organic synthesis, medicinal chemistry, etc., such as the synthesis of specific drugs or functional materials. Intermediates can be used to build more complex and functional molecular structures through the reactivity of each group.
    What are the main uses of strontium 5- [ (bis (carboxymethyl) amino] -2-carboxyl-4-cyano-3-thiophene acetate (1:2)
    5 - [ (Bis (hydroxymethyl) ethyl ether) - 2-hydroxypropyl-4-hydroxybutyl-3-aminoethyl sulfate (1:2) ], which is widely used.
    In the field of medicine, it can be used as a drug carrier. Due to its unique chemical structure, good solubility and stability, it can wrap drug molecules, help drugs to accurately deliver to the target, improve drug efficacy and reduce side effects. For example, in some anti-cancer drug preparations, with this substance, the drug can better reach tumor cells, enhance the killing of cancer cells, and reduce damage to normal cells.
    In the cosmetic industry, this substance is often used in skin care product formulations. It can enhance the moisturizing performance of the product, improve the hydration of the skin, and make the skin more hydrated, smooth and soft. Due to its gentle properties, it is suitable for a variety of skin types, creating a good nourishing environment for the skin and helping to maintain the healthy state of the skin.
    In industrial production, it can be used as a surfactant. With its unique molecular structure, it can reduce the surface tension of liquids, improve emulsification, dispersion and wetting properties. In the production of paints and inks, the addition of this substance can improve the dispersion of pigments, make the coating and ink apply more evenly, and improve product quality and performance. In the textile printing and dyeing industry, as an auxiliary agent, it can help dyes better adhere to fibers, improve dyeing effect and fastness.
    What is the preparation method of 5- [ (bis (carboxymethyl) amino] -2-carboxyl-4-cyano-3-thiophene acetate strontium salt (1:2)
    To prepare 5 - [ (bis (hydroxymethyl) acetamide) - 2 - hydroxymethyl - 4 - hydroxy - 3 - formylacrylate lactone (1:2), the method is as follows:
    Prepare various drugs first, and the required materials should be carefully selected to ensure their purity and purity. Take an appropriate amount of starting materials. The choice of this raw material is related to success or failure, and it must be carefully screened.
    In a clean vessel, put an appropriate amount of solvent, which is mild in nature and soluble with all substances. Then slowly add the relevant reagents, and the action should be slow to prevent overreaction. When controlling the temperature of the reaction, it should not be high or low. It should be controlled by a precise method, so that the temperature is constant within a certain range. This range is determined according to the experience of predecessors and the properties of various things.
    When reacting, it is necessary to carefully observe, observe its color change, state change, smell its odor, and if there is any abnormality, quickly find the cause and correct it. When the reaction is asymptotically completed, the product should be analyzed by an appropriate method, or filtered, distilled, or extracted, and the appropriate one should be used.
    The product has been obtained and needs to be refined. By recrystallization or column chromatography, its impurities should be removed to make the product pure to the required standard.
    The whole process requires caution, the slightest bit of sparsity, or failure. The operator should be familiar with all skills and understand the properties of all things, so that the pure 5- [ (bis (hydroxymethyl) acetamide) - 2-hydroxymethyl-4-hydroxy-3-formylacrylate (1:2) can be obtained.
    What are the physicochemical properties of strontium acetate (1:2) 5- [ (bis (carboxymethyl) amino] -2-carboxyl-4-cyano-3-thiophene acetate)
    The physical properties of 5 - [ (bis (benzylamino) urea) ] -2 -benzyl-4-urea-3-imidazole acetic acid hydrochloride (1:2) can be said as follows in "Tiangong Kaiwu".
    In the physical properties of this compound, its appearance is often in a specific form, or it is crystalline and has a certain color, which is the appearance that can be recognized by the naked eye. Its melting point is a key physical constant. At a specific temperature, the substance changes from solid to liquid. The determination of this temperature is extremely important for identification and purity judgment. Solubility is also a key point. In different solvents, its dissolution status varies. In water, alcohols, organic solvents, etc., it is either soluble, slightly soluble, or insoluble, which is related to its ability to disperse and react in different media.
    Chemical properties, due to the presence of a variety of groups, have unique reactivity. The benzyl group can participate in reactions such as nucleophilic substitution, and its benzene ring structure gives certain stability and electronic effects. The urea group and the imidazole acetate hydrochloride part also have unique chemical behaviors. The urea group can be complexed with metal ions, or hydrolyzed under specific conditions. In imidazole acetate hydrochloride, the imidazole ring is basic and can react with acids or electrophilic reagents. The form of hydrochloride affects its ionization degree and chemical reactivity. In the fields of organic synthesis, medicinal chemistry, or as a key intermediate, its chemical properties can lead to the construction of more complex molecular structures.
    5- [ (Bis (carboxymethyl) amino] -2-carboxyl-4-cyano-3-thiophene acetate strontium salt (1:2) What are the precautions during use?
    5 - [ (Bis (hydroxymethyl) acetamide) - 2-hydroxymethyl-4-hydroxy-3-methoxybenzoic anhydride (1:2) ] During the application process, the following general matters should be paid attention to:
    First, this material has a specific chemical activity, and the established safety procedures must be followed during operation. Do not touch it with your bare hands, and you must wear suitable protective gloves to avoid the drug from staining the skin, causing discomfort and even injury. A protective mask should also be worn on the face to prevent the drug from splashing into the eyes and damaging the eyesight.
    Second, due to its chemical properties, it has strict requirements on the storage environment. It should be placed in a dry, cool and well-ventilated place, away from fire and heat sources. Excessive humidity or abnormal temperature may cause chemical reactions to occur, resulting in variation in quality and performance.
    Third, when preparing, be sure to precisely control the dose. A slight deviation in the proportion of this compound may have a significant impact on the expected effect. It is necessary to operate according to a specific formula and process, and use accurate measuring instruments to achieve the ideal ratio.
    Fourth, the ventilation conditions of the application site are crucial. If the ventilation is not smooth, the volatile gaseous substances of the drug may accumulate, which will not only affect the health of the workers, but also cause safety accidents.
    Fifth, after use, properly dispose of the remaining drugs and packaging. Do not discard at will to prevent pollution to the environment. It should be sorted and recycled or treated harmlessly in accordance with relevant regulations.
    After all, the use of this compound requires rigorous and meticulous attention to the operation specifications of each link to ensure safety and effectiveness.