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2,5-Dibutoxy-4-(Morpholin-4-Yl)Benzenediazonium Tetrachlorozincate (2:1)
Linshang Chemical
|
HS Code |
131661 |
| Chemical Formula | C28H44N6O6ZnCl4 |
| Molecular Weight | 780.81 g/mol |
| Appearance | Solid |
| Solubility | Soluble in some organic solvents |
| Stability | Stable under normal conditions |
| Hazardous Nature | May be harmful if swallowed, inhaled or in contact with skin |
| Application | Used in certain chemical reactions |
As an accredited 2,5-Dibutoxy-4-(Morpholin-4-Yl)Benzenediazonium Tetrachlorozincate (2:1) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | One - gram pack of 2,5 - dibutoxy - 4 - (morpholin - 4 - yl)benzenediazonium Tetrachlorozincate (2:1). |
| Storage | Store 2,5 - dibutoxy - 4 - (morpholin - 4 - yl)benzenediazonium Tetrachlorozincate (2:1) in a cool, dry place away from heat and ignition sources. Keep it in a tightly sealed container to prevent moisture absorption and decomposition. Avoid exposure to sunlight and incompatible substances, as it may be reactive. |
| Shipping | 2,5 - dibutoxy - 4 - (morpholin - 4 - yl)benzenediazonium Tetrachlorozincate (2:1) is shipped in accordance with chemical regulations. Packed securely to prevent breakage, it's transported by approved carriers to ensure safe delivery. |
Competitive 2,5-Dibutoxy-4-(Morpholin-4-Yl)Benzenediazonium Tetrachlorozincate (2:1) prices that fit your budget—flexible terms and customized quotes for every order.
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What are the chemical properties of 2,5-dibutoxy-4- (morpholine-4-yl) benzodiazotetrachlorozincate (2:1)
2% 2C5-diacetyl-4- (pyridine-4-yl) quinoline tetrazolium blue (2:1) is a rather special chemical substance. It has many unique chemical properties.
Among this compound, the 2,5-diacetyl moiety endows it with certain chemical activity and spatial structure characteristics. The presence of acetyl groups can participate in a variety of chemical reactions, such as nucleophilic substitution reactions. Because of its electrophilicity, the carbonyl of acetyl groups is easy to attract nucleophilic reagents to attack, resulting in various derivatization reactions, which can be used to construct more complex chemical structures. The
4- (pyridine-4-yl) part also affects its properties. The pyridine ring has certain alkalinity and aromaticity. The alkalinity makes the compound react with acids under specific conditions to form salt compounds and change its physical and chemical properties, such as solubility. The aromaticity endows it with certain stability, making it relatively stable under common conditions, and it is not prone to reactions such as ring opening and other structural damage. The
quinoline structure, as the core skeleton, provides a rigid planar structure for the whole molecule, which makes an important contribution to the conjugation system of the molecule, which in turn affects its optical properties. The compound may have certain fluorescence properties. Due to the existence of the conjugated system, it is conducive to electron transition and can emit fluorescence under suitable excitation conditions. This property may have potential applications in the fields of fluorescence detection and biological imaging.
The tetrazolium blue part increases the complexity and functionality of the compound. The tetrazolium ring can participate in a variety of reactions, such as forming complexes with metal ions. In the ratio of (2:1), the charge distribution and spatial structure of the whole compound can be determined, which affects its aggregation state in solution and interaction with other substances. It may be used as a chromogenic agent in some biochemical detection systems to take advantage of its color change characteristics after reacting with specific substances to achieve qualitative or quantitative analysis of the target.
Among this compound, the 2,5-diacetyl moiety endows it with certain chemical activity and spatial structure characteristics. The presence of acetyl groups can participate in a variety of chemical reactions, such as nucleophilic substitution reactions. Because of its electrophilicity, the carbonyl of acetyl groups is easy to attract nucleophilic reagents to attack, resulting in various derivatization reactions, which can be used to construct more complex chemical structures. The
4- (pyridine-4-yl) part also affects its properties. The pyridine ring has certain alkalinity and aromaticity. The alkalinity makes the compound react with acids under specific conditions to form salt compounds and change its physical and chemical properties, such as solubility. The aromaticity endows it with certain stability, making it relatively stable under common conditions, and it is not prone to reactions such as ring opening and other structural damage. The
quinoline structure, as the core skeleton, provides a rigid planar structure for the whole molecule, which makes an important contribution to the conjugation system of the molecule, which in turn affects its optical properties. The compound may have certain fluorescence properties. Due to the existence of the conjugated system, it is conducive to electron transition and can emit fluorescence under suitable excitation conditions. This property may have potential applications in the fields of fluorescence detection and biological imaging.
The tetrazolium blue part increases the complexity and functionality of the compound. The tetrazolium ring can participate in a variety of reactions, such as forming complexes with metal ions. In the ratio of (2:1), the charge distribution and spatial structure of the whole compound can be determined, which affects its aggregation state in solution and interaction with other substances. It may be used as a chromogenic agent in some biochemical detection systems to take advantage of its color change characteristics after reacting with specific substances to achieve qualitative or quantitative analysis of the target.
What are the main uses of 2,5-dibutoxy-4- (morpholine-4-yl) benzodiazotetrachlorozincate (2:1)
2% 2C5-diethoxy-4- (furan-4-yl) quinoline diazotetrafluoroborate (2:1) is an organic compound, which is widely used in chemical and scientific research fields. Its main uses are as follows:
First, in the field of organic synthetic chemistry, this compound is often used as a key intermediate. Because of its structure containing diazo groups and quinoline structures, it is active and can participate in a variety of chemical reactions, such as coupling reactions. With such reactions, many organic molecules with complex structures can be constructed, laying the foundation for the synthesis of new drugs, functional materials, etc. For example, in the preparation of specific quinoline-containing drug molecules, it can be used as a starting material to precisely construct the required molecular structure through a series of reactions, greatly expanding the pathways and possibilities of organic synthesis.
Second, in the field of materials science, it plays an important role. The compound's unique optical and electrical properties make it very popular in the preparation of optoelectronic device materials. After proper treatment and modification, it can be applied to organic Light Emitting Diode (OLED), solar cells and other devices. In OLED, it can be used as a luminescent material or an electron transmission material to help improve the luminous efficiency and stability of the device; in the field of solar cells, it may help to improve the photoelectric conversion efficiency and promote the research and development and progress of new high-efficiency optoelectronic devices.
Third, in the field of dye chemistry, 2% 2C5-diethoxy-4- (furan-4-yl) quinoline diazonium tetrafluoroborate (2:1) has unique color and good dyeing properties due to structural characteristics. It can be used to synthesize new dyes and dye fabrics, leather and other materials. It may endow materials with bright colors and good light resistance and washable fastness, meeting the needs of high-quality dyes in textile, leather and other industries, and promoting innovative development in the field of dye chemistry.
First, in the field of organic synthetic chemistry, this compound is often used as a key intermediate. Because of its structure containing diazo groups and quinoline structures, it is active and can participate in a variety of chemical reactions, such as coupling reactions. With such reactions, many organic molecules with complex structures can be constructed, laying the foundation for the synthesis of new drugs, functional materials, etc. For example, in the preparation of specific quinoline-containing drug molecules, it can be used as a starting material to precisely construct the required molecular structure through a series of reactions, greatly expanding the pathways and possibilities of organic synthesis.
Second, in the field of materials science, it plays an important role. The compound's unique optical and electrical properties make it very popular in the preparation of optoelectronic device materials. After proper treatment and modification, it can be applied to organic Light Emitting Diode (OLED), solar cells and other devices. In OLED, it can be used as a luminescent material or an electron transmission material to help improve the luminous efficiency and stability of the device; in the field of solar cells, it may help to improve the photoelectric conversion efficiency and promote the research and development and progress of new high-efficiency optoelectronic devices.
Third, in the field of dye chemistry, 2% 2C5-diethoxy-4- (furan-4-yl) quinoline diazonium tetrafluoroborate (2:1) has unique color and good dyeing properties due to structural characteristics. It can be used to synthesize new dyes and dye fabrics, leather and other materials. It may endow materials with bright colors and good light resistance and washable fastness, meeting the needs of high-quality dyes in textile, leather and other industries, and promoting innovative development in the field of dye chemistry.
What is the synthesis method of 2,5-dibutoxy-4- (morpholine-4-yl) benzodiazotetrachlorozincate (2:1)
To prepare 2,5-dihydroxy-4- (furan-4-yl) quinoline tetrachloroplatinate (2:1), the method is as follows:
First take an appropriate amount of furan derivative and place it in a clean reactor. The kettle must be carefully washed and dried to prevent impurities from disturbing it. Then add a specific quinoline-containing structural compound. When the ratio of the two is precisely prepared, according to the reaction mechanism and past experience, a specific molar ratio is preferred to ensure that the reaction proceeds efficiently in the desired direction.
Then, add an appropriate amount of tetrachloroplatinic acid solution. The concentration and dosage of tetrachloroplatinic acid are also crucial, and need to be carefully determined according to the scale of the reaction system and the amount of expected product. When adding, slowly drop in, and at the same time stir at a constant speed with a delicate stirring device to quickly mix the solution, so that the reactants are fully contacted, so that the reaction can occur uniformly.
The control of the reaction temperature is the key. When the temperature of the reaction system is maintained within a certain range with a precise temperature control device. If it is too low, the reaction will be slow, and if it is too high, it may cause a cluster of side reactions, which will damage the purity and yield of the product. At this temperature, the reaction will take several hours, during which time close attention should be paid to the signs of the reaction, such as the change of color, the generation of precipitation, etc.
When the reaction is asymptotically completed, the product is precipitated from the reaction mixture by suitable separation means, such as filtration, extraction, etc. The precipitated product still contains impurities and must be purified by multiple recrystallization. Select a suitable solvent to dissolve and crystallize the product. After several operations, a pure 2,5-dihydroxy-4- (furan-4-yl) quinoline tetrachloroplatinate (2:1) can be obtained. The whole process requires fine operation, and the parameter control of each link needs to be accurate to obtain the ideal product.
First take an appropriate amount of furan derivative and place it in a clean reactor. The kettle must be carefully washed and dried to prevent impurities from disturbing it. Then add a specific quinoline-containing structural compound. When the ratio of the two is precisely prepared, according to the reaction mechanism and past experience, a specific molar ratio is preferred to ensure that the reaction proceeds efficiently in the desired direction.
Then, add an appropriate amount of tetrachloroplatinic acid solution. The concentration and dosage of tetrachloroplatinic acid are also crucial, and need to be carefully determined according to the scale of the reaction system and the amount of expected product. When adding, slowly drop in, and at the same time stir at a constant speed with a delicate stirring device to quickly mix the solution, so that the reactants are fully contacted, so that the reaction can occur uniformly.
The control of the reaction temperature is the key. When the temperature of the reaction system is maintained within a certain range with a precise temperature control device. If it is too low, the reaction will be slow, and if it is too high, it may cause a cluster of side reactions, which will damage the purity and yield of the product. At this temperature, the reaction will take several hours, during which time close attention should be paid to the signs of the reaction, such as the change of color, the generation of precipitation, etc.
When the reaction is asymptotically completed, the product is precipitated from the reaction mixture by suitable separation means, such as filtration, extraction, etc. The precipitated product still contains impurities and must be purified by multiple recrystallization. Select a suitable solvent to dissolve and crystallize the product. After several operations, a pure 2,5-dihydroxy-4- (furan-4-yl) quinoline tetrachloroplatinate (2:1) can be obtained. The whole process requires fine operation, and the parameter control of each link needs to be accurate to obtain the ideal product.
What are the precautions for storing and transporting 2,5-dibutoxy-4- (morpholine-4-yl) benzodiazotetrachlorozincate (2:1)?
2% 2C5-diacetyl-4- (furan-4-yl) quinoxaline tetrafluoroboronic acid (2:1) has many points to pay attention to during storage and transportation, and must not be underestimated.
Its chemical properties are relatively special, and when stored, the first environment is dry. This compound is prone to reaction in contact with water, causing it to deteriorate and its efficacy is greatly reduced. Therefore, a dry and well-ventilated place should be selected, away from water sources and humid places. If conditions permit, it can be placed in a sealed container with a desiccant to prevent moisture from invading.
Temperature is also a key factor. It is necessary to maintain a suitable temperature to avoid too high or too low. If the temperature is too high, it may cause the compound to decompose and evaporate; if the temperature is too low, it may change its morphology and affect its chemical activity. Generally speaking, it should be stored in a cool place, and the specific temperature should be determined according to its physical and chemical properties and relevant instructions.
When transporting, the packaging must be strong and tight. Because it has a certain chemical activity, if the packaging is not good, the packaging may be damaged during transportation due to bumps and collisions, and leakage may occur, causing danger. The packaging materials used must be able to withstand certain external impact and chemical corrosion, and should be well marked to clearly indicate the characteristics and precautions of the contents.
In addition, this compound may have certain toxicity and irritation. Whether it is storage or transportation, relevant personnel should take protective measures, such as wearing appropriate protective equipment, including gloves, protective glasses and masks, to avoid direct contact and inhalation to prevent health damage. At the same time, a complete emergency plan should be formulated. If there is an accident such as leakage, it can be handled quickly and properly to minimize the harm.
Its chemical properties are relatively special, and when stored, the first environment is dry. This compound is prone to reaction in contact with water, causing it to deteriorate and its efficacy is greatly reduced. Therefore, a dry and well-ventilated place should be selected, away from water sources and humid places. If conditions permit, it can be placed in a sealed container with a desiccant to prevent moisture from invading.
Temperature is also a key factor. It is necessary to maintain a suitable temperature to avoid too high or too low. If the temperature is too high, it may cause the compound to decompose and evaporate; if the temperature is too low, it may change its morphology and affect its chemical activity. Generally speaking, it should be stored in a cool place, and the specific temperature should be determined according to its physical and chemical properties and relevant instructions.
When transporting, the packaging must be strong and tight. Because it has a certain chemical activity, if the packaging is not good, the packaging may be damaged during transportation due to bumps and collisions, and leakage may occur, causing danger. The packaging materials used must be able to withstand certain external impact and chemical corrosion, and should be well marked to clearly indicate the characteristics and precautions of the contents.
In addition, this compound may have certain toxicity and irritation. Whether it is storage or transportation, relevant personnel should take protective measures, such as wearing appropriate protective equipment, including gloves, protective glasses and masks, to avoid direct contact and inhalation to prevent health damage. At the same time, a complete emergency plan should be formulated. If there is an accident such as leakage, it can be handled quickly and properly to minimize the harm.
What are the safety risks of 2,5-dibutoxy-4- (morpholine-4-yl) benzodiazotetrachlorozincate (2:1)?
2% 2C5-diacetoxy-4- (morpholine-4-yl) quinoline diazotetrafluoroborate (2:1) is a chemical substance that poses many safety risks, as detailed below:
1. Toxicity risk
This substance may be toxic, and exposure routes are diverse, such as inhalation of its dust, vapor, or skin contact, accidental ingestion, etc., may cause poisoning. After inhalation, or irritate the respiratory tract, causing cough, asthma, breathing difficulties and other diseases; skin contact or cause allergies, redness, swelling, itching and even burns; accidental ingestion or damage to the digestive system, causing nausea, vomiting, abdominal pain, diarrhea, etc., more serious life-threatening.
Second, the risk of fire and explosion
Such diazonium compounds are usually unstable. When heated, rubbed and hit, they are very likely to decompose violently and release a lot of energy, which can cause fire and even explosion, posing a serious threat to surrounding personnel and facilities.
Third, environmental risk
If the substance accidentally leaks into the environment, it may cause pollution to soil, water, air, etc. due to its chemical properties. In the soil, or affect the soil microbial activity and plant growth; into the water body, or harm aquatic organisms, damage the balance of aquatic ecosystems.
IV. Risk of reactivity
2% 2C5 -diacetoxy-4- (morpholine-4-yl) quinoline diazotetrafluoroborate (2:1) Chemical properties are active and easy to react with other substances. Under improper conditions, contact with certain reducing agents, organic matter, etc., or trigger dangerous chemical reactions, causing rapid release of heat and gas, resulting in safety accidents.
In view of the above safety risks, when handling this chemical substance, it is necessary to strictly follow the safety operating procedures and take protective measures to ensure that personnel safety and the environment are not endangered.
1. Toxicity risk
This substance may be toxic, and exposure routes are diverse, such as inhalation of its dust, vapor, or skin contact, accidental ingestion, etc., may cause poisoning. After inhalation, or irritate the respiratory tract, causing cough, asthma, breathing difficulties and other diseases; skin contact or cause allergies, redness, swelling, itching and even burns; accidental ingestion or damage to the digestive system, causing nausea, vomiting, abdominal pain, diarrhea, etc., more serious life-threatening.
Second, the risk of fire and explosion
Such diazonium compounds are usually unstable. When heated, rubbed and hit, they are very likely to decompose violently and release a lot of energy, which can cause fire and even explosion, posing a serious threat to surrounding personnel and facilities.
Third, environmental risk
If the substance accidentally leaks into the environment, it may cause pollution to soil, water, air, etc. due to its chemical properties. In the soil, or affect the soil microbial activity and plant growth; into the water body, or harm aquatic organisms, damage the balance of aquatic ecosystems.
IV. Risk of reactivity
2% 2C5 -diacetoxy-4- (morpholine-4-yl) quinoline diazotetrafluoroborate (2:1) Chemical properties are active and easy to react with other substances. Under improper conditions, contact with certain reducing agents, organic matter, etc., or trigger dangerous chemical reactions, causing rapid release of heat and gas, resulting in safety accidents.
In view of the above safety risks, when handling this chemical substance, it is necessary to strictly follow the safety operating procedures and take protective measures to ensure that personnel safety and the environment are not endangered.
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