As a leading 1,3-Benzenedicarboxamide, N,N'-Bis(2,3-Dihydroxypropyl)-5-[(Hydroxyacetyl)(2-Hydroxyethyl)Amino]-2,4,6-Triiodo-, (R*,S*)- 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 1,3-benzenedicarboxamide, N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodo-, (r *, s *) -
The 1% 2C3 - benzenedicarboxamide%2C + N% 2Cn% 27 - bis% 282% 2C3 - dihydroxypropyl% 29 - 5 - %5B%28hydroxyacetyl%29%282 - hydroxyethyl%29amino%5D - 2% 2C4% 2C6 - triiodo -% 2C +% 28r% 2A% 2Cs% 2A% 29 - has a complex chemical structure.
The main structure of this compound is 1,3 - benzodiformamide. At the 5th position of the benzene ring, there is an amino group composed of hydroxyacetyl group and 2 - hydroxyethyl group. And at the 2nd, 4th and 6th positions of the benzene ring, each is connected to an iodine atom. Furthermore, N and N 'positions are connected with 2,3-dihydroxypropyl groups, respectively. The label of% 28r% 2A% 2Cs% 2A% 29 - refers to the fact that the molecule contains a chiral center, and this chiral center configuration is a combination of r and s configurations.
From this point of view, this compound contains polyiodine atoms, or has specific chemical properties and applications, and because of the existence of chiral centers, it may affect its biological activity, solubility and many other properties. The polyhydroxyl part of its structure may also affect its physical and chemical properties, such as hydrophilicity.
What are the main uses of 1,3-benzenedicarboxamide, N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodo-, (r *, s *) -
1% 2C3 - benzenedicarboxamide, N, n '- bis (2,3 - dihydroxypropyl) - 5 - [ (hydroxyacetyl) (2 - hydroxyethyl) amino] - 2,4,6 - triiodo -, (r *, s *) - This substance is a special organic compound. Its main uses are quite extensive, and it is often used as a contrast agent in the field of medical imaging. Because the iodine atoms contained in it have good X-ray absorption properties, it can help doctors clearly observe the morphology, structure and blood flow of internal organs and tissues of the human body. In cardiovascular angiography, the vascular pathway can be accurately developed, allowing doctors to accurately determine whether there are stenosis, blockage and other lesions in blood vessels, so as to formulate treatment plans in time. In urography, it can help doctors understand the morphology and function of the kidney, ureter and bladder, which is of great significance for the diagnosis of urinary system diseases.
And in the field of scientific research, it may be used as a raw material or intermediate for specific chemical reactions. With its unique chemical structure, it can participate in many organic synthesis reactions, help scientists create new compounds, expand the research scope of organic chemistry, and provide the possibility for the development of more curative drugs and materials with excellent performance. This compound plays an indispensable role in the fields of medicine and scientific research.
What is the safety of 1,3-benzenedicarboxamide, N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodo-, (r *, s *) -
1% 2C3 - benzenedicarboxamide, N, n '- bis (2,3 - dihydroxypropyl) - 5 - [ (hydroxyacetyl) (2 - hydroxyethyl) amino] - 2,4,6 - triiodo -, (r *, s *) - This object is related to safety and is a crucial consideration. In the past, "Tiangong Kaiwu" said: "All things in the world need to be observed for their properties and their use in order to avoid disasters and seek safety." This substance is no exception.
In terms of safety characteristics, it needs to be carefully investigated. First, looking at its chemical composition, many functional groups are juxtaposed, and the existence of groups such as 2,3-dihydroxypropyl, hydroxyacetyl, and 2-hydroxyethyl may cause the substance to react with surrounding substances under specific conditions. For example, the method of casting in "Tiangong Kaiwu", the material touches or changes. If this substance encounters acid and alkali, it may cause chemical changes, or produce heat and gas, endangering safety.
Second, consider its toxicological properties. Although the specific toxicity data is not known in detail, it contains iodine and has a complex structure, which cannot be prevented. In the past, man-made substances were also afraid of the harm of poisons. This substance may enter the body through the mouth, skin, or respiratory tract, and may affect human organs, such as hurting the viscera, damaging qi and blood.
Third, in terms of storage and transportation safety. Because of its special chemical structure, there should be requirements for environmental conditions. If the temperature and humidity are improper, it may decompose and deteriorate. Just like the storage method of the objects contained in "Tiangong Kaiqi", it exists according to the nature. This substance also needs to be stored and transported in a suitable environment to prevent it from causing potential safety hazards due to changes in the environment.
What are the synthesis methods of 1,3-benzenedicarboxamide, N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodo-, (r *, s *) -
In order to obtain 1% 2C3-phthalamide, N, N '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodo-, (R *, S *) -this product, the synthesis method has also been explored in many ways throughout the ages.
In the past, or starting with benzene diformic anhydride, first use a specific reagent to react with hydroxyl-containing propyl compounds to form an amide structure. This process requires careful temperature control and the selection of suitable solvents to obtain better yields. As for the introduction of triiodine groups, iodization reagents are often used, and with the help of catalysts, they are gradually introduced through multiple reaction steps. The key 5 - [ (hydroxyacetyl) (2-hydroxyethyl) amino] part also needs to be carefully planned for synthesis.
During the reaction process, many factors can affect the purity and yield of the product. If the temperature is high, if it is too high, side reactions will occur frequently and the product will be impure; if it is too low, the reaction rate will be slow and take a long time. In addition, the nature of the solvent, the size of the polarity, and the solubility are all closely related to the progress of the reaction.
Today's synthesis method may be optimized on the basis of the past. If a more efficient catalyst is used, the reaction rate can be accelerated and the selectivity can be improved, so that the yield of the target product can be improved. Or in the reaction conditions, new technologies can be used to precisely adjust parameters such as temperature and pressure to make the reaction more smooth. And the means of separation and purification are constantly innovated to obtain high-purity products. All these are the keys to the synthesis of this compound, which requires careful study and careful practice by researchers to obtain satisfactory results.
1,3-benzenedicarboxamide, N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodo-, (r *, s *) - What are the advantages over other similar compounds
1% 2C3-benzodiformamide, N, N '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodo-, (R *, S *) - This product is superior to other similar compounds in terms of stability.
It has a unique molecular structure and can remain stable under changing environmental conditions. It is not easily deteriorated by external factors such as temperature and humidity, light, etc. This is one of its advantages.
Furthermore, solubility is also its advantage. In a variety of common solvents, it exhibits good solubility and can be rapidly and uniformly dispersed. When preparing various preparations, it greatly facilitates the operation process, making the preparation easier and smoother. Other compounds may be difficult to match.
In terms of pharmacological activity, this compound is outstanding. It can accurately act on specific targets, showing efficient pharmacological effects, and relatively minor side effects. In medical applications, it can bring better therapeutic effects to patients while reducing adverse reactions, which is beyond the reach of his analogues.
From a safety perspective, after many rigorous tests and verifications, its safety is quite high, and it has little obvious toxicity and irritation within the normal dosage range. It can provide users with a reliable safety guarantee, which is undoubtedly more advantageous than some similar substances.