Chemical Formula | C7H6F3N |
Molar Mass | 161.124 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 162 - 164 °C |
Density | 1.234 g/cm³ |
Flash Point | 52 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Odor | Aminic odor |
Refractive Index | 1.455 - 1.457 |
Chemical Formula | C7H6F3N |
Molar Mass | 161.124 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | Approx. 172 - 174 °C |
Density | 1.268 g/cm³ |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | Approx. 65 °C |
Odor | Aminelike odor |
What are the main uses of 3,4,5-trifluorobenzamine?
3,4,5-Trihydroxybenzoic acid, also known as gallic acid, has a wide range of main uses.
In the field of medicine, it has many effects. It can be used as an antibacterial drug, which has the effect of inhibiting many bacteria and fungi, and can help the human body resist the invasion of bacteria and maintain health. It also has antioxidant properties, which can remove free radicals in the body, slow down cell aging, and reduce the risk of disease.
In the food industry, it is a commonly used antioxidant. It can prevent oxidative deterioration of food, extend the shelf life, and has no adverse effects on food flavor, color, etc. In easily oxidized foods such as oils and meats, it can effectively prevent rancidity and discoloration.
In the chemical field, it is an important chemical raw material. It can be used to make ink, which can react with iron salts to form a black substance, making the ink write smoothly and have a long-lasting color. It can also be used as a tanning agent to help leather tanning and improve the quality and durability of leather.
In the cosmetic industry, it is used in skin care products due to its antioxidant and antibacterial properties. It can resist skin aging, reduce wrinkles and pigmentation, regulate skin oil secretion, and prevent skin problems such as acne.
In short, 3,4,5-trihydroxybenzoic acid plays an important role in many fields such as medicine, food, chemical industry, and cosmetics. With the development of science and technology, its application prospects will also be broader.
What are the physical properties of 3,4,5-trifluorobenzyl amine?
3,4,5-Trihydroxybenzoic acid, also known as gallic acid, has the following physical properties:
Gallic acid is white or light brown crystalline and has a slightly acidic taste. Its melting point is 253 ° C. When heated to 250 ° C, it will decompose into pyrogallic acid and carbon dioxide. It loses crystalline water at 100 ° C and has a density of 1.694g/cm ³.
This substance is slightly soluble in cold water, easily soluble in hot water, ethanol, ether, and also soluble in glycerol and acetone, but almost insoluble in benzene, chloroform, and petroleum ether. Its aqueous solution will appear blue-black when exposed to ferric chloride test solution, and it has strong reductivity, especially in alkaline media. Due to the presence of multiple hydroxyl groups in its molecules, gallic acid has a certain degree of hydrophilicity. At room temperature and pressure, gallic acid is relatively stable, but contact with strong oxidants should be avoided to prevent oxidation reactions. These physical properties make gallic acid unique in many fields. For example, in the field of medicine, it can be used as a raw material for antibacterial and antiviral drugs; in the food industry, it can be used as an antioxidant to extend the shelf life of food; in the chemical industry, it can also be used for the preparation of ink and other products.
Is the chemical properties of 3,4,5-trifluorobenzyl amine stable?
3,4,5-Trihydroxybenzaldehyde, which is an organic compound. The stability of its chemical properties needs to be viewed from multiple ends.
In terms of structure, the hydroxyl group and the aldehyde group coexist on a benzene ring. The hydroxyl group has the conjugation effect of electron giving, and the aldehyde group has the induction effect of electron withdrawing. The hydroxyl group can increase the electron cloud density of the benzene ring, making the benzene ring more prone to electrophilic substitution, which affects the stability of the substance to a certain extent. However, the conjugation system of the benzene ring itself gives it a certain stability.
From the perspective of reactivity, the aldehyde group is quite active, prone to oxidation, and can be oxidized to a carboxyl group, which significantly affects its stability. In case of common oxidants, such as oxygen in the air, under suitable conditions, the aldehyde group may be oxidized, causing its structure to change. Hydroxyl groups can also participate in many reactions, such as reacting with sodium metal to release hydrogen, and esterification reactions can also occur, which all indicate that their chemical properties are not extremely stable.
In addition, external environmental factors also affect its stability. When the temperature increases, the molecular thermal movement intensifies, the reactivity is enhanced, and the chemical reaction is more likely to occur, and the stability is reduced. Under light conditions, some compounds will undergo photochemical reactions due to photoexcitation, and 3,4,5-trihydroxybenzaldehyde may also be affected by this.
In summary, the chemical properties of 3,4,5-trihydroxybenzaldehyde are not very stable, and the activities of aldehyde and hydroxyl groups and external environmental factors can easily cause its structure and properties to change.
What are the preparation methods of 3,4,5-trifluorobenzyl amine?
3,4,5-Trihydroxybenzoic acid, also known as gallic acid, is prepared by many methods, and the following are common ones:
First, it is obtained by hydrolysis of gallnut. The gall is formed by the horned aphid or the egg aphid in its host salt skin wood, green bran poplar or red bran poplar and other trees. After crushing the gall, put it in an acid-resistant container, add water and add an appropriate amount of sulfuric acid, heat it to a specific temperature and maintain it for a period of time, the tannins in the gall will be hydrolyzed to form gallic acid and glucose. Then through neutralization, filtration, concentration, crystallization and other steps, pure gallic acid can be obtained. This method has a wide source of raw materials and a relatively mature process. However, it is necessary to pay attention to the use of sulfuric acid, and be careful when operating to prevent danger.
Second, the method of chemical synthesis. Using methyl gallate as raw material and hydrolyzing under alkaline conditions, gallic acid can be prepared. The specific operation is to dissolve methyl gallate in an appropriate amount of organic solvent, add a certain amount of alkali, and heat and reflux for a certain period of time. After the reaction is completed, the target product can be obtained after acidification, extraction, distillation and other treatments. The synthesis route of this method is clear, and the purity of the product is easy to control. However, the raw material methyl gallate needs to be prepared or purchased in advance, and the cost may be higher.
Third, biological fermentation method. Certain microorganisms have the ability to synthesize gallic acid. Select suitable strains, such as specific molds or bacteria, and culture medium containing tannins as the main carbon source. Under suitable temperature, pH value and other conditions, tannin can be converted into gallic acid during the growth and metabolism of microorganisms. After fermentation, gallic acid is harvested through solid-liquid separation, extraction, purification and other processes. This method is green and environmentally friendly, and the conditions are mild. However, the requirements for bacterial species screening and culture are quite high, and the fermentation process also needs to be precisely controlled.
What is the price range of 3,4,5-trifluorobenzamine in the market?
The price of 3,4,5-trihydroxybenzoic acid in the market is difficult to determine. The price of trihydroxybenzoic acid often varies due to various factors, such as the supply and demand of the market, the amount of production, the quality of the product, the difficulty of making it, and even the luck.
In the past, if the product was prosperous and the demand was small, the price might be quite low, only tens of dollars per catty; however, if the product was thin and prosperous, the price would rise sharply, or hundreds of dollars per catty, or even thousands of gold.
And its price varies from place to place. In the vicinity of the product, because it is easy to obtain, the price may be slightly cheaper; in the distance, after being transported and trafficked, all kinds of fees increase, and the price also rises.
In addition, the method of making also affects its price. If the method of making is simple and saves labor, the cost will drop, and the price will also drop; if the method of making is complicated and labor costs, the cost will be high, and the price will be higher.
Therefore, if you want to know the exact price, you should go to the city in person, consult various merchants, observe their supply and demand, and measure their various conditions, so that you can know the approximate price. However, this price is not constant, and you must always pay attention to it in order to get a real-time price.