Name | diatrizoic acid |
Synonyms | Diatrizoic acid diatrizoic acid DIATRIZOIC ACID USP DIAZTRIZOICACID,DIHYDRATE DIATRIZOIC ACID DIHYDRATE DIATRIZOICACID,DIHYDRATE,USP 3,5-DIACETAMIDO-2,4,6-TRIIODOBENZIOCACID 3,5-Diacetamido-2,4,6-triiodobenzoic acid 3,5-Diacetamido-2,4,6-triiodobenzioc acid 3,5-bis(acetylamino)-2,4,6-triiodobenzoic acid Benzoic acid, 3,5-bis(acetylamino)-2,4,6-triiodo-, dihydrate 3,5-DIACETAMIDO- 2,4,6-TRIIODOBENZOIC ACID (DIATRIZOIC ACID DIHYDRATE) |
CAS | 50978-11-5 117-96-4 |
EINECS | 204-223-6 |
InChI | InChI=1S/C11H9I3N2O4/c1-3(17)15-9-6(12)5(11(19)20)7(13)10(8(9)14)16-4(2)18/h1-2H3,(H,15,17)(H,16,18)(H,19,20) |
InChIKey | JHQKUXXJPHSPOL-UHFFFAOYSA-N |
Molecular Formula | C11H9I3N2O4.2H2O |
Molar Mass | 649.93 |
Density | 2.619g/cm3 |
Boling Point | 614.1°C at 760 mmHg |
Flash Point | 325.2°C |
Solubility | Very slightly soluble in water and in ethanol (96 per cent). It dissolves in dilute solutions of alkali hydroxides. |
Vapor Presure | 6.19E-16mmHg at 25°C |
Appearance | neat |
pKa | pKa 3.4 (Uncertain) |
Storage Condition | 2-8°C |
Refractive Index | 1.802 |
Physical and Chemical Properties | Colorless crystalline powder, odorless, slightly bitter taste. Melting point> 300 °c. Insoluble in water, ethanol-soluble, insoluble in ether, soluble in sodium hydroxide solution and sodium salt formation. FIG. 1 shows the structural formula of pantothenic acid. |
Use | Diagnostic medication for urography, cardiovascular, cerebral and peripheral vascular imaging |
WGK Germany | 3 |
HS Code | 2924296000 |
This product is 3, 5-diacetamido-2, 4, 6-triiodobenzoic acid dihydrate. Calculated as dry product, containing C11H913N2O, not less than 98.5%.
take l.Og of this product, add water 20ml, shake for several minutes, filter, and determine according to law (General rule 0631), the pH value should be 2.5~3.5.
take 4.8g of this product, Add 10ml of sodium hydroxide solution to dissolve the solution should be colorless; If the color is colored, compare with the control solution (take 5ml of Yellow 3 or orange 2 Standard Colorimetric solution, add 5ml of water, shake well) comparison, not deeper.
take 2.0ml of the solution under the color of the alkaline solution, dilute it to 10ml with water, add dilute acetic acid until it is acidic to litmus paper, and add potassium iodide 0. = 5G, after shaking and dissolving, add 1ml of starch indicator solution, shake well; If color is developed, compare with the control solution (take the same amount of sample, use the same method, water lm = l instead of starch indicator liquid lml) comparison should not be deeper.
take 2.0g of this product, add 4ml of sodium hydroxide solution to dissolve, Add 30ml of water, Dropwise add 3ml of dilute nitric acid, stir for several minutes, make the diatrizoate acid precipitate, filter, and wash the precipitate with a small amount of water, combine the washing solution and filtrate, dilute to 50ml with water, shake well, and filter repeatedly if necessary; Separate the filtrate to 20ml and check with chloride method (General rule 0801), not more concentrated (0.005%) than the control solution made from of standard sodium chloride solution.
Take 20ml of the remaining filtrate under the halide item, add 1ml of chloroform, 3ml of dilute nitric acid and 1ml of concentrated hydrogen peroxide solution, shake, stand and delaminate, if the chloroform layer is colored, with 0.0013% potassium chloride solution (equivalent to 10ug of 1 per 1ml) 2.0ml after adding water to 20ml, the control solution prepared by the same method should not be deeper (0.0025%).
take this product l. Add 5ml water and 5ml sodium hydroxide solution to dissolve, add water to 100ml, shake, take 10ml, add sodium nitrite titration solution (0.lmol/L) 5ml with hydrochloric acid solution (9-100)l0ml, shake, place for 10 minutes, add 2.5% Ammonium sulfamate solution 5ml, shake, place for 5 minutes, add 2ml of basic naphthol test solution and 15ml of sodium hydroxide test solution, add water to 50ml, shake well, measure absorbance at the wavelength of 485nm according to UV-visible spectrophotometry (General rule 0401), not more than 0.25.
take this product, add methanol-concentrated ammonia solution (97:3) to dissolve and dilute to make a solution containing about 50mg per 1 ml, as a test solution; Take an appropriate amount of precision, quantitative dilution with methanol-concentrated ammonia solution (97:3) was made to contain O per 1 ml. 1 mg solution, as a control solution. According to the thin layer chromatography (General 0502) test, absorb the above two solutions each 5 u1, respectively, on the same high performance silica gel GF254 thin layer plate, with anhydrous formic acid-methyl ketone-toluene (20:25:60) is the developing solvent. After spreading, it is dried and inspected under UV light (254nm). Test solution such as impurity spots, compared with the control solution of the main spot, not deeper.
take this product, dry to constant weight at 130°C, weight loss shall not exceed 6.0% (General rule 0831).
take l.Og of this product and check it according to law (General rule 0841). The residue left shall not exceed 0.1%.
take the residue left under the item of ignition residue, add hydrochloric acid (lml), dry on a water bath, add a proper amount of dilute hydrochloric acid (lml) and water, heat on the water bath, filter, wash the Crucible with water, the filtrate and the washing solution are combined and added with water to make 25ml, which shall be checked according to law (General rule 0807), and shall not be deeper (0.001%) compared with ml of standard iron solution prepared by the same method.
This product l.Og, inspection according to law (General Principles 0821 second law), containing heavy metals shall not exceed 10 parts per million.
take this product about 0.4g, precision weighing, Add 30ml of sodium hydroxide solution and zinc powder l.Og, refluxing for 30 minutes, cooling, condenser tube with a small amount of water washing, filtering, flask and filter water washing 3 times, each 15ml, combined wash and filtrate, add 5ml of glacial acetic acid and 5 drops of eosin sodium indicator solution, and use silver nitrate titration solution (0.lmol/L titration. Each 1 ml of silver nitrate titration solution (0.1 mol/L) corresponds to 20.46mg of C1H913N204.
diagnostic medication.
light shielding, sealed storage.
This product is a sterilized aqueous solution made of diatrizoate acid and isomolecular meglumine. Containing meglumine diatrizoate (C11H9I3N204 • C7H17N05) shall be between 95.0% and 105.0% of the labeled amount.
This product is colorless to light yellow clear liquid.
take an appropriate amount of this product (about 6g equivalent to meglumine diatrizoate), put it in a 100ml measuring flask, dilute it with water to the scale, shake it well, and take 10ml for precision measurement, according to the method under the item of diatrizoate acid, from "Add 30ml of sodium hydroxide test solution and 1.0g of zinc powder", the determination was carried out according to law. Each 1 ml of silver nitrate titration solution (0.1 mol/L) corresponds to 26.97mg of C11H9I3N204 .C7H17N05.
diagnostic medication.
light shielding, closed storage.
This product is a sterilized aqueous solution after neutralized with sodium hydroxide. Containing sodium diatrizoate (C11H9I3N204) shall be between 95.0% and 105.0% of label load.
This product is colorless to light yellow clear liquid.
take an appropriate amount of this product (about 5g of sodium diatrizoate), put it in a 100ml measuring flask, dilute it with water to the scale, shake it well, and take 10ml for precision measurement, according to the method under the item of diatrizoate acid, from "Add 30ml of sodium hydroxide test solution and 1.0g of zinc powder", the determination was carried out according to law. Each 1 ml of silver nitrate titration solution (0.1 mol/L) corresponds to 21.20mg of C11H8I3N2Na04.
diagnostic medication.
(l ) lml:0.3g (2)20ml:10g
light shielding, closed storage.
use | pantothenic acid is a diagnostic drug and contrast agent. But pantothenic acid is not directly used for angiography, but is formulated into sodium pantothenate and meglumine diatrizoate injection for clinical angiography, used for urinary tract, cardiovascular, cerebrovascular and peripheral angiography. For usage, refer to sodium pantothenate and meglumine diatrizoate. Do not use it for those who are allergic to iodine. diagnostic medication, used for urinary system, cardiovascular, cerebral tube and peripheral angiography |
sodium pantothenate | sodium pantothenate is an iodine benzoic acid salt, ionic hypertonic contrast agent. After intravenous injection, it is quickly filtered through the glomerulus in its original shape and excreted with urine. This product has low viscosity and large adverse reactions. It is not suitable for angiography. It is often combined with meglumine diatrizoate for angiography. After oral administration, it is less absorbed from the gastrointestinal tract. After intravenous injection and plasma protein binding is not obvious. The highest distribution in the body is in the kidney, followed by the liver, spleen, stomach, small intestine, heart, large intestine and muscle. There are still trace amounts in the blood circulation, which can be maintained for about 4 days. 95% of the dose is discharged from the urine through the kidney in its original form, 1% ~ 2% is discharged from feces, and a very small amount can be detected in tears and saliva. Drugs can also enter the placenta and milk. [Purpose] Mainly used for urography, also used for cardiac large blood vessels and peripheral angiography, retrograde pyelography, and can be injected into the organ cavity or fistula angiography. [usage and dosage] 1. intravenous pyelography: 20~30ml of 50% injection, slow intravenous injection for 1~3 minutes, and photography for 5, 10 and 15 minutes after injection. 2. retrograde pyelography: dilute into 20% solution with sterilized water for injection, use 6~10ml on one side, and reduce it for children. 3. cardiac angiography: 40ml 50%, rapid intravenous injection. 4. peripheral angiography: 50% injection, 40ml for arteriography, 20ml for upper limb venography and 10ml for lower limb venography. [adverse reactions] many adverse reactions of pantothenate can be attributed to the high osmotic pressure produced by its ionic drugs. In addition, the use of contrast agents, injection speed, drug concentration, volume and viscosity, etc., are closely related to the adverse reactions. Most adverse reactions occur within 5~10 minutes after drug injection, but they can also be delayed. |
contrast agent | contrast agent is one of the most commonly used drugs in interventional radiology and is mostly excreted by the kidneys. As an ideal contrast agent, it should have the following characteristics: ① high content of contrast components; ② simple synthesis and high yield; ③ good stability in vitro and in vivo; ④ infinite water solubility; ⑤ low viscosity; ⑥ no biological activity. In the 1940s and 1950s, in order to improve the safety of contrast agents, ionic contrast agents such as pantothenic acid, iodaric acid, and methylpantothenic acid were invented. This is the first breakthrough in the development of modern contrast agents. These contrast agents have low toxicity and high concentration, and are suitable for urography. From the late 60s to the early 70s, a non-ionic monomer contrast agent, mepanthumine, appeared, characterized by low osmotic pressure and good tolerance. This is the first generation of non-ionic contrast agents and the development of modern contrast agents. The second breakthrough. In view of the shortcomings of the first generation of non-ionic contrast agents such as unstable performance, from the mid-1970s to the 1980s, the second and third generation of new non-ionic contrast agents were successively developed, namely iopamidol, Iohexol, Youweixian, Aesoxian, etc. These contrast agents have the advantages of low toxicity, stable performance, isotonic, and good tolerance. This is the third breakthrough in the development of modern contrast agents. The successful development and development of contrast agents have promoted the progress of imaging technology and the development of interventional radiology. |
Preparation method | It is prepared by iodination of m-diaminobenzoic acid and iodine monochloride, and then acylation with acetic anhydride. |