Molecular Formula | C6H6Cl2N2O4S2 |
Molar Mass | 305.16 |
Density | 1.7263 (rough estimate) |
Melting Point | 239-241° (patent, mp 228.5-229°) |
Boling Point | 590.5±60.0 °C(Predicted) |
Flash Point | 115.9°C |
Solubility | Acetonitrile (Slightly), Chloroform, DMSO (Slightly), Methanol |
Vapor Presure | 0.0079mmHg at 25°C |
Appearance | Solid |
Color | White to Off-White |
pKa | pKa 7.4 (Uncertain);8.6 (Uncertain) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.6000 (estimate) |
Physical and Chemical Properties | White or nearly white crystalline powder. Melting point 239-241 °c. Soluble in ethanol, soluble in alkaline solution, almost insoluble in water or chloroform. No odor, slightly bitter taste. |
Use | Used as an intermediate |
Hazard Symbols | Xn - Harmful |
Risk Codes | 63 - Possible risk of harm to the unborn child |
Safety Description | 36 - Wear suitable protective clothing. |
RTECS | CZ9200000 |
HS Code | 2935904000 |
The melting point of this product (General 0612) is 238~242.
This product is 4,5-two gas isophthalamide. Calculated as dry product, containing no less than 98.0% of C6H6C12N204S2.
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.277 ml | 16.385 ml | 32.77 ml |
5 mM | 0.655 ml | 3.277 ml | 6.554 ml |
10 mM | 0.328 ml | 1.638 ml | 3.277 ml |
5 mM | 0.066 ml | 0.328 ml | 0.655 ml |
take l.Og of this product, add 10ml of sodium hydroxide solution to dissolve, the solution should be clarified.
take 0.25g of this product, add 25ml of water, shake for 5 minutes, filter, take the filtrate to check according to law (General rule 0801), and compare with the control solution made of 7.0ml of standard sodium chloride solution, no more concentrated (0.028%).
take this product, add mobile phase to dissolve and dilute to make a solution containing 2mg per 1 ml as a test solution; Take appropriate amount of precision, A solution containing 40ug per 1 ml was prepared as a control solution by quantitative dilution with mobile phase. According to the test of high performance liquid chromatography (General rule 0512), silica gel bonded with decylsilane was used as the filler; Phosphate buffer solution was used (5.52 of water was added to dissolve the anhydrous disodium hydrogen phosphate 5.68g and sodium dihydrogen phosphate g).-Acetonitrile (1:1) as mobile phase; Detection wavelength was 280nm. The control solution 10 u1 was taken and injected into the human liquid chromatograph, and the flow rate was adjusted so that the retention time of the main peak was about 7 minutes. Then the test solution and the control solution are respectively injected into the liquid chromatograph, and the chromatogram is recorded to 2 times of the retention time of the main component peak.
Impurity peak, and the sum of each impurity peak area shall not be greater than the main peak area of the control solution (2.0%).
take this product, dry to constant weight at 105°C, weight loss shall not exceed 1.0% (General rule 0831).
not more than 0.1% (General rule 0841).
take this product L. 0g, inspection according to law (General Principles 0821 third law), containing heavy metals shall not exceed 10 parts per million.
take this product about 0.3g, precision weighing, according to the nitrogen determination method (General 0704 first method) determination. Each 1 ml of sulfuric acid titration solution (0.05mol/L) corresponds to 15.26mg of C6H6C12N204S2.
carbonic anhydrase inhibitor.
light shielding, sealed storage.
This product contains two gas phenalamine (C6H6Cl2N204S2) should be 93.0% to 107.0% of the label amount.
This product is white tablet.
should be in accordance with the relevant provisions under The tablet item (General rule 0101).
Take 10 tablets of this product, precision weighing, fine, precision weighing an appropriate amount (about 50mg equivalent to dichlorofinalamine), put it in a 100ml measuring flask, add 50ml of 0.4% sodium hydroxide solution, fully shake to dissolve the diamine, dilute to the scale with 0.4% sodium hydroxide solution, shake well, filter, and take a precise amount. Dilute the filtrate to a standard with 0.4% sodium hydroxide solution. Shake the filtrate to a standard, then use UV-Vis spectrophotometry (General rule 0401), the absorbance was measured at a wavelength of 284mn and calculated as the absorption coefficient of C6H6Cl2N204S2 was 43.4.
Same as dichlorofinamine.
25mg
light shielding, sealed storage.