Molecular Formula | C22H23NO7 |
Molar Mass | 413.42 |
Density | 1.395 |
Melting Point | 174-176°C(lit.) |
Boling Point | 532.6°C (rough estimate) |
Specific Rotation(α) | -200 º (c=1 in chloroform) |
Flash Point | 308.5°C |
Water Solubility | 302.9mg/L(25 ºC) |
Solubility | Practically insoluble in water, soluble in acetone, slightly soluble in ethanol (96 per cent). It dissolves in strong acids; on dilution of the solution with water, the base may be precipitated. |
Vapor Presure | 4.83E-14mmHg at 25°C |
Appearance | Crystalline solid |
Color | Orthorhombic prisms or stout needles from alc |
Merck | 13,6752 |
pKa | 7.8(at 25℃) |
Storage Condition | -20°C Freezer, Under Inert Atmosphere |
Refractive Index | 1.5614 (estimate) |
Physical and Chemical Properties | Colorless crystalline powder or glossy prismatic or flaky crystals; Odorless and tasteless. Almost insoluble in water, slightly soluble in ethanol and ether, soluble in chloroform. |
Hazard Symbols | Xn - Harmful![]() |
Risk Codes | 22 - Harmful if swallowed |
Safety Description | 24/25 - Avoid contact with skin and eyes. |
UN IDs | 1544 |
WGK Germany | 3 |
RTECS | RD2625000 |
HS Code | 29329990 |
Hazard Class | 6.1(b) |
Packing Group | III |
Toxicity | cyt-ham:lng 100 mg/L ATSUDG (4),41,80 |
This product is (S-R 'S')]-6, 7-dimethoxy-3-(5,6, 7, 8-tetrahydro-6-methyl-4-methoxy-1, 3-dioxolene [4,5-g]-5-isoquinolyl)-1(3H)-isobenzofuranone. Calculated as dried product, the content of C22H23N07 shall not be less than 99.0%.
The melting point of this product (General 0612) is 174~177°C.
take this product, precision weighing, plus O. 1 mol/L hydrochloric acid solution was dissolved and quantitatively diluted to give a solution containing about 20mg per 1 ml, which was measured according to law (General 0621). The specific rotation was 42 ° to 48 °.
take 0.2g of this product, add acetone 10ml to dissolve, the solution should be clear and colorless; If the color is colored, compared with the yellow No. 2 Standard Colorimetric liquid (General rule 0901 first method), not deeper.
take this product, add the mobile phase to dissolve and dilute to make a solution containing lmg per lml as a test solution; Take lml for precision measurement and put it in a 100ml measuring flask, dilute to the scale with the mobile phase, shake, and serve as a control solution. According to the high performance liquid chromatography (General 0512) test, using eighteen alkyl silane bonded silica gel as filler; Methanol -0.lmol /L sodium dihydrogen phosphate solution (85:15) as mobile phase; The detection wavelength was 290nm. The number of the theoretical plates shall not be less than 2000 based on the calculation of the Ding peak. 20 u1 of test solution and 20 u1 of control solution were respectively injected into human liquid chromatograph, and the chromatogram was recorded to 2.5 times of the retention time of principal component peak. If there are impurity peaks in the chromatogram of the test solution, the sum of each impurity peak area shall not be greater than the main peak area of the control solution (1.0%).
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 about 0.3g of this product, precision weighing, add glacial acetic acid 10ml dissolved, add crystal violet indicator solution 1 drop, with perchloric acid titration solution (0.1 mol/L) titration to a clear blue color of the solution, and the results of the titration were corrected with a blank test. Each 1 ml of perchloric acid titration solution (0.1 mol/L) corresponds to 41.34mg of C22H23NO7.
antitussive drugs.
light shielding, sealed storage.
This product contains 93.0% ~ 107.0% of the label amount of nacrine (C22H23N07).
This product is sugar-coated tablets, White after removing the coating.
take an appropriate amount of fine powder of this product (about 20mg equivalent to that of nacrodine), add 10ml of chloroform, stir to dissolve nacrosine, filter, and evaporate the filtrate on a water bath, the residue showed the same reaction according to the test of identification (1) and (2) under the nacrine.
Take 30 tablets of this product, remove the coating, precision weighing, fine, precision weighing an appropriate amount (about equivalent to 0.lg), add chloroform 20ml, shake, dissolve nacropin, filter, wash the container and filter with chloroform for 8 times, 5ml each time, combine the wash solution and filtrate, add glacial acetic acid 10ml, crystal violet indicator solution 1 drop, titrated with perchloric acid titration solution (0.05mol/L) to a clear blue solution, and the titration results were corrected with a blank test. Per 1 ml of perchloric acid titration solution (0.05mol/L) corresponds to 20.67mg of C22H23N07.
same as that of Codin.
lOmg