Name | antazoline hydrochloride |
Synonyms | ANTAZOLINE HCL Antazoline HCL LABOTEST-BB LT00134672 antazoline hydrochloride Phenazoline hydrochloride 2-(N-PHENYL-N-BENZYL-AMINOMETHYL)-IMIDAZOLINE HCL 2-(N-BENZYLANILINOMETHYL) IMIDAZOLINE HYDROCHLORIDE 2-Phenyl-benzyl-amino-methylimidazolin hydrochloride 2-(N-BENZYLANILINOMETHYL)-2-IMIDAZOLINE HYDROCHLORIDE N-Benzyl-N-(2-imidazolin-2-ylmethy)aniline hydrochloride BENZYL-(4,5-DIHYDRO-1H-IMIDAZOL-2-YLMETHYL)-PHENYL-AMINE HCL 2-{[benzyl(phenyl)amino]methyl}-4,5-dihydro-1H-imidazol-3-ium |
CAS | 2508-72-7 |
EINECS | 219-719-8 |
InChI | InChI=1/C17H19N3/c1-3-7-15(8-4-1)13-20(14-17-18-11-12-19-17)16-9-5-2-6-10-16/h1-10H,11-14H2,(H,18,19)/p+1 |
Molecular Formula | C17H20ClN3 |
Molar Mass | 301.81 |
Melting Point | 238 °C |
Boling Point | 475.5°C at 760 mmHg |
Flash Point | 241.4°C |
Solubility | Soluble in water (100 mM), alcohol (40 mg/ml), methanol, and ethanol (50 mg/ml). Insolu |
Vapor Presure | 3.31E-09mmHg at 25°C |
Appearance | Powder |
Color | White to Off-White |
Merck | 14,680 |
Storage Condition | Inert atmosphere,Room Temperature |
MDL | MFCD00058145 |
Use | Anti-cholamine, with anticholinergic and local anesthetic effects, can be used for anti-allergic and anti-arrhythmic |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
WGK Germany | 3 |
RTECS | NJ2150000 |
This product is 4, 5-dihydro-n-phenyl-1-benzyl-1-imidazole-2-methylamine hydrochloride. The content of C17H19N3 • HCl shall not be less than 98.0% calculated on a dry basis.
take this product l.Og, add water 100ml to dissolve, according to the law (General 0631),pH value should be 5.0~6.5.
take this product, add mobile phase to dissolve and dilute to make about 0.1 mg of the solution was used as a test solution, and an appropriate amount was quantitatively diluted with a mobile phase to prepare a solution containing 1% per 1 ml as a control solution. According to the test of high performance liquid chromatography (General 0512), silica gel bonded with eighteen alkyl silane was used as the filler, and 0.02mol/L ammonium acetate solution (adjusted to pH 3.5 with glacial acetic acid)-methanol (57:43) as mobile phase, the detection wavelength was 242nm. The number of theoretical plates shall not be less than 5000 based on the calculation of the antazoline peak, and the separation degree between the antazoline peak and the adjacent impurity peak shall meet the requirements. 20ul of the test solution and the control solution were respectively injected into the human liquid chromatograph, and the chromatogram was recorded to 2 times of the retention time of the main 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).
take l.Og of this product and check it according to law (General rule 0841). The residue left shall not exceed 0.1%.
The residue left under the item of taking the ignition residue shall not contain more than 20 parts per million of heavy metal when examined by law (General rule 0821, Law II).
take this product about 0.2g, precision weighing, add glacial acetic acid 20ml, add mercury acetate test solution 5ml, according to the potential titration method (General rule 0701), with perchloric acid titration solution (0.1 mol/L) titration, 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 30.18mg of C17H19N3. Hc1.
antihistamines.
light shielding, sealed storage.
This product contains antazoline hydrochloride (C17H19N3 • HCI) should be 93.0% ~ 107.0% of the label amount.
This product is white tablet.
Take 20 tablets of this product, precision weighing, fine grinding, precision weighing an appropriate amount (equivalent to 0.lg of tarazoline hydrochloride), put it in a 200ml measuring flask, add 0.1 mol/L hydrochloric acid solution about 160ml, shake, warm to dissolve the antazoline hydrochloride, cool, with 0. Dilute 1 mol/L hydrochloric acid solution to the scale, shake well, filter, take 2ml of continuous filtrate accurately, put it in a 100ml measuring flask, use 0. Dilute 1 mol/L hydrochloric acid solution to the scale, shake well, as the test solution, according to UV-visible spectrophotometry (General 0401), at the wavelength of 241nm absorbance; separately take the reference product of antazoline hydrochloride, precision weighing, add 0.lmol/L hydrochloric acid solution is dissolved and quantitatively diluted to make a solution containing about 10ug per lml, which is determined and calculated by the same method.
The same as that of antazoline hydrochloride.
O.lg
light shielding, sealed storage.