Name | Pipecuronium bromide |
Synonyms | 257-740-4 Pipecurium bromide 4,4'-[(2b,3a,5a,16b,17b)-3,17-Bis(acetyloxy)androstane-2,16-diyl]bis(1,1-dimethylpiperazinium) Dibromide (2beta,9xi,14xi,16beta,17beta)-3,17-bis(acetyloxy)-2,16-bis(4,4-dimethylpiperazin-4-ium-1-yl)androstane dibromide (2beta,3alpha,5alpha,16beta,17beta)-3,17-Diacetoxy-2,16-bis(4,4-dimethylpiperazin-4-ium-1-yl)androstane dibromide (2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(acetyloxy)-2,16-bis(4,4-dimethylpiperazin-4-ium-1-yl)androstane dibromide 4,4'-((2Beta,3Alpha,5Alpha,16Beta,17Beta)-3,17-Bis(Acetyloxy)Androstane-2,16-Diyl)Bis(1,1-Dimethyl-Piperazinium) Dibromide |
CAS | 52212-02-9 |
EINECS | 257-740-4 |
InChI | InChI=1/C35H62N4O4.2BrH/c1-24(40)42-32-21-26-9-10-27-28(35(26,4)23-31(32)37-15-19-39(7,8)20-16-37)11-12-34(3)29(27)22-30(33(34)43-25(2)41)36-13-17-38(5,6)18-14-36;;/h26-33H,9-23H2,1-8H3;2*1H/q+2;;/p-2/t26?,27-,28?,29?,30+,31+,32?,33+,34+,35+;;/m1../s1 |
Molecular Formula | C35H62Br2N4O4 |
Molar Mass | 762.69918 |
Storage Condition | Room Temprature |
This product is 4,4 '-( 3a, 17b-dihydroxy-5a-andrographole-2b, 16B, dibasic release) BIS [1,1-dimethylpiperidine 3,17-diacetate. Pipecuronium bromide (C35H62Br2N404) should be between 97.0% and 102.0% based on anhydrous and solvent-free calculations.
take this product, weigh it precisely, add water to dissolve and quantitatively dilute it into a solution containing 10 mg pipecuronium bromide per 1 ml, and determine it according to law (General rule 0621), the specific rotation was 7.0 ° to 11.0 °.
take this product, add water to make a solution containing 2mg per lml, according to the law (General 0631),pH value should be 5.0~7.0.
take this product and add water to make a solution containing 2mg per lml. The solution should be clear, colorless or almost colorless.
take lOOmg of this product, put it in a 10ml measuring flask, add the mobile phase to dissolve and dilute to the scale, shake well, as a test solution; Take appropriate amount with precision, quantitative dilution with mobile phase was made to contain O per 1 ml. 1 mg solution, as a control solution. The control solution (1 ml) was accurately weighed, placed in a 20ml measuring flask, diluted to the scale with mobile phase, and shaken to obtain a sensitivity solution. According to the chromatographic conditions under the content determination item, the sensitivity solution 20ul is injected into the human liquid chromatograph, the signal and noise of the main component peak height is injected into the human liquid chromatograph, and the chromatogram is recorded to 4 times of the retention time of the main component peak. If there are impurity peaks in the chromatogram of the test solution, the area of a single impurity peak shall not be greater than the area of the main peak of the control solution (1.0%), the sum of each impurity peak area shall not be greater than 1.5 times (1.5%) of the main peak area of the control solution. The chromatographic peaks in the chromatogram of the test solution which are smaller than the main peak area of the sensitivity solution are ignored.
take this product about O.lg, precision weighing, put in 10ml headspace bottle, add water lml seal, shake to dissolve, as a test solution; Respectively, take alcohol, acetone, the appropriate amount of acetonitrile and tetrahydrofuran was precisely weighed and water was added to prepare the stock solution; The appropriate amount of dichloromethane was additionally precisely weighed and N,N-dimethylmethylimine was added to prepare the stock solution; accurately take appropriate amount of each stock solution, mix, and dilute with water to make a solution containing 0.3mg of methanol, 0.5mg of acetone, 0.041mg of acetonitrile, 0.06mg of dichloromethane and 0.072mg of tetrahydrofuran per 1 ml, precision take 1 ml into 10ml headspace bottle, sealed, as a reference solution. According to the test for determination of residual solvents (General rule 0861 second method), the capillary column fixed with 6% cyanopropyl phenyl-94% dimethyl polysiloxane was used as the column, and the temperature was increased by program, the initial temperature was 40°C, and the temperature was maintained for 6 minutes, then, the temperature was increased to 180°C at a rate of 10°C per minute for 5 minutes; The detector temperature was 250°C; The inlet temperature was 200°C; And the equilibrium temperature of the headspace bottle was 80°C; the equilibration time was 30 minutes. Take the reference solution into the headspace, the separation degree of each peak should meet the requirements. The test solution and the reference solution were injected by Headspace, and the chromatograms were recorded. According to the external standard method, the residual amount of methanol, acetone, acetonitrile, dichloromethane and tetrahydrofuran shall be in accordance with the provisions.
take this product, according to the determination of moisture (General 0832 first method 1), the water content shall not exceed 10.0%.
take this product 2.0g, inspection according to law (General Principles 0821 second law), containing heavy metals shall not exceed 20 parts per million.
measured by high performance liquid chromatography (General 0512).
silica gel bonded with decylsilane was used as the filler, and 0.02mol/L sodium heptane sulfonate solution (containing 0.5% triethylamine, adjusted to pH 3.5 with phosphoric acid)-methanol (49:51) as the mobile phase; the detection wavelength was 210nm. The number of theoretical plates shall not be less than 2000 according to the peak of pipecu bromide ammonium.
take an appropriate amount of this product, precision weigh, add mobile phase to dissolve and dilute to make a solution containing about 0.4mg per 1 ml, as a test solution, take 20ul for precision, injection of human liquid chromatograph, record chromatogram; Another appropriate amount of pipecuronium bromide reference substance, the same method for determination. According to the external standard method to calculate the peak area, that is.
muscle relaxant.
sealed and stored in a cool and dry place.
This product is a sterile freeze-dried product prepared by adding appropriate amount of pipecuonium bromide and mannitol, containing pipecuonium bromide (C35H62Br2N404) should be 90.0% ~ 110.0% of the label amount.
This product is white or off-white powder.
with pipecuonium bromide.
4mg
It was sealed and stored in a dry place at 2-8°C.
дЄ≠жЦЗеРНзІ∞: | еУМеЇУжЇійУµ |
дЄ≠жЦЗеРМдєЙиѓН: | еУМеПѓжЭЊ;4,4'-[(2ќТ,3ќС,5ќС,16ќТ,17ќТ)-3,17-еПМ(дєЩйЕ∞ж∞ІеЯЇ)йЫДзФЊзГЈ-2,16-дЇЪеЯЇ]еПМ(1,1-дЇМзФ≤еЯЇеУМеЧ™йФЪ)дЇМжЇіеМЦзЙ©;еУМеЇУжЇійУµ;йШњзЂѓ;жЇіеМЦеР°еУМиАГе∞Љ |
иЛ±жЦЗеРНзІ∞: | Pipecuronium bromide |
иЛ±жЦЗеРМдєЙиѓН: | pipecuronium bromide;4,4'-((2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(acetyloxy)androstane-2,16-diyl)bis(1,1-dimethyl-piperazinium) dibromide;4,4'-[(2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(acetoxy)androstane-2,16-diyl]bis[1,1-dimethylpiperazinium] dibromide;PIPECURIUM BROMIDE;Pipecuronium;PIPECURINIUM BROMIDE;4пЉМ4вАЩ-[(2ќ≤пЉМ3ќ±пЉМ5ќ±пЉМ16ќ≤пЉМ17ќ≤)-3пЉМ17-Bis(acetoxy)andrc~tane-2пЉМ16-diyl]bis(1пЉМ1-dimethylpiperazinium)dibromide;Ardtm |
CASеПЈ: | 52212-02-9 |
еИЖе≠РеЉП: | C35H62Br2N4O4 |
еИЖе≠РйЗП: | 762.69918 |
EINECSеПЈ: | 257-740-4 |
зЫЄеЕ≥з±їеИЂ: | иВМиВЙжЭЊеЉЫиНѓ;йЇїйЖЙзФ®иНѓ;иНѓзЙ©;еОЯжЦЩиНѓ |
MolжЦЗдї∂: | 52212-02-9.mol |
зЖФзВє | 262-264¬∞ (dec) |
жѓФжЧЛеЕЙеЇ¶ | D25 +8.1¬∞ (c = 1 in water) |
ж¶Вињ∞ | еУМеЇУжЇійУµ(PipecuroniumBromide)еПИеРНењЕеПѓжЭЊпЉМдЄЇеРЂжЬЙдЄ§дЄ™е≠£йУµзЪДзФЊз±їеМЦеРИзЙ©пЉМе±ЮйХњжХИйЭЮеОїжЮБжАІиВМиВЙжЭЊеЉЫз±їиНѓзЙ©гАВеУМеЇУжЇійУµдЄїи¶БдљњзФ®дЇОеЕ®иЇЂйЇїйЖЙињЗз®ЛдЄ≠иВМиВЙжЭЊеЉЫпЉМе§ЪзФ®дЇОжЧ∂йЧіеЬ®40еИЖйТЯдї•дЄКзЪДжЙЛжЬѓйЇїйЖЙпЉМзЙєеИЂжШѓеЇФзФ®дЇОењГи°АзЃ°зЦЊзЧЕжВ£иАЕеБЪењГи°АзЃ°жИЦйЭЮењГи°АзЃ°з≠ЙжЙЛжЬѓдЄ≠гАВ |
зФЯзЙ©жіїжАІ | Pipecuronium bromide жШѓдЄАзІНжЬЙжХИзЪДйХњжХИйЭЮеОїжЮБеМЦзФЊдљУз•ЮзїПиВМиВЙйШїжїЮеЙВ (NMBA)пЉМжШѓдЄАзІНеПМе≠£йУµеМЦеРИзЙ©гАВPipecuronium bromide жШѓдЄАзІНеКЯиГљеЉЇе§ІзЪДзЂЮдЇЙжАІ nAChR жЛЃжКЧеЙВпЉМKd дЄЇ 3.06 ќЉMгАВ |
йЭ∂зВє | nAChR |
дљУе§Цз†Фз©∂ | Sugammadex has a high affinity for Pipecuronium bromide. As Pipecuronium bromide is about 6 to 7 times more potent than Rocuronium, fewer molecules are required to achieve a comparative blockade than in the case of Rocuronium. |
дљУеЖЕз†Фз©∂ | The average ED 95 is 0.045mg/kg (0.035-0.059 mg/kg) of Pipecuronium bromide, the onset of action varies between 2 and 6.3 minutes, depending on the dose and the background anesthesia. Pipecuronium bromide does not liberate histamine, it has no cardiovascular side effects even in doses of 3√Ч ED 95 , and anaphylaxis does not appear to be a problem. Carboxymethylated ќ≥-cyclodextrin shows efficient and complete reversal of the Pipecuronium bromide induced neuromuscular block in an ex vivo rat diaphragm experiment. |
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жѓТжАІ | LD50 in mice, rats (mg/kg): 29.7, 172.6 i.v.; 70.6, 449.6 i.p.; 60.5, 455.8 s.c. (K√°rp√°ti, Biro) |
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