Rocuronium bromide CAS NO.119302-91-9

product information

rocuronium bromide basic information

non-depolarizing muscle relaxants pharmacological effects pharmacokinetics indications clinical evaluation precautions chemical properties application production methods

product name:	rocuronium bromide
synonyms:	rocuronium bromide;[3-hydroxy-10,13-dimethyl-2-morpholin-4-yl-16-(1-prop-2-enyl-2,3,4,5-tetrahydropyrrol-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl] acetate bromide;rocuroniun bromide;1-[(2b,3a,5a,16b,17b)-17-(acetyloxy)-3-hydroxy-2-(4-morpholinyl)androstan-16-yl]-1-(2-propenyl)pyrrolidinium bromide;esmeron;org-9426;zemuron;rocuronium bromide／1-[17b-(acetyloxy)-3a-hydroxy2b-(4-morpholinyl)-5a-androstan-16b-yl]-1-(2-propenyl)pyrrolidinium bromide
cas:	119302-91-9
mf:	c32h53brn2o4
mw:	609.68
einecs:	214-776-5
product categories:	intermediates & fine chemicals;pharmaceuticals;acetylcholine receptor;heterocycles;steroids;steroid and hormone
mol file:	119302-91-9.mol

rocuronium bromide chemical properties

mp	162-1640c
storage temp.	room temp
cas database reference	119302-91-9(cas database reference)

safety information

msds information

rocuronium bromide usage and synthesis

non-depolarizing muscle relaxants	rocuronium bromide, together with pancuronium, vecuronium, atracurium, and pipecuronium are current commonly used several kinds of clinically non-depolarizing muscle relaxants with rocuronium bromide having the fastest onset which can provide the ideal conditions of muscle relaxant within 60~90 s. the binding between non-depolarizing muscle relaxants with motor endplate cholinergic receptor will not change the membrane potential of the motion endplate, but instead hinder the binding between acetylcholine and its receptors, and making muscle relaxation occur. the muscle relaxant drugs in the event before, unlike depolarizing muscle relaxants, won’t lead to muscle twitching caused by the contraction of muscle fiber bundles before the occurrence of muscle relaxation. rocuronium bromide is the derivative of vecuronium, and they have similar role. however, the strength of rocuronium bromide is only one seventh of that of vecuronium. intravenous injection of it has a rapid onset, with the cannula can be carried out within 60 to 90 seconds and the action being lasted as long as 30 to 40 minutes. it has no significant effect on vegetation nervous and cardiovascular, but can reduce the intraocular pressure. it has no histamine release effect and sympathetic ganglion blocking effect. it is commonly used in clinical tracheal intubation, can also be used for the maintenance of muscle relaxation in various kinds of surgeries. when being applied to cannula, use a single injection of 0.6mg/kg and a maintenance dose of 0.15mg/kg. this product can have cross-allergic reaction with other muscle relaxants, and thus should be used with caution. patients of liver and kidney dysfunction and the elderly people should use with caution.
pharmacological effects	neuromuscular junction includes motor nerve terminals and motor endplates. under physiological conditions, when the transmission of nerve impulses to the motor nerve terminals, causing the fusion of vesicle located at motor nerve terminal with the nerve membrane and further discharge of acetylcholine in the vesicular. after leaving the nerve terminal, acetylcholine binds to the acetylcholine receptors located at motor endplate, causing the open of ion channels, and the influx of na+, resulting in the depolarization of muscle cell, further triggering muscle contraction. according to the difference of muscle relaxants’ nerve impulse disturbances on neuromuscular binding regions, the muscle relaxants are classified into depolarizing muscle relaxants and non-depolarizing muscle relaxants. rocuronium bromide is a kind of non-depolarizing neuromuscular blocking agents with a similar chemical structure as vecuronium and pancuronium. being similar as other non-depolarizing drugs, it competitively binds to the cholinergic receptor located in the motor nerve terminals for antagonism of acetylcholine. this medicine is fast-acting, but acts more slowly than succinylcholine with a big range of safety. it has a long duration of action and is in dose-dependent manner. among the non-depolarizing neuromuscular blocking agents, rocuronium bromide has a most rapid onset with providing an excellent condition for the cannula after intravenous injection for as short as 60 s whose onset time is a bit longer than succinylcholine though, but is two times as fast as vecuronium and tracrium. therefore, for the inner rapid intubation, rocuronium bromide is a good alternative to succinylcholine. however, succinylcholine has a short duration (typically less than 10min) which is much shorter than this product which can last for at least 30min. in this perspective, vecuronium tracrium is similar as atracurium. compared with other muscle relaxants, the inhibition effect of rocuronium bromide on motor nerve terminal is weaker than that of d-tubocurarine chloride and pancuronium, but similar as vecuronium. intravenous anesthesia does not affect the neuromuscular blocking effect of the product nor influence the process. the median effective dose for children (ed50) and 95% effective doses are 170, 303μg/kg, respectively. after injection of the product for 600μg/kg, the onset time of 90% and 100% neuromuscular blocking are 0.8 and 1.3min, respectively. 25% recovery of neuromuscular conduction requires a time of 27min. elderly patients (over 70 years) has a similar onset time with young people, but has a prolonged reaction time, a reduced plasma clearance rate and volume of distribution. kidney transplant patients with renal failure have a longer volume of distribution and elimination half-life for this product than normal person. but there have been no evidences of prolonged intramuscular nerve blocking effect. for the neuromuscular blockage onset time of intravenous injection of this product for 0.6mg/kg, it is longer for patients suffering liver cirrhosis than normal patients (158s ± 56s to 108s ± 36s) with the elimination half-life being 97min ± 37min and 88min ± 18min, respectively.
pharmacokinetics	after intravenous injection, the relation of plasma concentration-time exhibits three indices with the average distribution half-life of 73 (66 to 80) minutes, the steady-state volume of distribution of 203 (119 ~ 214) ml/kg, plasma clearance rate being 3.9 (± 1.3) ml/kg/min. a comparative study shows that the elderly people and patients suffering liver disease or renal insufficiency have a decreased plasma clearance rate, but the change in most studies has no statistically significance. it has reported that some patients with liver disease have an average elimination half-life being prolonged for about 30 minutes. this product is mainly eliminated through biliary excretion. within several hours, 30% to 40% of the administrated drug is excreted as prototype through the bile.
indications	rocuronium bromide belongs to an adjuvant drug for general anesthesia used for tracheal intubation during routine induction of anesthesia for the maintenance of muscle relaxation of surgery.
clinical evaluation	in anesthetized patients, the strength of producing muscle relaxation effect of rocuronium bromide is 6-8 times weaker than that of vecuronium and atracurium 6-8 times but with a more rapid onset. this product is usually injected at a dose of 0.5 ~ 0.9mg/kg with producing a valid trachea inset effect within 1 minute and having a duration of action similar as vecuronium and atracurium. compared with succinylcholine, this product has a relatively rapid onset as well as a significantly prolonged clinical duration of action.
precautions	this product can lead to respiratory paralysis. thereby, the patient applied with this drug should apply artificial respiratory support before the full restoration of self-respiratory capability. because this product is always applied simultaneously with other drugs, even without the existence of known induced-drug during anesthesia, malignant hyperthermia can still occur. therefore, the clinicians should be familiar with its early signs and be able to accurately diagnose and treat malignant hyperthermia before any kinds of anesthesia. animal studies have demonstrated that rocuronium bromide is not a predisposing factor for malignant hyperthermia. the above information is edited by the chemicalbook of dai xiongfeng.
chemical properties	crystallization; melting temperature of 161~169 °c. [α] d20 + 18.7 ° (c = 1.03, chloroform).
application	1. it is a kind of muscle relaxants and a kind of non-depolarizing neuromuscular blocking agents. it is used as the adjuvant drugs for general anesthesia and conventional intubation of both inpatient and outpatient. it can keep the muscle relaxation during the process of mechanical ventilation and surgery. 2. it is used as a kind of skeletal muscle relaxants (non-depolarizing)
production methods	(2α, 3α, 5α, 16α, 17β) -2,3,16,17- diglycidyl androst-17-ol acetate (i) is refluxed together with aqueous solution of pyrrolidine for 1h, resulting in 17-ketone (ii ) and sodium borohydride; stir them together in methanol and perform reduction reaction to give compound (iii); reflux together with morphine solution for 3d to obtain compound (iv). partially acetylated, and then reacted with allyl bromide to obtain the product.
chemical properties	off-white solid
usage	aminosteroid, competitive neuromuscular blocker

company information

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