Chemical Properties Clinical evaluation Pharmacological effects Uses Mechanism of action Pharmacokinetics Indications Precautions Production methods Non-depolarizing muscle relaxants
ChemicalBook > CAS DataBase List > Rocuronium bromide

Rocuronium bromide

Chemical Properties Clinical evaluation Pharmacological effects Uses Mechanism of action Pharmacokinetics Indications Precautions Production methods Non-depolarizing muscle relaxants
Product Name
Rocuronium bromide
CAS No.
119302-91-9
Chemical Name
Rocuronium bromide
Synonyms
Zemuron;Esmeron;1-[17B-(acetyloxy)-3a-hydroxy-2B-(4-morpholinyl)-;1-[(2b,3a,5a,16b,17b)-17-(Acetyloxy)-3-hydroxy-2-(4-morpholinyl)androstan-16-yl]-1-(2-propenyl)pyrrolidinium Bromide;Rocuronium Bromide/1-[17B-(acetyloxy)-3a-hydroxy2B-(4-morpholinyl)-5a-androstan-16B-yl]-1-(2-propenyl)pyrrolidinium bromide;Eslax;Org-9426;Esmeron:Zemuron;ROCURONIUM BROMIDE;ROCURONIUN BROMIDE
CBNumber
CB2222507
Molecular Formula
C32H53BrN2O4
Formula Weight
609.68
MOL File
119302-91-9.mol
More
Less

Rocuronium bromide Property

Melting point:
162-1640C
alpha 
D20 +18.7° (c = 1.03 in CHCl3)
storage temp. 
Inert atmosphere,2-8°C
solubility 
H2O: soluble100mg/mL, clear, light yellow
form 
Powder to Crystal
color 
White to Yellow
Merck 
14,8246
Stability:
Hygroscopic
InChIKey
OYTJKRAYGYRUJK-FMCCZJBLSA-M
CAS DataBase Reference
119302-91-9(CAS DataBase Reference)
More
Less

Safety

WGK Germany 
3
HS Code 
2934990002
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H312Harmful in contact with skin

H330Fatal if inhaled

H331Toxic if inhaled

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P284Wear respiratory protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P310Immediately call a POISON CENTER or doctor/physician.

P311Call a POISON CENTER or doctor/physician.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P320Specific treatment is urgent (see … on this label).

P321Specific treatment (see … on this label).

P322Specific measures (see …on this label).

P330Rinse mouth.

P363Wash contaminated clothing before reuse.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
R5155
Product name
Rocuronium bromide
Purity
≥98% (perchloric acid titration)
Packaging
50mg
Price
$153
Updated
2024/03/01
Sigma-Aldrich
Product number
PHR2397
Product name
Rocuronium Bromide
Purity
Pharmaceutical Secondary Standard; Certified Reference Material
Packaging
500MG
Price
$194
Updated
2024/03/01
Sigma-Aldrich
Product number
1604905
Product name
Rocuronium bromide
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
250mg
Price
$436
Updated
2024/03/01
TCI Chemical
Product number
R0099
Product name
Rocuronium Bromide
Purity
>98.0%(T)
Packaging
100mg
Price
$132
Updated
2024/03/01
Cayman Chemical
Product number
23698
Product name
Rocuronium (bromide)
Purity
≥98%
Packaging
5mg
Price
$32
Updated
2024/03/01
More
Less

Rocuronium bromide Chemical Properties,Usage,Production

Chemical Properties

Crystallization; melting temperature of 161~169 °C. [α] D20 + 18.7 ° (C = 1.03, chloroform).

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.

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.

Uses

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)

Mechanism of action

It was designed to be a weaker antagonist at the neuromuscular junction than pancuronium; hence its monoquaternary structure and its having an allyl group and a pyrrolidine group attached to the D ring quaternary nitrogen atom. Rocuronium has a rapid onset and intermediate duration of action.
There is considered to be a risk of allergic reaction to the drug in some patients (particularly those with asthma), but a similar incidence of allergic reactions has been observed by using other members of the same drug class (non-depolarizing neuromuscular blocking drugs).
The γ-cyclodextrin derivative sugammadex (trade name Bridion) has been recently introduced as a novel agent to reverse the action of rocuronium.Sugammadex has been in use since 2009 in many European countries; however, it was turned down for approval twice by the US FDA due to concerns over allergic reactions and bleeding,but finally approved the medication for use during surgical procedures in the United States on December 15, 2015. Neostigmine can also be used as a reversal agent of rocuronium but is not as effective as sugammadex. Neostigmine is often still used due to its low cost compared with sugammadex.

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.

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.

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.

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.

Chemical Properties

Off-white Solid

Uses

A non-depolarizing neuromuscular blocker used in anesthesia to help insert breathing tubes.

Uses

Aminosteroid, competitive neuromuscular blocker

Description

Rocuronium bromide is a short-acting nondepolarizing steroidal neuromuscular blocker introduced in the U.S.A as Zemuron and in the United Kingdom as Esmeron. k is indicated for use as an adjunct to general anesthesia to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. Rocuroniurn bromide has a significantly more rapid onset than other intermediate acting neuromuscular blockers, comparable to succinylcholine but with a very stable cardiovascular profile and has an improved side effect profile. It has been reported that good to excellent intubation conditions were achieved only one minute after a bolus dose of 600μg/kg of rocuronium bromide. It has a short duration of action, therefore, is useful for rapid sequence intubation without unacceptable delays in the spontaneous recovery of neuromuscular function.

Originator

Organon (Netherlands)

Uses

Aminosteroid, competitive neuromuscular blocker.

Definition

ChEBI: Rocuronium bromide is the organic bromide salt of a 5alpha androstane compound having 3alpha-hydroxy-, 17beta-acetoxy-, 2beta-morpholino- and 16beta-N-allyllyrrolidinium substituents. It has a role as a neuromuscular agent and a muscle relaxant. It is an organic bromide salt and a quaternary ammonium salt. It contains a rocuronium. It derives from a hydride of a 5alpha-androstane.

brand name

Zemuron (Organon).

Biological Functions

Rocuronium bromide (Zemuron) is a recently approved amino steroid neuromuscular blocking agent. It has a rapid onset of action (1 minute), but its duration of action is intermediate (55 minutes), about that of vecuronium. On rare occasions, it may release histamine and cause cardiac irregularities. Rapacuronium bromide (Raplon) is the most recent neuromuscular blocking agent approved by the United States Food and Drug Administration (FDA). It is an analogue of vecuronium and is thus categorized as an amino steroid. It has a rapid onset of action (1.5 minutes) and a short to intermediate duration of action (20 minutes).This makes it a suitable alternative to mivacurium or succinylcholine for short procedures. It is eliminated mainly by the liver.Adverse effects are dose dependent; they include tachycardia, hypotension, and bronchospasm. These effects may be related to the ability of the drug to release a small amount of histamine.

Clinical Use

Muscle relaxant in general anaesthesia, medium duration

Side effects

Common side effects of Rocuronium bromide include anaphylactic reactions, residual neuromuscular weakness, critical illness myopathy and polyneuropathy. Systemic anaphylactic reactions should be suspected in any patient who develops sudden cardiovascular collapse with cutaneous signs of anaphylactic reaction after Rocuronium bromide administration. Adverse effects of residual neuromuscular blockade have been shown to increase postoperative morbidity and mortality. The inability to fully reverse the effects of neuromuscular blockade may result in an increased risk of postoperative respiratory dysfunction, including hypoxia, need for mechanical ventilation, and increased length of hospital stay. Prolonged infusion of neuromuscular blockade may prolong skeletal muscle weakness due to myopathy caused by critical illness, in patients on steroids or with multiple organ failure. Rocuronium bromide has been shown to be very stable and has no effect on heart rate or blood pressure.

Safety

Limited information on the use of rocuronium during breastfeeding indicates that no adverse infant effects occur. Because it is short acting, highly polar and poorly absorbed orally, it is not likely to reach the breastmilk in high concentration or to reach the bloodstream of the infant. When a combination of anesthetic agents is used for a procedure, follow the recommendations for the most problematic medication used during the procedure. General anesthesia for cesarean section using rocuronium as a component may delay the onset of lactation.

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced muscle relaxant effect.
Anti-arrhythmics: procainamide enhances muscle relaxant effect.
Antibacterials: effect enhanced by aminoglycosides, clindamycin, polymyxins and piperacillin.
Antiepileptics: muscle relaxant effects antagonised by carbamazepine; effects reduced by long-term use of fosphenytoin and phenytoin but might be increased by acute use.
Botulinum toxin: neuromuscular block enhanced (risk of toxicity).

Metabolism

Rocuronium is metabolised by the liver to a less active metabolite, 17-desacetylrocuronium which is reported to have weak neuromuscular blocking effect.
Up to 40% of a dose may be excreted in the urine within 24 hours; rocuronium is also excreted in the bile. After injection of a radiolabelled dose of rocuronium bromide, excretion of the radiolabel is on average 47% in urine and 43% in faeces after 9 days. Approximately 50% is recovered as the parent compound. No metabolites are detected in plasma.

Rocuronium bromide Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Rocuronium bromide Suppliers

Jinan Sunshine Pharmaceutical Co.,Ltd.
Tel
531-82812892
Fax
0531-82812892
Email
sunshinepharm0531@163.com
Country
China
ProdList
68
Advantage
58
Yunfei Pharmaceutical(Shenzhen) Co., Ltd.
Tel
0755-61160828 15994832653
Fax
0755-61160828
Email
hulixiu@yunfeipharma.com
Country
China
ProdList
249
Advantage
58
Shandong RuiYue Biotechnology Co., Ltd.
Tel
0531-88581623 18805314509
Fax
0531-88581623
Email
1456922171@126.com
Country
China
ProdList
68
Advantage
50
Nanjing zehe Pharmaceutical Technology Co., Ltd
Tel
17768115366
Email
henry124604479@163.com
Country
China
ProdList
289
Advantage
58
Shanghai Yatan Pharmaceutical Research and Development Co. LTD
Tel
021-58003085 15865876430
Fax
QQ1060196522
Email
hujy@neutanpharma.com
Country
China
ProdList
291
Advantage
58
Beijing Mesochem Technology Co., Ltd.
Tel
010-57862036 18811083386
Email
msales@mesochem.com
Country
China
ProdList
188
Advantage
58
Beijing Zhongshuo Pharmaceutical Technology Development Co., Ltd
Tel
010-53679529 13801208576
Fax
010-64215766
Email
sales.2@chinazhongshuo.com
Country
China
ProdList
100
Advantage
65
YICHANG TIANRUI BIOPHARM CO., LTD
Tel
0717-4065884 18671799682
Email
yctr@renfu.com.cn
Country
China
ProdList
25
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6013
Advantage
61
More
Less

View Lastest Price from Rocuronium bromide manufacturers

Biopole Pharmatech Co., Ltd.
Product
Rocuronium bromide 119302-91-9
Price
US $0.00/g
Min. Order
1g
Purity
0.99
Supply Ability
100kg
Release date
2024-01-19
Hebei Yanxi Chemical Co., Ltd.
Product
Rocuronium Bromide 119302-91-9
Price
US $3000.00/kg
Min. Order
10kg
Purity
99.0%~101.0%
Supply Ability
100kg/month
Release date
2023-09-08
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Rocuronium bromide 119302-91-9
Price
US $0.00/g
Min. Order
1g
Purity
98%-102%; USP
Supply Ability
10KGS
Release date
2021-07-30

119302-91-9, Rocuronium bromideRelated Search:


  • ROCURONIUM 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
  • [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
  • Rocuronium Bromide/1-[17B-(acetyloxy)-3a-hydroxy2B-(4-morpholinyl)-5a-androstan-16B-yl]-1-(2-propenyl)pyrrolidinium bromide
  • 1-[17B-(acetyloxy)-3a-hydroxy2B-(4-morpholinyl)-5a -androstan-16B-yl]-1-(2-propenyl)pyrrolidinium bromide
  • 1-[17B-(acetyloxy)-3a-hydroxy-2B-(4-morpholinyl)-
  • 1-[(2,3a,5a,16,17)-17-(Acetyloxy)-3-hydroxy-2-(4-morpholinyl)androstan-16-yl]-1-(2-propenyl)pyrrolidinium Bromide
  • 1-[(2β,3α,5α,16β,17β)-17-(Acetyloxy)-3-hydroxy-2-(4-morpholinyl)andrcstan-16-y1]-1-propenylpyrrolidinium bromide
  • Esmeron:Zemuron
  • Eslax
  • Rocuronium Bromide (250 mg)
  • RocuroniuM BroMide IsoMers
  • 1-[(1S,2S,4S,5S,7S,10R,11S,13S,14R,15S)-14-(acetyloxy)-5-hydroxy-2,15-diMethyl-4-(Morpholin-4-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-13-yl]-1-(prop-2-en-1-yl)pyrrolidin-1-iuM
  • 1-[(2β,3α,5α,16β,17β)-17-(Acetyloxy)-3-hydroxy-2-(4-Morpholinyl)androstan-16-yl]-1-(2-propenyl)pyrrolidiniuM BroMide
  • 1-((2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-17-acetoxy-3-hydroxy-10,13-diMethyl-2-Morpholinohexadecahydro-1H-cyclopenta[a]phenanthren-16-yl)-1-allylpyrrolidin-1-iuM broMide
  • RocuroniuM BroMideAPI
  • Pyrrolidinium, 1-[(2β,3α,5α,16β,17β)-17-(acetyloxy)-3-hydroxy-2-(4-morpholinyl)androstan-16-yl]-1-(2-propenyl)-, bromide
  • Rocuronium hydrobromide
  • 1-[17β-(Acetyloxy)-3α-hydroxy-2β-(morpholin-4-yl)-5α-androstan-16β-yl]-1-(prop-2-enyl)pyrrolidinium bromide
  • Rocuronium bromide CRS
  • Rocuronium for peak identification CRS
  • Rocuronium Bromide &gt
  • ORG 9426 (Bromide)
  • Rocuronium dibromide
  • Rocuronium bromide USP/EP/BP
  • Rocuronium Bromide Crude
  • Rocuronium bromide Impurity 47
  • Rocuronium Bromide (ORG 9426 Bromide)
  • Rocuronium for peak identification (Y0000527)
  • Rocuronium Bromide (COLD SHIPMENT REQUIRED) (1604905)
  • Rocuronium Bromide USP/IP/PH.Eur
  • 119302-91-9
  • 19302-91-9
  • 119032-86-2
  • BrC32H53N2O4
  • C34H57NO4
  • C32H53BrNO4
  • C32H53N2O4Br
  • C32H53BrN2O4
  • 1
  • Heterocycles
  • Steroids
  • Steroid and Hormone
  • Acetylcholine receptor
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • APIs
  • 119302-91-9
  • API