Remifentanil Hydrochloride

Remifentanil Hydrochloride Structure
CAS No.
132539-07-2
Chemical Name:
Remifentanil Hydrochloride
Synonyms
Ultiva;GI 87084;GI 87084B;Unii-5V444H5wic;Remifentanil HCl;Remifentanil Hydrochloride;remifnetanil hydrochloride;Remifentanyl Hydrochloride;WFBMIPUMYUHANP-UHFFFAOYSA-N;Remifentanil (hydrochloride) (CRM)
CBNumber:
CB31105671
Molecular Formula:
C20H28N2O5.ClH
Molecular Weight:
412.911
MOL File:
132539-07-2.mol
Modify Date:
2023/6/8 9:02:37

Remifentanil Hydrochloride Properties

Melting point 195-197°C
Flash point 9°C
storage temp. 2-8°C
solubility PBS (pH 7.2): 10 mg/ml
form A neat solid
CAS DataBase Reference 132539-07-2

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02, GHS06, GHS08
Signal word  Danger
Hazard statements  H225-H301+H311+H331-H370
Precautionary statements  P210-P260-P280-P301+P310-P311
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  1
NFPA 704
0
4 0

Remifentanil Hydrochloride Chemical Properties,Uses,Production

Description

Ultiva was launched in Germany and the US for use in general anesthesia and immediate post-operative pain management. This compound can be prepared via the Michael addition of a 4,4-disubstituted piperidine to methyl acrylate. It behaves as a specific μ-opiod agonist that is about 30 times more potent than its chemical relative alfentanil. While its pharmacodynamic properties are similar to other μ agonists, remifentanil has unique pharmacokinetic properties. It has a rapid onset (1.6 min) and a rapid offset (5.4 min) independent of duration of administration. This has been attributed to its rapid catabolism by general esterases to the corresponding acrylic acid derivative. The metabolite has 0.01 to 0.0005 times the activity of remifentanil and is excreted via the kidneys (80% recovery).

Chemical Properties

White Solid

Uses

Labelled synthetic mu-opioid agonist. This is a controlled substance (opiate)

Pharmacokinetics

Remifentanil is much like alfentanil in its pharmacodynamic effects. It is a selective μ opioid agonist with 15 to 20 times greater potency than alfentanil. Remifentanil has an onset of action of 1 to 3 minutes when given intravenously. Its unique property is its rapid offset of action, which is independent of the duration of administration of the compound. Thus, it is very useful for titration of antinociceptive effect, followed by a rapid and predictable recovery time of 3 to 5 minutes. The short duration of action is a result of the ester group, which has been rationally designed into the substituent on the piperidine nitrogen. This ester group is rapidly hydrolyzed to the inactive carboxylic acid by serum and tissue esterases, making the drug's duration of action essentially independent of the liver or renal function of the patient. Remifentanil is used extensively for analgesia associated with general anesthesia procedures. It often is used in combination with injectable general anesthetic agents, such as midazolam or propofol.

Remifentanil Hydrochloride Preparation Products And Raw materials

132539-07-2(Remifentanil Hydrochloride)Related Search:

Remifentanil Hydrochloride 4-(Methoxycarbonyl)-4-[(1-oxopropyl)phenylamino]-1-piperidinepropanoic Acid Methyl Ester Hydrochloride GI 87084 Remifentanyl Hydrochloride Ultiva GI 87084B 1-Piperidinepropanoic acid, 4-(methoxycarbonyl)-4-((1-oxopropyl)phenylamino)-, methyl ester, monohydrochloride Remifentanil HCl Unii-5V444H5wic WFBMIPUMYUHANP-UHFFFAOYSA-N REMIFENTANIL HYDROCHLORIDE SOLUTION remifnetanil hydrochloride Remifentanil (hydrochloride) (CRM) Remifentanil HydrochlorideQ: What is Remifentanil Hydrochloride Q: What is the CAS Number of Remifentanil Hydrochloride Q: What is the storage condition of Remifentanil Hydrochloride Q: What are the applications of Remifentanil Hydrochloride 33,72-difluoro-N,N′-dimethyl-5-oxo-2,8-dioxa-4,6-diaza-1(4),9(4)-dipyridina-3(1,4),7(1,4)-dibenzenanonaphane-12,92-dicarboxamide 132539-07-2 C20H29ClN2O5 C20H28N2O5ClH Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals