OXYCODONE

OXYCODONE Basic information
Product Name:OXYCODONE
Synonyms:OXYCODONE;14-Hydroxydihydrocodeinone;4,5-alpha-epoxy-14-hydroxy-3-methoxy-17-methyl-morphinan-6-on;4,5alpha-epoxy-14-hydroxy-3-methoxy-17-methyl-morphinan-6-on;4,5alpha-Epoxy-14-hydroxy-3-methoxy-17-methylmorphinan-6-one;endone;eubine(france);Eucodalum
CAS:76-42-6
MF:C18H21NO4
MW:315.36
EINECS:200-960-2
Product Categories:API;phartmaceutical intermediate
Mol File:76-42-6.mol
OXYCODONE Structure
OXYCODONE Chemical Properties
Melting point 218-220°
Boiling point 454.92°C (rough estimate)
density 1.2164 (rough estimate)
refractive index 1.5740 (estimate)
Fp 9℃
storage temp. 2-8°C
solubility DMF: 20 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 10 mg/ml
form A neat solid
pka8.53(at 25℃)
color Long rods from EtOH
EPA Substance Registry SystemMorphinan-6-one, 4,5-epoxy-14-hydroxy-3-methoxy-17-methyl-, (5.alpha.)- (76-42-6)
Safety Information
Hazard Codes F,T
Risk Statements 11-23/24/25-39/23/24/25
Safety Statements 7-16-36/37-45
RIDADR 1544
WGK Germany 1
HazardClass 6.1(a)
PackingGroup II
HS Code 2939110000
Hazardous Substances Data76-42-6(Hazardous Substances Data)
ToxicityLD50 intraperitoneal in mouse: 320mg/kg
MSDS Information
OXYCODONE Usage And Synthesis
DescriptionOxycodone (Item No. 15465) is an analytical reference material categorized as an opioid. Oxycodone is regulated as a Schedule II compound in the United States. This product is intended for research and forensic applications.
OriginatorOxyfast,Purdue Pharma, L.P.
UsesAnalgesic (narcotic).
Definitionoxycodone: An opioid, C18H21N2,similar in structure to codeine butwith a –OH group in codeine replacedby a carbonyl group. It is ananalgesic often used for the treatmentof chronic pain. It is also usedillegally and is a controlled substancein most countries.
Brand nameOxycontin (Purdue); Roxicodone (Roxane); Roxicodone (Xanodyne).
Therapeutic FunctionNarcotic analgesic
Biological FunctionsOxycodone is nearly 10 times as strong as codeine, with absorption equal to that of orally administered morphine. Neither hydromorphone nor oxycodone is approved for use in children, and hydromorphone is contraindicated in obstetrical analgesia and in asthmatics.
General DescriptionOxycodone is synthesized from the natural opium alkaloidthebaine. Oxycodone is the 14 beta-hydroxyl version of hydrocodone.This additional functional group gives oxycodonegreater potency (1.5 times orally) than hydrocodone presumablyby increasing receptor affinity. The oral bioavailabilityof oxycodone is 65% to 87%. The metabolism of oxycodonefollows the similar pattern of opioid metabolism withN-demethylation, O-demethylation, and their glucuronides allidentified. Per the manufacturer, the analgesic effect of oxycodonecorrelates well with oxycodone plasma concentrations,not the minimal amount of oxymorphone formed, thusoxycodone is not assumed to be a prodrug. There are no largescalestudies of oxycodone used for analgesia in CYP2D6poor metabolizers that can confirm this.
Oxycodone is marketed in combination with acetaminophen(Percocet), aspirin (Percodan), and ibuprofen(Combunox). It has been available for over 50 years as animmediate-release tablet, and in 1995 an extended-releasetablet was approved by the FDA (OxyContin). OxyContin ismanufactured in eight strengths from 10 to 160 mg, and thehigh-dose preparations quickly became attractive to drugabusers. The extended-release tablets are crushed and theninjected or snorted to give an immediate high. The DrugAbuse Warning Network (DAWN) is a public health surveillancesystem that monitors drug-related emergency roomvisits and drug-related deaths. In 1995, they estimated that598,542 emergency room visits involved the nonmedical useof a pharmaceutical (e.g., antidepressant, anxiolytic, stimulant).Of these ER visits, 160,363 visits were attributed toopiates with an estimated 42,810 involving oxycodone or anoxycodone combination. Methadone and hydrocodone/combinationswere estimated to be similar to oxycodone.
PharmacologyOxycodone is a potent semisynthetic opioid that has been in use for many years. In addition to actions at the MOP receptor, it may also have analgesic effects mediated via the KOP receptor, resulting in incomplete crosstolerance with morphine. It has a good oral bioavailability, and its plasma concentrations are more predictable than those of morphine after oral administration. It is available in both long- and short-acting oral preparations and, more recently, in a parenteral formulation. Oral oxycodone is roughly 1.5 times more potent than oral morphine.
Safety ProfilePoison by intraperitoneal route. Moderately toxic by subcutaneous route. When heated to decomposition it emits toxic fumes of NOx.
OXYCODONE-D3,1.0MG/MLINMETHANOL OXYCODONE HYDROCHLORIDE OXYCODONE IMPURITY D Oxycodone terephthalate Oxycodone-d3 Hydrochloride OXYCODONE-D3,100/MLINMETHANOL OXYCODONE-D3 OXYCODONE HYDROCHLORIDE CONTROLLED SUBSTANCE OXYCODONE (D3, 98%) 1.0 MG/ML IN METHANOL OXYCODONE (D3, 98%) 100 UG/ML IN METHANOL OXYCODONE CONTROLLED SUBSTANCE CII USP(CRM STANDARD) OXYCODONE HYDROCHLORIDE, [7,8-3H],OXYCODONE [7,8-3H] HYDROCHLORIDE OXYCODONE-D6,1.0MG/MLINMETHANOL component of Percodan OXYCODONE CHLORHYDRATE REFERENCE SPECTRUM FPC(CRM STANDARD) OXYCODONE (D6, 98%) 1.0 MG/ML IN METHANOL OXYCODONE-D6,100/MLINMETHANOL Oxycodone BSA Conjugate BSA

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