23095-84-3 Usage
Description
(5alpha,6alpha)-3-hydroxy-17-methyl-7,8-didehydro-4,5-epoxymorphinan-6-yl hydrogen sulfate, also known as Morphine 6-sulfate, is a derivative of morphine, a naturally occurring opioid analgesic. It possesses potent analgesic properties and is used in the treatment of moderate to severe pain.
Uses
Used in Pain Management:
Morphine 6-sulfate is used as an analgesic agent for the treatment of moderate to severe pain. Its potent pain-relieving effects make it a valuable component in pain management therapies.
Used in Addiction Treatment:
Morphine 6-sulfate is also used in the treatment of addiction, particularly opioid dependence. Its controlled administration can help manage withdrawal symptoms and support recovery efforts.
Used in Safe Inhaled Delivery:
Morphine 6-sulfate is utilized in compositions, methods, and kits for safe inhaled delivery of targeted opioids. This innovative approach allows for precise and controlled administration of the drug, reducing the risk of misuse and ensuring optimal therapeutic outcomes for pain and addiction treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 23095-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,9 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23095-84:
(7*2)+(6*3)+(5*0)+(4*9)+(3*5)+(2*8)+(1*4)=103
103 % 10 = 3
So 23095-84-3 is a valid CAS Registry Number.
23095-84-3Relevant articles and documents
Sulfate esters of morphine derivatives: Synthesis and characterization
Váradi, András,Gergely, András,Béni, Szabolcs,Jankovics, Péter,Noszál, Béla,Hosztafi, Sándor
, p. 65 - 72 (2012/03/09)
Sixteen 3-O- and 6-O-sulfate esters of morphine, codeine and some of their N-methyl quaternary derivatives were synthesized by means of sulfation with pyridine-SO3 complex and sulfuric acid/N,N′- dicyclohexylcarbodiimide. Complete 1H- and 13C-NMR assignments are given for each of the synthesized compounds based on one- and two-dimensional homo- and heteronuclear measurements. Comparative analysis of chiral properties by circular dichroism and optical rotatory dispersion revealed characteristic differences in the spectra due to changes in charge, polarity and intramolecular association by strong hydrogen bonds in aqueous solution. The synthesized sulfate esters are prospective peripheral analgesics lacking central side effects and are also useful as reference substances for various analytical studies involving sulfate ester metabolites.