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Oxymorphazone, a semi-synthetic opioid analgesic derived from morphine, is a potent μ-opioid receptor agonist. It is known for its potentially strong analgesic effects, making it a valuable asset for pain relief. While its potential use in treating opioid addiction and dependence is under research due to its ability to activate opioid receptors without inducing the same level of euphoria and physical dependence as other opioids, it also carries a risk of abuse and dependence, necessitating careful monitoring and regulation.

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  • 73697-35-5 Structure
  • Basic information

    1. Product Name: oxymorphazone
    2. Synonyms: oxymorphazone;4,5α-Epoxy-3,14-dihydroxy-17-methylmorphinan-6-one hydrazone
    3. CAS NO:73697-35-5
    4. Molecular Formula: C17H21N3O3
    5. Molecular Weight: 315.36694
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73697-35-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 555.42°C at 760 mmHg
    3. Flash Point: 289.708°C
    4. Appearance: /
    5. Density: 1.688g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.816
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: oxymorphazone(CAS DataBase Reference)
    11. NIST Chemistry Reference: oxymorphazone(73697-35-5)
    12. EPA Substance Registry System: oxymorphazone(73697-35-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 73697-35-5(Hazardous Substances Data)

73697-35-5 Usage

Uses

Used in Pain Management:
Oxymorphazone is used as a potent analgesic for the management of severe pain. Its strong affinity for the μ-opioid receptors makes it effective in providing relief for various types of pain, including postoperative and chronic pain conditions.
Used in Opioid Addiction Research:
Oxymorphazone is being investigated as a potential medication for treating opioid addiction and dependence. It is used as a research compound to explore its ability to activate opioid receptors without producing the same level of euphoria and physical dependence associated with other opioids, offering a possible alternative for managing opioid use disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 73697-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,9 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73697-35:
(7*7)+(6*3)+(5*6)+(4*9)+(3*7)+(2*3)+(1*5)=165
165 % 10 = 5
So 73697-35-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H21N3O3/c1-20-7-6-16-13-9-2-3-11(21)14(13)23-15(16)10(19-18)4-5-17(16,22)12(20)8-9/h2-3,12,15,21-22H,4-8,18H2,1H3/b19-10+/t12-,15+,16+,17-/m1/s1

73697-35-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,4aS,7E,7aR,12bS)-7-hydrazinylidene-3-methyl-2,4,5,6,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diol

1.2 Other means of identification

Product number -
Other names Morphinan-6-one,4,5-epoxy-3,14-dihydroxy-17-methyl-,hydrazone,(5alpha)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73697-35-5 SDS

73697-35-5Upstream product

73697-35-5Downstream Products

73697-35-5Relevant articles and documents

Long-Acting Opiate Agonists and Antagonists: 14-Hydroxydihydromorphinone Hydrazones

Pasternak, Gavril W.,Hahn, Elliot F.

, p. 674 - 676 (2007/10/02)

Two new long-acting hydrazone derivatives of 14-hydroxydihydromorphinones have been synthesized, oxymorphazone and naltrexazone.Both derivatives show high affinity for opiate binding sites in vitro, similar to naloxazone, the hydrazone analogue of naloxone.Sodium and manganese shifts imply that naltrexazone, like naloxazone, is a pure antagonist.By contrast, oxymorphazone inhibition of receptor binding is dramatically reduced by sodium and potentiated by manganese, suggesting it is an agonist.When given in vivo, all agents produce a significant inhibition of receptor binding for over 24 h despite extensive washing of the brain homogenates.Oxymorphone, naltrexone, and naloxone are without effect.Twenty-four hours after in vivo administration of oxymorphazone, 82percent of mice are still analgetic compared to only 17percent of oxymorphone-treated mice (p 0.005).Twenty-four hours after naltrexazone or naloxazone treatment all mice were protected from morphine analgesia (12 mg/kg; p 0.005), while naltrexone- and naloxone-treated animals did not differ significantly from saline-treated controls.

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