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CAS

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6829-98-7

Imipramine N-Oxide, also known as Imipramine N-Oxide Monohydrate, is a metabolite of Imipramine. It is a white crystalline solid with chemical properties that contribute to its effectiveness as a pharmaceutical compound.

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  • 5H-Dibenz[b,f]azepine-5-propanamine,10,11-dihydro-N,N-dimethyl-, N-oxide

    Cas No: 6829-98-7

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  • 6829-98-7 Structure

  • Basic information

    1. Product Name: IMIPRAMINE N-OXIDE
    2. Synonyms: IPNO;Imipraminoxide;Imipramine N-Oxide Monohydrate;5H-Dibenzb,fazepine-5-propanamine, 10,11-dihydro-N,N-dimethyl-, N-oxide;10,11-Dihydro-N,N-dimethyl-5H-dibenz[b,f]azepine-5-propanamine N-Oxide Monohydrate;5-[3-(Dimethylamino)propyl]-10,11-dihydro-5H-dibenz[b,f]azepine 5-oxide Monohydrate;Imipraminoxide Monohydrate;10,11-Dihydro-N,N-dimethyl-5H-dibenz[b,f]azepine-5-propan-1-amine oxide
    3. CAS NO:6829-98-7
    4. Molecular Formula: C19H24N2O
    5. Molecular Weight: 296.41
    6. EINECS: 229-907-1
    7. Product Categories: Various Metabolites and Impurities;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals
    8. Mol File: 6829-98-7.mol

  • Chemical Properties

    1. Melting Point: 93-95°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: -20°C Freezer
    8. Solubility: Chloroform (Slightly), Methanol (Slightly)
    9. Stability: Hygroscopic
    10. CAS DataBase Reference: IMIPRAMINE N-OXIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: IMIPRAMINE N-OXIDE(6829-98-7)
    12. EPA Substance Registry System: IMIPRAMINE N-OXIDE(6829-98-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. RIDADR: 3249
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 6.1(b)
    8. PackingGroup: III
    9. Hazardous Substances Data: 6829-98-7(Hazardous Substances Data)

6829-98-7 Usage

Uses

Used in Pharmaceutical Industry:
Imipramine N-Oxide is used as an antidepressant for treating various forms of depression. As a metabolite of Imipramine, it plays a role in the therapeutic effects of the parent compound, helping to alleviate symptoms of depression and improve the overall well-being of patients.

Check Digit Verification of cas no

The CAS Registry Mumber 6829-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,2 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6829-98:
(6*6)+(5*8)+(4*2)+(3*9)+(2*9)+(1*8)=137
137 % 10 = 7
So 6829-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H24N2O.H2O/c1-21(2,22)15-7-14-20-18-10-5-3-8-16(18)12-13-17-9-4-6-11-19(17)20;/h3-6,8-11H,7,12-15H2,1-2H3;1H2

6829-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N,N-dimethylpropan-1-amine oxide

1.2 Other means of identification

Product number -
Other names Elepsin

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:6829-98-7 SDS

6829-98-7Downstream Products

6829-98-7Relevant articles and documents

A chemoselective deoxygenation of N-oxides by sodium borohydride-Raney nickel in water

Gowda, Narendra B.,Rao, Gopal Krishna,Ramakrishna, Ramesha A.

supporting information; experimental part, p. 5690 - 5693 (2010/11/05)

A simple and convenient protocol for deoxygenation of aliphatic and aromatic N-oxides to the corresponding amines in good to excellent yield using sodium borohydride-Raney nickel in water is reported. Other functional moieties such as alkenes, halides, ethers, and amides are unaffected under the present reaction condition.

Metabolism of imipramine by microorganisms

Hufford,Capiton,Clark,Baker

, p. 151 - 155 (2007/10/02)

The microbial metabolism of imipramine was studied using selected fungal organisms. The major microbial metabolites were isolated, and their structures were established by spectroscopic analyses (particularly 13C-NMR) and by comparison with authentic samples. The microbial metabolites identified included 2-hydroxyimipramine, 10-hydroxyimipramine, iminodibenzyl, imipramine-N-oxide, and desipramine; these metabolites also have been found in mammalian metabolism studies.

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